CINXE.COM

Substituted cathinone - Wikipedia

<!DOCTYPE html> <html class="client-nojs vector-feature-language-in-header-enabled vector-feature-language-in-main-page-header-disabled vector-feature-sticky-header-disabled vector-feature-page-tools-pinned-disabled vector-feature-toc-pinned-clientpref-1 vector-feature-main-menu-pinned-disabled vector-feature-limited-width-clientpref-1 vector-feature-limited-width-content-enabled vector-feature-custom-font-size-clientpref-1 vector-feature-appearance-pinned-clientpref-1 vector-feature-night-mode-enabled skin-theme-clientpref-day vector-toc-available" lang="en" dir="ltr"> <head> <meta charset="UTF-8"> <title>Substituted cathinone - Wikipedia</title> <script>(function(){var className="client-js vector-feature-language-in-header-enabled vector-feature-language-in-main-page-header-disabled vector-feature-sticky-header-disabled vector-feature-page-tools-pinned-disabled vector-feature-toc-pinned-clientpref-1 vector-feature-main-menu-pinned-disabled vector-feature-limited-width-clientpref-1 vector-feature-limited-width-content-enabled vector-feature-custom-font-size-clientpref-1 vector-feature-appearance-pinned-clientpref-1 vector-feature-night-mode-enabled skin-theme-clientpref-day vector-toc-available";var cookie=document.cookie.match(/(?:^|; )enwikimwclientpreferences=([^;]+)/);if(cookie){cookie[1].split('%2C').forEach(function(pref){className=className.replace(new RegExp('(^| )'+pref.replace(/-clientpref-\w+$|[^\w-]+/g,'')+'-clientpref-\\w+( |$)'),'$1'+pref+'$2');});}document.documentElement.className=className;}());RLCONF={"wgBreakFrames":false,"wgSeparatorTransformTable":["",""],"wgDigitTransformTable":["",""],"wgDefaultDateFormat":"dmy", "wgMonthNames":["","January","February","March","April","May","June","July","August","September","October","November","December"],"wgRequestId":"76a4749e-b51d-4a27-81cb-820fd75b1d66","wgCanonicalNamespace":"","wgCanonicalSpecialPageName":false,"wgNamespaceNumber":0,"wgPageName":"Substituted_cathinone","wgTitle":"Substituted cathinone","wgCurRevisionId":1256601547,"wgRevisionId":1256601547,"wgArticleId":25835853,"wgIsArticle":true,"wgIsRedirect":false,"wgAction":"view","wgUserName":null,"wgUserGroups":["*"],"wgCategories":["CS1 Finnish-language sources (fi)","Webarchive template wayback links","Articles with short description","Short description matches Wikidata","Use dmy dates from October 2021","Wikipedia articles needing clarification from September 2024","Chemical classes of psychoactive drugs","Cathinones"],"wgPageViewLanguage":"en","wgPageContentLanguage":"en","wgPageContentModel":"wikitext","wgRelevantPageName":"Substituted_cathinone","wgRelevantArticleId":25835853, "wgIsProbablyEditable":true,"wgRelevantPageIsProbablyEditable":true,"wgRestrictionEdit":[],"wgRestrictionMove":[],"wgNoticeProject":"wikipedia","wgCiteReferencePreviewsActive":false,"wgFlaggedRevsParams":{"tags":{"status":{"levels":1}}},"wgMediaViewerOnClick":true,"wgMediaViewerEnabledByDefault":true,"wgPopupsFlags":0,"wgVisualEditor":{"pageLanguageCode":"en","pageLanguageDir":"ltr","pageVariantFallbacks":"en"},"wgMFDisplayWikibaseDescriptions":{"search":true,"watchlist":true,"tagline":false,"nearby":true},"wgWMESchemaEditAttemptStepOversample":false,"wgWMEPageLength":60000,"wgRelatedArticlesCompat":[],"wgCentralAuthMobileDomain":false,"wgEditSubmitButtonLabelPublish":true,"wgULSPosition":"interlanguage","wgULSisCompactLinksEnabled":false,"wgVector2022LanguageInHeader":true,"wgULSisLanguageSelectorEmpty":false,"wgWikibaseItemId":"Q7632116","wgCheckUserClientHintsHeadersJsApi":["brands","architecture","bitness","fullVersionList","mobile","model","platform","platformVersion"], "GEHomepageSuggestedEditsEnableTopics":true,"wgGETopicsMatchModeEnabled":false,"wgGEStructuredTaskRejectionReasonTextInputEnabled":false,"wgGELevelingUpEnabledForUser":false};RLSTATE={"ext.globalCssJs.user.styles":"ready","site.styles":"ready","user.styles":"ready","ext.globalCssJs.user":"ready","user":"ready","user.options":"loading","ext.cite.styles":"ready","skins.vector.search.codex.styles":"ready","skins.vector.styles":"ready","skins.vector.icons":"ready","jquery.tablesorter.styles":"ready","jquery.makeCollapsible.styles":"ready","ext.wikimediamessages.styles":"ready","ext.visualEditor.desktopArticleTarget.noscript":"ready","ext.uls.interlanguage":"ready","wikibase.client.init":"ready","ext.wikimediaBadges":"ready"};RLPAGEMODULES=["ext.cite.ux-enhancements","mediawiki.page.media","site","mediawiki.page.ready","jquery.tablesorter","jquery.makeCollapsible","mediawiki.toc","skins.vector.js","ext.centralNotice.geoIP","ext.centralNotice.startUp","ext.gadget.ReferenceTooltips", "ext.gadget.switcher","ext.urlShortener.toolbar","ext.centralauth.centralautologin","mmv.bootstrap","ext.popups","ext.visualEditor.desktopArticleTarget.init","ext.visualEditor.targetLoader","ext.echo.centralauth","ext.eventLogging","ext.wikimediaEvents","ext.navigationTiming","ext.uls.interface","ext.cx.eventlogging.campaigns","ext.cx.uls.quick.actions","wikibase.client.vector-2022","ext.checkUser.clientHints","ext.growthExperiments.SuggestedEditSession","wikibase.sidebar.tracking"];</script> <script>(RLQ=window.RLQ||[]).push(function(){mw.loader.impl(function(){return["user.options@12s5i",function($,jQuery,require,module){mw.user.tokens.set({"patrolToken":"+\\","watchToken":"+\\","csrfToken":"+\\"}); }];});});</script> <link rel="stylesheet" href="/w/load.php?lang=en&amp;modules=ext.cite.styles%7Cext.uls.interlanguage%7Cext.visualEditor.desktopArticleTarget.noscript%7Cext.wikimediaBadges%7Cext.wikimediamessages.styles%7Cjquery.makeCollapsible.styles%7Cjquery.tablesorter.styles%7Cskins.vector.icons%2Cstyles%7Cskins.vector.search.codex.styles%7Cwikibase.client.init&amp;only=styles&amp;skin=vector-2022"> <script async="" src="/w/load.php?lang=en&amp;modules=startup&amp;only=scripts&amp;raw=1&amp;skin=vector-2022"></script> <meta name="ResourceLoaderDynamicStyles" content=""> <link rel="stylesheet" href="/w/load.php?lang=en&amp;modules=site.styles&amp;only=styles&amp;skin=vector-2022"> <meta name="generator" content="MediaWiki 1.44.0-wmf.4"> <meta name="referrer" content="origin"> <meta name="referrer" content="origin-when-cross-origin"> <meta name="robots" content="max-image-preview:standard"> <meta name="format-detection" content="telephone=no"> <meta property="og:image" content="https://upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/1200px-Cathinone.svg.png"> <meta property="og:image:width" content="1200"> <meta property="og:image:height" content="729"> <meta property="og:image" content="https://upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/800px-Cathinone.svg.png"> <meta property="og:image:width" content="800"> <meta property="og:image:height" content="486"> <meta property="og:image" content="https://upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/640px-Cathinone.svg.png"> <meta property="og:image:width" content="640"> <meta property="og:image:height" content="389"> <meta name="viewport" content="width=1120"> <meta property="og:title" content="Substituted cathinone - Wikipedia"> <meta property="og:type" content="website"> <link rel="preconnect" href="//upload.wikimedia.org"> <link rel="alternate" media="only screen and (max-width: 640px)" href="//en.m.wikipedia.org/wiki/Substituted_cathinone"> <link rel="alternate" type="application/x-wiki" title="Edit this page" href="/w/index.php?title=Substituted_cathinone&amp;action=edit"> <link rel="apple-touch-icon" href="/static/apple-touch/wikipedia.png"> <link rel="icon" href="/static/favicon/wikipedia.ico"> <link rel="search" type="application/opensearchdescription+xml" href="/w/rest.php/v1/search" title="Wikipedia (en)"> <link rel="EditURI" type="application/rsd+xml" href="//en.wikipedia.org/w/api.php?action=rsd"> <link rel="canonical" href="https://en.wikipedia.org/wiki/Substituted_cathinone"> <link rel="license" href="https://creativecommons.org/licenses/by-sa/4.0/deed.en"> <link rel="alternate" type="application/atom+xml" title="Wikipedia Atom feed" href="/w/index.php?title=Special:RecentChanges&amp;feed=atom"> <link rel="dns-prefetch" href="//meta.wikimedia.org" /> <link rel="dns-prefetch" href="//login.wikimedia.org"> </head> <body class="skin--responsive skin-vector skin-vector-search-vue mediawiki ltr sitedir-ltr mw-hide-empty-elt ns-0 ns-subject mw-editable page-Substituted_cathinone rootpage-Substituted_cathinone skin-vector-2022 action-view"><a class="mw-jump-link" href="#bodyContent">Jump to content</a> <div class="vector-header-container"> <header class="vector-header mw-header"> <div class="vector-header-start"> <nav class="vector-main-menu-landmark" aria-label="Site"> <div id="vector-main-menu-dropdown" class="vector-dropdown vector-main-menu-dropdown vector-button-flush-left vector-button-flush-right" > <input type="checkbox" id="vector-main-menu-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-main-menu-dropdown" class="vector-dropdown-checkbox " aria-label="Main menu" > <label id="vector-main-menu-dropdown-label" for="vector-main-menu-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--icon-only " aria-hidden="true" ><span class="vector-icon mw-ui-icon-menu mw-ui-icon-wikimedia-menu"></span> <span class="vector-dropdown-label-text">Main menu</span> </label> <div class="vector-dropdown-content"> <div id="vector-main-menu-unpinned-container" class="vector-unpinned-container"> <div id="vector-main-menu" class="vector-main-menu vector-pinnable-element"> <div class="vector-pinnable-header vector-main-menu-pinnable-header vector-pinnable-header-unpinned" data-feature-name="main-menu-pinned" data-pinnable-element-id="vector-main-menu" data-pinned-container-id="vector-main-menu-pinned-container" data-unpinned-container-id="vector-main-menu-unpinned-container" > <div class="vector-pinnable-header-label">Main menu</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-main-menu.pin">move to sidebar</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-main-menu.unpin">hide</button> </div> <div id="p-navigation" class="vector-menu mw-portlet mw-portlet-navigation" > <div class="vector-menu-heading"> Navigation </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="n-mainpage-description" class="mw-list-item"><a href="/wiki/Main_Page" title="Visit the main page [z]" accesskey="z"><span>Main page</span></a></li><li id="n-contents" class="mw-list-item"><a href="/wiki/Wikipedia:Contents" title="Guides to browsing Wikipedia"><span>Contents</span></a></li><li id="n-currentevents" class="mw-list-item"><a href="/wiki/Portal:Current_events" title="Articles related to current events"><span>Current events</span></a></li><li id="n-randompage" class="mw-list-item"><a href="/wiki/Special:Random" title="Visit a randomly selected article [x]" accesskey="x"><span>Random article</span></a></li><li id="n-aboutsite" class="mw-list-item"><a href="/wiki/Wikipedia:About" title="Learn about Wikipedia and how it works"><span>About Wikipedia</span></a></li><li id="n-contactpage" class="mw-list-item"><a href="//en.wikipedia.org/wiki/Wikipedia:Contact_us" title="How to contact Wikipedia"><span>Contact us</span></a></li> </ul> </div> </div> <div id="p-interaction" class="vector-menu mw-portlet mw-portlet-interaction" > <div class="vector-menu-heading"> Contribute </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="n-help" class="mw-list-item"><a href="/wiki/Help:Contents" title="Guidance on how to use and edit Wikipedia"><span>Help</span></a></li><li id="n-introduction" class="mw-list-item"><a href="/wiki/Help:Introduction" title="Learn how to edit Wikipedia"><span>Learn to edit</span></a></li><li id="n-portal" class="mw-list-item"><a href="/wiki/Wikipedia:Community_portal" title="The hub for editors"><span>Community portal</span></a></li><li id="n-recentchanges" class="mw-list-item"><a href="/wiki/Special:RecentChanges" title="A list of recent changes to Wikipedia [r]" accesskey="r"><span>Recent changes</span></a></li><li id="n-upload" class="mw-list-item"><a href="/wiki/Wikipedia:File_upload_wizard" title="Add images or other media for use on Wikipedia"><span>Upload file</span></a></li> </ul> </div> </div> </div> </div> </div> </div> </nav> <a href="/wiki/Main_Page" class="mw-logo"> <img class="mw-logo-icon" src="/static/images/icons/wikipedia.png" alt="" aria-hidden="true" height="50" width="50"> <span class="mw-logo-container skin-invert"> <img class="mw-logo-wordmark" alt="Wikipedia" src="/static/images/mobile/copyright/wikipedia-wordmark-en.svg" style="width: 7.5em; height: 1.125em;"> <img class="mw-logo-tagline" alt="The Free Encyclopedia" src="/static/images/mobile/copyright/wikipedia-tagline-en.svg" width="117" height="13" style="width: 7.3125em; height: 0.8125em;"> </span> </a> </div> <div class="vector-header-end"> <div id="p-search" role="search" class="vector-search-box-vue vector-search-box-collapses vector-search-box-show-thumbnail vector-search-box-auto-expand-width vector-search-box"> <a href="/wiki/Special:Search" class="cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--icon-only search-toggle" title="Search Wikipedia [f]" accesskey="f"><span class="vector-icon mw-ui-icon-search mw-ui-icon-wikimedia-search"></span> <span>Search</span> </a> <div class="vector-typeahead-search-container"> <div class="cdx-typeahead-search cdx-typeahead-search--show-thumbnail cdx-typeahead-search--auto-expand-width"> <form action="/w/index.php" id="searchform" class="cdx-search-input cdx-search-input--has-end-button"> <div id="simpleSearch" class="cdx-search-input__input-wrapper" data-search-loc="header-moved"> <div class="cdx-text-input cdx-text-input--has-start-icon"> <input class="cdx-text-input__input" type="search" name="search" placeholder="Search Wikipedia" aria-label="Search Wikipedia" autocapitalize="sentences" title="Search Wikipedia [f]" accesskey="f" id="searchInput" > <span class="cdx-text-input__icon cdx-text-input__start-icon"></span> </div> <input type="hidden" name="title" value="Special:Search"> </div> <button class="cdx-button cdx-search-input__end-button">Search</button> </form> </div> </div> </div> <nav class="vector-user-links vector-user-links-wide" aria-label="Personal tools"> <div class="vector-user-links-main"> <div id="p-vector-user-menu-preferences" class="vector-menu mw-portlet emptyPortlet" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> </ul> </div> </div> <div id="p-vector-user-menu-userpage" class="vector-menu mw-portlet emptyPortlet" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> </ul> </div> </div> <nav class="vector-appearance-landmark" aria-label="Appearance"> <div id="vector-appearance-dropdown" class="vector-dropdown " title="Change the appearance of the page&#039;s font size, width, and color" > <input type="checkbox" id="vector-appearance-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-appearance-dropdown" class="vector-dropdown-checkbox " aria-label="Appearance" > <label id="vector-appearance-dropdown-label" for="vector-appearance-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--icon-only " aria-hidden="true" ><span class="vector-icon mw-ui-icon-appearance mw-ui-icon-wikimedia-appearance"></span> <span class="vector-dropdown-label-text">Appearance</span> </label> <div class="vector-dropdown-content"> <div id="vector-appearance-unpinned-container" class="vector-unpinned-container"> </div> </div> </div> </nav> <div id="p-vector-user-menu-notifications" class="vector-menu mw-portlet emptyPortlet" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> </ul> </div> </div> <div id="p-vector-user-menu-overflow" class="vector-menu mw-portlet" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="pt-sitesupport-2" class="user-links-collapsible-item mw-list-item user-links-collapsible-item"><a data-mw="interface" href="https://donate.wikimedia.org/wiki/Special:FundraiserRedirector?utm_source=donate&amp;utm_medium=sidebar&amp;utm_campaign=C13_en.wikipedia.org&amp;uselang=en" class=""><span>Donate</span></a> </li> <li id="pt-createaccount-2" class="user-links-collapsible-item mw-list-item user-links-collapsible-item"><a data-mw="interface" href="/w/index.php?title=Special:CreateAccount&amp;returnto=Substituted+cathinone" title="You are encouraged to create an account and log in; however, it is not mandatory" class=""><span>Create account</span></a> </li> <li id="pt-login-2" class="user-links-collapsible-item mw-list-item user-links-collapsible-item"><a data-mw="interface" href="/w/index.php?title=Special:UserLogin&amp;returnto=Substituted+cathinone" title="You&#039;re encouraged to log in; however, it&#039;s not mandatory. [o]" accesskey="o" class=""><span>Log in</span></a> </li> </ul> </div> </div> </div> <div id="vector-user-links-dropdown" class="vector-dropdown vector-user-menu vector-button-flush-right vector-user-menu-logged-out" title="Log in and more options" > <input type="checkbox" id="vector-user-links-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-user-links-dropdown" class="vector-dropdown-checkbox " aria-label="Personal tools" > <label id="vector-user-links-dropdown-label" for="vector-user-links-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--icon-only " aria-hidden="true" ><span class="vector-icon mw-ui-icon-ellipsis mw-ui-icon-wikimedia-ellipsis"></span> <span class="vector-dropdown-label-text">Personal tools</span> </label> <div class="vector-dropdown-content"> <div id="p-personal" class="vector-menu mw-portlet mw-portlet-personal user-links-collapsible-item" title="User menu" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="pt-sitesupport" class="user-links-collapsible-item mw-list-item"><a href="https://donate.wikimedia.org/wiki/Special:FundraiserRedirector?utm_source=donate&amp;utm_medium=sidebar&amp;utm_campaign=C13_en.wikipedia.org&amp;uselang=en"><span>Donate</span></a></li><li id="pt-createaccount" class="user-links-collapsible-item mw-list-item"><a href="/w/index.php?title=Special:CreateAccount&amp;returnto=Substituted+cathinone" title="You are encouraged to create an account and log in; however, it is not mandatory"><span class="vector-icon mw-ui-icon-userAdd mw-ui-icon-wikimedia-userAdd"></span> <span>Create account</span></a></li><li id="pt-login" class="user-links-collapsible-item mw-list-item"><a href="/w/index.php?title=Special:UserLogin&amp;returnto=Substituted+cathinone" title="You&#039;re encouraged to log in; however, it&#039;s not mandatory. [o]" accesskey="o"><span class="vector-icon mw-ui-icon-logIn mw-ui-icon-wikimedia-logIn"></span> <span>Log in</span></a></li> </ul> </div> </div> <div id="p-user-menu-anon-editor" class="vector-menu mw-portlet mw-portlet-user-menu-anon-editor" > <div class="vector-menu-heading"> Pages for logged out editors <a href="/wiki/Help:Introduction" aria-label="Learn more about editing"><span>learn more</span></a> </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="pt-anoncontribs" class="mw-list-item"><a href="/wiki/Special:MyContributions" title="A list of edits made from this IP address [y]" accesskey="y"><span>Contributions</span></a></li><li id="pt-anontalk" class="mw-list-item"><a href="/wiki/Special:MyTalk" title="Discussion about edits from this IP address [n]" accesskey="n"><span>Talk</span></a></li> </ul> </div> </div> </div> </div> </nav> </div> </header> </div> <div class="mw-page-container"> <div class="mw-page-container-inner"> <div class="vector-sitenotice-container"> <div id="siteNotice"><!-- CentralNotice --></div> </div> <div class="vector-column-start"> <div class="vector-main-menu-container"> <div id="mw-navigation"> <nav id="mw-panel" class="vector-main-menu-landmark" aria-label="Site"> <div id="vector-main-menu-pinned-container" class="vector-pinned-container"> </div> </nav> </div> </div> <div class="vector-sticky-pinned-container"> <nav id="mw-panel-toc" aria-label="Contents" data-event-name="ui.sidebar-toc" class="mw-table-of-contents-container vector-toc-landmark"> <div id="vector-toc-pinned-container" class="vector-pinned-container"> <div id="vector-toc" class="vector-toc vector-pinnable-element"> <div class="vector-pinnable-header vector-toc-pinnable-header vector-pinnable-header-pinned" data-feature-name="toc-pinned" data-pinnable-element-id="vector-toc" > <h2 class="vector-pinnable-header-label">Contents</h2> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-toc.pin">move to sidebar</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-toc.unpin">hide</button> </div> <ul class="vector-toc-contents" id="mw-panel-toc-list"> <li id="toc-mw-content-text" class="vector-toc-list-item vector-toc-level-1"> <a href="#" class="vector-toc-link"> <div class="vector-toc-text">(Top)</div> </a> </li> <li id="toc-List_of_substituted_cathinones" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#List_of_substituted_cathinones"> <div class="vector-toc-text"> <span class="vector-toc-numb">1</span> <span>List of substituted cathinones</span> </div> </a> <ul id="toc-List_of_substituted_cathinones-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Legality" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#Legality"> <div class="vector-toc-text"> <span class="vector-toc-numb">2</span> <span>Legality</span> </div> </a> <ul id="toc-Legality-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-See_also" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#See_also"> <div class="vector-toc-text"> <span class="vector-toc-numb">3</span> <span>See also</span> </div> </a> <ul id="toc-See_also-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-References" class="vector-toc-list-item vector-toc-level-1 vector-toc-list-item-expanded"> <a class="vector-toc-link" href="#References"> <div class="vector-toc-text"> <span class="vector-toc-numb">4</span> <span>References</span> </div> </a> <ul id="toc-References-sublist" class="vector-toc-list"> </ul> </li> </ul> </div> </div> </nav> </div> </div> <div class="mw-content-container"> <main id="content" class="mw-body"> <header class="mw-body-header vector-page-titlebar"> <nav aria-label="Contents" class="vector-toc-landmark"> <div id="vector-page-titlebar-toc" class="vector-dropdown vector-page-titlebar-toc vector-button-flush-left" > <input type="checkbox" id="vector-page-titlebar-toc-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-page-titlebar-toc" class="vector-dropdown-checkbox " aria-label="Toggle the table of contents" > <label id="vector-page-titlebar-toc-label" for="vector-page-titlebar-toc-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--icon-only " aria-hidden="true" ><span class="vector-icon mw-ui-icon-listBullet mw-ui-icon-wikimedia-listBullet"></span> <span class="vector-dropdown-label-text">Toggle the table of contents</span> </label> <div class="vector-dropdown-content"> <div id="vector-page-titlebar-toc-unpinned-container" class="vector-unpinned-container"> </div> </div> </div> </nav> <h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Substituted cathinone</span></h1> <div id="p-lang-btn" class="vector-dropdown mw-portlet mw-portlet-lang" > <input type="checkbox" id="p-lang-btn-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-p-lang-btn" class="vector-dropdown-checkbox mw-interlanguage-selector" aria-label="Go to an article in another language. Available in 6 languages" > <label id="p-lang-btn-label" for="p-lang-btn-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--action-progressive mw-portlet-lang-heading-6" aria-hidden="true" ><span class="vector-icon mw-ui-icon-language-progressive mw-ui-icon-wikimedia-language-progressive"></span> <span class="vector-dropdown-label-text">6 languages</span> </label> <div class="vector-dropdown-content"> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="interlanguage-link interwiki-fa mw-list-item"><a href="https://fa.wikipedia.org/wiki/%DA%A9%D8%A7%D8%AA%DB%8C%D9%86%D9%88%D9%86_%D8%A7%D8%B3%D8%AA%D8%AE%D9%84%D8%A7%D9%81%DB%8C" title="کاتینون استخلافی – Persian" lang="fa" hreflang="fa" data-title="کاتینون استخلافی" data-language-autonym="فارسی" data-language-local-name="Persian" class="interlanguage-link-target"><span>فارسی</span></a></li><li class="interlanguage-link interwiki-hr mw-list-item"><a href="https://hr.wikipedia.org/wiki/Katinoni" title="Katinoni – Croatian" lang="hr" hreflang="hr" data-title="Katinoni" data-language-autonym="Hrvatski" data-language-local-name="Croatian" class="interlanguage-link-target"><span>Hrvatski</span></a></li><li class="interlanguage-link interwiki-it mw-list-item"><a href="https://it.wikipedia.org/wiki/Catinone_sostituito" title="Catinone sostituito – Italian" lang="it" hreflang="it" data-title="Catinone sostituito" data-language-autonym="Italiano" data-language-local-name="Italian" class="interlanguage-link-target"><span>Italiano</span></a></li><li class="interlanguage-link interwiki-pl mw-list-item"><a href="https://pl.wikipedia.org/wiki/Pochodne_katynonu" title="Pochodne katynonu – Polish" lang="pl" hreflang="pl" data-title="Pochodne katynonu" data-language-autonym="Polski" data-language-local-name="Polish" class="interlanguage-link-target"><span>Polski</span></a></li><li class="interlanguage-link interwiki-ru mw-list-item"><a href="https://ru.wikipedia.org/wiki/%D0%9A%D0%B0%D1%82%D0%B8%D0%BD%D0%BE%D0%BD%D1%8B" title="Катиноны – Russian" lang="ru" hreflang="ru" data-title="Катиноны" data-language-autonym="Русский" data-language-local-name="Russian" class="interlanguage-link-target"><span>Русский</span></a></li><li class="interlanguage-link interwiki-zh mw-list-item"><a href="https://zh.wikipedia.org/wiki/%E5%8D%A1%E8%A5%BF%E9%85%AE%E8%A1%8D%E7%94%9F%E7%89%A9" title="卡西酮衍生物 – Chinese" lang="zh" hreflang="zh" data-title="卡西酮衍生物" data-language-autonym="中文" data-language-local-name="Chinese" class="interlanguage-link-target"><span>中文</span></a></li> </ul> <div class="after-portlet after-portlet-lang"><span class="wb-langlinks-edit wb-langlinks-link"><a href="https://www.wikidata.org/wiki/Special:EntityPage/Q7632116#sitelinks-wikipedia" title="Edit interlanguage links" class="wbc-editpage">Edit links</a></span></div> </div> </div> </div> </header> <div class="vector-page-toolbar"> <div class="vector-page-toolbar-container"> <div id="left-navigation"> <nav aria-label="Namespaces"> <div id="p-associated-pages" class="vector-menu vector-menu-tabs mw-portlet mw-portlet-associated-pages" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-nstab-main" class="selected vector-tab-noicon mw-list-item"><a href="/wiki/Substituted_cathinone" title="View the content page [c]" accesskey="c"><span>Article</span></a></li><li id="ca-talk" class="vector-tab-noicon mw-list-item"><a href="/wiki/Talk:Substituted_cathinone" rel="discussion" title="Discuss improvements to the content page [t]" accesskey="t"><span>Talk</span></a></li> </ul> </div> </div> <div id="vector-variants-dropdown" class="vector-dropdown emptyPortlet" > <input type="checkbox" id="vector-variants-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-variants-dropdown" class="vector-dropdown-checkbox " aria-label="Change language variant" > <label id="vector-variants-dropdown-label" for="vector-variants-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet" aria-hidden="true" ><span class="vector-dropdown-label-text">English</span> </label> <div class="vector-dropdown-content"> <div id="p-variants" class="vector-menu mw-portlet mw-portlet-variants emptyPortlet" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> </ul> </div> </div> </div> </div> </nav> </div> <div id="right-navigation" class="vector-collapsible"> <nav aria-label="Views"> <div id="p-views" class="vector-menu vector-menu-tabs mw-portlet mw-portlet-views" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-view" class="selected vector-tab-noicon mw-list-item"><a href="/wiki/Substituted_cathinone"><span>Read</span></a></li><li id="ca-edit" class="vector-tab-noicon mw-list-item"><a href="/w/index.php?title=Substituted_cathinone&amp;action=edit" title="Edit this page [e]" accesskey="e"><span>Edit</span></a></li><li id="ca-history" class="vector-tab-noicon mw-list-item"><a href="/w/index.php?title=Substituted_cathinone&amp;action=history" title="Past revisions of this page [h]" accesskey="h"><span>View history</span></a></li> </ul> </div> </div> </nav> <nav class="vector-page-tools-landmark" aria-label="Page tools"> <div id="vector-page-tools-dropdown" class="vector-dropdown vector-page-tools-dropdown" > <input type="checkbox" id="vector-page-tools-dropdown-checkbox" role="button" aria-haspopup="true" data-event-name="ui.dropdown-vector-page-tools-dropdown" class="vector-dropdown-checkbox " aria-label="Tools" > <label id="vector-page-tools-dropdown-label" for="vector-page-tools-dropdown-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet" aria-hidden="true" ><span class="vector-dropdown-label-text">Tools</span> </label> <div class="vector-dropdown-content"> <div id="vector-page-tools-unpinned-container" class="vector-unpinned-container"> <div id="vector-page-tools" class="vector-page-tools vector-pinnable-element"> <div class="vector-pinnable-header vector-page-tools-pinnable-header vector-pinnable-header-unpinned" data-feature-name="page-tools-pinned" data-pinnable-element-id="vector-page-tools" data-pinned-container-id="vector-page-tools-pinned-container" data-unpinned-container-id="vector-page-tools-unpinned-container" > <div class="vector-pinnable-header-label">Tools</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-page-tools.pin">move to sidebar</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-page-tools.unpin">hide</button> </div> <div id="p-cactions" class="vector-menu mw-portlet mw-portlet-cactions emptyPortlet vector-has-collapsible-items" title="More options" > <div class="vector-menu-heading"> Actions </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-more-view" class="selected vector-more-collapsible-item mw-list-item"><a href="/wiki/Substituted_cathinone"><span>Read</span></a></li><li id="ca-more-edit" class="vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Substituted_cathinone&amp;action=edit" title="Edit this page [e]" accesskey="e"><span>Edit</span></a></li><li id="ca-more-history" class="vector-more-collapsible-item mw-list-item"><a href="/w/index.php?title=Substituted_cathinone&amp;action=history"><span>View history</span></a></li> </ul> </div> </div> <div id="p-tb" class="vector-menu mw-portlet mw-portlet-tb" > <div class="vector-menu-heading"> General </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="t-whatlinkshere" class="mw-list-item"><a href="/wiki/Special:WhatLinksHere/Substituted_cathinone" title="List of all English Wikipedia pages containing links to this page [j]" accesskey="j"><span>What links here</span></a></li><li id="t-recentchangeslinked" class="mw-list-item"><a href="/wiki/Special:RecentChangesLinked/Substituted_cathinone" rel="nofollow" title="Recent changes in pages linked from this page [k]" accesskey="k"><span>Related changes</span></a></li><li id="t-upload" class="mw-list-item"><a href="/wiki/Wikipedia:File_Upload_Wizard" title="Upload files [u]" accesskey="u"><span>Upload file</span></a></li><li id="t-specialpages" class="mw-list-item"><a href="/wiki/Special:SpecialPages" title="A list of all special pages [q]" accesskey="q"><span>Special pages</span></a></li><li id="t-permalink" class="mw-list-item"><a href="/w/index.php?title=Substituted_cathinone&amp;oldid=1256601547" title="Permanent link to this revision of this page"><span>Permanent link</span></a></li><li id="t-info" class="mw-list-item"><a href="/w/index.php?title=Substituted_cathinone&amp;action=info" title="More information about this page"><span>Page information</span></a></li><li id="t-cite" class="mw-list-item"><a href="/w/index.php?title=Special:CiteThisPage&amp;page=Substituted_cathinone&amp;id=1256601547&amp;wpFormIdentifier=titleform" title="Information on how to cite this page"><span>Cite this page</span></a></li><li id="t-urlshortener" class="mw-list-item"><a href="/w/index.php?title=Special:UrlShortener&amp;url=https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FSubstituted_cathinone"><span>Get shortened URL</span></a></li><li id="t-urlshortener-qrcode" class="mw-list-item"><a href="/w/index.php?title=Special:QrCode&amp;url=https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FSubstituted_cathinone"><span>Download QR code</span></a></li> </ul> </div> </div> <div id="p-coll-print_export" class="vector-menu mw-portlet mw-portlet-coll-print_export" > <div class="vector-menu-heading"> Print/export </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="coll-download-as-rl" class="mw-list-item"><a href="/w/index.php?title=Special:DownloadAsPdf&amp;page=Substituted_cathinone&amp;action=show-download-screen" title="Download this page as a PDF file"><span>Download as PDF</span></a></li><li id="t-print" class="mw-list-item"><a href="/w/index.php?title=Substituted_cathinone&amp;printable=yes" title="Printable version of this page [p]" accesskey="p"><span>Printable version</span></a></li> </ul> </div> </div> <div id="p-wikibase-otherprojects" class="vector-menu mw-portlet mw-portlet-wikibase-otherprojects" > <div class="vector-menu-heading"> In other projects </div> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="wb-otherproject-link wb-otherproject-commons mw-list-item"><a href="https://commons.wikimedia.org/wiki/Category:Cathinones" hreflang="en"><span>Wikimedia Commons</span></a></li><li id="t-wikibase" class="wb-otherproject-link wb-otherproject-wikibase-dataitem mw-list-item"><a href="https://www.wikidata.org/wiki/Special:EntityPage/Q7632116" title="Structured data on this page hosted by Wikidata [g]" accesskey="g"><span>Wikidata item</span></a></li> </ul> </div> </div> </div> </div> </div> </div> </nav> </div> </div> </div> <div class="vector-column-end"> <div class="vector-sticky-pinned-container"> <nav class="vector-page-tools-landmark" aria-label="Page tools"> <div id="vector-page-tools-pinned-container" class="vector-pinned-container"> </div> </nav> <nav class="vector-appearance-landmark" aria-label="Appearance"> <div id="vector-appearance-pinned-container" class="vector-pinned-container"> <div id="vector-appearance" class="vector-appearance vector-pinnable-element"> <div class="vector-pinnable-header vector-appearance-pinnable-header vector-pinnable-header-pinned" data-feature-name="appearance-pinned" data-pinnable-element-id="vector-appearance" data-pinned-container-id="vector-appearance-pinned-container" data-unpinned-container-id="vector-appearance-unpinned-container" > <div class="vector-pinnable-header-label">Appearance</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-appearance.pin">move to sidebar</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-appearance.unpin">hide</button> </div> </div> </div> </nav> </div> </div> <div id="bodyContent" class="vector-body" aria-labelledby="firstHeading" data-mw-ve-target-container> <div class="vector-body-before-content"> <div class="mw-indicators"> </div> <div id="siteSub" class="noprint">From Wikipedia, the free encyclopedia</div> </div> <div id="contentSub"><div id="mw-content-subtitle"></div></div> <div id="mw-content-text" class="mw-body-content"><div class="mw-content-ltr mw-parser-output" lang="en" dir="ltr"><div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Class of chemical compounds</div> <p class="mw-empty-elt"> </p> <figure typeof="mw:File/Thumb"><a href="/wiki/File:Cathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/200px-Cathinone.svg.png" decoding="async" width="200" height="121" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/300px-Cathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/400px-Cathinone.svg.png 2x" data-file-width="1230" data-file-height="747" /></a><figcaption><a href="/wiki/Cathinone" title="Cathinone">Cathinone</a></figcaption></figure> <figure typeof="mw:File/Thumb"><a href="/wiki/File:Substituted_cathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d7/Substituted_cathinone.svg/200px-Substituted_cathinone.svg.png" decoding="async" width="200" height="95" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d7/Substituted_cathinone.svg/300px-Substituted_cathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d7/Substituted_cathinone.svg/400px-Substituted_cathinone.svg.png 2x" data-file-width="1586" data-file-height="757" /></a><figcaption>General chemical structure of substituted cathinones, with R<sub>1</sub>-R<sub>4</sub> defined in text</figcaption></figure> <p><b>Substituted cathinones</b>, or simply <b>cathinones</b>, which include some <a href="/wiki/Stimulant" title="Stimulant">stimulants</a> and <a href="/wiki/Empathogen-entactogen" class="mw-redirect" title="Empathogen-entactogen">entactogens</a>, are <a href="/wiki/Chemical_derivative" class="mw-redirect" title="Chemical derivative">derivatives</a> of <a href="/wiki/Cathinone" title="Cathinone">cathinone</a>. They feature a <a href="/wiki/Substituted_phenethylamine" title="Substituted phenethylamine">phenethylamine</a> core with an <a href="/wiki/Alkyl" class="mw-redirect" title="Alkyl">alkyl</a> <a href="/wiki/Functional_group" title="Functional group">group</a> attached to the <a href="/wiki/Alpha_and_beta_carbon" class="mw-redirect" title="Alpha and beta carbon">alpha carbon</a>, and a <a href="/wiki/Ketone" title="Ketone">ketone</a> group attached to the <a href="/wiki/Alpha_and_beta_carbon" class="mw-redirect" title="Alpha and beta carbon">beta carbon</a>, along with additional <a href="/wiki/Substitution_reaction" title="Substitution reaction">substitutions</a>.<sup id="cite_ref-1" class="reference"><a href="#cite_note-1"><span class="cite-bracket">&#91;</span>1<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-2" class="reference"><a href="#cite_note-2"><span class="cite-bracket">&#91;</span>2<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">&#91;</span>3<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">&#91;</span>4<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">&#91;</span>5<span class="cite-bracket">&#93;</span></a></sup> Cathinone occurs naturally in the plant <a href="/wiki/Khat" title="Khat">khat</a> whose leaves are chewed as a recreational drug.<sup id="cite_ref-pmid21698275_6-0" class="reference"><a href="#cite_note-pmid21698275-6"><span class="cite-bracket">&#91;</span>6<span class="cite-bracket">&#93;</span></a></sup> </p><p>Substituted cathinones act as <a href="/wiki/Monoamine_releasing_agent" title="Monoamine releasing agent">monoamine releasing agents</a> and/or <a href="/wiki/Monoamine_reuptake_inhibitor" title="Monoamine reuptake inhibitor">monoamine reuptake inhibitors</a>, including of <a href="/wiki/Norepinephrine" title="Norepinephrine">norepinephrine</a>, <a href="/wiki/Dopamine" title="Dopamine">dopamine</a>, and/or <a href="/wiki/Serotonin" title="Serotonin">serotonin</a>.<sup id="cite_ref-RothmanBaumann2003_7-0" class="reference"><a href="#cite_note-RothmanBaumann2003-7"><span class="cite-bracket">&#91;</span>7<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-RothmanBaumann2006_8-0" class="reference"><a href="#cite_note-RothmanBaumann2006-8"><span class="cite-bracket">&#91;</span>8<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-ReithBLoughHong2015_9-0" class="reference"><a href="#cite_note-ReithBLoughHong2015-9"><span class="cite-bracket">&#91;</span>9<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-RothmanBaumann2005_10-0" class="reference"><a href="#cite_note-RothmanBaumann2005-10"><span class="cite-bracket">&#91;</span>10<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-RothmanBaumannDersch2001_11-0" class="reference"><a href="#cite_note-RothmanBaumannDersch2001-11"><span class="cite-bracket">&#91;</span>11<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-BaumannAyestasPartilla2012_12-0" class="reference"><a href="#cite_note-BaumannAyestasPartilla2012-12"><span class="cite-bracket">&#91;</span>12<span class="cite-bracket">&#93;</span></a></sup> In contrast to <a href="/wiki/Substituted_amphetamine" title="Substituted amphetamine">substituted amphetamines</a>, substituted cathinones do not act as <a href="/wiki/Agonist" title="Agonist">agonists</a> of the human <a href="/wiki/Trace_amine-associated_receptor_1" class="mw-redirect" title="Trace amine-associated receptor 1">trace amine-associated receptor 1</a> (TAAR1).<sup id="cite_ref-KuropkaZawadzkiSzpot2023_13-0" class="reference"><a href="#cite_note-KuropkaZawadzkiSzpot2023-13"><span class="cite-bracket">&#91;</span>13<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-SimmlerBuchyChaboz2016_14-0" class="reference"><a href="#cite_note-SimmlerBuchyChaboz2016-14"><span class="cite-bracket">&#91;</span>14<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-SimmlerRickliHoener2014_15-0" class="reference"><a href="#cite_note-SimmlerRickliHoener2014-15"><span class="cite-bracket">&#91;</span>15<span class="cite-bracket">&#93;</span></a></sup> This may potentiate their stimulating and <a href="/wiki/Drug_addiction" class="mw-redirect" title="Drug addiction">addictive</a> effects.<sup id="cite_ref-KuropkaZawadzkiSzpot2023_13-1" class="reference"><a href="#cite_note-KuropkaZawadzkiSzpot2023-13"><span class="cite-bracket">&#91;</span>13<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-SimmlerBuchyChaboz2016_14-1" class="reference"><a href="#cite_note-SimmlerBuchyChaboz2016-14"><span class="cite-bracket">&#91;</span>14<span class="cite-bracket">&#93;</span></a></sup> </p> <meta property="mw:PageProp/toc" /> <div class="mw-heading mw-heading2"><h2 id="List_of_substituted_cathinones">List of substituted cathinones</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Substituted_cathinone&amp;action=edit&amp;section=1" title="Edit section: List of substituted cathinones"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>The derivatives may be produced by substitutions at four locations of the cathinone molecule: </p> <ul><li>R<sub>1</sub> = hydrogen, or any combination of one or more alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents</li> <li>R<sub>2</sub> = hydrogen or any alkyl group</li> <li>R<sub>3</sub> = hydrogen, any alkyl group, or incorporation in a cyclic structure</li> <li>R<sub>4</sub> = hydrogen, any alkyl group, or incorporation in a cyclic structure</li></ul> <p>The following table displays notable derivatives that have been reported:<sup id="cite_ref-16" class="reference"><a href="#cite_note-16"><span class="cite-bracket">&#91;</span>16<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-17" class="reference"><a href="#cite_note-17"><span class="cite-bracket">&#91;</span>17<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-18" class="reference"><a href="#cite_note-18"><span class="cite-bracket">&#91;</span>18<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-19" class="reference"><a href="#cite_note-19"><span class="cite-bracket">&#91;</span>19<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-20" class="reference"><a href="#cite_note-20"><span class="cite-bracket">&#91;</span>20<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-21" class="reference"><a href="#cite_note-21"><span class="cite-bracket">&#91;</span>21<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-22" class="reference"><a href="#cite_note-22"><span class="cite-bracket">&#91;</span>22<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-23" class="reference"><a href="#cite_note-23"><span class="cite-bracket">&#91;</span>23<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-24" class="reference"><a href="#cite_note-24"><span class="cite-bracket">&#91;</span>24<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-25" class="reference"><a href="#cite_note-25"><span class="cite-bracket">&#91;</span>25<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-26" class="reference"><a href="#cite_note-26"><span class="cite-bracket">&#91;</span>26<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-27" class="reference"><a href="#cite_note-27"><span class="cite-bracket">&#91;</span>27<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-28" class="reference"><a href="#cite_note-28"><span class="cite-bracket">&#91;</span>28<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-pmid27863142_29-0" class="reference"><a href="#cite_note-pmid27863142-29"><span class="cite-bracket">&#91;</span>29<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-30" class="reference"><a href="#cite_note-30"><span class="cite-bracket">&#91;</span>30<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-31" class="reference"><a href="#cite_note-31"><span class="cite-bracket">&#91;</span>31<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-pmid29367861_32-0" class="reference"><a href="#cite_note-pmid29367861-32"><span class="cite-bracket">&#91;</span>32<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-pmid29426062_33-0" class="reference"><a href="#cite_note-pmid29426062-33"><span class="cite-bracket">&#91;</span>33<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-pmid30925345_34-0" class="reference"><a href="#cite_note-pmid30925345-34"><span class="cite-bracket">&#91;</span>34<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-pmid32882537_35-0" class="reference"><a href="#cite_note-pmid32882537-35"><span class="cite-bracket">&#91;</span>35<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-pmid33385148_36-0" class="reference"><a href="#cite_note-pmid33385148-36"><span class="cite-bracket">&#91;</span>36<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-37" class="reference"><a href="#cite_note-37"><span class="cite-bracket">&#91;</span>37<span class="cite-bracket">&#93;</span></a></sup> </p><p><br /> </p> <table class="wikitable sortable"> <tbody><tr> <th scope="col"><b>Structure</b> </th> <th scope="col"><b>Compound</b> </th> <th scope="col" class="unsortable"><b>R<sub>1</sub></b> </th> <th scope="col" class="unsortable"><b>R<sub>2</sub></b> </th> <th scope="col" class="unsortable"><b>R<sub>3</sub></b> </th> <th scope="col" class="unsortable"><b>R<sub>4</sub></b> </th> <th scope="col"><b>CAS number</b> </th></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Cathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/120px-Cathinone.svg.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/180px-Cathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/33/Cathinone.svg/240px-Cathinone.svg.png 2x" data-file-width="1230" data-file-height="747" /></a></span></td> <td><a href="/wiki/Cathinone" title="Cathinone">Cathinone</a></td> <td>H</td> <td><a href="/wiki/Methyl" class="mw-redirect" title="Methyl">Me</a></td> <td>H</td> <td><a href="/wiki/Hydrogen" title="Hydrogen">H</a></td> <td>71031-15-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Methcathinone_skeletal.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/49/Methcathinone_skeletal.svg/120px-Methcathinone_skeletal.svg.png" decoding="async" width="120" height="78" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/49/Methcathinone_skeletal.svg/180px-Methcathinone_skeletal.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/49/Methcathinone_skeletal.svg/240px-Methcathinone_skeletal.svg.png 2x" data-file-width="948" data-file-height="614" /></a></span></td> <td><a href="/wiki/Methcathinone" title="Methcathinone">Methcathinone</a></td> <td>H</td> <td>Me</td> <td>H</td> <td>Me</td> <td>5650-44-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Ethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Ethcathinone.svg/120px-Ethcathinone.svg.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Ethcathinone.svg/180px-Ethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Ethcathinone.svg/240px-Ethcathinone.svg.png 2x" data-file-width="1233" data-file-height="767" /></a></span></td> <td><a href="/wiki/Ethcathinone" title="Ethcathinone">Ethcathinone</a></td> <td>H</td> <td>Me</td> <td>H</td> <td><a href="/wiki/Ethyl_group" title="Ethyl group">Et</a></td> <td>51553-17-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Propylcathinone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/22/Propylcathinone_structure.png/120px-Propylcathinone_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/22/Propylcathinone_structure.png/180px-Propylcathinone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/22/Propylcathinone_structure.png/240px-Propylcathinone_structure.png 2x" data-file-width="1000" data-file-height="506" /></a></span></td> <td>Propylcathinone</td> <td>H</td> <td>Me</td> <td>H</td> <td><a href="/wiki/Propyl" class="mw-redirect" title="Propyl">nPr</a></td> <td>52597-14-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Buphedrone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/70/Buphedrone.svg/120px-Buphedrone.svg.png" decoding="async" width="120" height="77" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/70/Buphedrone.svg/180px-Buphedrone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/70/Buphedrone.svg/240px-Buphedrone.svg.png 2x" data-file-width="292" data-file-height="187" /></a></span></td> <td><a href="/wiki/Buphedrone" title="Buphedrone">Buphedrone</a></td> <td>H</td> <td>Et</td> <td>H</td> <td>Me</td> <td>408332-79-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-Ethylbuphedrone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/60/N-Ethylbuphedrone.svg/120px-N-Ethylbuphedrone.svg.png" decoding="async" width="120" height="72" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/60/N-Ethylbuphedrone.svg/180px-N-Ethylbuphedrone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/60/N-Ethylbuphedrone.svg/240px-N-Ethylbuphedrone.svg.png 2x" data-file-width="512" data-file-height="306" /></a></span></td> <td>N-Ethylbuphedrone (<a href="/wiki/N-Ethylbuphedrone" title="N-Ethylbuphedrone">NEB</a>)</td> <td>H</td> <td>Et</td> <td>H</td> <td>Et</td> <td>1354631-28-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Methylethylbuphedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/15/Methylethylbuphedrone_structure.png/120px-Methylethylbuphedrone_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/15/Methylethylbuphedrone_structure.png/180px-Methylethylbuphedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/15/Methylethylbuphedrone_structure.png/240px-Methylethylbuphedrone_structure.png 2x" data-file-width="1000" data-file-height="573" /></a></span></td> <td>N-Methyl-N-ethylbuphedrone</td> <td>H</td> <td>Et</td> <td>Me</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Pentedrone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Pentedrone.svg/120px-Pentedrone.svg.png" decoding="async" width="120" height="99" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Pentedrone.svg/180px-Pentedrone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2e/Pentedrone.svg/240px-Pentedrone.svg.png 2x" data-file-width="292" data-file-height="240" /></a></span></td> <td><a href="/wiki/Pentedrone" title="Pentedrone">Pentedrone</a></td> <td>H</td> <td>nPr</td> <td>H</td> <td>Me</td> <td>879722-57-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-Ethylpentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/56/N-Ethylpentedrone_structure.png/120px-N-Ethylpentedrone_structure.png" decoding="async" width="120" height="86" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/56/N-Ethylpentedrone_structure.png/180px-N-Ethylpentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/56/N-Ethylpentedrone_structure.png/240px-N-Ethylpentedrone_structure.png 2x" data-file-width="1000" data-file-height="720" /></a></span></td> <td><a href="/wiki/N-Ethylpentedrone" title="N-Ethylpentedrone">N-Ethylpentedrone</a></td> <td>H</td> <td>nPr</td> <td>H</td> <td>Et</td> <td>18268-16-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-Isopropylpentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cd/N-Isopropylpentedrone_structure.png/120px-N-Isopropylpentedrone_structure.png" decoding="async" width="120" height="86" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cd/N-Isopropylpentedrone_structure.png/180px-N-Isopropylpentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cd/N-Isopropylpentedrone_structure.png/240px-N-Isopropylpentedrone_structure.png 2x" data-file-width="1000" data-file-height="720" /></a></span></td> <td>N-Isopropylpentedrone</td> <td>H</td> <td>nPr</td> <td>H</td> <td>iPr</td> <td>18268-14-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Hexedrone.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/5a/Hexedrone.png/120px-Hexedrone.png" decoding="async" width="120" height="111" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/5a/Hexedrone.png/180px-Hexedrone.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/5a/Hexedrone.png/240px-Hexedrone.png 2x" data-file-width="1000" data-file-height="921" /></a></span></td> <td><a href="/wiki/Hexedrone" title="Hexedrone">Hexedrone</a></td> <td>H</td> <td>nBu</td> <td>H</td> <td>Me</td> <td>2169446-41-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Ethylhexedrone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/57/Ethylhexedrone.svg/120px-Ethylhexedrone.svg.png" decoding="async" width="120" height="97" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/57/Ethylhexedrone.svg/180px-Ethylhexedrone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/57/Ethylhexedrone.svg/240px-Ethylhexedrone.svg.png 2x" data-file-width="445" data-file-height="360" /></a></span></td> <td>N-<a href="/wiki/Ethyl-Hexedrone" class="mw-redirect" title="Ethyl-Hexedrone">Ethylhexedrone</a></td> <td>H</td> <td>nBu</td> <td>H</td> <td>Et</td> <td>18410-62-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Butylhexedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/ea/Butylhexedrone_structure.png/120px-Butylhexedrone_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/ea/Butylhexedrone_structure.png/180px-Butylhexedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/ea/Butylhexedrone_structure.png/240px-Butylhexedrone_structure.png 2x" data-file-width="1000" data-file-height="633" /></a></span></td> <td>N-Butylhexedrone</td> <td>H</td> <td>nBu</td> <td>H</td> <td>nBu</td> <td>18296-66-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Isobutylhexedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/07/Isobutylhexedrone_structure.png/120px-Isobutylhexedrone_structure.png" decoding="async" width="120" height="85" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/07/Isobutylhexedrone_structure.png/180px-Isobutylhexedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/07/Isobutylhexedrone_structure.png/240px-Isobutylhexedrone_structure.png 2x" data-file-width="1000" data-file-height="706" /></a></span></td> <td>N-Isobutylhexedrone (NDH)</td> <td>H</td> <td>nBu</td> <td>H</td> <td><a href="/wiki/Isobutyl" class="mw-redirect" title="Isobutyl"><i>i</i>-Bu</a></td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Isohexedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/5e/Isohexedrone_structure.png/120px-Isohexedrone_structure.png" decoding="async" width="120" height="100" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/5e/Isohexedrone_structure.png/180px-Isohexedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/5e/Isohexedrone_structure.png/240px-Isohexedrone_structure.png 2x" data-file-width="1000" data-file-height="830" /></a></span></td> <td>Isohexedrone</td> <td>H</td> <td>iBu</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-ethylheptedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0d/N-ethylheptedrone_structure.png/120px-N-ethylheptedrone_structure.png" decoding="async" width="120" height="114" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0d/N-ethylheptedrone_structure.png/180px-N-ethylheptedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0d/N-ethylheptedrone_structure.png/240px-N-ethylheptedrone_structure.png 2x" data-file-width="1000" data-file-height="950" /></a></span></td> <td><a href="/wiki/N-Ethylheptedrone" title="N-Ethylheptedrone">N-Ethylheptedrone</a></td> <td>H</td> <td>nPe</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Octedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Octedrone_structure.png/120px-Octedrone_structure.png" decoding="async" width="120" height="123" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Octedrone_structure.png/180px-Octedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Octedrone_structure.png/240px-Octedrone_structure.png 2x" data-file-width="1000" data-file-height="1029" /></a></span></td> <td>Octedrone</td> <td>H</td> <td><a href="/wiki/Hexyl" class="mw-redirect" title="Hexyl">hexyl</a></td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Dimethylcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/07/Dimethylcathinone.svg/120px-Dimethylcathinone.svg.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/07/Dimethylcathinone.svg/180px-Dimethylcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/07/Dimethylcathinone.svg/240px-Dimethylcathinone.svg.png 2x" data-file-width="331" data-file-height="209" /></a></span></td> <td><a href="/wiki/Dimethylcathinone" class="mw-redirect" title="Dimethylcathinone">Dimethylcathinone</a></td> <td>H</td> <td>Me</td> <td>Me</td> <td>Me</td> <td>15351-09-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Amfepramone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/Amfepramone.svg/120px-Amfepramone.svg.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/Amfepramone.svg/180px-Amfepramone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/24/Amfepramone.svg/240px-Amfepramone.svg.png 2x" data-file-width="357" data-file-height="210" /></a></span></td> <td><a href="/wiki/Diethylpropion" class="mw-redirect" title="Diethylpropion">Diethylpropion</a></td> <td>H</td> <td>Me</td> <td>Et</td> <td>Et</td> <td>134-80-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NN-methylethylcathinone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/NN-methylethylcathinone_structure.png/120px-NN-methylethylcathinone_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/NN-methylethylcathinone_structure.png/180px-NN-methylethylcathinone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a8/NN-methylethylcathinone_structure.png/240px-NN-methylethylcathinone_structure.png 2x" data-file-width="1000" data-file-height="573" /></a></span></td> <td>N-Methyl-N-ethylcathinone</td> <td>H</td> <td>Me</td> <td>Me</td> <td>Et</td> <td>1157739-24-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bupropion_1.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/48/Bupropion_1.svg/120px-Bupropion_1.svg.png" decoding="async" width="120" height="57" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/48/Bupropion_1.svg/180px-Bupropion_1.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/48/Bupropion_1.svg/240px-Bupropion_1.svg.png 2x" data-file-width="512" data-file-height="242" /></a></span></td> <td><a href="/wiki/Bupropion" title="Bupropion">Bupropion</a></td> <td>3-Cl</td> <td>Me</td> <td>H</td> <td><a href="/wiki/Tert-butyl" class="mw-redirect" title="Tert-butyl"><i>t</i>-Bu</a></td> <td>34911-55-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Hydroxybupropion.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e1/Hydroxybupropion.svg/120px-Hydroxybupropion.svg.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e1/Hydroxybupropion.svg/180px-Hydroxybupropion.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e1/Hydroxybupropion.svg/240px-Hydroxybupropion.svg.png 2x" data-file-width="1240" data-file-height="610" /></a></span></td> <td><a href="/wiki/Hydroxybupropion" title="Hydroxybupropion">Hydroxybupropion</a></td> <td>3-Cl</td> <td>Me</td> <td>H</td> <td>2-Me-3-OH-propan-2-yl</td> <td>357399-43-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Methylmethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/4-Methylmethcathinone.svg/120px-4-Methylmethcathinone.svg.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/4-Methylmethcathinone.svg/180px-4-Methylmethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/b9/4-Methylmethcathinone.svg/240px-4-Methylmethcathinone.svg.png 2x" data-file-width="245" data-file-height="134" /></a></span></td> <td><a href="/wiki/Mephedrone" title="Mephedrone">Mephedrone</a></td> <td>4-Me</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1189805-46-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-MMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c0/2-MMC_structure.png/120px-2-MMC_structure.png" decoding="async" width="120" height="79" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c0/2-MMC_structure.png/180px-2-MMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c0/2-MMC_structure.png/240px-2-MMC_structure.png 2x" data-file-width="1000" data-file-height="660" /></a></span></td> <td><a href="/wiki/2-MMC" class="mw-redirect" title="2-MMC">2-MMC</a></td> <td>2-Me</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1246911-71-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-MEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4f/2-MEC_structure.png/120px-2-MEC_structure.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4f/2-MEC_structure.png/180px-2-MEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4f/2-MEC_structure.png/240px-2-MEC_structure.png 2x" data-file-width="1012" data-file-height="556" /></a></span></td> <td>2-MEC</td> <td>2-Me</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1439439-84-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-EMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cd/2-EMC_structure.png/120px-2-EMC_structure.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cd/2-EMC_structure.png/180px-2-EMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cd/2-EMC_structure.png/240px-2-EMC_structure.png 2x" data-file-width="971" data-file-height="679" /></a></span></td> <td>2-EMC</td> <td>2-Et</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-EEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/82/2-EEC_structure.png/120px-2-EEC_structure.png" decoding="async" width="120" height="72" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/82/2-EEC_structure.png/180px-2-EEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/82/2-EEC_structure.png/240px-2-EEC_structure.png 2x" data-file-width="1006" data-file-height="606" /></a></span></td> <td>2-EEC</td> <td>2-Et</td> <td>Me</td> <td>H</td> <td>Et</td> <td>2446466-59-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-methylmethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/ad/3-methylmethcathinone.svg/120px-3-methylmethcathinone.svg.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/ad/3-methylmethcathinone.svg/180px-3-methylmethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/ad/3-methylmethcathinone.svg/240px-3-methylmethcathinone.svg.png 2x" data-file-width="342" data-file-height="188" /></a></span></td> <td><a href="/wiki/3-Methylmethcathinone" title="3-Methylmethcathinone">3-MMC</a></td> <td>3-Me</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1246816-62-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-MEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/47/3-MEC_structure.png/120px-3-MEC_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/47/3-MEC_structure.png/180px-3-MEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/47/3-MEC_structure.png/240px-3-MEC_structure.png 2x" data-file-width="1127" data-file-height="565" /></a></span></td> <td>3-MEC</td> <td>3-Me</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1439439-83-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-MPC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/23/3-MPC_structure.png/120px-3-MPC_structure.png" decoding="async" width="120" height="56" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/23/3-MPC_structure.png/180px-3-MPC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/23/3-MPC_structure.png/240px-3-MPC_structure.png 2x" data-file-width="1399" data-file-height="653" /></a></span></td> <td>3-MPC</td> <td>3-Me</td> <td>Me</td> <td>H</td> <td>nPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-EMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/63/3-EMC_structure.png/120px-3-EMC_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/63/3-EMC_structure.png/180px-3-EMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/63/3-EMC_structure.png/240px-3-EMC_structure.png 2x" data-file-width="1136" data-file-height="566" /></a></span></td> <td>3-EMC</td> <td>3-Et</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-EEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/5d/3-EEC_structure.png/120px-3-EEC_structure.png" decoding="async" width="120" height="53" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/5d/3-EEC_structure.png/180px-3-EEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/5d/3-EEC_structure.png/240px-3-EEC_structure.png 2x" data-file-width="1265" data-file-height="558" /></a></span></td> <td>3-EEC</td> <td>3-Et</td> <td>Me</td> <td>H</td> <td>Et</td> <td>2446466-61-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Ethylmethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/4-Ethylmethcathinone.svg/120px-4-Ethylmethcathinone.svg.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/4-Ethylmethcathinone.svg/180px-4-Ethylmethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/04/4-Ethylmethcathinone.svg/240px-4-Ethylmethcathinone.svg.png 2x" data-file-width="515" data-file-height="260" /></a></span></td> <td><a href="/wiki/4-Ethylmethcathinone" title="4-Ethylmethcathinone">4-EMC</a></td> <td>4-Et</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1225622-14-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-EEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cb/4-EEC_structure.png/120px-4-EEC_structure.png" decoding="async" width="120" height="54" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cb/4-EEC_structure.png/180px-4-EEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cb/4-EEC_structure.png/240px-4-EEC_structure.png 2x" data-file-width="1256" data-file-height="561" /></a></span></td> <td>4-EEC</td> <td>4-Et</td> <td>Me</td> <td>H</td> <td>Et</td> <td>2446466-62-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Methylcathinone.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/99/4-Methylcathinone.png/120px-4-Methylcathinone.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/99/4-Methylcathinone.png/180px-4-Methylcathinone.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/99/4-Methylcathinone.png/240px-4-Methylcathinone.png 2x" data-file-width="270" data-file-height="188" /></a></span></td> <td><a href="/wiki/4-Methylcathinone" title="4-Methylcathinone">4-MC</a></td> <td>4-Me</td> <td>Me</td> <td>H</td> <td>H</td> <td>31952-47-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Benzedrone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/Benzedrone.svg/120px-Benzedrone.svg.png" decoding="async" width="120" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/Benzedrone.svg/180px-Benzedrone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/04/Benzedrone.svg/240px-Benzedrone.svg.png 2x" data-file-width="445" data-file-height="187" /></a></span></td> <td><a href="/wiki/Benzedrone" title="Benzedrone">Benzedrone</a></td> <td>4-Me</td> <td>Me</td> <td>H</td> <td><a href="/wiki/Benzyl" class="mw-redirect" title="Benzyl">Bn</a></td> <td>1225617-75-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2%27-MeO-benzedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e8/2%27-MeO-benzedrone_structure.png/120px-2%27-MeO-benzedrone_structure.png" decoding="async" width="120" height="55" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e8/2%27-MeO-benzedrone_structure.png/180px-2%27-MeO-benzedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e8/2%27-MeO-benzedrone_structure.png/240px-2%27-MeO-benzedrone_structure.png 2x" data-file-width="1393" data-file-height="639" /></a></span></td> <td>2'-MeO-Benzedrone</td> <td>4-Me</td> <td>Me</td> <td>H</td> <td>2-MeO-Bn</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,N-DM-Benzedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/2%2CN-DM-Benzedrone_structure.png/120px-2%2CN-DM-Benzedrone_structure.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/2%2CN-DM-Benzedrone_structure.png/180px-2%2CN-DM-Benzedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1e/2%2CN-DM-Benzedrone_structure.png/240px-2%2CN-DM-Benzedrone_structure.png 2x" data-file-width="1383" data-file-height="675" /></a></span></td> <td>2,N-Dimethylbenzedrone</td> <td>2-Me</td> <td>Me</td> <td>Me</td> <td>Bn</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,N-DM-Benzedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a7/3%2CN-DM-Benzedrone_structure.png/120px-3%2CN-DM-Benzedrone_structure.png" decoding="async" width="120" height="54" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a7/3%2CN-DM-Benzedrone_structure.png/180px-3%2CN-DM-Benzedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a7/3%2CN-DM-Benzedrone_structure.png/240px-3%2CN-DM-Benzedrone_structure.png 2x" data-file-width="1509" data-file-height="679" /></a></span></td> <td>3,N-Dimethylbenzedrone</td> <td>3-Me</td> <td>Me</td> <td>Me</td> <td>Bn</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4,N-DM-Benzedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/52/4%2CN-DM-Benzedrone_structure.png/120px-4%2CN-DM-Benzedrone_structure.png" decoding="async" width="120" height="54" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/52/4%2CN-DM-Benzedrone_structure.png/180px-4%2CN-DM-Benzedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/52/4%2CN-DM-Benzedrone_structure.png/240px-4%2CN-DM-Benzedrone_structure.png 2x" data-file-width="1507" data-file-height="681" /></a></span></td> <td>4,N-Dimethylbenzedrone</td> <td>4-Me</td> <td>Me</td> <td>Me</td> <td>Bn</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MEC.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/b4/4-MEC.svg/120px-4-MEC.svg.png" decoding="async" width="120" height="57" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/b4/4-MEC.svg/180px-4-MEC.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/b4/4-MEC.svg/240px-4-MEC.svg.png 2x" data-file-width="357" data-file-height="169" /></a></span></td> <td><a href="/wiki/4-Methylethcathinone" title="4-Methylethcathinone">4-MEC</a></td> <td>4-Me</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1225617-18-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-methyl-propylcathinone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/20/4-methyl-propylcathinone_structure.png/120px-4-methyl-propylcathinone_structure.png" decoding="async" width="120" height="53" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/20/4-methyl-propylcathinone_structure.png/180px-4-methyl-propylcathinone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/20/4-methyl-propylcathinone_structure.png/240px-4-methyl-propylcathinone_structure.png 2x" data-file-width="1262" data-file-height="553" /></a></span></td> <td>4-MPC</td> <td>4-Me</td> <td>Me</td> <td>H</td> <td>nPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NN-DMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/NN-DMMC_structure.png/120px-NN-DMMC_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/NN-DMMC_structure.png/180px-NN-DMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/b9/NN-DMMC_structure.png/240px-NN-DMMC_structure.png 2x" data-file-width="988" data-file-height="562" /></a></span></td> <td>N,N-DMMC</td> <td>4-Me</td> <td>Me</td> <td>Me</td> <td>Me</td> <td>1448845-14-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NN-MEMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e4/NN-MEMC_structure.png/120px-NN-MEMC_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e4/NN-MEMC_structure.png/180px-NN-MEMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e4/NN-MEMC_structure.png/240px-NN-MEMC_structure.png 2x" data-file-width="1135" data-file-height="574" /></a></span></td> <td>N,N-MEMC</td> <td>4-Me</td> <td>Me</td> <td>Me</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NN-DEMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6d/NN-DEMC_structure.png/120px-NN-DEMC_structure.png" decoding="async" width="120" height="65" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6d/NN-DEMC_structure.png/180px-NN-DEMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6d/NN-DEMC_structure.png/240px-NN-DEMC_structure.png 2x" data-file-width="1145" data-file-height="624" /></a></span></td> <td>N,N-DEMC</td> <td>4-Me</td> <td>Me</td> <td>Et</td> <td>Et</td> <td>676316-90-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MEAP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-MEAP.svg/120px-4-MEAP.svg.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-MEAP.svg/180px-4-MEAP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-MEAP.svg/240px-4-MEAP.svg.png 2x" data-file-width="990" data-file-height="625" /></a></span></td> <td><a href="/wiki/4-MEAP" class="mw-redirect" title="4-MEAP">4-MEAP</a></td> <td>4-Me</td> <td>Pr</td> <td>H</td> <td>Et</td> <td>746540-82-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-EDMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/da/4-EDMC_structure.png/120px-4-EDMC_structure.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/da/4-EDMC_structure.png/180px-4-EDMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/da/4-EDMC_structure.png/240px-4-EDMC_structure.png 2x" data-file-width="1136" data-file-height="557" /></a></span></td> <td>EDMC</td> <td>4-Et</td> <td>Me</td> <td>Me</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,3-DMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/36/2%2C3-DMMC_structure.png/120px-2%2C3-DMMC_structure.png" decoding="async" width="120" height="72" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/36/2%2C3-DMMC_structure.png/180px-2%2C3-DMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/36/2%2C3-DMMC_structure.png/240px-2%2C3-DMMC_structure.png 2x" data-file-width="1091" data-file-height="655" /></a></span></td> <td>2,3-DMMC</td> <td>2,3-dimethyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,3-DMEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/80/2%2C3-DMEC_structure.png/120px-2%2C3-DMEC_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/80/2%2C3-DMEC_structure.png/180px-2%2C3-DMEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/80/2%2C3-DMEC_structure.png/240px-2%2C3-DMEC_structure.png 2x" data-file-width="1230" data-file-height="613" /></a></span></td> <td>2,3-DMEC</td> <td>2,3-dimethyl</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,4-DMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4b/2%2C4-DMMC_structure.png/120px-2%2C4-DMMC_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4b/2%2C4-DMMC_structure.png/180px-2%2C4-DMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4b/2%2C4-DMMC_structure.png/240px-2%2C4-DMMC_structure.png 2x" data-file-width="999" data-file-height="562" /></a></span></td> <td>2,4-DMMC</td> <td>2,4-dimethyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1225623-63-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,4-DMEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/43/2%2C4-DMEC_structure.png/120px-2%2C4-DMEC_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/43/2%2C4-DMEC_structure.png/180px-2%2C4-DMEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/43/2%2C4-DMEC_structure.png/240px-2%2C4-DMEC_structure.png 2x" data-file-width="1129" data-file-height="566" /></a></span></td> <td>2,4-DMEC</td> <td>2,4-dimethyl</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1225913-88-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,5-DMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/81/2%2C5-DMMC_structure.png/120px-2%2C5-DMMC_structure.png" decoding="async" width="120" height="97" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/81/2%2C5-DMMC_structure.png/180px-2%2C5-DMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/81/2%2C5-DMMC_structure.png/240px-2%2C5-DMMC_structure.png 2x" data-file-width="965" data-file-height="781" /></a></span></td> <td>2,5-DMMC</td> <td>2,5-dimethyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,5-DMEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d4/2%2C5-DMEC_structure.png/120px-2%2C5-DMEC_structure.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d4/2%2C5-DMEC_structure.png/180px-2%2C5-DMEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d4/2%2C5-DMEC_structure.png/240px-2%2C5-DMEC_structure.png 2x" data-file-width="1103" data-file-height="771" /></a></span></td> <td>2,5-DMEC</td> <td>2,5-dimethyl</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,6-DMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1f/2%2C6-DMMC_structure.png/120px-2%2C6-DMMC_structure.png" decoding="async" width="120" height="82" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1f/2%2C6-DMMC_structure.png/180px-2%2C6-DMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1f/2%2C6-DMMC_structure.png/240px-2%2C6-DMMC_structure.png 2x" data-file-width="953" data-file-height="649" /></a></span></td> <td>2,6-DMMC</td> <td>2,6-dimethyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,6-DMEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/2%2C6-DMEC_structure.png/120px-2%2C6-DMEC_structure.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/2%2C6-DMEC_structure.png/180px-2%2C6-DMEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2e/2%2C6-DMEC_structure.png/240px-2%2C6-DMEC_structure.png 2x" data-file-width="1093" data-file-height="661" /></a></span></td> <td>2,6-DMEC</td> <td>2,6-dimethyl</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DMMC.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f2/3%2C4-DMMC.svg/120px-3%2C4-DMMC.svg.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f2/3%2C4-DMMC.svg/180px-3%2C4-DMMC.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f2/3%2C4-DMMC.svg/240px-3%2C4-DMMC.svg.png 2x" data-file-width="449" data-file-height="247" /></a></span></td> <td><a href="/wiki/3,4-Dimethylmethcathinone" title="3,4-Dimethylmethcathinone">3,4-DMMC</a></td> <td>3,4-dimethyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1082110-00-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DMEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4e/3%2C4-DMEC_structure.png/120px-3%2C4-DMEC_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4e/3%2C4-DMEC_structure.png/180px-3%2C4-DMEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4e/3%2C4-DMEC_structure.png/240px-3%2C4-DMEC_structure.png 2x" data-file-width="1148" data-file-height="570" /></a></span></td> <td>3,4-DMEC</td> <td>3,4-dimethyl</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1225811-81-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,5-DMEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7a/3%2C5-DMEC_structure.png/120px-3%2C5-DMEC_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7a/3%2C5-DMEC_structure.png/180px-3%2C5-DMEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7a/3%2C5-DMEC_structure.png/240px-3%2C5-DMEC_structure.png 2x" data-file-width="1227" data-file-height="781" /></a></span></td> <td>3,5-DMEC</td> <td>3,5-dimethyl</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:245-TMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4f/245-TMMC_structure.png/120px-245-TMMC_structure.png" decoding="async" width="120" height="85" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4f/245-TMMC_structure.png/180px-245-TMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4f/245-TMMC_structure.png/240px-245-TMMC_structure.png 2x" data-file-width="994" data-file-height="705" /></a></span></td> <td>2,4,5-TMMC</td> <td>2,4,5-trimethyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1368603-85-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:245-TMOMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/44/245-TMOMC_structure.png/120px-245-TMOMC_structure.png" decoding="async" width="120" height="88" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/44/245-TMOMC_structure.png/180px-245-TMOMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/44/245-TMOMC_structure.png/240px-245-TMOMC_structure.png 2x" data-file-width="1135" data-file-height="832" /></a></span></td> <td>2,4,5-TMOMC</td> <td>2,4,5-trimethoxy</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:345-TMOMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/03/345-TMOMC_structure.png/120px-345-TMOMC_structure.png" decoding="async" width="120" height="82" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/03/345-TMOMC_structure.png/180px-345-TMOMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/03/345-TMOMC_structure.png/240px-345-TMOMC_structure.png 2x" data-file-width="1127" data-file-height="768" /></a></span></td> <td>3,4,5-TMOMC</td> <td>3,4,5-trimethoxy</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Methoxymethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/75/4-Methoxymethcathinone.svg/120px-4-Methoxymethcathinone.svg.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/75/4-Methoxymethcathinone.svg/180px-4-Methoxymethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/75/4-Methoxymethcathinone.svg/240px-4-Methoxymethcathinone.svg.png 2x" data-file-width="512" data-file-height="257" /></a></span></td> <td><a href="/wiki/Methedrone" title="Methedrone">Methedrone</a></td> <td>4-<a href="/wiki/Methoxy" class="mw-redirect" title="Methoxy">MeO</a></td> <td>Me</td> <td>H</td> <td>Me</td> <td>530-54-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Dimethedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/5f/Dimethedrone_structure.png/120px-Dimethedrone_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/5f/Dimethedrone_structure.png/180px-Dimethedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/5f/Dimethedrone_structure.png/240px-Dimethedrone_structure.png 2x" data-file-width="1146" data-file-height="580" /></a></span></td> <td>Dimethedrone</td> <td>4-<a href="/wiki/Methoxy" class="mw-redirect" title="Methoxy">MeO</a></td> <td>Me</td> <td>Me</td> <td>Me</td> <td>91564-39-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Ethedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4e/Ethedrone_structure.png/120px-Ethedrone_structure.png" decoding="async" width="120" height="55" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4e/Ethedrone_structure.png/180px-Ethedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4e/Ethedrone_structure.png/240px-Ethedrone_structure.png 2x" data-file-width="1263" data-file-height="582" /></a></span></td> <td>Ethedrone</td> <td>4-MeO</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-MOMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/54/2-MOMC_structure.png/120px-2-MOMC_structure.png" decoding="async" width="120" height="82" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/54/2-MOMC_structure.png/180px-2-MOMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/54/2-MOMC_structure.png/240px-2-MOMC_structure.png 2x" data-file-width="878" data-file-height="603" /></a></span></td> <td>2-MOMC</td> <td>2-MeO</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-MOMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-MOMC_structure.png/120px-3-MOMC_structure.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-MOMC_structure.png/180px-3-MOMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-MOMC_structure.png/240px-3-MOMC_structure.png 2x" data-file-width="1127" data-file-height="554" /></a></span></td> <td>3-MOMC</td> <td>3-MeO</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1435933-70-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-fluorocathinone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c7/3-fluorocathinone_structure.png/120px-3-fluorocathinone_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c7/3-fluorocathinone_structure.png/180px-3-fluorocathinone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c7/3-fluorocathinone_structure.png/240px-3-fluorocathinone_structure.png 2x" data-file-width="993" data-file-height="560" /></a></span></td> <td>3-FC</td> <td>3-F</td> <td>Me</td> <td>H</td> <td>H</td> <td>1082949-91-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-fluorocathinone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9e/4-fluorocathinone_structure.png/120px-4-fluorocathinone_structure.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9e/4-fluorocathinone_structure.png/180px-4-fluorocathinone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9e/4-fluorocathinone_structure.png/240px-4-fluorocathinone_structure.png 2x" data-file-width="997" data-file-height="587" /></a></span></td> <td>4-FC</td> <td>4-F</td> <td>Me</td> <td>H</td> <td>H</td> <td>80096-51-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-FMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2a/2-FMC_structure.png/120px-2-FMC_structure.png" decoding="async" width="120" height="77" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2a/2-FMC_structure.png/180px-2-FMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2a/2-FMC_structure.png/240px-2-FMC_structure.png 2x" data-file-width="861" data-file-height="550" /></a></span></td> <td>2-FMC</td> <td>2-F</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1186137-35-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-FEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/ab/2-FEC_structure.png/120px-2-FEC_structure.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/ab/2-FEC_structure.png/180px-2-FEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/ab/2-FEC_structure.png/240px-2-FEC_structure.png 2x" data-file-width="979" data-file-height="540" /></a></span></td> <td>2-FEC</td> <td>2-F</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-fluoromethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/82/3-fluoromethcathinone.svg/120px-3-fluoromethcathinone.svg.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/82/3-fluoromethcathinone.svg/180px-3-fluoromethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/82/3-fluoromethcathinone.svg/240px-3-fluoromethcathinone.svg.png 2x" data-file-width="512" data-file-height="271" /></a></span></td> <td><a href="/wiki/3-Fluoromethcathinone" title="3-Fluoromethcathinone">3-FMC</a></td> <td>3-F</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1049677-77-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-FEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/98/3-FEC_structure.png/120px-3-FEC_structure.png" decoding="async" width="120" height="58" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/98/3-FEC_structure.png/180px-3-FEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/98/3-FEC_structure.png/240px-3-FEC_structure.png 2x" data-file-width="1133" data-file-height="550" /></a></span></td> <td>3-FEC</td> <td>3-F</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-CMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/77/2-CMC_structure.png/120px-2-CMC_structure.png" decoding="async" width="120" height="74" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/77/2-CMC_structure.png/180px-2-CMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/77/2-CMC_structure.png/240px-2-CMC_structure.png 2x" data-file-width="862" data-file-height="534" /></a></span></td> <td>2-CMC</td> <td>2-Cl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-BMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/63/2-BMC_structure.png/120px-2-BMC_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/63/2-BMC_structure.png/180px-2-BMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/63/2-BMC_structure.png/240px-2-BMC_structure.png 2x" data-file-width="867" data-file-height="547" /></a></span></td> <td>2-BMC</td> <td>2-Br</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-IMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/2-IMC_structure.png/120px-2-IMC_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/2-IMC_structure.png/180px-2-IMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/21/2-IMC_structure.png/240px-2-IMC_structure.png 2x" data-file-width="894" data-file-height="560" /></a></span></td> <td>2-IMC</td> <td>2-I</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-TFMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/88/2-TFMMC_structure.png/120px-2-TFMMC_structure.png" decoding="async" width="120" height="97" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/88/2-TFMMC_structure.png/180px-2-TFMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/88/2-TFMMC_structure.png/240px-2-TFMMC_structure.png 2x" data-file-width="868" data-file-height="699" /></a></span></td> <td>2-TFMAP</td> <td>2-CF<sub>3</sub></td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-Chloromethcathinone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1d/3-Chloromethcathinone_structure.png/120px-3-Chloromethcathinone_structure.png" decoding="async" width="120" height="72" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1d/3-Chloromethcathinone_structure.png/180px-3-Chloromethcathinone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1d/3-Chloromethcathinone_structure.png/240px-3-Chloromethcathinone_structure.png 2x" data-file-width="796" data-file-height="476" /></a></span></td> <td><a href="/wiki/Clophedrone" class="mw-redirect" title="Clophedrone">Clophedrone</a></td> <td>3-Cl</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1049677-59-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-CEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/b2/3-CEC_structure.png/120px-3-CEC_structure.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/b2/3-CEC_structure.png/180px-3-CEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/b2/3-CEC_structure.png/240px-3-CEC_structure.png 2x" data-file-width="1137" data-file-height="559" /></a></span></td> <td><a href="/w/index.php?title=3-Chloroethcathinone&amp;action=edit&amp;redlink=1" class="new" title="3-Chloroethcathinone (page does not exist)">3-CEC</a></td> <td>3-Cl</td> <td>Me</td> <td>H</td> <td>Et</td> <td>2150476-60-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-BMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/19/3-BMC_structure.png/120px-3-BMC_structure.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/19/3-BMC_structure.png/180px-3-BMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/19/3-BMC_structure.png/240px-3-BMC_structure.png 2x" data-file-width="1015" data-file-height="558" /></a></span></td> <td>3-BMC</td> <td>3-Br</td> <td>Me</td> <td>H</td> <td>Me</td> <td>676487-42-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-IMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9a/3-IMC_structure.png/120px-3-IMC_structure.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9a/3-IMC_structure.png/180px-3-IMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9a/3-IMC_structure.png/240px-3-IMC_structure.png 2x" data-file-width="973" data-file-height="570" /></a></span></td> <td>3-IMC</td> <td>3-I</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-TFMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/ed/3-TFMMC_structure.png/120px-3-TFMMC_structure.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/ed/3-TFMMC_structure.png/180px-3-TFMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/ed/3-TFMMC_structure.png/240px-3-TFMMC_structure.png 2x" data-file-width="1138" data-file-height="563" /></a></span></td> <td>3-TFMAP</td> <td>3-CF<sub>3</sub></td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-fluoromethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/09/4-fluoromethcathinone.svg/120px-4-fluoromethcathinone.svg.png" decoding="async" width="120" height="67" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/09/4-fluoromethcathinone.svg/180px-4-fluoromethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/09/4-fluoromethcathinone.svg/240px-4-fluoromethcathinone.svg.png 2x" data-file-width="512" data-file-height="287" /></a></span></td> <td><a href="/wiki/Flephedrone" title="Flephedrone">Flephedrone</a></td> <td>4-<a href="/wiki/Fluorine" title="Fluorine">F</a></td> <td>Me</td> <td>H</td> <td>Me</td> <td>447-40-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Fluoroethcathinone_Structure.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cb/4-Fluoroethcathinone_Structure.svg/120px-4-Fluoroethcathinone_Structure.svg.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cb/4-Fluoroethcathinone_Structure.svg/180px-4-Fluoroethcathinone_Structure.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cb/4-Fluoroethcathinone_Structure.svg/240px-4-Fluoroethcathinone_Structure.svg.png 2x" data-file-width="512" data-file-height="256" /></a></span></td> <td><a href="/wiki/4-Fluoroethcathinone" title="4-Fluoroethcathinone">4-FEC</a></td> <td>4-F</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1225625-74-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Chloromethcathinone.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e6/4-Chloromethcathinone.png/120px-4-Chloromethcathinone.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e6/4-Chloromethcathinone.png/180px-4-Chloromethcathinone.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e6/4-Chloromethcathinone.png/240px-4-Chloromethcathinone.png 2x" data-file-width="296" data-file-height="185" /></a></span></td> <td><a href="/wiki/4-Chloromethcathinone" title="4-Chloromethcathinone">Clephedrone</a></td> <td>4-Cl</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1225843-86-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2Cl-NEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/14/2Cl-NEC_structure.png/120px-2Cl-NEC_structure.png" decoding="async" width="120" height="67" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/14/2Cl-NEC_structure.png/180px-2Cl-NEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/14/2Cl-NEC_structure.png/240px-2Cl-NEC_structure.png 2x" data-file-width="1091" data-file-height="605" /></a></span></td> <td>2-CEC</td> <td>2-Cl</td> <td>Me</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-CEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7b/4-CEC_structure.png/120px-4-CEC_structure.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7b/4-CEC_structure.png/180px-4-CEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7b/4-CEC_structure.png/240px-4-CEC_structure.png 2x" data-file-width="1151" data-file-height="590" /></a></span></td> <td>4-CEC</td> <td>4-Cl</td> <td>Me</td> <td>H</td> <td>Et</td> <td>14919-85-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2Cl-NiPC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c4/2Cl-NiPC_structure.png/120px-2Cl-NiPC_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c4/2Cl-NiPC_structure.png/180px-2Cl-NiPC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c4/2Cl-NiPC_structure.png/240px-2Cl-NiPC_structure.png 2x" data-file-width="1093" data-file-height="619" /></a></span></td> <td>2-CiPC</td> <td>2-Cl</td> <td>Me</td> <td>H</td> <td>iPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3Cl-NiPC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8f/3Cl-NiPC_structure.png/120px-3Cl-NiPC_structure.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8f/3Cl-NiPC_structure.png/180px-3Cl-NiPC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8f/3Cl-NiPC_structure.png/240px-3Cl-NiPC_structure.png 2x" data-file-width="1307" data-file-height="645" /></a></span></td> <td>3-CiPC</td> <td>3-Cl</td> <td>Me</td> <td>H</td> <td>iPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-CiPC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f7/4-CiPC_structure.png/120px-4-CiPC_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f7/4-CiPC_structure.png/180px-4-CiPC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f7/4-CiPC_structure.png/240px-4-CiPC_structure.png 2x" data-file-width="1145" data-file-height="582" /></a></span></td> <td>4-CiPC</td> <td>4-Cl</td> <td>Me</td> <td>H</td> <td>iPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-CBC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/07/4-CBC_structure.png/120px-4-CBC_structure.png" decoding="async" width="120" height="51" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/07/4-CBC_structure.png/180px-4-CBC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/07/4-CBC_structure.png/240px-4-CBC_structure.png 2x" data-file-width="1409" data-file-height="593" /></a></span></td> <td>4-CBC</td> <td>4-Cl</td> <td>Me</td> <td>H</td> <td>nBu</td> <td>1225621-71-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2Cl-DMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/2Cl-DMC_structure.png/120px-2Cl-DMC_structure.png" decoding="async" width="120" height="78" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/2Cl-DMC_structure.png/180px-2Cl-DMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7f/2Cl-DMC_structure.png/240px-2Cl-DMC_structure.png 2x" data-file-width="935" data-file-height="609" /></a></span></td> <td>2-CDMC</td> <td>2-Cl</td> <td>Me</td> <td>Me</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3Cl-DMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/3Cl-DMC_structure.png/120px-3Cl-DMC_structure.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/3Cl-DMC_structure.png/180px-3Cl-DMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/13/3Cl-DMC_structure.png/240px-3Cl-DMC_structure.png 2x" data-file-width="1165" data-file-height="637" /></a></span></td> <td>3-CDMC</td> <td>3-Cl</td> <td>Me</td> <td>Me</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-CDMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2f/4-CDMC_structure.png/120px-4-CDMC_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2f/4-CDMC_structure.png/180px-4-CDMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2f/4-CDMC_structure.png/240px-4-CDMC_structure.png 2x" data-file-width="1041" data-file-height="588" /></a></span></td> <td>4-CDMC</td> <td>4-Cl</td> <td>Me</td> <td>Me</td> <td>Me</td> <td>1157667-29-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-bromomethcathinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-bromomethcathinone.svg/120px-4-bromomethcathinone.svg.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-bromomethcathinone.svg/180px-4-bromomethcathinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-bromomethcathinone.svg/240px-4-bromomethcathinone.svg.png 2x" data-file-width="512" data-file-height="271" /></a></span></td> <td><a href="/wiki/Brephedrone" class="mw-redirect" title="Brephedrone">Brephedrone</a></td> <td>4-<a href="/wiki/Bromine" title="Bromine">Br</a></td> <td>Me</td> <td>H</td> <td>Me</td> <td>486459-03-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-BEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/47/4-BEC_structure.png/120px-4-BEC_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/47/4-BEC_structure.png/180px-4-BEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/47/4-BEC_structure.png/240px-4-BEC_structure.png 2x" data-file-width="1169" data-file-height="591" /></a></span></td> <td>4-BEC</td> <td>4-Br</td> <td>Me</td> <td>H</td> <td>Et</td> <td>135333-26-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-IMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/4-IMC_structure.png/120px-4-IMC_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/4-IMC_structure.png/180px-4-IMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1e/4-IMC_structure.png/240px-4-IMC_structure.png 2x" data-file-width="1011" data-file-height="580" /></a></span></td> <td>4-IMC</td> <td>4-I</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-TFMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4a/4-TFMMC_structure.png/120px-4-TFMMC_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4a/4-TFMMC_structure.png/180px-4-TFMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4a/4-TFMMC_structure.png/240px-4-TFMMC_structure.png 2x" data-file-width="1152" data-file-height="733" /></a></span></td> <td>4-TFMAP</td> <td>4-CF<sub>3</sub></td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-EFMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/3a/4-EFMC_structure.png/120px-4-EFMC_structure.png" decoding="async" width="120" height="55" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/3a/4-EFMC_structure.png/180px-4-EFMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/3a/4-EFMC_structure.png/240px-4-EFMC_structure.png 2x" data-file-width="1277" data-file-height="584" /></a></span></td> <td>4-EFMC</td> <td>4-(2-fluoroethyl)</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MTMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/34/4-MTMC_structure.png/120px-4-MTMC_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/34/4-MTMC_structure.png/180px-4-MTMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/34/4-MTMC_structure.png/240px-4-MTMC_structure.png 2x" data-file-width="1130" data-file-height="578" /></a></span></td> <td>4-MTMC</td> <td>4-SCH<sub>3</sub></td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MSMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/4-MSMC_structure.png/120px-4-MSMC_structure.png" decoding="async" width="120" height="77" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/4-MSMC_structure.png/180px-4-MSMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9d/4-MSMC_structure.png/240px-4-MSMC_structure.png 2x" data-file-width="1134" data-file-height="725" /></a></span></td> <td>4-MSMC</td> <td>4-SO<sub>2</sub>CH<sub>3</sub></td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-PHMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/4-PHMC_structure.png/120px-4-PHMC_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/4-PHMC_structure.png/180px-4-PHMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7f/4-PHMC_structure.png/240px-4-PHMC_structure.png 2x" data-file-width="1265" data-file-height="799" /></a></span></td> <td>4-PHMC</td> <td>4-phenyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Mexedrone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f1/Mexedrone.svg/120px-Mexedrone.svg.png" decoding="async" width="120" height="87" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f1/Mexedrone.svg/180px-Mexedrone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f1/Mexedrone.svg/240px-Mexedrone.svg.png 2x" data-file-width="512" data-file-height="370" /></a></span></td> <td><a href="/wiki/Mexedrone" title="Mexedrone">Mexedrone</a></td> <td>4-Me</td> <td>methoxymethyl</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-FMMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/32/3%2C4-FMMC_structure.png/120px-3%2C4-FMMC_structure.png" decoding="async" width="120" height="65" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/32/3%2C4-FMMC_structure.png/180px-3%2C4-FMMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/32/3%2C4-FMMC_structure.png/240px-3%2C4-FMMC_structure.png 2x" data-file-width="1033" data-file-height="561" /></a></span></td> <td>FMMC</td> <td>3-F-4-Me</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1696642-00-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-MFMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/99/3%2C4-MFMC_structure.png/120px-3%2C4-MFMC_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/99/3%2C4-MFMC_structure.png/180px-3%2C4-MFMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/99/3%2C4-MFMC_structure.png/240px-3%2C4-MFMC_structure.png 2x" data-file-width="1007" data-file-height="576" /></a></span></td> <td>MFMC</td> <td>3-Me-4-F</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1368943-21-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Cl-3-MMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/67/4-Cl-3-MMC_structure.png/120px-4-Cl-3-MMC_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/67/4-Cl-3-MMC_structure.png/180px-4-Cl-3-MMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/67/4-Cl-3-MMC_structure.png/240px-4-Cl-3-MMC_structure.png 2x" data-file-width="1187" data-file-height="671" /></a></span></td> <td><a href="/wiki/4-Cl-3-MMC" title="4-Cl-3-MMC">4-Cl-3-MMC</a></td> <td>3-Me-4-Cl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-MMOMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/67/3%2C4-MMOMC_structure.png/120px-3%2C4-MMOMC_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/67/3%2C4-MMOMC_structure.png/180px-3%2C4-MMOMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/67/3%2C4-MMOMC_structure.png/240px-3%2C4-MMOMC_structure.png 2x" data-file-width="1137" data-file-height="582" /></a></span></td> <td>MMOMC</td> <td>3-Me-4-MeO</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DCMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1f/3%2C4-DCMC_structure.png/120px-3%2C4-DCMC_structure.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1f/3%2C4-DCMC_structure.png/180px-3%2C4-DCMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1f/3%2C4-DCMC_structure.png/240px-3%2C4-DCMC_structure.png 2x" data-file-width="1028" data-file-height="603" /></a></span></td> <td>3,4-DCMC</td> <td>3,4-dichloro</td> <td>Me</td> <td>H</td> <td>Me</td> <td>802281-39-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DCEC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/37/3%2C4-DCEC_structure.png/120px-3%2C4-DCEC_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/37/3%2C4-DCEC_structure.png/180px-3%2C4-DCEC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/37/3%2C4-DCEC_structure.png/240px-3%2C4-DCEC_structure.png 2x" data-file-width="1339" data-file-height="679" /></a></span></td> <td>3,4-DCEC</td> <td>3,4-dichloro</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1225618-63-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,5-DCMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/3%2C5-DCMC_structure.png/120px-3%2C5-DCMC_structure.png" decoding="async" width="120" height="85" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/3%2C5-DCMC_structure.png/180px-3%2C5-DCMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/3%2C5-DCMC_structure.png/240px-3%2C5-DCMC_structure.png 2x" data-file-width="1046" data-file-height="741" /></a></span></td> <td>3,5-DCMC</td> <td>3,5-dichloro</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,5-DFMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/87/3%2C5-DFMC_structure.png/120px-3%2C5-DFMC_structure.png" decoding="async" width="120" height="87" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/87/3%2C5-DFMC_structure.png/180px-3%2C5-DFMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/87/3%2C5-DFMC_structure.png/240px-3%2C5-DFMC_structure.png 2x" data-file-width="1035" data-file-height="751" /></a></span></td> <td><a href="/wiki/3,5-DFMC" class="mw-redirect" title="3,5-DFMC">3,5-DFMC</a></td> <td>3,5-difluoro</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1430343-55-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,5-DMOMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/78/2%2C5-DMOMC_structure.png/120px-2%2C5-DMOMC_structure.png" decoding="async" width="120" height="116" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/78/2%2C5-DMOMC_structure.png/180px-2%2C5-DMOMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/78/2%2C5-DMOMC_structure.png/240px-2%2C5-DMOMC_structure.png 2x" data-file-width="867" data-file-height="837" /></a></span></td> <td>2,5-DMOMC</td> <td>2,5-dimethoxy</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk2CC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/42/Bk2CC_structure.png/120px-Bk2CC_structure.png" decoding="async" width="120" height="101" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/42/Bk2CC_structure.png/180px-Bk2CC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/42/Bk2CC_structure.png/240px-Bk2CC_structure.png 2x" data-file-width="1011" data-file-height="847" /></a></span></td> <td>βk-2C-C</td> <td>2,5-dimethoxy-4-chloro</td> <td>H</td> <td>H</td> <td>H</td> <td>1538191-15-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:%CE%92k-2C-B-skeletal.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/96/%CE%92k-2C-B-skeletal.svg/120px-%CE%92k-2C-B-skeletal.svg.png" decoding="async" width="120" height="82" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/96/%CE%92k-2C-B-skeletal.svg/180px-%CE%92k-2C-B-skeletal.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/96/%CE%92k-2C-B-skeletal.svg/240px-%CE%92k-2C-B-skeletal.svg.png 2x" data-file-width="736" data-file-height="500" /></a></span></td> <td><a href="/wiki/%CE%92k-2C-B" title="Βk-2C-B">βk-2C-B</a></td> <td>2,5-dimethoxy-4-bromo</td> <td>H</td> <td>H</td> <td>H</td> <td>807631-09-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk2CI_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0e/Bk2CI_structure.png/120px-Bk2CI_structure.png" decoding="async" width="120" height="102" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0e/Bk2CI_structure.png/180px-Bk2CI_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0e/Bk2CI_structure.png/240px-Bk2CI_structure.png 2x" data-file-width="998" data-file-height="851" /></a></span></td> <td>βk-2C-I</td> <td>2,5-dimethoxy-4-iodo</td> <td>H</td> <td>H</td> <td>H</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk2CD_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/37/Bk2CD_structure.png/120px-Bk2CD_structure.png" decoding="async" width="120" height="103" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/37/Bk2CD_structure.png/180px-Bk2CD_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/37/Bk2CD_structure.png/240px-Bk2CD_structure.png 2x" data-file-width="987" data-file-height="850" /></a></span></td> <td>βk-2C-D</td> <td>2,5-dimethoxy-4-methyl</td> <td>H</td> <td>H</td> <td>H</td> <td>1368627-25-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk2CE_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/Bk2CE_structure.png/120px-Bk2CE_structure.png" decoding="async" width="120" height="91" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/Bk2CE_structure.png/180px-Bk2CE_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1e/Bk2CE_structure.png/240px-Bk2CE_structure.png 2x" data-file-width="1124" data-file-height="855" /></a></span></td> <td>βk-2C-E</td> <td>2,5-dimethoxy-4-ethyl</td> <td>H</td> <td>H</td> <td>H</td> <td>1517021-02-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk2CP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a4/Bk2CP_structure.png/120px-Bk2CP_structure.png" decoding="async" width="120" height="80" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a4/Bk2CP_structure.png/180px-Bk2CP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a4/Bk2CP_structure.png/240px-Bk2CP_structure.png 2x" data-file-width="1265" data-file-height="843" /></a></span></td> <td>βk-2C-P</td> <td>2,5-dimethoxy-4-propyl</td> <td>H</td> <td>H</td> <td>H</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk2CiP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d5/Bk2CiP_structure.png/120px-Bk2CiP_structure.png" decoding="async" width="120" height="91" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d5/Bk2CiP_structure.png/180px-Bk2CiP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d5/Bk2CiP_structure.png/240px-Bk2CiP_structure.png 2x" data-file-width="1126" data-file-height="854" /></a></span></td> <td>βk-2C-iP</td> <td>2,5-dimethoxy-4-isopropyl</td> <td>H</td> <td>H</td> <td>H</td> <td>1511033-62-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkDOB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/15/BkDOB_structure.png/120px-BkDOB_structure.png" decoding="async" width="120" height="100" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/15/BkDOB_structure.png/180px-BkDOB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/15/BkDOB_structure.png/240px-BkDOB_structure.png 2x" data-file-width="1019" data-file-height="852" /></a></span></td> <td>βk-DOB</td> <td>2,5-dimethoxy-4-bromo</td> <td>Me</td> <td>H</td> <td>H</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkMDOM_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1d/BkMDOM_structure.png/120px-BkMDOM_structure.png" decoding="async" width="120" height="102" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1d/BkMDOM_structure.png/180px-BkMDOM_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1d/BkMDOM_structure.png/240px-BkMDOM_structure.png 2x" data-file-width="1009" data-file-height="854" /></a></span></td> <td>βk-MDOM</td> <td>2,5-dimethoxy-4-methyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDC.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6b/MDC.png/120px-MDC.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6b/MDC.png/180px-MDC.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6b/MDC.png/240px-MDC.png 2x" data-file-width="760" data-file-height="388" /></a></span></td> <td><a href="/wiki/Methylenedioxycathinone" title="Methylenedioxycathinone">βk-MDA</a></td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>H</td> <td>80535-73-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkMDAc_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0a/BkMDAc_structure.png/120px-BkMDAc_structure.png" decoding="async" width="120" height="55" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0a/BkMDAc_structure.png/180px-BkMDAc_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0a/BkMDAc_structure.png/240px-BkMDAc_structure.png 2x" data-file-width="1231" data-file-height="565" /></a></span></td> <td>N-Acetyl-βk-MDA</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>acetyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,3-MDMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/5a/2%2C3-MDMC_structure.png/120px-2%2C3-MDMC_structure.png" decoding="async" width="120" height="67" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/5a/2%2C3-MDMC_structure.png/180px-2%2C3-MDMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/5a/2%2C3-MDMC_structure.png/240px-2%2C3-MDMC_structure.png 2x" data-file-width="1016" data-file-height="567" /></a></span></td> <td>2,3-MDMC</td> <td>2,3-methylenedioxy</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1427205-87-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Methylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Methylone.svg/120px-Methylone.svg.png" decoding="async" width="120" height="55" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Methylone.svg/180px-Methylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d1/Methylone.svg/240px-Methylone.svg.png 2x" data-file-width="503" data-file-height="229" /></a></span></td> <td><a href="/wiki/Methylone" title="Methylone">Methylone</a></td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>Me</td> <td>186028-79-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Dimethylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Dimethylone.svg/120px-Dimethylone.svg.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Dimethylone.svg/180px-Dimethylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Dimethylone.svg/240px-Dimethylone.svg.png 2x" data-file-width="500" data-file-height="260" /></a></span></td> <td><a href="/wiki/Dimethylone" title="Dimethylone">Dimethylone</a></td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>Me</td> <td>Me</td> <td>109367-07-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NAc-Methylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/df/NAc-Methylone_structure.png/120px-NAc-Methylone_structure.png" decoding="async" width="120" height="58" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/df/NAc-Methylone_structure.png/180px-NAc-Methylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/df/NAc-Methylone_structure.png/240px-NAc-Methylone_structure.png 2x" data-file-width="1215" data-file-height="585" /></a></span></td> <td>N-Acetylmethylone</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>acetyl</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NOH-Methylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a5/NOH-Methylone_structure.png/120px-NOH-Methylone_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a5/NOH-Methylone_structure.png/180px-NOH-Methylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a5/NOH-Methylone_structure.png/240px-NOH-Methylone_structure.png 2x" data-file-width="1165" data-file-height="585" /></a></span></td> <td>N-Hydroxymethylone</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>hydroxy</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk-MDEA.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Bk-MDEA.svg/120px-Bk-MDEA.svg.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Bk-MDEA.svg/180px-Bk-MDEA.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/65/Bk-MDEA.svg/240px-Bk-MDEA.svg.png 2x" data-file-width="379" data-file-height="189" /></a></span></td> <td><a href="/wiki/Ethylone" title="Ethylone">Ethylone</a></td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1112937-64-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Diethylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f7/Diethylone_structure.png/120px-Diethylone_structure.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f7/Diethylone_structure.png/180px-Diethylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f7/Diethylone_structure.png/240px-Diethylone_structure.png 2x" data-file-width="1239" data-file-height="644" /></a></span></td> <td>Diethylone</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>Et</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NAc-Ethylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e4/NAc-Ethylone_structure.png/120px-NAc-Ethylone_structure.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e4/NAc-Ethylone_structure.png/180px-NAc-Ethylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e4/NAc-Ethylone_structure.png/240px-NAc-Ethylone_structure.png 2x" data-file-width="1220" data-file-height="650" /></a></span></td> <td>N-Acetylethylone</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>acetyl</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkMDiP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/59/BkMDiP_structure.png/120px-BkMDiP_structure.png" decoding="async" width="120" height="56" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/59/BkMDiP_structure.png/180px-BkMDiP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/59/BkMDiP_structure.png/240px-BkMDiP_structure.png 2x" data-file-width="1233" data-file-height="575" /></a></span></td> <td>N-Isopropyl-βk-MDA</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>iPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkMDtB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/08/BkMDtB_structure.png/120px-BkMDtB_structure.png" decoding="async" width="120" height="56" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/08/BkMDtB_structure.png/180px-BkMDtB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/08/BkMDtB_structure.png/240px-BkMDtB_structure.png 2x" data-file-width="1219" data-file-height="564" /></a></span></td> <td>MDPT</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>t-Bu</td> <td>186028-84-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BMDP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/86/BMDP_structure.png/120px-BMDP_structure.png" decoding="async" width="120" height="53" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/86/BMDP_structure.png/180px-BMDP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/86/BMDP_structure.png/240px-BMDP_structure.png 2x" data-file-width="1494" data-file-height="654" /></a></span></td> <td><a href="/wiki/Benzylone" title="Benzylone">Benzylone</a> (BMDP)</td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>Bn</td> <td>1823274-68-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-Cyclohexylmethylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f3/N-Cyclohexylmethylone_structure.png/120px-N-Cyclohexylmethylone_structure.png" decoding="async" width="120" height="51" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f3/N-Cyclohexylmethylone_structure.png/180px-N-Cyclohexylmethylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f3/N-Cyclohexylmethylone_structure.png/240px-N-Cyclohexylmethylone_structure.png 2x" data-file-width="1493" data-file-height="639" /></a></span></td> <td><a href="/wiki/N-Cyclohexylmethylone" title="N-Cyclohexylmethylone">N-Cyclohexylmethylone</a></td> <td>3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>cyclohexyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-EDMC_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/ca/3%2C4-EDMC_structure.png/120px-3%2C4-EDMC_structure.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/ca/3%2C4-EDMC_structure.png/180px-3%2C4-EDMC_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/ca/3%2C4-EDMC_structure.png/240px-3%2C4-EDMC_structure.png 2x" data-file-width="1151" data-file-height="614" /></a></span></td> <td>3,4-EDMC</td> <td>3,4-ethylenedioxy</td> <td>Me</td> <td>H</td> <td>Me</td> <td>30253-44-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkIMP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/BkIMP_structure.png/120px-BkIMP_structure.png" decoding="async" width="120" height="63" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/BkIMP_structure.png/180px-BkIMP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d6/BkIMP_structure.png/240px-BkIMP_structure.png 2x" data-file-width="1118" data-file-height="591" /></a></span></td> <td>βk-IMP</td> <td>3,4-trimethylene</td> <td>Me</td> <td>H</td> <td>Me</td> <td>100608-69-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkIEB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c9/BkIEB_structure.png/120px-BkIEB_structure.png" decoding="async" width="120" height="55" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c9/BkIEB_structure.png/180px-BkIEB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c9/BkIEB_structure.png/240px-BkIEB_structure.png 2x" data-file-width="1246" data-file-height="575" /></a></span></td> <td>βk-IBP</td> <td>3,4-trimethylene</td> <td>Et</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkIEV_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e1/BkIEV_structure.png/120px-BkIEV_structure.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e1/BkIEV_structure.png/180px-BkIEV_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e1/BkIEV_structure.png/240px-BkIEV_structure.png 2x" data-file-width="1264" data-file-height="744" /></a></span></td> <td>βk-IVP</td> <td>3,4-trimethylene</td> <td>nPr</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-fluorobuphedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-fluorobuphedrone_structure.png/120px-3-fluorobuphedrone_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-fluorobuphedrone_structure.png/180px-3-fluorobuphedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-fluorobuphedrone_structure.png/240px-3-fluorobuphedrone_structure.png 2x" data-file-width="1025" data-file-height="579" /></a></span></td> <td>3-Fluorobuphedrone</td> <td>3-F</td> <td>Et</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-fluorobuphedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/32/4-fluorobuphedrone_structure.png/120px-4-fluorobuphedrone_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/32/4-fluorobuphedrone_structure.png/180px-4-fluorobuphedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/32/4-fluorobuphedrone_structure.png/240px-4-fluorobuphedrone_structure.png 2x" data-file-width="1034" data-file-height="596" /></a></span></td> <td>4-Fluorobuphedrone</td> <td>4-F</td> <td>Et</td> <td>H</td> <td>Me</td> <td>1368599-12-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-bromobuphedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/df/4-bromobuphedrone_structure.png/120px-4-bromobuphedrone_structure.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/df/4-bromobuphedrone_structure.png/180px-4-bromobuphedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/df/4-bromobuphedrone_structure.png/240px-4-bromobuphedrone_structure.png 2x" data-file-width="1036" data-file-height="601" /></a></span></td> <td>4-Bromobuphedrone</td> <td>4-Br</td> <td>Et</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-Methylbuphedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/60/3-Methylbuphedrone_structure.png/120px-3-Methylbuphedrone_structure.png" decoding="async" width="120" height="67" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/60/3-Methylbuphedrone_structure.png/180px-3-Methylbuphedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/60/3-Methylbuphedrone_structure.png/240px-3-Methylbuphedrone_structure.png 2x" data-file-width="1439" data-file-height="798" /></a></span></td> <td>3-Methylbuphedrone</td> <td>3-Me</td> <td>Et</td> <td>H</td> <td>Me</td> <td>1797911-07-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Methylbuphedrone.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/4-Methylbuphedrone.png/120px-4-Methylbuphedrone.png" decoding="async" width="120" height="74" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/4-Methylbuphedrone.png/180px-4-Methylbuphedrone.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9d/4-Methylbuphedrone.png/240px-4-Methylbuphedrone.png 2x" data-file-width="306" data-file-height="188" /></a></span></td> <td><a href="/wiki/4-Methylbuphedrone" title="4-Methylbuphedrone">4-Me-MABP</a></td> <td>4-Me</td> <td>Et</td> <td>H</td> <td>Me</td> <td>1336911-98-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Me-NEB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/4-Me-NEB_structure.png/120px-4-Me-NEB_structure.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/4-Me-NEB_structure.png/180px-4-Me-NEB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/13/4-Me-NEB_structure.png/240px-4-Me-NEB_structure.png 2x" data-file-width="1151" data-file-height="590" /></a></span></td> <td>4-Me-NEB</td> <td>4-Me</td> <td>Et</td> <td>H</td> <td>Et</td> <td>18268-19-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2F-NEB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/25/2F-NEB_structure.png/120px-2F-NEB_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/25/2F-NEB_structure.png/180px-2F-NEB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/25/2F-NEB_structure.png/240px-2F-NEB_structure.png 2x" data-file-width="1107" data-file-height="639" /></a></span></td> <td>2-F-NEB</td> <td>2-F</td> <td>Et</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3F-NEB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/51/3F-NEB_structure.png/120px-3F-NEB_structure.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/51/3F-NEB_structure.png/180px-3F-NEB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/51/3F-NEB_structure.png/240px-3F-NEB_structure.png 2x" data-file-width="1267" data-file-height="657" /></a></span></td> <td><a href="/wiki/3F-NEB" title="3F-NEB">3F-NEB</a></td> <td>3-F</td> <td>Et</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-F-NEB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/03/4-F-NEB_structure.png/120px-4-F-NEB_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/03/4-F-NEB_structure.png/180px-4-F-NEB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/03/4-F-NEB_structure.png/240px-4-F-NEB_structure.png 2x" data-file-width="1151" data-file-height="589" /></a></span></td> <td>4-F-NEB</td> <td>4-F</td> <td>Et</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Me-DMB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f6/4-Me-DMB_structure.png/120px-4-Me-DMB_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f6/4-Me-DMB_structure.png/180px-4-Me-DMB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f6/4-Me-DMB_structure.png/240px-4-Me-DMB_structure.png 2x" data-file-width="1011" data-file-height="580" /></a></span></td> <td>4-Me-DMB</td> <td>4-Me</td> <td>Et</td> <td>Me</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DMEB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9a/3%2C4-DMEB_structure.png/120px-3%2C4-DMEB_structure.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9a/3%2C4-DMEB_structure.png/180px-3%2C4-DMEB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9a/3%2C4-DMEB_structure.png/240px-3%2C4-DMEB_structure.png 2x" data-file-width="1145" data-file-height="588" /></a></span></td> <td>3,4-DMEB</td> <td>3,4-dimethyl</td> <td>Et</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-methoxybuphedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/72/4-methoxybuphedrone_structure.png/120px-4-methoxybuphedrone_structure.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/72/4-methoxybuphedrone_structure.png/180px-4-methoxybuphedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/72/4-methoxybuphedrone_structure.png/240px-4-methoxybuphedrone_structure.png 2x" data-file-width="1126" data-file-height="604" /></a></span></td> <td>4-Methoxybuphedrone</td> <td>4-MeO</td> <td>Et</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk-MBDB.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/30/Bk-MBDB.svg/120px-Bk-MBDB.svg.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/30/Bk-MBDB.svg/180px-Bk-MBDB.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/30/Bk-MBDB.svg/240px-Bk-MBDB.svg.png 2x" data-file-width="254" data-file-height="128" /></a></span></td> <td><a href="/wiki/Butylone" title="Butylone">Butylone</a></td> <td>3,4-methylenedioxy</td> <td>Et</td> <td>H</td> <td>Me</td> <td>802575-11-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Eutylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c9/Eutylone.svg/120px-Eutylone.svg.png" decoding="async" width="120" height="54" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c9/Eutylone.svg/180px-Eutylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c9/Eutylone.svg/240px-Eutylone.svg.png 2x" data-file-width="425" data-file-height="192" /></a></span></td> <td><a href="/wiki/Eutylone" title="Eutylone">Eutylone</a></td> <td>3,4-methylenedioxy</td> <td>Et</td> <td>H</td> <td>Et</td> <td>802855-66-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkPBDB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4f/BkPBDB_structure.png/120px-BkPBDB_structure.png" decoding="async" width="120" height="50" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4f/BkPBDB_structure.png/180px-BkPBDB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4f/BkPBDB_structure.png/240px-BkPBDB_structure.png 2x" data-file-width="1353" data-file-height="564" /></a></span></td> <td>βk-PBDB</td> <td>3,4-methylenedioxy</td> <td>Et</td> <td>H</td> <td>nPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bn-4-Me-MABP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/17/Bn-4-Me-MABP_structure.png/120px-Bn-4-Me-MABP_structure.png" decoding="async" width="120" height="53" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/17/Bn-4-Me-MABP_structure.png/180px-Bn-4-Me-MABP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/17/Bn-4-Me-MABP_structure.png/240px-Bn-4-Me-MABP_structure.png 2x" data-file-width="1416" data-file-height="629" /></a></span></td> <td>Bn-4-MeMABP</td> <td>4-Me</td> <td>Et</td> <td>H</td> <td>Bn</td> <td>1445751-39-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BMDB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/de/BMDB_structure.png/120px-BMDB_structure.png" decoding="async" width="120" height="52" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/de/BMDB_structure.png/180px-BMDB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/de/BMDB_structure.png/240px-BMDB_structure.png 2x" data-file-width="1491" data-file-height="647" /></a></span></td> <td>BMDB</td> <td>3,4-methylenedioxy</td> <td>Et</td> <td>H</td> <td>Bn</td> <td>1445751-47-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-Cyclohexylbutylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/3b/N-Cyclohexylbutylone_structure.png/120px-N-Cyclohexylbutylone_structure.png" decoding="async" width="120" height="52" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/3b/N-Cyclohexylbutylone_structure.png/180px-N-Cyclohexylbutylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/3b/N-Cyclohexylbutylone_structure.png/240px-N-Cyclohexylbutylone_structure.png 2x" data-file-width="1469" data-file-height="639" /></a></span></td> <td>N-Cyclohexylbutylone</td> <td>3,4-methylenedioxy</td> <td>Et</td> <td>H</td> <td>cyclohexyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Dibutylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/Dibutylone.svg/120px-Dibutylone.svg.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/Dibutylone.svg/180px-Dibutylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/04/Dibutylone.svg/240px-Dibutylone.svg.png 2x" data-file-width="512" data-file-height="257" /></a></span></td> <td><a href="/wiki/Dibutylone" title="Dibutylone">βk-DMBDB</a></td> <td>3,4-methylenedioxy</td> <td>Et</td> <td>Me</td> <td>Me</td> <td>802286-83-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkMMDMA_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/BkMMDMA_structure.png/120px-BkMMDMA_structure.png" decoding="async" width="120" height="89" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2e/BkMMDMA_structure.png/180px-BkMMDMA_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2e/BkMMDMA_structure.png/240px-BkMMDMA_structure.png 2x" data-file-width="406" data-file-height="302" /></a></span></td> <td><a href="/wiki/5-Methoxymethylone" title="5-Methoxymethylone">βk-MMDMA</a></td> <td>3,4-methylenedioxy-5-MeO</td> <td>Me</td> <td>H</td> <td>Me</td> <td>2230716-98-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-methoxymethylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/50/2-methoxymethylone_structure.png/120px-2-methoxymethylone_structure.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/50/2-methoxymethylone_structure.png/180px-2-methoxymethylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/50/2-methoxymethylone_structure.png/240px-2-methoxymethylone_structure.png 2x" data-file-width="1092" data-file-height="627" /></a></span></td> <td>βk-MMDMA-2</td> <td>2-MeO-3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BkDMMDA_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/BkDMMDA_structure.png/120px-BkDMMDA_structure.png" decoding="async" width="120" height="92" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/04/BkDMMDA_structure.png/180px-BkDMMDA_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/04/BkDMMDA_structure.png/240px-BkDMMDA_structure.png 2x" data-file-width="1106" data-file-height="851" /></a></span></td> <td>βk-DMMDA</td> <td>2,5-diMeO-3,4-methylenedioxy</td> <td>Me</td> <td>H</td> <td>H</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-methylmethylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/96/5-methylmethylone_structure.png/120px-5-methylmethylone_structure.png" decoding="async" width="120" height="80" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/96/5-methylmethylone_structure.png/180px-5-methylmethylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/96/5-methylmethylone_structure.png/240px-5-methylmethylone_structure.png 2x" data-file-width="1121" data-file-height="744" /></a></span></td> <td>5-Methylmethylone</td> <td>3,4-methylenedioxy-5-Me</td> <td>Me</td> <td>H</td> <td>Me</td> <td>1364933-83-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-Methylethylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/5-Methylethylone.svg/120px-5-Methylethylone.svg.png" decoding="async" width="120" height="79" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/5-Methylethylone.svg/180px-5-Methylethylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9d/5-Methylethylone.svg/240px-5-Methylethylone.svg.png 2x" data-file-width="1140" data-file-height="750" /></a></span></td> <td><a href="/wiki/5-Methylethylone" title="5-Methylethylone">5-Methylethylone</a></td> <td>3,4-methylenedioxy-5-Me</td> <td>Me</td> <td>H</td> <td>Et</td> <td>1364933-82-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-methylbutylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8e/2-methylbutylone_structure.png/120px-2-methylbutylone_structure.png" decoding="async" width="120" height="63" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8e/2-methylbutylone_structure.png/180px-2-methylbutylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8e/2-methylbutylone_structure.png/240px-2-methylbutylone_structure.png 2x" data-file-width="1129" data-file-height="596" /></a></span></td> <td>2-Methylbutylone</td> <td>2-Me-3,4-methylenedioxy</td> <td>Et</td> <td>H</td> <td>Me</td> <td>1364933-86-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-methylbutylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d9/5-methylbutylone_structure.png/120px-5-methylbutylone_structure.png" decoding="async" width="120" height="79" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d9/5-methylbutylone_structure.png/180px-5-methylbutylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d9/5-methylbutylone_structure.png/240px-5-methylbutylone_structure.png 2x" data-file-width="1113" data-file-height="731" /></a></span></td> <td>5-Methylbutylone</td> <td>3,4-methylenedioxy-5-Me</td> <td>Et</td> <td>H</td> <td>Me</td> <td>1354631-29-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Pentylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/85/Pentylone.svg/120px-Pentylone.svg.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/85/Pentylone.svg/180px-Pentylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/85/Pentylone.svg/240px-Pentylone.svg.png 2x" data-file-width="377" data-file-height="240" /></a></span></td> <td><a href="/wiki/Pentylone" title="Pentylone">Pentylone</a></td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td>H</td> <td>Me</td> <td>698963-77-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-Ethylpentylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/N-Ethylpentylone.svg/120px-N-Ethylpentylone.svg.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/N-Ethylpentylone.svg/180px-N-Ethylpentylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2b/N-Ethylpentylone.svg/240px-N-Ethylpentylone.svg.png 2x" data-file-width="565" data-file-height="325" /></a></span></td> <td><a href="/wiki/N-Ethylpentylone" title="N-Ethylpentylone">N-Ethylpentylone</a></td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td>H</td> <td>Et</td> <td>727641-67-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-propylpentylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/27/N-propylpentylone_structure.png/120px-N-propylpentylone_structure.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/27/N-propylpentylone_structure.png/180px-N-propylpentylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/27/N-propylpentylone_structure.png/240px-N-propylpentylone_structure.png 2x" data-file-width="1391" data-file-height="738" /></a></span></td> <td>N-propylpentylone</td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td>H</td> <td>nPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-butylpentylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/N-butylpentylone_structure.png/120px-N-butylpentylone_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9d/N-butylpentylone_structure.png/180px-N-butylpentylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9d/N-butylpentylone_structure.png/240px-N-butylpentylone_structure.png 2x" data-file-width="1490" data-file-height="747" /></a></span></td> <td>N-butylpentylone</td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td>H</td> <td>nBu</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,3-Dipentylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/62/2%2C3-Dipentylone_structure.png/120px-2%2C3-Dipentylone_structure.png" decoding="async" width="120" height="85" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/62/2%2C3-Dipentylone_structure.png/180px-2%2C3-Dipentylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/62/2%2C3-Dipentylone_structure.png/240px-2%2C3-Dipentylone_structure.png 2x" data-file-width="1105" data-file-height="785" /></a></span></td> <td>2,3-Dipentylone</td> <td>2,3-methylenedioxy</td> <td>nPr</td> <td>Me</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Dipentylone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/11/Dipentylone.svg/120px-Dipentylone.svg.png" decoding="async" width="120" height="78" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/11/Dipentylone.svg/180px-Dipentylone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/11/Dipentylone.svg/240px-Dipentylone.svg.png 2x" data-file-width="500" data-file-height="325" /></a></span></td> <td><a href="/wiki/Dipentylone" title="Dipentylone">Dipentylone</a></td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td>Me</td> <td>Me</td> <td>17763-13-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:NN-diethyl-pentylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/06/NN-diethyl-pentylone_structure.png/120px-NN-diethyl-pentylone_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/06/NN-diethyl-pentylone_structure.png/180px-NN-diethyl-pentylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/06/NN-diethyl-pentylone_structure.png/240px-NN-diethyl-pentylone_structure.png 2x" data-file-width="1323" data-file-height="829" /></a></span></td> <td>N,N-Diethylnorpentylone</td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td>Et</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Hexylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/Hexylone_structure.png/120px-Hexylone_structure.png" decoding="async" width="120" height="85" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/Hexylone_structure.png/180px-Hexylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/ff/Hexylone_structure.png/240px-Hexylone_structure.png 2x" data-file-width="1145" data-file-height="813" /></a></span></td> <td>Hexylone</td> <td>3,4-methylenedioxy</td> <td>nBu</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Isohexylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/16/Isohexylone_structure.png/120px-Isohexylone_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/16/Isohexylone_structure.png/180px-Isohexylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/16/Isohexylone_structure.png/240px-Isohexylone_structure.png 2x" data-file-width="1221" data-file-height="775" /></a></span></td> <td><a href="/wiki/Isohexylone" title="Isohexylone">Isohexylone</a></td> <td>3,4-methylenedioxy</td> <td>iBu</td> <td>H</td> <td>Me</td> <td>1157947-89-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Isoheptylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/bd/Isoheptylone_structure.png/120px-Isoheptylone_structure.png" decoding="async" width="120" height="88" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/bd/Isoheptylone_structure.png/180px-Isoheptylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/bd/Isoheptylone_structure.png/240px-Isoheptylone_structure.png 2x" data-file-width="1212" data-file-height="886" /></a></span></td> <td>Isoheptylone</td> <td>3,4-methylenedioxy</td> <td>iPe</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-ethylhexylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c5/N-ethylhexylone_structure.png/120px-N-ethylhexylone_structure.png" decoding="async" width="120" height="77" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c5/N-ethylhexylone_structure.png/180px-N-ethylhexylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c5/N-ethylhexylone_structure.png/240px-N-ethylhexylone_structure.png 2x" data-file-width="1263" data-file-height="813" /></a></span></td> <td><a href="/wiki/N-Ethylhexylone" title="N-Ethylhexylone">N-Ethylhexylone</a></td> <td>3,4-methylenedioxy</td> <td>nBu</td> <td>H</td> <td>Et</td> <td>27912-41-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:N-ethylheptylone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d8/N-ethylheptylone_structure.png/120px-N-ethylheptylone_structure.png" decoding="async" width="120" height="91" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d8/N-ethylheptylone_structure.png/180px-N-ethylheptylone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d8/N-ethylheptylone_structure.png/240px-N-ethylheptylone_structure.png 2x" data-file-width="1270" data-file-height="968" /></a></span></td> <td><a href="/wiki/N-Ethylheptylone" title="N-Ethylheptylone">N-Ethylheptylone</a></td> <td>3,4-methylenedioxy</td> <td>nPe</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MEAP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-MEAP.svg/120px-4-MEAP.svg.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-MEAP.svg/180px-4-MEAP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/ff/4-MEAP.svg/240px-4-MEAP.svg.png 2x" data-file-width="990" data-file-height="625" /></a></span></td> <td><a href="/wiki/4-Methyl-%CE%B1-ethylaminopentiophenone" title="4-Methyl-α-ethylaminopentiophenone">4-MEAP</a></td> <td>4-Me</td> <td>nPr</td> <td>H</td> <td>Et</td> <td>746540-82-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DMEP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/99/3%2C4-DMEP_structure.png/120px-3%2C4-DMEP_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/99/3%2C4-DMEP_structure.png/180px-3%2C4-DMEP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/99/3%2C4-DMEP_structure.png/240px-3%2C4-DMEP_structure.png 2x" data-file-width="1152" data-file-height="729" /></a></span></td> <td>3,4-DMEP</td> <td>3,4-dimethyl</td> <td>nPr</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2F-Pentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/ba/2F-Pentedrone_structure.png/120px-2F-Pentedrone_structure.png" decoding="async" width="120" height="98" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/ba/2F-Pentedrone_structure.png/180px-2F-Pentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/ba/2F-Pentedrone_structure.png/240px-2F-Pentedrone_structure.png 2x" data-file-width="963" data-file-height="783" /></a></span></td> <td>2-F-Pentedrone</td> <td>2-F</td> <td>nPr</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3F-Pentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/fe/3F-Pentedrone_structure.png/120px-3F-Pentedrone_structure.png" decoding="async" width="120" height="85" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/fe/3F-Pentedrone_structure.png/180px-3F-Pentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/fe/3F-Pentedrone_structure.png/240px-3F-Pentedrone_structure.png 2x" data-file-width="1119" data-file-height="789" /></a></span></td> <td>3-F-Pentedrone</td> <td>3-F</td> <td>nPr</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-fluoropentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/ae/4-fluoropentedrone_structure.png/120px-4-fluoropentedrone_structure.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/ae/4-fluoropentedrone_structure.png/180px-4-fluoropentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/ae/4-fluoropentedrone_structure.png/240px-4-fluoropentedrone_structure.png 2x" data-file-width="1020" data-file-height="714" /></a></span></td> <td>4-F-Pentedrone</td> <td>4-F</td> <td>nPr</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-chloropentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/73/4-chloropentedrone_structure.png/120px-4-chloropentedrone_structure.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/73/4-chloropentedrone_structure.png/180px-4-chloropentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/73/4-chloropentedrone_structure.png/240px-4-chloropentedrone_structure.png 2x" data-file-width="1050" data-file-height="733" /></a></span></td> <td>4-Cl-Pentedrone</td> <td>4-Cl</td> <td>nPr</td> <td>H</td> <td>Me</td> <td>2167949-43-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Methylpentedrone.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/4-Methylpentedrone.png/120px-4-Methylpentedrone.png" decoding="async" width="120" height="90" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d1/4-Methylpentedrone.png/180px-4-Methylpentedrone.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d1/4-Methylpentedrone.png/240px-4-Methylpentedrone.png 2x" data-file-width="306" data-file-height="230" /></a></span></td> <td><a href="/wiki/4-Methylpentedrone" title="4-Methylpentedrone">4-Methylpentedrone</a></td> <td>4-Me</td> <td>nPr</td> <td>H</td> <td>Me</td> <td>1373918-61-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:DL-4662_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/ac/DL-4662_structure.png/120px-DL-4662_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/ac/DL-4662_structure.png/180px-DL-4662_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/ac/DL-4662_structure.png/240px-DL-4662_structure.png 2x" data-file-width="1277" data-file-height="727" /></a></span></td> <td>DL-4662</td> <td>3,4-dimethoxy</td> <td>nPr</td> <td>H</td> <td>Et</td> <td>1674389-55-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4F-NiP-pentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/fb/4F-NiP-pentedrone_structure.png/120px-4F-NiP-pentedrone_structure.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/fb/4F-NiP-pentedrone_structure.png/180px-4F-NiP-pentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/fb/4F-NiP-pentedrone_structure.png/240px-4F-NiP-pentedrone_structure.png 2x" data-file-width="1152" data-file-height="701" /></a></span></td> <td>4-F-iPr-norpentedrone</td> <td>4-F</td> <td>nPr</td> <td>H</td> <td>iPr</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4Cl-NtB-pentedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/14/4Cl-NtB-pentedrone_structure.png/120px-4Cl-NtB-pentedrone_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/14/4Cl-NtB-pentedrone_structure.png/180px-4Cl-NtB-pentedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/14/4Cl-NtB-pentedrone_structure.png/240px-4Cl-NtB-pentedrone_structure.png 2x" data-file-width="1164" data-file-height="728" /></a></span></td> <td>3-CBV</td> <td>3-Cl</td> <td>nPr</td> <td>H</td> <td>tBu</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-methylhexedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/4-methylhexedrone_structure.png/120px-4-methylhexedrone_structure.png" decoding="async" width="120" height="96" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/4-methylhexedrone_structure.png/180px-4-methylhexedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/13/4-methylhexedrone_structure.png/240px-4-methylhexedrone_structure.png 2x" data-file-width="1002" data-file-height="799" /></a></span></td> <td>4-methylhexedrone</td> <td>4-Me</td> <td>nBu</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-methyl-N-ethylhexedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/52/4-methyl-N-ethylhexedrone_structure.png/120px-4-methyl-N-ethylhexedrone_structure.png" decoding="async" width="120" height="82" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/52/4-methyl-N-ethylhexedrone_structure.png/180px-4-methyl-N-ethylhexedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/52/4-methyl-N-ethylhexedrone_structure.png/240px-4-methyl-N-ethylhexedrone_structure.png 2x" data-file-width="1162" data-file-height="791" /></a></span></td> <td>MEH</td> <td>4-Me</td> <td>nBu</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3F-NEH_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/61/3F-NEH_structure.png/120px-3F-NEH_structure.png" decoding="async" width="120" height="82" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/61/3F-NEH_structure.png/180px-3F-NEH_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/61/3F-NEH_structure.png/240px-3F-NEH_structure.png 2x" data-file-width="1229" data-file-height="839" /></a></span></td> <td><a href="/wiki/3F-NEH" title="3F-NEH">3F-NEH</a></td> <td>3-F</td> <td>nBu</td> <td>H</td> <td>Et</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-fluorohexedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/fa/4-fluorohexedrone_structure.png/120px-4-fluorohexedrone_structure.png" decoding="async" width="120" height="92" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/fa/4-fluorohexedrone_structure.png/180px-4-fluorohexedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/fa/4-fluorohexedrone_structure.png/240px-4-fluorohexedrone_structure.png 2x" data-file-width="1053" data-file-height="807" /></a></span></td> <td>4-F-hexedrone</td> <td>4-F</td> <td>nBu</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-fluorooctedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/80/4-fluorooctedrone_structure.png/120px-4-fluorooctedrone_structure.png" decoding="async" width="120" height="105" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/80/4-fluorooctedrone_structure.png/180px-4-fluorooctedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/80/4-fluorooctedrone_structure.png/240px-4-fluorooctedrone_structure.png 2x" data-file-width="978" data-file-height="853" /></a></span></td> <td>4-F-octedrone</td> <td>4-F</td> <td>hexyl</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-phenylmephedrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6b/Alpha-phenylmephedrone_structure.png/120px-Alpha-phenylmephedrone_structure.png" decoding="async" width="120" height="97" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6b/Alpha-phenylmephedrone_structure.png/180px-Alpha-phenylmephedrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6b/Alpha-phenylmephedrone_structure.png/240px-Alpha-phenylmephedrone_structure.png 2x" data-file-width="996" data-file-height="803" /></a></span></td> <td>α-phenylmephedrone</td> <td>4-Me</td> <td>phenyl</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk-EPE_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Bk-EPE_structure.png/120px-Bk-EPE_structure.png" decoding="async" width="120" height="94" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Bk-EPE_structure.png/180px-Bk-EPE_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Bk-EPE_structure.png/240px-Bk-EPE_structure.png 2x" data-file-width="994" data-file-height="782" /></a></span></td> <td><a href="/wiki/2-(Ethylamino)-1,2-diphenylethanone" title="2-(Ethylamino)-1,2-diphenylethanone">βk-Ephenidine</a></td> <td>H</td> <td>phenyl</td> <td>H</td> <td>Et</td> <td>22312-16-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk-methamnetamine.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/98/Bk-methamnetamine.svg/120px-Bk-methamnetamine.svg.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/98/Bk-methamnetamine.svg/180px-Bk-methamnetamine.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/98/Bk-methamnetamine.svg/240px-Bk-methamnetamine.svg.png 2x" data-file-width="515" data-file-height="255" /></a></span></td> <td><a href="/wiki/BMAPN" title="BMAPN">BMAPN</a></td> <td>β-naphthyl instead of phenyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Thiothinone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8d/Thiothinone.svg/120px-Thiothinone.svg.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8d/Thiothinone.svg/180px-Thiothinone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8d/Thiothinone.svg/240px-Thiothinone.svg.png 2x" data-file-width="512" data-file-height="296" /></a></span></td> <td><a href="/wiki/Thiothinone" title="Thiothinone">βk-Methiopropamine</a></td> <td>thiophen-2-yl instead of phenyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td>24065-17-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5ClbkMPA_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/62/5ClbkMPA_structure.png/120px-5ClbkMPA_structure.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/62/5ClbkMPA_structure.png/180px-5ClbkMPA_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/62/5ClbkMPA_structure.png/240px-5ClbkMPA_structure.png 2x" data-file-width="1151" data-file-height="616" /></a></span></td> <td><a href="/wiki/5-Cl-bk-MPA" title="5-Cl-bk-MPA">5-Cl-bk-MPA</a></td> <td>5-chlorothiophen-2-yl instead of phenyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk-5-MAPB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e9/Bk-5-MAPB_structure.png/120px-Bk-5-MAPB_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e9/Bk-5-MAPB_structure.png/180px-Bk-5-MAPB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e9/Bk-5-MAPB_structure.png/240px-Bk-5-MAPB_structure.png 2x" data-file-width="1109" data-file-height="566" /></a></span></td> <td><a href="/wiki/BK-5-MAPB" title="BK-5-MAPB">βk-5-MAPB</a></td> <td>benzofuran-5-yl instead of phenyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk-6-MAPB_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/3d/Bk-6-MAPB_structure.png/120px-Bk-6-MAPB_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/3d/Bk-6-MAPB_structure.png/180px-Bk-6-MAPB_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/3d/Bk-6-MAPB_structure.png/240px-Bk-6-MAPB_structure.png 2x" data-file-width="1105" data-file-height="557" /></a></span></td> <td>βk-6-MAPB</td> <td>benzofuran-6-yl instead of phenyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Bk-5-IT_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/Bk-5-IT_structure.png/120px-Bk-5-IT_structure.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/b9/Bk-5-IT_structure.png/180px-Bk-5-IT_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/b9/Bk-5-IT_structure.png/240px-Bk-5-IT_structure.png 2x" data-file-width="1094" data-file-height="663" /></a></span></td> <td>βk-5-IT</td> <td>indol-5-yl instead of phenyl</td> <td>Me</td> <td>H</td> <td>H</td> <td>1369231-36-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:BK-5F-NM-AMT_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/62/BK-5F-NM-AMT_structure.png/120px-BK-5F-NM-AMT_structure.png" decoding="async" width="120" height="98" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/62/BK-5F-NM-AMT_structure.png/180px-BK-5F-NM-AMT_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/62/BK-5F-NM-AMT_structure.png/240px-BK-5F-NM-AMT_structure.png 2x" data-file-width="1114" data-file-height="910" /></a></span></td> <td>βk-5F-NM-AMT<sup id="cite_ref-38" class="reference"><a href="#cite_note-38"><span class="cite-bracket">&#91;</span>38<span class="cite-bracket">&#93;</span></a></sup></td> <td>5-fluoroindol-3-yl instead of phenyl</td> <td>Me</td> <td>H</td> <td>Me</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Phthalprop.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6a/Phthalprop.svg/120px-Phthalprop.svg.png" decoding="async" width="120" height="72" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6a/Phthalprop.svg/180px-Phthalprop.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6a/Phthalprop.svg/240px-Phthalprop.svg.png 2x" data-file-width="206" data-file-height="124" /></a></span></td> <td><a href="/wiki/%CE%91-Phthalimidopropiophenone" class="mw-redirect" title="Α-Phthalimidopropiophenone">α-Phthalimidopropiophenone</a></td> <td>H</td> <td>Me</td> <td colspan="2">phthalimido</td> <td>19437-20-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:PPPO_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e0/PPPO_structure.png/120px-PPPO_structure.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e0/PPPO_structure.png/180px-PPPO_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e0/PPPO_structure.png/240px-PPPO_structure.png 2x" data-file-width="1013" data-file-height="616" /></a></span></td> <td>PPPO</td> <td>H</td> <td>Me</td> <td colspan="2">piperidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:PPBO_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/ec/PPBO_structure.png/120px-PPBO_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/ec/PPBO_structure.png/180px-PPBO_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/ec/PPBO_structure.png/240px-PPBO_structure.png 2x" data-file-width="1004" data-file-height="624" /></a></span></td> <td>PPBO</td> <td>H</td> <td>Et</td> <td colspan="2">piperidinyl</td> <td>92728-82-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:FPPVO_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7a/FPPVO_structure.png/120px-FPPVO_structure.png" decoding="async" width="120" height="80" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7a/FPPVO_structure.png/180px-FPPVO_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7a/FPPVO_structure.png/240px-FPPVO_structure.png 2x" data-file-width="1142" data-file-height="764" /></a></span></td> <td>FPPVO</td> <td>4-F</td> <td>nPr</td> <td colspan="2">piperidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-Pr-PipVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a1/3%2C4-Pr-PipVP_structure.png/120px-3%2C4-Pr-PipVP_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a1/3%2C4-Pr-PipVP_structure.png/180px-3%2C4-Pr-PipVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a1/3%2C4-Pr-PipVP_structure.png/240px-3%2C4-Pr-PipVP_structure.png 2x" data-file-width="1323" data-file-height="828" /></a></span></td> <td><a href="/wiki/3,4-Pr-PipVP" title="3,4-Pr-PipVP">3,4-Pr-PipVP</a></td> <td>3,4-trimethylene</td> <td>nPr</td> <td colspan="2">piperidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPV-azepane_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/40/MDPV-azepane_structure.png/120px-MDPV-azepane_structure.png" decoding="async" width="120" height="72" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/40/MDPV-azepane_structure.png/180px-MDPV-azepane_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/40/MDPV-azepane_structure.png/240px-MDPV-azepane_structure.png 2x" data-file-width="1297" data-file-height="782" /></a></span></td> <td>MDPV-azepane</td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td colspan="2"><a href="/wiki/Azepane" title="Azepane">azepane</a></td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Caccure907_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/bd/Caccure907_structure.png/120px-Caccure907_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/bd/Caccure907_structure.png/180px-Caccure907_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/bd/Caccure907_structure.png/240px-Caccure907_structure.png 2x" data-file-width="1279" data-file-height="655" /></a></span></td> <td>Caccure 907</td> <td>4-SCH<sub>3</sub></td> <td>α,α-di-Me</td> <td colspan="2">morpholinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:A-PPP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/be/A-PPP.svg/120px-A-PPP.svg.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/be/A-PPP.svg/180px-A-PPP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/be/A-PPP.svg/240px-A-PPP.svg.png 2x" data-file-width="512" data-file-height="298" /></a></span></td> <td><a href="/wiki/Alpha-Pyrrolidinopropiophenone" class="mw-redirect" title="Alpha-Pyrrolidinopropiophenone">α-PPP</a></td> <td>H</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>19134-50-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:%CE%91-PBP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0c/%CE%91-PBP.svg/120px-%CE%91-PBP.svg.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0c/%CE%91-PBP.svg/180px-%CE%91-PBP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0c/%CE%91-PBP.svg/240px-%CE%91-PBP.svg.png 2x" data-file-width="512" data-file-height="298" /></a></span></td> <td><a href="/wiki/Alpha-Pyrrolidinobutiophenone" class="mw-redirect" title="Alpha-Pyrrolidinobutiophenone">α-PBP</a></td> <td>H</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td>13415-54-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-Pyrrolidinopentiophenone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c2/Alpha-Pyrrolidinopentiophenone.svg/120px-Alpha-Pyrrolidinopentiophenone.svg.png" decoding="async" width="120" height="88" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c2/Alpha-Pyrrolidinopentiophenone.svg/180px-Alpha-Pyrrolidinopentiophenone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c2/Alpha-Pyrrolidinopentiophenone.svg/240px-Alpha-Pyrrolidinopentiophenone.svg.png 2x" data-file-width="512" data-file-height="375" /></a></span></td> <td><a href="/wiki/Alpha-Pyrrolidinopentiophenone" class="mw-redirect" title="Alpha-Pyrrolidinopentiophenone">α-PVP</a> (O-2387)</td> <td>H</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>14530-33-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:%CE%91-PHP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/%CE%91-PHP.svg/120px-%CE%91-PHP.svg.png" decoding="async" width="120" height="98" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/%CE%91-PHP.svg/180px-%CE%91-PHP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/24/%CE%91-PHP.svg/240px-%CE%91-PHP.svg.png 2x" data-file-width="512" data-file-height="416" /></a></span></td> <td><a href="/wiki/Alpha-Pyrrolidinohexiophenone" class="mw-redirect" title="Alpha-Pyrrolidinohexiophenone">α-PHP</a></td> <td>H</td> <td><a href="/wiki/Butyl" class="mw-redirect" title="Butyl">nBu</a></td> <td colspan="2">pyrrolidinyl</td> <td>13415-86-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-PHiP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0b/Alpha-PHiP_structure.png/120px-Alpha-PHiP_structure.png" decoding="async" width="120" height="88" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0b/Alpha-PHiP_structure.png/180px-Alpha-PHiP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0b/Alpha-PHiP_structure.png/240px-Alpha-PHiP_structure.png 2x" data-file-width="983" data-file-height="724" /></a></span></td> <td><a href="/wiki/%CE%91-PHiP" title="Α-PHiP">α-PHiP</a></td> <td>H</td> <td>iBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-Pyrrolidinoheptaphenone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/29/Alpha-Pyrrolidinoheptaphenone.svg/120px-Alpha-Pyrrolidinoheptaphenone.svg.png" decoding="async" width="120" height="117" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/29/Alpha-Pyrrolidinoheptaphenone.svg/180px-Alpha-Pyrrolidinoheptaphenone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/29/Alpha-Pyrrolidinoheptaphenone.svg/240px-Alpha-Pyrrolidinoheptaphenone.svg.png 2x" data-file-width="850" data-file-height="830" /></a></span></td> <td><a href="/wiki/%CE%91-Pyrrolidinoheptaphenone" title="Α-Pyrrolidinoheptaphenone">α-PEP</a> (α-PHPP)</td> <td>H</td> <td><a href="/wiki/Pentyl" class="mw-redirect" title="Pentyl">nPe</a></td> <td colspan="2">pyrrolidinyl</td> <td>13415-83-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-POP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/38/Alpha-POP_structure.png/120px-Alpha-POP_structure.png" decoding="async" width="120" height="120" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/38/Alpha-POP_structure.png/180px-Alpha-POP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/38/Alpha-POP_structure.png/240px-Alpha-POP_structure.png 2x" data-file-width="854" data-file-height="856" /></a></span></td> <td>α-POP</td> <td>H</td> <td><a href="/wiki/Hexyl" class="mw-redirect" title="Hexyl">hexyl</a></td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-PNP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/Alpha-PNP_structure.png/120px-Alpha-PNP_structure.png" decoding="async" width="120" height="139" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/Alpha-PNP_structure.png/180px-Alpha-PNP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2b/Alpha-PNP_structure.png/240px-Alpha-PNP_structure.png 2x" data-file-width="739" data-file-height="854" /></a></span></td> <td>α-PNP</td> <td>H</td> <td><a href="/wiki/Heptyl" class="mw-redirect" title="Heptyl">heptyl</a></td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Diphenylpyrrolidinylethanone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/Diphenylpyrrolidinylethanone_structure.png/120px-Diphenylpyrrolidinylethanone_structure.png" decoding="async" width="120" height="95" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c3/Diphenylpyrrolidinylethanone_structure.png/180px-Diphenylpyrrolidinylethanone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c3/Diphenylpyrrolidinylethanone_structure.png/240px-Diphenylpyrrolidinylethanone_structure.png 2x" data-file-width="977" data-file-height="773" /></a></span></td> <td>DPPE (<a href="/wiki/Alpha-D2PV" class="mw-redirect" title="Alpha-D2PV">Alpha-D2PV</a>)</td> <td>H</td> <td>phenyl</td> <td colspan="2">pyrrolidinyl</td> <td>27590-61-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-PcPeP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f2/Alpha-PcPeP_structure.png/120px-Alpha-PcPeP_structure.png" decoding="async" width="120" height="87" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f2/Alpha-PcPeP_structure.png/180px-Alpha-PcPeP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f2/Alpha-PcPeP_structure.png/240px-Alpha-PcPeP_structure.png 2x" data-file-width="971" data-file-height="705" /></a></span></td> <td>α-PcPeP</td> <td>H</td> <td><a href="/wiki/Cyclopentyl" class="mw-redirect" title="Cyclopentyl">cyclopentyl</a></td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-PCYP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2a/Alpha-PCYP_structure.png/120px-Alpha-PCYP_structure.png" decoding="async" width="120" height="97" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2a/Alpha-PCYP_structure.png/180px-Alpha-PCYP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2a/Alpha-PCYP_structure.png/240px-Alpha-PCYP_structure.png 2x" data-file-width="740" data-file-height="600" /></a></span></td> <td><a href="/wiki/%CE%91-PCYP" title="Α-PCYP">α-PCYP</a></td> <td>H</td> <td><a href="/wiki/Cyclohexyl" class="mw-redirect" title="Cyclohexyl">cyclohexyl</a></td> <td colspan="2">pyrrolidinyl</td> <td>1803168-11-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2-Me-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0b/2-Me-PPP_structure.png/120px-2-Me-PPP_structure.png" decoding="async" width="120" height="68" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0b/2-Me-PPP_structure.png/180px-2-Me-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0b/2-Me-PPP_structure.png/240px-2-Me-PPP_structure.png 2x" data-file-width="979" data-file-height="554" /></a></span></td> <td>2-MePPP</td> <td>2-Me</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>2092429-83-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-Me-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/3-Me-PPP_structure.png/120px-3-Me-PPP_structure.png" decoding="async" width="120" height="63" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/21/3-Me-PPP_structure.png/180px-3-Me-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/21/3-Me-PPP_structure.png/240px-3-Me-PPP_structure.png 2x" data-file-width="1081" data-file-height="566" /></a></span></td> <td>3-MePPP</td> <td>3-Me</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>1214940-01-8 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:PMPPP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/PMPPP.svg/120px-PMPPP.svg.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/PMPPP.svg/180px-PMPPP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7f/PMPPP.svg/240px-PMPPP.svg.png 2x" data-file-width="512" data-file-height="264" /></a></span></td> <td><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinopropiophenone" title="4&#39;-Methyl-α-pyrrolidinopropiophenone">4-MePPP</a></td> <td>4-Me</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>1313393-58-6 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3MeO-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6b/3MeO-PPP_structure.png/120px-3MeO-PPP_structure.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6b/3MeO-PPP_structure.png/180px-3MeO-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6b/3MeO-PPP_structure.png/240px-3MeO-PPP_structure.png 2x" data-file-width="1221" data-file-height="635" /></a></span></td> <td>3-MeO-PPP</td> <td>3-MeO</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MOPPP_SVG.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/87/MOPPP_SVG.svg/120px-MOPPP_SVG.svg.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/87/MOPPP_SVG.svg/180px-MOPPP_SVG.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/87/MOPPP_SVG.svg/240px-MOPPP_SVG.svg.png 2x" data-file-width="512" data-file-height="250" /></a></span></td> <td><a href="/wiki/4%27-Methoxy-%CE%B1-pyrrolidinopropiophenone" title="4&#39;-Methoxy-α-pyrrolidinopropiophenone">MOPPP</a></td> <td>4-MeO</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>478243-09-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-F-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/53/3-F-PPP_structure.png/120px-3-F-PPP_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/53/3-F-PPP_structure.png/180px-3-F-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/53/3-F-PPP_structure.png/240px-3-F-PPP_structure.png 2x" data-file-width="1109" data-file-height="560" /></a></span></td> <td>3-F-PPP</td> <td>3-F</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>1214939-99-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-F-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a5/4-F-PPP_structure.png/120px-4-F-PPP_structure.png" decoding="async" width="120" height="65" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a5/4-F-PPP_structure.png/180px-4-F-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a5/4-F-PPP_structure.png/240px-4-F-PPP_structure.png 2x" data-file-width="1131" data-file-height="613" /></a></span></td> <td>FPPP</td> <td>4-F</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>28117-76-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Cl-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1f/4-Cl-PPP_structure.png/120px-4-Cl-PPP_structure.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1f/4-Cl-PPP_structure.png/180px-4-Cl-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1f/4-Cl-PPP_structure.png/240px-4-Cl-PPP_structure.png 2x" data-file-width="1126" data-file-height="598" /></a></span></td> <td>Cl-PPP</td> <td>4-Cl</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>93307-24-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-Br-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/39/3-Br-PPP_structure.png/120px-3-Br-PPP_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/39/3-Br-PPP_structure.png/180px-3-Br-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/39/3-Br-PPP_structure.png/240px-3-Br-PPP_structure.png 2x" data-file-width="1307" data-file-height="666" /></a></span></td> <td>3-Br-PPP</td> <td>3-Br</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4Br-PPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/4Br-PPP_structure.png/120px-4Br-PPP_structure.png" decoding="async" width="120" height="64" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/1e/4Br-PPP_structure.png/180px-4Br-PPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/1e/4Br-PPP_structure.png/240px-4Br-PPP_structure.png 2x" data-file-width="1275" data-file-height="677" /></a></span></td> <td>Br-PPP</td> <td>4-Br</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,3-DMPPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/ca/2%2C3-DMPPP_structure.png/120px-2%2C3-DMPPP_structure.png" decoding="async" width="120" height="65" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/ca/2%2C3-DMPPP_structure.png/180px-2%2C3-DMPPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/ca/2%2C3-DMPPP_structure.png/240px-2%2C3-DMPPP_structure.png 2x" data-file-width="1223" data-file-height="661" /></a></span></td> <td>2,3-DMPPP</td> <td>2,3-dimethyl</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,4-DMPPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/ad/2%2C4-DMPPP_structure.png/120px-2%2C4-DMPPP_structure.png" decoding="async" width="120" height="63" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/ad/2%2C4-DMPPP_structure.png/180px-2%2C4-DMPPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/ad/2%2C4-DMPPP_structure.png/240px-2%2C4-DMPPP_structure.png 2x" data-file-width="1124" data-file-height="588" /></a></span></td> <td>2,4-DMPPP</td> <td>2,4-dimethyl</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DMPPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f6/3%2C4-DMPPP_structure.png/120px-3%2C4-DMPPP_structure.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f6/3%2C4-DMPPP_structure.png/180px-3%2C4-DMPPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f6/3%2C4-DMPPP_structure.png/240px-3%2C4-DMPPP_structure.png 2x" data-file-width="1222" data-file-height="668" /></a></span></td> <td>3,4-DMPPP</td> <td>3,4-dimethyl</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-Me-PBP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/fb/3-Me-PBP_structure.png/120px-3-Me-PBP_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/fb/3-Me-PBP_structure.png/180px-3-Me-PBP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/fb/3-Me-PBP_structure.png/240px-3-Me-PBP_structure.png 2x" data-file-width="1102" data-file-height="562" /></a></span></td> <td>3-MPBP</td> <td>3-Me</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td>1373918-60-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-F-PBP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/83/3-F-PBP_structure.png/120px-3-F-PBP_structure.png" decoding="async" width="120" height="61" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/83/3-F-PBP_structure.png/180px-3-F-PBP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/83/3-F-PBP_structure.png/240px-3-F-PBP_structure.png 2x" data-file-width="1112" data-file-height="566" /></a></span></td> <td>3-F-PBP</td> <td>3-F</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td>1373918-59-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MPBP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9e/MPBP.svg/120px-MPBP.svg.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9e/MPBP.svg/180px-MPBP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9e/MPBP.svg/240px-MPBP.svg.png 2x" data-file-width="512" data-file-height="264" /></a></span></td> <td><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinobutiophenone" title="4&#39;-Methyl-α-pyrrolidinobutiophenone">MPBP</a></td> <td>4-Me</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td>732180-91-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-F-PBP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/4-F-PBP_structure.png/120px-4-F-PBP_structure.png" decoding="async" width="120" height="65" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/4-F-PBP_structure.png/180px-4-F-PBP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/4c/4-F-PBP_structure.png/240px-4-F-PBP_structure.png 2x" data-file-width="1122" data-file-height="607" /></a></span></td> <td>FPBP</td> <td>4-F</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td>1373918-67-2 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Et-PBP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/5c/4-Et-PBP_structure.png/120px-4-Et-PBP_structure.png" decoding="async" width="120" height="55" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/5c/4-Et-PBP_structure.png/180px-4-Et-PBP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/5c/4-Et-PBP_structure.png/240px-4-Et-PBP_structure.png 2x" data-file-width="1228" data-file-height="567" /></a></span></td> <td>EPBP</td> <td>4-Et</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MeO-PBP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c9/4-MeO-PBP_structure.png/120px-4-MeO-PBP_structure.png" decoding="async" width="120" height="57" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c9/4-MeO-PBP_structure.png/180px-4-MeO-PBP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c9/4-MeO-PBP_structure.png/240px-4-MeO-PBP_structure.png 2x" data-file-width="1232" data-file-height="588" /></a></span></td> <td>MOPBP</td> <td>4-MeO</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MMOPBP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0c/MMOPBP_structure.png/120px-MMOPBP_structure.png" decoding="async" width="120" height="58" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0c/MMOPBP_structure.png/180px-MMOPBP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0c/MMOPBP_structure.png/240px-MMOPBP_structure.png 2x" data-file-width="1228" data-file-height="595" /></a></span></td> <td>MMOPBP</td> <td>3-Me-4-MeO</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:O-2384_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f2/O-2384_structure.png/120px-O-2384_structure.png" decoding="async" width="120" height="62" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f2/O-2384_structure.png/180px-O-2384_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f2/O-2384_structure.png/240px-O-2384_structure.png 2x" data-file-width="1139" data-file-height="591" /></a></span></td> <td>O-2384</td> <td>3,4-dichloro</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td>850352-65-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2Me-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/14/2Me-PVP_structure.png/120px-2Me-PVP_structure.png" decoding="async" width="120" height="88" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/14/2Me-PVP_structure.png/180px-2Me-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/14/2Me-PVP_structure.png/240px-2Me-PVP_structure.png 2x" data-file-width="1000" data-file-height="730" /></a></span></td> <td><a href="/wiki/2-Me-PVP" title="2-Me-PVP">2-Me-PVP</a></td> <td>2-Me</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>850352-54-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3Me-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/74/3Me-PVP_structure.png/120px-3Me-PVP_structure.png" decoding="async" width="120" height="80" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/74/3Me-PVP_structure.png/180px-3Me-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/74/3Me-PVP_structure.png/240px-3Me-PVP_structure.png 2x" data-file-width="1215" data-file-height="805" /></a></span></td> <td><a href="/wiki/3-Me-PVP" title="3-Me-PVP">3-Me-PVP</a></td> <td>3-Me</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>13415-85-5 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Pyrovalerone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/22/Pyrovalerone.svg/120px-Pyrovalerone.svg.png" decoding="async" width="120" height="78" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/22/Pyrovalerone.svg/180px-Pyrovalerone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/22/Pyrovalerone.svg/240px-Pyrovalerone.svg.png 2x" data-file-width="512" data-file-height="332" /></a></span></td> <td><a href="/wiki/Pyrovalerone" title="Pyrovalerone">Pyrovalerone</a> (O-2371)</td> <td>4-Me</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>3563-49-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Et-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/79/4-Et-PVP_structure.png/120px-4-Et-PVP_structure.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/79/4-Et-PVP_structure.png/180px-4-Et-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/79/4-Et-PVP_structure.png/240px-4-Et-PVP_structure.png 2x" data-file-width="1336" data-file-height="787" /></a></span></td> <td><a href="/wiki/4-Et-PVP" title="4-Et-PVP">4-Et-PVP</a></td> <td>4-Et</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-F-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/3-F-PVP_structure.png/120px-3-F-PVP_structure.png" decoding="async" width="120" height="77" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/3-F-PVP_structure.png/180px-3-F-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/24/3-F-PVP_structure.png/240px-3-F-PVP_structure.png 2x" data-file-width="1126" data-file-height="719" /></a></span></td> <td><a href="/wiki/3F-PVP" title="3F-PVP">3F-PVP</a></td> <td>3-F</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>2725852-55-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:FPVP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/FPVP.svg/120px-FPVP.svg.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/FPVP.svg/180px-FPVP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2b/FPVP.svg/240px-FPVP.svg.png 2x" data-file-width="512" data-file-height="325" /></a></span></td> <td><a href="/wiki/4%27-Fluoro-%CE%B1-Pyrrolidinopentiophenone" class="mw-redirect" title="4&#39;-Fluoro-α-Pyrrolidinopentiophenone">FPVP</a></td> <td>4-F</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>850352-31-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2Cl-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/47/2Cl-PVP_structure.png/120px-2Cl-PVP_structure.png" decoding="async" width="120" height="89" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/47/2Cl-PVP_structure.png/180px-2Cl-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/47/2Cl-PVP_structure.png/240px-2Cl-PVP_structure.png 2x" data-file-width="1077" data-file-height="803" /></a></span></td> <td>2-Cl-PVP</td> <td>2-Cl</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3Cl-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/bf/3Cl-PVP_structure.png/120px-3Cl-PVP_structure.png" decoding="async" width="120" height="72" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/bf/3Cl-PVP_structure.png/180px-3Cl-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/bf/3Cl-PVP_structure.png/240px-3Cl-PVP_structure.png 2x" data-file-width="1289" data-file-height="777" /></a></span></td> <td>3-Cl-PVP</td> <td>3-Cl</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Cl-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c8/4-Cl-PVP_structure.png/120px-4-Cl-PVP_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c8/4-Cl-PVP_structure.png/180px-4-Cl-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c8/4-Cl-PVP_structure.png/240px-4-Cl-PVP_structure.png 2x" data-file-width="1118" data-file-height="704" /></a></span></td> <td><a href="/wiki/4-Cl-PVP" class="mw-redirect" title="4-Cl-PVP">4-Cl-PVP</a></td> <td>4-Cl</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>5537-17-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-Br-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-Br-PVP_structure.png/120px-3-Br-PVP_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-Br-PVP_structure.png/180px-3-Br-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/68/3-Br-PVP_structure.png/240px-3-Br-PVP_structure.png 2x" data-file-width="1292" data-file-height="816" /></a></span></td> <td>3-Br-PVP</td> <td>3-Br</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Br-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/5/59/4-Br-PVP_structure.png/120px-4-Br-PVP_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/5/59/4-Br-PVP_structure.png/180px-4-Br-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/5/59/4-Br-PVP_structure.png/240px-4-Br-PVP_structure.png 2x" data-file-width="1112" data-file-height="705" /></a></span></td> <td>4-Br-PVP</td> <td>4-Br</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MOPVP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c2/MOPVP.svg/120px-MOPVP.svg.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c2/MOPVP.svg/180px-MOPVP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c2/MOPVP.svg/240px-MOPVP.svg.png 2x" data-file-width="512" data-file-height="297" /></a></span></td> <td><a href="/wiki/4%27-Methoxy-%CE%B1-Pyrrolidinopentiophenone" class="mw-redirect" title="4&#39;-Methoxy-α-Pyrrolidinopentiophenone">MOPVP</a></td> <td>4-MeO</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>5537-19-9 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:DMPVP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/36/DMPVP.svg/120px-DMPVP.svg.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/36/DMPVP.svg/180px-DMPVP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/36/DMPVP.svg/240px-DMPVP.svg.png 2x" data-file-width="512" data-file-height="297" /></a></span></td> <td><a href="/wiki/3%27,4%27-Dimethoxy-%CE%B1-pyrrolidinopentiophenone" title="3&#39;,4&#39;-Dimethoxy-α-pyrrolidinopentiophenone">DMOPVP</a></td> <td>3,4-dimethoxy</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>850442-84-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-DMPVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cb/3%2C4-DMPVP_structure.png/120px-3%2C4-DMPVP_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cb/3%2C4-DMPVP_structure.png/180px-3%2C4-DMPVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cb/3%2C4-DMPVP_structure.png/240px-3%2C4-DMPVP_structure.png 2x" data-file-width="1126" data-file-height="709" /></a></span></td> <td>DMPVP</td> <td>3,4-dimethyl</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:O-2390_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/9e/O-2390_structure.png/120px-O-2390_structure.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/9e/O-2390_structure.png/180px-O-2390_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/9e/O-2390_structure.png/240px-O-2390_structure.png 2x" data-file-width="1149" data-file-height="698" /></a></span></td> <td><a href="/wiki/O-2390" title="O-2390">O-2390</a></td> <td>3,4-dichloro</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>850352-61-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MFPVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/MFPVP_structure.png/120px-MFPVP_structure.png" decoding="async" width="120" height="78" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7f/MFPVP_structure.png/180px-MFPVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7f/MFPVP_structure.png/240px-MFPVP_structure.png 2x" data-file-width="921" data-file-height="597" /></a></span></td> <td><a href="/wiki/MFPVP" title="MFPVP">MFPVP</a></td> <td>3-methyl-4-fluoro</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MPHP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/ca/MPHP.svg/120px-MPHP.svg.png" decoding="async" width="120" height="86" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/ca/MPHP.svg/180px-MPHP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/ca/MPHP.svg/240px-MPHP.svg.png 2x" data-file-width="512" data-file-height="368" /></a></span></td> <td><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinohexiophenone" title="4&#39;-Methyl-α-pyrrolidinohexiophenone">MPHP</a></td> <td>4-Me</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td>34138-58-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3F-PHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/3F-PHP_structure.png/120px-3F-PHP_structure.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/24/3F-PHP_structure.png/180px-3F-PHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/24/3F-PHP_structure.png/240px-3F-PHP_structure.png 2x" data-file-width="1213" data-file-height="847" /></a></span></td> <td><a href="/wiki/3F-PHP" title="3F-PHP">3F-PHP</a></td> <td>3-F</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-F-PHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/98/4-F-PHP_structure.png/120px-4-F-PHP_structure.png" decoding="async" width="120" height="83" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/98/4-F-PHP_structure.png/180px-4-F-PHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/98/4-F-PHP_structure.png/240px-4-F-PHP_structure.png 2x" data-file-width="1133" data-file-height="779" /></a></span></td> <td><a href="/wiki/4F-PHP" title="4F-PHP">4F-PHP</a></td> <td>4-F</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td>2230706-09-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Cl-PHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/39/4-Cl-PHP_structure.png/120px-4-Cl-PHP_structure.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/39/4-Cl-PHP_structure.png/180px-4-Cl-PHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/39/4-Cl-PHP_structure.png/240px-4-Cl-PHP_structure.png 2x" data-file-width="1135" data-file-height="790" /></a></span></td> <td><a href="/wiki/4-Cl-PHP" title="4-Cl-PHP">4-Cl-PHP</a></td> <td>4-Cl</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td>2748592-29-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:DMOPHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/3a/DMOPHP_structure.png/120px-DMOPHP_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/3a/DMOPHP_structure.png/180px-DMOPHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/3a/DMOPHP_structure.png/240px-DMOPHP_structure.png 2x" data-file-width="1245" data-file-height="780" /></a></span></td> <td>DMOPHP</td> <td>3,4-dimethoxy</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MFPHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/MFPHP_structure.png/120px-MFPHP_structure.png" decoding="async" width="120" height="87" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/MFPHP_structure.png/180px-MFPHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a8/MFPHP_structure.png/240px-MFPHP_structure.png 2x" data-file-width="847" data-file-height="615" /></a></span></td> <td>MFPHP</td> <td>3-Me-4-F</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-F-PiHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6f/3-F-PiHP_structure.png/120px-3-F-PiHP_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6f/3-F-PiHP_structure.png/180px-3-F-PiHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6f/3-F-PiHP_structure.png/240px-3-F-PiHP_structure.png 2x" data-file-width="1126" data-file-height="712" /></a></span></td> <td><a href="/wiki/3F-PiHP" title="3F-PiHP">3F-PiHP</a></td> <td>3-F</td> <td>iBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-F-PiHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/4-F-PiHP_structure.png/120px-4-F-PiHP_structure.png" decoding="async" width="120" height="76" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/4-F-PiHP_structure.png/180px-4-F-PiHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a8/4-F-PiHP_structure.png/240px-4-F-PiHP_structure.png 2x" data-file-width="1113" data-file-height="704" /></a></span></td> <td>4F-PiHP</td> <td>4-F</td> <td>iBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:O-2494_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/09/O-2494_structure.png/120px-O-2494_structure.png" decoding="async" width="120" height="77" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/09/O-2494_structure.png/180px-O-2494_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/09/O-2494_structure.png/240px-O-2494_structure.png 2x" data-file-width="1116" data-file-height="717" /></a></span></td> <td>O-2394</td> <td>4-Me</td> <td><a href="/wiki/Isobutyl" class="mw-redirect" title="Isobutyl">iBu</a></td> <td colspan="2">pyrrolidinyl</td> <td>850352-51-1 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-Me-PEP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cc/4-Me-PEP_structure.png/120px-4-Me-PEP_structure.png" decoding="async" width="120" height="102" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cc/4-Me-PEP_structure.png/180px-4-Me-PEP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cc/4-Me-PEP_structure.png/240px-4-Me-PEP_structure.png 2x" data-file-width="966" data-file-height="819" /></a></span></td> <td>MPEP</td> <td>4-Me</td> <td><a href="/wiki/Pentyl" class="mw-redirect" title="Pentyl">pentyl</a></td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-F-PEP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/6e/4-F-PEP_structure.png/120px-4-F-PEP_structure.png" decoding="async" width="120" height="101" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/6e/4-F-PEP_structure.png/180px-4-F-PEP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/6e/4-F-PEP_structure.png/240px-4-F-PEP_structure.png 2x" data-file-width="987" data-file-height="827" /></a></span></td> <td>4F-PV8</td> <td>4-F</td> <td>pentyl</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MeO-PEP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/3a/4-MeO-PEP_structure.png/120px-4-MeO-PEP_structure.png" decoding="async" width="120" height="92" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/3a/4-MeO-PEP_structure.png/180px-4-MeO-PEP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/3a/4-MeO-PEP_structure.png/240px-4-MeO-PEP_structure.png 2x" data-file-width="1079" data-file-height="826" /></a></span></td> <td>4-MeO-PV8</td> <td>4-MeO</td> <td>pentyl</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MFPEP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/MFPEP_structure.png/120px-MFPEP_structure.png" decoding="async" width="120" height="102" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2b/MFPEP_structure.png/180px-MFPEP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2b/MFPEP_structure.png/240px-MFPEP_structure.png 2x" data-file-width="842" data-file-height="716" /></a></span></td> <td>MFPEP</td> <td>3-Me-4-F</td> <td>pentyl</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MCPEP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/2/2a/MCPEP_structure.png/120px-MCPEP_structure.png" decoding="async" width="120" height="100" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/2/2a/MCPEP_structure.png/180px-MCPEP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/2/2a/MCPEP_structure.png/240px-MCPEP_structure.png 2x" data-file-width="878" data-file-height="731" /></a></span></td> <td>MCPEP</td> <td>3-Me-4-Cl</td> <td>pentyl</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:FPOP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/9/95/FPOP.svg/120px-FPOP.svg.png" decoding="async" width="120" height="107" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/9/95/FPOP.svg/180px-FPOP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/9/95/FPOP.svg/240px-FPOP.svg.png 2x" data-file-width="512" data-file-height="457" /></a></span></td> <td><a href="/wiki/4%27-Fluoro-%CE%B1-Pyrrolidinooctanophenone" class="mw-redirect" title="4&#39;-Fluoro-α-Pyrrolidinooctanophenone">4F-PV9</a></td> <td>4-F</td> <td><a href="/wiki/Hexyl" class="mw-redirect" title="Hexyl">hexyl</a></td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MeO-POP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a1/4-MeO-POP_structure.png/120px-4-MeO-POP_structure.png" decoding="async" width="120" height="98" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a1/4-MeO-POP_structure.png/180px-4-MeO-POP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a1/4-MeO-POP_structure.png/240px-4-MeO-POP_structure.png 2x" data-file-width="966" data-file-height="787" /></a></span></td> <td>4-MeO-PV9</td> <td>4-MeO</td> <td>hexyl</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-phenylpyrovalerone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cd/Alpha-phenylpyrovalerone_structure.png/120px-Alpha-phenylpyrovalerone_structure.png" decoding="async" width="120" height="86" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cd/Alpha-phenylpyrovalerone_structure.png/180px-Alpha-phenylpyrovalerone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cd/Alpha-phenylpyrovalerone_structure.png/240px-Alpha-phenylpyrovalerone_structure.png 2x" data-file-width="982" data-file-height="702" /></a></span></td> <td>α-Phenylpyrovalerone</td> <td>4-Me</td> <td><a href="/wiki/Phenyl" class="mw-redirect" title="Phenyl">phenyl</a></td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPPP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d4/MDPPP.svg/120px-MDPPP.svg.png" decoding="async" width="120" height="57" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d4/MDPPP.svg/180px-MDPPP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d4/MDPPP.svg/240px-MDPPP.svg.png 2x" data-file-width="512" data-file-height="243" /></a></span></td> <td><a href="/wiki/3%27,4%27-Methylenedioxy-%CE%B1-pyrrolidinopropiophenone" title="3&#39;,4&#39;-Methylenedioxy-α-pyrrolidinopropiophenone">MDPPP</a></td> <td>3,4-methylenedioxy</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td>783241-66-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDMPP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0d/MDMPP_structure.png/120px-MDMPP_structure.png" decoding="async" width="120" height="57" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0d/MDMPP_structure.png/180px-MDMPP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0d/MDMPP_structure.png/240px-MDMPP_structure.png 2x" data-file-width="1200" data-file-height="570" /></a></span></td> <td>MDMPP</td> <td>3,4-methylenedioxy</td> <td>α,α-di-Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3%27,4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7e/3%27%2C4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone.svg/120px-3%27%2C4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone.svg.png" decoding="async" width="120" height="57" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7e/3%27%2C4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone.svg/180px-3%27%2C4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7e/3%27%2C4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone.svg/240px-3%27%2C4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone.svg.png 2x" data-file-width="512" data-file-height="243" /></a></span></td> <td><a href="/wiki/3%27,4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone" title="3&#39;,4&#39;-Methylenedioxy-α-pyrrolidinobutiophenone">MDPBP</a></td> <td>3,4-methylenedioxy</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td>784985-33-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPV.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/7/7c/MDPV.svg/120px-MDPV.svg.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/7/7c/MDPV.svg/180px-MDPV.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/7/7c/MDPV.svg/240px-MDPV.svg.png 2x" data-file-width="512" data-file-height="303" /></a></span></td> <td><a href="/wiki/Methylenedioxypyrovalerone" title="Methylenedioxypyrovalerone">MDPV</a></td> <td>3,4-methylenedioxy</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>687603-66-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:2,3-MDPV_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/4/43/2%2C3-MDPV_structure.png/120px-2%2C3-MDPV_structure.png" decoding="async" width="120" height="77" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/4/43/2%2C3-MDPV_structure.png/180px-2%2C3-MDPV_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/4/43/2%2C3-MDPV_structure.png/240px-2%2C3-MDPV_structure.png 2x" data-file-width="1096" data-file-height="706" /></a></span></td> <td>2,3-MDPV</td> <td>2,3-methylenedioxy</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-Me-MDPV_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/ac/5-Me-MDPV_structure.png/120px-5-Me-MDPV_structure.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/ac/5-Me-MDPV_structure.png/180px-5-Me-MDPV_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/ac/5-Me-MDPV_structure.png/240px-5-Me-MDPV_structure.png 2x" data-file-width="1215" data-file-height="720" /></a></span></td> <td>5-Me-MDPV</td> <td>3,4-methylenedioxy-5-Me</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:6-Me-MDPV_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/6-Me-MDPV_structure.png/120px-6-Me-MDPV_structure.png" decoding="async" width="120" height="80" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a8/6-Me-MDPV_structure.png/180px-6-Me-MDPV_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a8/6-Me-MDPV_structure.png/240px-6-Me-MDPV_structure.png 2x" data-file-width="1095" data-file-height="733" /></a></span></td> <td>6-Me-MDPV</td> <td>2-Me-4,5-methylenedioxy</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:6-MeO-MDPV_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/37/6-MeO-MDPV_structure.png/120px-6-MeO-MDPV_structure.png" decoding="async" width="120" height="83" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/37/6-MeO-MDPV_structure.png/180px-6-MeO-MDPV_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/37/6-MeO-MDPV_structure.png/240px-6-MeO-MDPV_structure.png 2x" data-file-width="1118" data-file-height="776" /></a></span></td> <td>6-MeO-MDPV</td> <td>2-MeO-4,5-methylenedioxy</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:4-MeO-5-Br-2,3-MDPV_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/fd/4-MeO-5-Br-2%2C3-MDPV_structure.png/120px-4-MeO-5-Br-2%2C3-MDPV_structure.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/fd/4-MeO-5-Br-2%2C3-MDPV_structure.png/180px-4-MeO-5-Br-2%2C3-MDPV_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/fd/4-MeO-5-Br-2%2C3-MDPV_structure.png/240px-4-MeO-5-Br-2%2C3-MDPV_structure.png 2x" data-file-width="1236" data-file-height="749" /></a></span></td> <td>Br-MeO-MDPV</td> <td>2,3-methylenedioxy-4-MeO-5-Br</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPiVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c7/MDPiVP_structure.png/120px-MDPiVP_structure.png" decoding="async" width="120" height="57" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c7/MDPiVP_structure.png/180px-MDPiVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c7/MDPiVP_structure.png/240px-MDPiVP_structure.png 2x" data-file-width="1205" data-file-height="571" /></a></span></td> <td>MDPiVP</td> <td>3,4-methylenedioxy</td> <td>iPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPHP.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/ab/MDPHP.svg/120px-MDPHP.svg.png" decoding="async" width="120" height="79" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/ab/MDPHP.svg/180px-MDPHP.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/ab/MDPHP.svg/240px-MDPHP.svg.png 2x" data-file-width="512" data-file-height="336" /></a></span></td> <td><a href="/wiki/MDPHP" title="MDPHP">MDPHP</a></td> <td>3,4-methylenedioxy</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td>776994-64-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPHiP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/MDPHiP_structure.png/120px-MDPHiP_structure.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/68/MDPHiP_structure.png/180px-MDPHiP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/68/MDPHiP_structure.png/240px-MDPHiP_structure.png 2x" data-file-width="1301" data-file-height="771" /></a></span></td> <td>MDPHiP</td> <td>3,4-methylenedioxy</td> <td>iBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPEP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/e/e1/MDPEP_structure.png/120px-MDPEP_structure.png" decoding="async" width="120" height="94" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/e/e1/MDPEP_structure.png/180px-MDPEP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/e/e1/MDPEP_structure.png/240px-MDPEP_structure.png 2x" data-file-width="1052" data-file-height="821" /></a></span></td> <td><a href="/wiki/MDPEP" title="MDPEP">MDPEP</a> (MD-PV8)</td> <td>3,4-methylenedioxy</td> <td>pentyl</td> <td colspan="2">pyrrolidinyl</td> <td>24646-39-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:MDPOP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/b/bd/MDPOP_structure.png/120px-MDPOP_structure.png" decoding="async" width="120" height="98" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/b/bd/MDPOP_structure.png/180px-MDPOP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/b/bd/MDPOP_structure.png/240px-MDPOP_structure.png 2x" data-file-width="1050" data-file-height="858" /></a></span></td> <td>MDPOP (MD-PV9)</td> <td>3,4-methylenedioxy</td> <td>hexyl</td> <td colspan="2">pyrrolidinyl</td> <td>24646-40-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3,4-EtPV_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/02/3%2C4-EtPV_structure.png/120px-3%2C4-EtPV_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/02/3%2C4-EtPV_structure.png/180px-3%2C4-EtPV_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/02/3%2C4-EtPV_structure.png/240px-3%2C4-EtPV_structure.png 2x" data-file-width="1277" data-file-height="803" /></a></span></td> <td>3,4-EtPV</td> <td>3,4-dimethylene</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-PPDI_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/6/65/5-PPDI_structure.png/120px-5-PPDI_structure.png" decoding="async" width="120" height="59" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/6/65/5-PPDI_structure.png/180px-5-PPDI_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/6/65/5-PPDI_structure.png/240px-5-PPDI_structure.png 2x" data-file-width="1186" data-file-height="580" /></a></span></td> <td>5-PPDi</td> <td>3,4-trimethylene</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-BPDI_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/3/35/5-BPDI_structure.png/120px-5-BPDI_structure.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/3/35/5-BPDI_structure.png/180px-5-BPDI_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/3/35/5-BPDI_structure.png/240px-5-BPDI_structure.png 2x" data-file-width="1209" data-file-height="707" /></a></span></td> <td>Indanyl-α-PVP</td> <td>3,4-trimethylene</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>2748590-83-0 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-HPDI_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8c/5-HPDI_structure.png/120px-5-HPDI_structure.png" decoding="async" width="120" height="79" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8c/5-HPDI_structure.png/180px-5-HPDI_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8c/5-HPDI_structure.png/240px-5-HPDI_structure.png 2x" data-file-width="1201" data-file-height="791" /></a></span></td> <td><a href="/wiki/5-BPDi" title="5-BPDi">5-BPDi</a></td> <td>3,4-trimethylene</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Indapyrophenidone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Indapyrophenidone.svg/120px-Indapyrophenidone.svg.png" decoding="async" width="120" height="79" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Indapyrophenidone.svg/180px-Indapyrophenidone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8b/Indapyrophenidone.svg/240px-Indapyrophenidone.svg.png 2x" data-file-width="512" data-file-height="337" /></a></span></td> <td><a href="/wiki/Indapyrophenidone" title="Indapyrophenidone">IPPV</a></td> <td>3,4-trimethylene</td> <td>phenyl</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:TH-PBP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/8f/TH-PBP_structure.png/120px-TH-PBP_structure.png" decoding="async" width="120" height="60" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/8f/TH-PBP_structure.png/180px-TH-PBP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/8f/TH-PBP_structure.png/240px-TH-PBP_structure.png 2x" data-file-width="1372" data-file-height="685" /></a></span></td> <td>TH-PBP</td> <td>3,4-tetramethylene</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:TH-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/TH-PVP_structure.png/120px-TH-PVP_structure.png" decoding="async" width="120" height="73" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/13/TH-PVP_structure.png/180px-TH-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/13/TH-PVP_structure.png/240px-TH-PVP_structure.png 2x" data-file-width="1223" data-file-height="740" /></a></span></td> <td><a href="/wiki/TH-PVP" title="TH-PVP">TH-PVP</a></td> <td>3,4-tetramethylene</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>2304915-07-7 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:TH-PHP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cc/TH-PHP_structure.png/120px-TH-PHP_structure.png" decoding="async" width="120" height="75" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cc/TH-PHP_structure.png/180px-TH-PHP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cc/TH-PHP_structure.png/240px-TH-PHP_structure.png 2x" data-file-width="1246" data-file-height="780" /></a></span></td> <td>TH-PHP</td> <td>3,4-tetramethylene</td> <td>nBu</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:5-DBFPV.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/5-DBFPV.svg/120px-5-DBFPV.svg.png" decoding="async" width="120" height="71" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/5-DBFPV.svg/180px-5-DBFPV.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/5-DBFPV.svg/240px-5-DBFPV.svg.png 2x" data-file-width="512" data-file-height="303" /></a></span></td> <td><a href="/wiki/5-DBFPV" title="5-DBFPV">5-DBFPV</a></td> <td>2,3-dihydrobenzofuran-5-yl instead of Ph</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>1620807-94-4 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:3-BF-PVP_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/1/17/3-BF-PVP_structure.png/120px-3-BF-PVP_structure.png" decoding="async" width="120" height="74" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/1/17/3-BF-PVP_structure.png/180px-3-BF-PVP_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/1/17/3-BF-PVP_structure.png/240px-3-BF-PVP_structure.png 2x" data-file-width="1136" data-file-height="703" /></a></span></td> <td>3-BF-PVP</td> <td>benzofuran-3-yl instead of Ph</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Naphyrone.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/c/c4/Naphyrone.svg/120px-Naphyrone.svg.png" decoding="async" width="120" height="69" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/c4/Naphyrone.svg/180px-Naphyrone.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/c4/Naphyrone.svg/240px-Naphyrone.svg.png 2x" data-file-width="512" data-file-height="296" /></a></span></td> <td><a href="/wiki/Naphyrone" title="Naphyrone">Naphyrone</a> (O-2482)</td> <td>β-naphthyl instead of phenyl</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>850352-53-3 </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-naphyrone_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/Alpha-naphyrone_structure.png/120px-Alpha-naphyrone_structure.png" decoding="async" width="120" height="84" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/ff/Alpha-naphyrone_structure.png/180px-Alpha-naphyrone_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/ff/Alpha-naphyrone_structure.png/240px-Alpha-naphyrone_structure.png 2x" data-file-width="1093" data-file-height="768" /></a></span></td> <td>α-Naphyrone</td> <td>α-naphthyl instead of phenyl</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-PPT_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0c/Alpha-PPT_structure.png/120px-Alpha-PPT_structure.png" decoding="async" width="120" height="66" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0c/Alpha-PPT_structure.png/180px-Alpha-PPT_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0c/Alpha-PPT_structure.png/240px-Alpha-PPT_structure.png 2x" data-file-width="946" data-file-height="518" /></a></span></td> <td>α-PPT</td> <td>thiophen-2-yl instead of phenyl</td> <td>Me</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:Alpha-PBT_structure.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/0f/Alpha-PBT_structure.png/120px-Alpha-PBT_structure.png" decoding="async" width="120" height="70" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/0f/Alpha-PBT_structure.png/180px-Alpha-PBT_structure.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/0f/Alpha-PBT_structure.png/240px-Alpha-PBT_structure.png 2x" data-file-width="943" data-file-height="551" /></a></span></td> <td>α-PBT</td> <td>thiophen-2-yl instead of phenyl</td> <td>Et</td> <td colspan="2">pyrrolidinyl</td> <td> </td></tr> <tr> <td><span typeof="mw:File"><a href="/wiki/File:%CE%91-PVT.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/d/d9/%CE%91-PVT.svg/120px-%CE%91-PVT.svg.png" decoding="async" width="120" height="89" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/d/d9/%CE%91-PVT.svg/180px-%CE%91-PVT.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/d/d9/%CE%91-PVT.svg/240px-%CE%91-PVT.svg.png 2x" data-file-width="512" data-file-height="381" /></a></span></td> <td><a href="/wiki/Alpha-Pyrrolidinopentiothiophenone" class="mw-redirect" title="Alpha-Pyrrolidinopentiothiophenone">α-PVT</a></td> <td>thiophen-2-yl instead of phenyl</td> <td>nPr</td> <td colspan="2">pyrrolidinyl</td> <td>1400742-66-6 </td></tr> </tbody></table> <div class="mw-heading mw-heading2"><h2 id="Legality">Legality</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Substituted_cathinone&amp;action=edit&amp;section=2" title="Edit section: Legality"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>On 2 April 2010, the <a href="/wiki/Advisory_Council_on_the_Misuse_of_Drugs" title="Advisory Council on the Misuse of Drugs">Advisory Council on the Misuse of Drugs</a> in the <a href="/wiki/United_Kingdom" title="United Kingdom">UK</a> announced that a broad structure-based ban of this entire class of compounds would be instituted, following extensive publicity around grey-market sales and <a href="/wiki/Recreational_drug_use" title="Recreational drug use">recreational use</a> of <a href="/wiki/Mephedrone" title="Mephedrone">mephedrone</a>, a common member of the family. This ban covers compounds with the aforementioned general structure, with 28 compounds specifically named.<sup id="cite_ref-ACMD2010_39-0" class="reference"><a href="#cite_note-ACMD2010-39"><span class="cite-bracket">&#91;</span>39<span class="cite-bracket">&#93;</span></a></sup> </p> <style data-mw-deduplicate="TemplateStyles:r1244412712">.mw-parser-output .templatequote{overflow:hidden;margin:1em 0;padding:0 32px}.mw-parser-output .templatequotecite{line-height:1.5em;text-align:left;margin-top:0}@media(min-width:500px){.mw-parser-output .templatequotecite{padding-left:1.6em}}</style><blockquote class="templatequote"><p>"Any compound (not being bupropion or a substance for the time being specified in paragraph 2.2) structurally derived from 2-amino-1-phenyl-1-propanone by modification in any of the following ways, that is to say, </p><p>(i) by substitution in the phenyl ring to any extent with alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents, whether or not further substituted in the phenyl ring by one or more other univalent substituents; </p><p>(ii) by substitution at the 3-position with an alkyl substituent; </p><p> (iii) by substitution at the nitrogen atom with alkyl or dialkyl groups, or by inclusion of the nitrogen atom in a cyclic structure."</p><div class="templatequotecite">—&#8202;<cite>ACMD, 2 April 2010</cite></div></blockquote> <p>This text was added as an amendment to the <a href="/wiki/Misuse_of_Drugs_Act_1971" title="Misuse of Drugs Act 1971">Misuse of Drugs Act 1971</a>, to come into force on 16 April 2010.<sup id="cite_ref-40" class="reference"><a href="#cite_note-40"><span class="cite-bracket">&#91;</span>40<span class="cite-bracket">&#93;</span></a></sup> Note that four of the above compounds (cathinone, methcathinone, diethylpropion and pyrovalerone) were already illegal in the UK at the time the ACMD report was issued. Two compounds were specifically excluded from the ban, these being bupropion because of its common use in medicine and relative lack of abuse potential, and naphyrone because its structure falls outside the generic definition and not enough evidence was yet available to justify a ban. </p><p>Naphyrone analogues were subsequently banned in July 2010 following a further review by the ACMD,<sup id="cite_ref-41" class="reference"><a href="#cite_note-41"><span class="cite-bracket">&#91;</span>41<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-42" class="reference"><a href="#cite_note-42"><span class="cite-bracket">&#91;</span>42<span class="cite-bracket">&#93;</span></a></sup> along with a further broad based structure ban even more expansive than the last.<sup id="cite_ref-43" class="reference"><a href="#cite_note-43"><span class="cite-bracket">&#91;</span>43<span class="cite-bracket">&#93;</span></a></sup><sup id="cite_ref-44" class="reference"><a href="#cite_note-44"><span class="cite-bracket">&#91;</span>44<span class="cite-bracket">&#93;</span></a></sup> </p> <link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1244412712"><blockquote class="templatequote"><p>"Any compound structurally derived from 2–aminopropan–1–one by substitution at the 1-position with any monocyclic, or fused-polycyclic ring system (not being a phenyl ring or alkylenedioxyphenyl ring system), whether or not the compound is </p><p>further modified in any of the following ways, that is to say— </p><p>(i) by substitution in the ring system to any extent with alkyl, alkoxy, haloalkyl or halide substituents, whether or not further substituted in the ring system by one or more other univalent substituents; </p><p>(ii) by substitution at the 3–position with an alkyl substituent; </p><p>(iii) by substitution at the 2-amino nitrogen atom with alkyl or dialkyl groups, or </p><p> by inclusion of the 2-amino nitrogen atom in a cyclic structure".</p><div class="templatequotecite">—&#8202;<cite>Home Office, 13 July 2010.</cite></div></blockquote> <figure typeof="mw:File/Thumb"><a href="/wiki/File:Naphyrone_general.png" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/f/f4/Naphyrone_general.png/180px-Naphyrone_general.png" decoding="async" width="180" height="131" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/f/f4/Naphyrone_general.png/270px-Naphyrone_general.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/f/f4/Naphyrone_general.png/360px-Naphyrone_general.png 2x" data-file-width="408" data-file-height="298" /></a><figcaption>General chemical structure of substituted naphyrones, with R<sub>1</sub>-R<sub>3</sub> defined in text</figcaption></figure><p>The substitutions in the general structure for naphyrone analogues subject to the ban may be described as follows: </p><ul><li>Cyc = any monocyclic, or fused-polycyclic ring system (not being a phenyl ring or alkylenedioxyphenyl ring system), including analogues where the ring system is substituted to any extent with alkyl, alkoxy, haloalkyl or halide substituents, whether or not further substituted in the ring system by one or more other univalent substituents</li> <li>R<sub>1</sub> = hydrogen or any alkyl group</li> <li>R<sub>2</sub> = hydrogen, any alkyl group, or incorporation in a cyclic structure</li> <li>R<sub>3</sub> = hydrogen, any alkyl group, or incorporation in a cyclic structure</li></ul> <p>More new derivatives have however continued to appear, with the UK reporting more novel cathinone derivatives detected in 2010 than any other country in Europe, with most of them first identified after the generic ban had gone into effect and thus already being illegal despite never having been previously reported.<sup id="cite_ref-45" class="reference"><a href="#cite_note-45"><span class="cite-bracket">&#91;</span>45<span class="cite-bracket">&#93;</span></a></sup> </p><p>In the United States, substituted cathinones are the psychoactive ingredients in "<a href="/wiki/Bath_salts_(drug)" title="Bath salts (drug)">bath salts</a>" which as of July 2011 were banned by at least 28 states, but not by the federal government.<sup id="cite_ref-46" class="reference"><a href="#cite_note-46"><span class="cite-bracket">&#91;</span>46<span class="cite-bracket">&#93;</span></a></sup> </p> <div class="mw-heading mw-heading2"><h2 id="See_also">See also</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Substituted_cathinone&amp;action=edit&amp;section=3" title="Edit section: See also"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/List_of_patent_claim_types#Markush" title="List of patent claim types">Markush structure</a></li> <li><a href="/wiki/Substituted_amphetamine" title="Substituted amphetamine">Substituted amphetamines</a></li> <li><a href="/wiki/Substituted_%CE%B2-hydroxyamphetamine" title="Substituted β-hydroxyamphetamine">Substituted β-hydroxyamphetamines</a></li> <li><a href="/wiki/Substituted_methylenedioxyphenethylamine" title="Substituted methylenedioxyphenethylamine">Substituted methylenedioxyphenethylamines</a></li> <li><a href="/wiki/Substituted_phenethylamine" title="Substituted phenethylamine">Substituted phenethylamines</a></li> <li><a href="/wiki/Substituted_phenylmorpholine" title="Substituted phenylmorpholine">Substituted phenylmorpholines</a></li> <li><a href="/wiki/Structural_scheduling_of_synthetic_cannabinoids" title="Structural scheduling of synthetic cannabinoids">Structural scheduling of synthetic cannabinoids</a></li> <li><a href="/wiki/Arylcyclohexylamine" title="Arylcyclohexylamine">Arylcyclohexylamines</a></li> <li><a href="/wiki/List_of_aminorex_analogues" title="List of aminorex analogues">List of aminorex analogues</a></li> <li><a href="/wiki/List_of_fentanyl_analogues" title="List of fentanyl analogues">List of fentanyl analogues</a></li> <li><a href="/wiki/List_of_methylphenidate_analogues" title="List of methylphenidate analogues">List of methylphenidate analogues</a></li></ul> <div class="mw-heading mw-heading2"><h2 id="References">References</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Substituted_cathinone&amp;action=edit&amp;section=4" title="Edit section: References"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <style data-mw-deduplicate="TemplateStyles:r1239543626">.mw-parser-output .reflist{margin-bottom:0.5em;list-style-type:decimal}@media screen{.mw-parser-output .reflist{font-size:90%}}.mw-parser-output .reflist .references{font-size:100%;margin-bottom:0;list-style-type:inherit}.mw-parser-output .reflist-columns-2{column-width:30em}.mw-parser-output .reflist-columns-3{column-width:25em}.mw-parser-output .reflist-columns{margin-top:0.3em}.mw-parser-output .reflist-columns ol{margin-top:0}.mw-parser-output .reflist-columns li{page-break-inside:avoid;break-inside:avoid-column}.mw-parser-output .reflist-upper-alpha{list-style-type:upper-alpha}.mw-parser-output .reflist-upper-roman{list-style-type:upper-roman}.mw-parser-output .reflist-lower-alpha{list-style-type:lower-alpha}.mw-parser-output .reflist-lower-greek{list-style-type:lower-greek}.mw-parser-output .reflist-lower-roman{list-style-type:lower-roman}</style><div class="reflist"> <div class="mw-references-wrap mw-references-columns"><ol class="references"> <li id="cite_note-1"><span class="mw-cite-backlink"><b><a href="#cite_ref-1">^</a></b></span> <span class="reference-text"><style data-mw-deduplicate="TemplateStyles:r1238218222">.mw-parser-output cite.citation{font-style:inherit;word-wrap:break-word}.mw-parser-output .citation q{quotes:"\"""\"""'""'"}.mw-parser-output .citation:target{background-color:rgba(0,127,255,0.133)}.mw-parser-output .id-lock-free.id-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/6/65/Lock-green.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-limited.id-lock-limited a,.mw-parser-output .id-lock-registration.id-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/d/d6/Lock-gray-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-subscription.id-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/a/aa/Lock-red-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/4/4c/Wikisource-logo.svg")right 0.1em center/12px no-repeat}body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-free a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-limited a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-registration a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-subscription a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .cs1-ws-icon a{background-size:contain;padding:0 1em 0 0}.mw-parser-output .cs1-code{color:inherit;background:inherit;border:none;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;color:var(--color-error,#d33)}.mw-parser-output .cs1-visible-error{color:var(--color-error,#d33)}.mw-parser-output .cs1-maint{display:none;color:#085;margin-left:0.3em}.mw-parser-output .cs1-kern-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right{padding-right:0.2em}.mw-parser-output .citation .mw-selflink{font-weight:inherit}@media screen{.mw-parser-output .cs1-format{font-size:95%}html.skin-theme-clientpref-night .mw-parser-output .cs1-maint{color:#18911f}}@media screen and (prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .cs1-maint{color:#18911f}}</style><cite id="CITEREFMeltzerButlerDeschampsMadras2006" class="citation journal cs1">Meltzer PC, Butler D, Deschamps JR, Madras BK (February 2006). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2602954">"1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) analogues: a promising class of monoamine uptake inhibitors"</a>. <i>Journal of Medicinal Chemistry</i>. <b>49</b> (4): 1420–32. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1021%2Fjm050797a">10.1021/jm050797a</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2602954">2602954</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/16480278">16480278</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Journal+of+Medicinal+Chemistry&amp;rft.atitle=1-%284-Methylphenyl%29-2-pyrrolidin-1-yl-pentan-1-one+%28Pyrovalerone%29+analogues%3A+a+promising+class+of+monoamine+uptake+inhibitors&amp;rft.volume=49&amp;rft.issue=4&amp;rft.pages=1420-32&amp;rft.date=2006-02&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC2602954%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F16480278&amp;rft_id=info%3Adoi%2F10.1021%2Fjm050797a&amp;rft.aulast=Meltzer&amp;rft.aufirst=PC&amp;rft.au=Butler%2C+D&amp;rft.au=Deschamps%2C+JR&amp;rft.au=Madras%2C+BK&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC2602954&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-2"><span class="mw-cite-backlink"><b><a href="#cite_ref-2">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFPaillet-LoilierCesbronLe_BoisselierBourgine2014" class="citation journal cs1">Paillet-Loilier M, Cesbron A, Le Boisselier R, Bourgine J, Debruyne D (2014). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043811">"Emerging drugs of abuse: current perspectives on substituted cathinones"</a>. <i>Substance Abuse and Rehabilitation</i>. <b>5</b>: 37–52. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://doi.org/10.2147%2FSAR.S37257">10.2147/SAR.S37257</a></span>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043811">4043811</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/24966713">24966713</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Substance+Abuse+and+Rehabilitation&amp;rft.atitle=Emerging+drugs+of+abuse%3A+current+perspectives+on+substituted+cathinones&amp;rft.volume=5&amp;rft.pages=37-52&amp;rft.date=2014&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC4043811%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F24966713&amp;rft_id=info%3Adoi%2F10.2147%2FSAR.S37257&amp;rft.aulast=Paillet-Loilier&amp;rft.aufirst=M&amp;rft.au=Cesbron%2C+A&amp;rft.au=Le+Boisselier%2C+R&amp;rft.au=Bourgine%2C+J&amp;rft.au=Debruyne%2C+D&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC4043811&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-3"><span class="mw-cite-backlink"><b><a href="#cite_ref-3">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSimmonsLeyrer-JacksonOliverHicks2018" class="citation journal cs1">Simmons SJ, Leyrer-Jackson JM, Oliver CF, Hicks C, Muschamp JW, Rawls SM, Olive MF (October 2018). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197900">"DARK Classics in Chemical Neuroscience: Cathinone-Derived Psychostimulants"</a>. <i>ACS Chemical Neuroscience</i>. <b>9</b> (10): 2379–2394. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1021%2Facschemneuro.8b00147">10.1021/acschemneuro.8b00147</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197900">6197900</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/29714473">29714473</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=ACS+Chemical+Neuroscience&amp;rft.atitle=DARK+Classics+in+Chemical+Neuroscience%3A+Cathinone-Derived+Psychostimulants&amp;rft.volume=9&amp;rft.issue=10&amp;rft.pages=2379-2394&amp;rft.date=2018-10&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC6197900%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F29714473&amp;rft_id=info%3Adoi%2F10.1021%2Facschemneuro.8b00147&amp;rft.aulast=Simmons&amp;rft.aufirst=SJ&amp;rft.au=Leyrer-Jackson%2C+JM&amp;rft.au=Oliver%2C+CF&amp;rft.au=Hicks%2C+C&amp;rft.au=Muschamp%2C+JW&amp;rft.au=Rawls%2C+SM&amp;rft.au=Olive%2C+MF&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC6197900&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-4"><span class="mw-cite-backlink"><b><a href="#cite_ref-4">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBeckBäckbergSignellHelander2018" class="citation journal cs1">Beck O, Bäckberg M, Signell P, Helander A (April 2018). <a rel="nofollow" class="external text" href="https://doi.org/10.1080%2F15563650.2017.1370097">"Intoxications in the STRIDA project involving a panorama of psychostimulant pyrovalerone derivatives, MDPV copycats"</a>. <i>Clinical Toxicology</i>. <b>56</b> (4): 256–263. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://doi.org/10.1080%2F15563650.2017.1370097">10.1080/15563650.2017.1370097</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/28895757">28895757</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a>&#160;<a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:3401681">3401681</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Clinical+Toxicology&amp;rft.atitle=Intoxications+in+the+STRIDA+project+involving+a+panorama+of+psychostimulant+pyrovalerone+derivatives%2C+MDPV+copycats&amp;rft.volume=56&amp;rft.issue=4&amp;rft.pages=256-263&amp;rft.date=2018-04&amp;rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A3401681%23id-name%3DS2CID&amp;rft_id=info%3Apmid%2F28895757&amp;rft_id=info%3Adoi%2F10.1080%2F15563650.2017.1370097&amp;rft.aulast=Beck&amp;rft.aufirst=O&amp;rft.au=B%C3%A4ckberg%2C+M&amp;rft.au=Signell%2C+P&amp;rft.au=Helander%2C+A&amp;rft_id=https%3A%2F%2Fdoi.org%2F10.1080%252F15563650.2017.1370097&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-5"><span class="mw-cite-backlink"><b><a href="#cite_ref-5">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMajchrzakCelińskiKuśKowalska2018" class="citation journal cs1">Majchrzak M, Celiński R, Kuś P, Kowalska T, Sajewicz M (2018). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754390">"The newest cathinone derivatives as designer drugs: an analytical and toxicological review"</a>. <i>Forensic Toxicology</i>. <b>36</b> (1): 33–50. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1007%2Fs11419-017-0385-6">10.1007/s11419-017-0385-6</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754390">5754390</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/29367861">29367861</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Forensic+Toxicology&amp;rft.atitle=The+newest+cathinone+derivatives+as+designer+drugs%3A+an+analytical+and+toxicological+review&amp;rft.volume=36&amp;rft.issue=1&amp;rft.pages=33-50&amp;rft.date=2018&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC5754390%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F29367861&amp;rft_id=info%3Adoi%2F10.1007%2Fs11419-017-0385-6&amp;rft.aulast=Majchrzak&amp;rft.aufirst=M&amp;rft.au=Celi%C5%84ski%2C+R&amp;rft.au=Ku%C5%9B%2C+P&amp;rft.au=Kowalska%2C+T&amp;rft.au=Sajewicz%2C+M&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC5754390&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-pmid21698275-6"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid21698275_6-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFColzatoRuizvan_den_WildenbergHommel2011" class="citation journal cs1">Colzato LS, Ruiz MJ, van den Wildenberg WP, Hommel B (2011). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115937">"Khat use is associated with impaired working memory and cognitive flexibility"</a>. <i>PLOS ONE</i>. <b>6</b> (6): e20602. <a href="/wiki/Bibcode_(identifier)" class="mw-redirect" title="Bibcode (identifier)">Bibcode</a>:<a rel="nofollow" class="external text" href="https://ui.adsabs.harvard.edu/abs/2011PLoSO...620602C">2011PLoSO...620602C</a>. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://doi.org/10.1371%2Fjournal.pone.0020602">10.1371/journal.pone.0020602</a></span>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3115937">3115937</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/21698275">21698275</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=PLOS+ONE&amp;rft.atitle=Khat+use+is+associated+with+impaired+working+memory+and+cognitive+flexibility&amp;rft.volume=6&amp;rft.issue=6&amp;rft.pages=e20602&amp;rft.date=2011&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC3115937%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F21698275&amp;rft_id=info%3Adoi%2F10.1371%2Fjournal.pone.0020602&amp;rft_id=info%3Abibcode%2F2011PLoSO...620602C&amp;rft.aulast=Colzato&amp;rft.aufirst=LS&amp;rft.au=Ruiz%2C+MJ&amp;rft.au=van+den+Wildenberg%2C+WP&amp;rft.au=Hommel%2C+B&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC3115937&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-RothmanBaumann2003-7"><span class="mw-cite-backlink"><b><a href="#cite_ref-RothmanBaumann2003_7-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRothmanBaumann2003" class="citation journal cs1">Rothman RB, Baumann MH (2003). "Monoamine transporters and psychostimulant drugs". <i>Eur. J. Pharmacol</i>. <b>479</b> (1–3): 23–40. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.ejphar.2003.08.054">10.1016/j.ejphar.2003.08.054</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/14612135">14612135</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Eur.+J.+Pharmacol.&amp;rft.atitle=Monoamine+transporters+and+psychostimulant+drugs&amp;rft.volume=479&amp;rft.issue=1%E2%80%933&amp;rft.pages=23-40&amp;rft.date=2003&amp;rft_id=info%3Adoi%2F10.1016%2Fj.ejphar.2003.08.054&amp;rft_id=info%3Apmid%2F14612135&amp;rft.aulast=Rothman&amp;rft.aufirst=RB&amp;rft.au=Baumann%2C+MH&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-RothmanBaumann2006-8"><span class="mw-cite-backlink"><b><a href="#cite_ref-RothmanBaumann2006_8-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRothmanBaumann2006" class="citation journal cs1">Rothman RB, Baumann MH (2006). "Therapeutic potential of monoamine transporter substrates". <i>Curr Top Med Chem</i>. <b>6</b> (17): 1845–1859. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.2174%2F156802606778249766">10.2174/156802606778249766</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/17017961">17017961</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Curr+Top+Med+Chem&amp;rft.atitle=Therapeutic+potential+of+monoamine+transporter+substrates&amp;rft.volume=6&amp;rft.issue=17&amp;rft.pages=1845-1859&amp;rft.date=2006&amp;rft_id=info%3Adoi%2F10.2174%2F156802606778249766&amp;rft_id=info%3Apmid%2F17017961&amp;rft.aulast=Rothman&amp;rft.aufirst=RB&amp;rft.au=Baumann%2C+MH&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-ReithBLoughHong2015-9"><span class="mw-cite-backlink"><b><a href="#cite_ref-ReithBLoughHong2015_9-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFReithBloughHongJones2015" class="citation journal cs1">Reith ME, Blough BE, Hong WC, Jones KT, Schmitt KC, Baumann MH, Partilla JS, Rothman RB, Katz JL (February 2015). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297708">"Behavioral, biological, and chemical perspectives on atypical agents targeting the dopamine transporter"</a>. <i>Drug and Alcohol Dependence</i>. <b>147</b>: 1–19. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.drugalcdep.2014.12.005">10.1016/j.drugalcdep.2014.12.005</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297708">4297708</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/25548026">25548026</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Drug+and+Alcohol+Dependence&amp;rft.atitle=Behavioral%2C+biological%2C+and+chemical+perspectives+on+atypical+agents+targeting+the+dopamine+transporter&amp;rft.volume=147&amp;rft.pages=1-19&amp;rft.date=2015-02&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC4297708%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F25548026&amp;rft_id=info%3Adoi%2F10.1016%2Fj.drugalcdep.2014.12.005&amp;rft.aulast=Reith&amp;rft.aufirst=ME&amp;rft.au=Blough%2C+BE&amp;rft.au=Hong%2C+WC&amp;rft.au=Jones%2C+KT&amp;rft.au=Schmitt%2C+KC&amp;rft.au=Baumann%2C+MH&amp;rft.au=Partilla%2C+JS&amp;rft.au=Rothman%2C+RB&amp;rft.au=Katz%2C+JL&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC4297708&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-RothmanBaumann2005-10"><span class="mw-cite-backlink"><b><a href="#cite_ref-RothmanBaumann2005_10-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRothmanBaumann2005" class="citation journal cs1">Rothman RB, Baumann MH (December 2005). "Targeted screening for biogenic amine transporters: potential applications for natural products". <i>Life Sciences</i>. <b>78</b> (5): 512–518. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.lfs.2005.09.001">10.1016/j.lfs.2005.09.001</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/16202429">16202429</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Life+Sciences&amp;rft.atitle=Targeted+screening+for+biogenic+amine+transporters%3A+potential+applications+for+natural+products&amp;rft.volume=78&amp;rft.issue=5&amp;rft.pages=512-518&amp;rft.date=2005-12&amp;rft_id=info%3Adoi%2F10.1016%2Fj.lfs.2005.09.001&amp;rft_id=info%3Apmid%2F16202429&amp;rft.aulast=Rothman&amp;rft.aufirst=RB&amp;rft.au=Baumann%2C+MH&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-RothmanBaumannDersch2001-11"><span class="mw-cite-backlink"><b><a href="#cite_ref-RothmanBaumannDersch2001_11-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRothmanBaumannDerschRomero2001" class="citation journal cs1">Rothman RB, Baumann MH, Dersch CM, Romero DV, Rice KC, Carroll FI, Partilla JS (January 2001). "Amphetamine-type central nervous system stimulants release norepinephrine more potently than they release dopamine and serotonin". <i>Synapse</i>. <b>39</b> (1): 32–41. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2F1098-2396%2820010101%2939%3A1%3C32%3A%3AAID-SYN5%3E3.0.CO%3B2-3">10.1002/1098-2396(20010101)39:1&#60;32::AID-SYN5&#62;3.0.CO&#59;2-3</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/11071707">11071707</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Synapse&amp;rft.atitle=Amphetamine-type+central+nervous+system+stimulants+release+norepinephrine+more+potently+than+they+release+dopamine+and+serotonin&amp;rft.volume=39&amp;rft.issue=1&amp;rft.pages=32-41&amp;rft.date=2001-01&amp;rft_id=info%3Adoi%2F10.1002%2F1098-2396%2820010101%2939%3A1%3C32%3A%3AAID-SYN5%3E3.0.CO%3B2-3&amp;rft_id=info%3Apmid%2F11071707&amp;rft.aulast=Rothman&amp;rft.aufirst=RB&amp;rft.au=Baumann%2C+MH&amp;rft.au=Dersch%2C+CM&amp;rft.au=Romero%2C+DV&amp;rft.au=Rice%2C+KC&amp;rft.au=Carroll%2C+FI&amp;rft.au=Partilla%2C+JS&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-BaumannAyestasPartilla2012-12"><span class="mw-cite-backlink"><b><a href="#cite_ref-BaumannAyestasPartilla2012_12-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBaumannAyestasPartillaSink2012" class="citation journal cs1">Baumann MH, Ayestas MA, Partilla JS, Sink JR, Shulgin AT, Daley PF, Brandt SD, Rothman RB, Ruoho AE, Cozzi NV (April 2012). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306880">"The designer methcathinone analogs, mephedrone and methylone, are substrates for monoamine transporters in brain tissue"</a>. <i>Neuropsychopharmacology</i>. <b>37</b> (5): 1192–203. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1038%2Fnpp.2011.304">10.1038/npp.2011.304</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306880">3306880</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/22169943">22169943</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Neuropsychopharmacology&amp;rft.atitle=The+designer+methcathinone+analogs%2C+mephedrone+and+methylone%2C+are+substrates+for+monoamine+transporters+in+brain+tissue&amp;rft.volume=37&amp;rft.issue=5&amp;rft.pages=1192-203&amp;rft.date=2012-04&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC3306880%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F22169943&amp;rft_id=info%3Adoi%2F10.1038%2Fnpp.2011.304&amp;rft.aulast=Baumann&amp;rft.aufirst=MH&amp;rft.au=Ayestas%2C+MA&amp;rft.au=Partilla%2C+JS&amp;rft.au=Sink%2C+JR&amp;rft.au=Shulgin%2C+AT&amp;rft.au=Daley%2C+PF&amp;rft.au=Brandt%2C+SD&amp;rft.au=Rothman%2C+RB&amp;rft.au=Ruoho%2C+AE&amp;rft.au=Cozzi%2C+NV&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC3306880&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-KuropkaZawadzkiSzpot2023-13"><span class="mw-cite-backlink">^ <a href="#cite_ref-KuropkaZawadzkiSzpot2023_13-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-KuropkaZawadzkiSzpot2023_13-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFKuropkaZawadzkiSzpot2023" class="citation journal cs1">Kuropka P, Zawadzki M, Szpot P (May 2023). "A narrative review of the neuropharmacology of synthetic cathinones-Popular alternatives to classical drugs of abuse". <i>Hum Psychopharmacol</i>. <b>38</b> (3): e2866. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2Fhup.2866">10.1002/hup.2866</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/36866677">36866677</a>. <q>Another feature that distinguishes [substituted cathinones (SCs)] from amphetamines is their negligible interaction with the trace amine associated receptor 1 (TAAR1). Activation of this receptor reduces the activity of dopaminergic neurones, thereby reducing psychostimulatory effects and addictive potential (Miller, 2011; Simmler et al., 2016). Amphetamines are potent agonists of this receptor, making them likely to self‐inhibit their stimulating effects. In contrast, SCs show negligible activity towards TAAR1 (Kolaczynska et al., 2021; Rickli et al., 2015; Simmler et al., 2014, 2016). [...] The lack of self‐regulation by TAAR1 may partly explain the higher addictive potential of SCs compared to amphetamines (Miller, 2011; Simmler et al., 2013).</q></cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Hum+Psychopharmacol&amp;rft.atitle=A+narrative+review+of+the+neuropharmacology+of+synthetic+cathinones-Popular+alternatives+to+classical+drugs+of+abuse&amp;rft.volume=38&amp;rft.issue=3&amp;rft.pages=e2866&amp;rft.date=2023-05&amp;rft_id=info%3Adoi%2F10.1002%2Fhup.2866&amp;rft_id=info%3Apmid%2F36866677&amp;rft.aulast=Kuropka&amp;rft.aufirst=P&amp;rft.au=Zawadzki%2C+M&amp;rft.au=Szpot%2C+P&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-SimmlerBuchyChaboz2016-14"><span class="mw-cite-backlink">^ <a href="#cite_ref-SimmlerBuchyChaboz2016_14-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-SimmlerBuchyChaboz2016_14-1"><sup><i><b>b</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSimmlerBuchyChabozHoener2016" class="citation journal cs1">Simmler LD, Buchy D, Chaboz S, Hoener MC, Liechti ME (April 2016). "In Vitro Characterization of Psychoactive Substances at Rat, Mouse, and Human Trace Amine-Associated Receptor 1". <i>J Pharmacol Exp Ther</i>. <b>357</b> (1): 134–144. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1124%2Fjpet.115.229765">10.1124/jpet.115.229765</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/26791601">26791601</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=J+Pharmacol+Exp+Ther&amp;rft.atitle=In+Vitro+Characterization+of+Psychoactive+Substances+at+Rat%2C+Mouse%2C+and+Human+Trace+Amine-Associated+Receptor+1&amp;rft.volume=357&amp;rft.issue=1&amp;rft.pages=134-144&amp;rft.date=2016-04&amp;rft_id=info%3Adoi%2F10.1124%2Fjpet.115.229765&amp;rft_id=info%3Apmid%2F26791601&amp;rft.aulast=Simmler&amp;rft.aufirst=LD&amp;rft.au=Buchy%2C+D&amp;rft.au=Chaboz%2C+S&amp;rft.au=Hoener%2C+MC&amp;rft.au=Liechti%2C+ME&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-SimmlerRickliHoener2014-15"><span class="mw-cite-backlink"><b><a href="#cite_ref-SimmlerRickliHoener2014_15-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFSimmlerRickliHoenerLiechti2014" class="citation journal cs1">Simmler LD, Rickli A, Hoener MC, Liechti ME (April 2014). "Monoamine transporter and receptor interaction profiles of a new series of designer cathinones". <i>Neuropharmacology</i>. <b>79</b>: 152–160. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.neuropharm.2013.11.008">10.1016/j.neuropharm.2013.11.008</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/24275046">24275046</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Neuropharmacology&amp;rft.atitle=Monoamine+transporter+and+receptor+interaction+profiles+of+a+new+series+of+designer+cathinones&amp;rft.volume=79&amp;rft.pages=152-160&amp;rft.date=2014-04&amp;rft_id=info%3Adoi%2F10.1016%2Fj.neuropharm.2013.11.008&amp;rft_id=info%3Apmid%2F24275046&amp;rft.aulast=Simmler&amp;rft.aufirst=LD&amp;rft.au=Rickli%2C+A&amp;rft.au=Hoener%2C+MC&amp;rft.au=Liechti%2C+ME&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-16"><span class="mw-cite-backlink"><b><a href="#cite_ref-16">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/550/2008_Implementation_report_281411.pdf">Europol 2008 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-17"><span class="mw-cite-backlink"><b><a href="#cite_ref-17">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/553/2009_Implementation_report_281420.pdf">Europol 2009 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-18"><span class="mw-cite-backlink"><b><a href="#cite_ref-18">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/644/EMCDDA-Europol_Annual_Report_2010A_281336.pdf">Europol 2010 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-19"><span class="mw-cite-backlink"><b><a href="#cite_ref-19">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/689/EMCDDA-Europol_Annual_Report_2011_2012_final_335568.pdf">Europol 2011 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-20"><span class="mw-cite-backlink"><b><a href="#cite_ref-20">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/734/EMCDDA-Europol_2012_Annual_Report_final_439477.pdf">Europol 2012 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-21"><span class="mw-cite-backlink"><b><a href="#cite_ref-21">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/814/TDAN14001ENN_475519.pdf">Europol 2013 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-22"><span class="mw-cite-backlink"><b><a href="#cite_ref-22">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/1018/TDAN15001ENN.pdf">Europol 2014 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-23"><span class="mw-cite-backlink"><b><a href="#cite_ref-23">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/2880/TDAS16001ENN.pdf">Europol 2015 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-24"><span class="mw-cite-backlink"><b><a href="#cite_ref-24">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/4724/TDAN17001ENN_PDFWEB.pdf">Europol 2016 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-25"><span class="mw-cite-backlink"><b><a href="#cite_ref-25">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/system/files/publications/9282/20183924_TDAN18001ENN_PDF.pdf">Europol 2017 Annual Report on the implementation of Council Decision 2005/387/JHA</a></span> </li> <li id="cite_note-26"><span class="mw-cite-backlink"><b><a href="#cite_ref-26">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFEuropean_Monitoring_Center_for_Drugs_and_Drug_Addiction2020" class="citation book cs1">European Monitoring Center for Drugs and Drug Addiction (December 2020). <a rel="nofollow" class="external text" href="https://www.emcdda.europa.eu/system/files/publications/13464/20205648_TD0320796ENN_PDF_rev.pdf"><i>New psychoactive substances: global markets, glocal threats and the COVID-19 pandemic. An update from the EU Early Warning System</i></a> <span class="cs1-format">(PDF)</span>. Luxembourg: Publications Office of the European Union. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.2810%2F921262">10.2810/921262</a>. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a>&#160;<a href="/wiki/Special:BookSources/9789294975584" title="Special:BookSources/9789294975584"><bdi>9789294975584</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&amp;rft.genre=book&amp;rft.btitle=New+psychoactive+substances%3A+global+markets%2C+glocal+threats+and+the+COVID-19+pandemic.+An+update+from+the+EU+Early+Warning+System&amp;rft.place=Luxembourg&amp;rft.pub=Publications+Office+of+the+European+Union&amp;rft.date=2020-12&amp;rft_id=info%3Adoi%2F10.2810%2F921262&amp;rft.isbn=9789294975584&amp;rft.au=European+Monitoring+Center+for+Drugs+and+Drug+Addiction&amp;rft_id=https%3A%2F%2Fwww.emcdda.europa.eu%2Fsystem%2Ffiles%2Fpublications%2F13464%2F20205648_TD0320796ENN_PDF_rev.pdf&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-27"><span class="mw-cite-backlink"><b><a href="#cite_ref-27">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMaurerKraemerSpringerStaack2004" class="citation journal cs1">Maurer HH, Kraemer T, Springer D, Staack RF (April 2004). "Chemistry, pharmacology, toxicology, and hepatic metabolism of designer drugs of the amphetamine (ecstasy), piperazine, and pyrrolidinophenone types: a synopsis". <i>Therapeutic Drug Monitoring</i>. <b>26</b> (2): 127–31. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1097%2F00007691-200404000-00007">10.1097/00007691-200404000-00007</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/15228152">15228152</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a>&#160;<a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:9255084">9255084</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Therapeutic+Drug+Monitoring&amp;rft.atitle=Chemistry%2C+pharmacology%2C+toxicology%2C+and+hepatic+metabolism+of+designer+drugs+of+the+amphetamine+%28ecstasy%29%2C+piperazine%2C+and+pyrrolidinophenone+types%3A+a+synopsis&amp;rft.volume=26&amp;rft.issue=2&amp;rft.pages=127-31&amp;rft.date=2004-04&amp;rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A9255084%23id-name%3DS2CID&amp;rft_id=info%3Apmid%2F15228152&amp;rft_id=info%3Adoi%2F10.1097%2F00007691-200404000-00007&amp;rft.aulast=Maurer&amp;rft.aufirst=HH&amp;rft.au=Kraemer%2C+T&amp;rft.au=Springer%2C+D&amp;rft.au=Staack%2C+RF&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-28"><span class="mw-cite-backlink"><b><a href="#cite_ref-28">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFDavisRands-TrevorBoydEdirisinghe2012" class="citation journal cs1">Davis S, Rands-Trevor K, Boyd S, Edirisinghe M (April 2012). "The characterisation of two halogenated cathinone analogues: 3,5-difluoromethcathinone and 3,5-dichloromethcathinone". <i>Forensic Science International</i>. <b>217</b> (1–3): 139–45. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.forsciint.2011.10.042">10.1016/j.forsciint.2011.10.042</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/22088945">22088945</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Forensic+Science+International&amp;rft.atitle=The+characterisation+of+two+halogenated+cathinone+analogues%3A+3%2C5-difluoromethcathinone+and+3%2C5-dichloromethcathinone&amp;rft.volume=217&amp;rft.issue=1%E2%80%933&amp;rft.pages=139-45&amp;rft.date=2012-04&amp;rft_id=info%3Adoi%2F10.1016%2Fj.forsciint.2011.10.042&amp;rft_id=info%3Apmid%2F22088945&amp;rft.aulast=Davis&amp;rft.aufirst=S&amp;rft.au=Rands-Trevor%2C+K&amp;rft.au=Boyd%2C+S&amp;rft.au=Edirisinghe%2C+M&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-pmid27863142-29"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid27863142_29-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFLiuJiaLiHua2017" class="citation journal cs1">Liu C, Jia W, Li T, Hua Z, Qian Z (August 2017). "Identification and analytical characterization of nine synthetic cathinone derivatives N-ethylhexedrone, 4-Cl-pentedrone, 4-Cl-α-EAPP, propylone, N-ethylnorpentylone, 6-MeO-bk-MDMA, α-PiHP, 4-Cl-α-PHP, and 4-F-α-PHP". <i>Drug Testing and Analysis</i>. <b>9</b> (8): 1162–1171. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2Fdta.2136">10.1002/dta.2136</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/27863142">27863142</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Drug+Testing+and+Analysis&amp;rft.atitle=Identification+and+analytical+characterization+of+nine+synthetic+cathinone+derivatives+N-ethylhexedrone%2C+4-Cl-pentedrone%2C+4-Cl-%CE%B1-EAPP%2C+propylone%2C+N-ethylnorpentylone%2C+6-MeO-bk-MDMA%2C+%CE%B1-PiHP%2C+4-Cl-%CE%B1-PHP%2C+and+4-F-%CE%B1-PHP&amp;rft.volume=9&amp;rft.issue=8&amp;rft.pages=1162-1171&amp;rft.date=2017-08&amp;rft_id=info%3Adoi%2F10.1002%2Fdta.2136&amp;rft_id=info%3Apmid%2F27863142&amp;rft.aulast=Liu&amp;rft.aufirst=C&amp;rft.au=Jia%2C+W&amp;rft.au=Li%2C+T&amp;rft.au=Hua%2C+Z&amp;rft.au=Qian%2C+Z&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-30"><span class="mw-cite-backlink"><b><a href="#cite_ref-30">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFBłażewiczBednarekPopławskaOlech2019" class="citation journal cs1">Błażewicz A, Bednarek E, Popławska M, Olech N, Sitkowski J, Kozerski L (2019). <a rel="nofollow" class="external text" href="https://doi.org/10.1007%2Fs11419-018-00463-w">"Identification and structural characterization of synthetic cathinones: N-propylcathinone, 2,4-dimethylmethcathinone, 2,4-dimethylethcathinone, 2,4-dimethyl-α-pyrrolidinopropiophenone, 4-bromo-α-pyrrolidinopropiophenone, 1-(2,3-dihydro-1H-inden-5-yl)-2-(pyrrolidin-1-yl)hexan-1-one and 2,4-dimethylisocathinone"</a>. <i>Forensic Toxicol</i>. <b>37</b> (2): 288–307. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://doi.org/10.1007%2Fs11419-018-00463-w">10.1007/s11419-018-00463-w</a></span>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a>&#160;<a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:59618061">59618061</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Forensic+Toxicol&amp;rft.atitle=Identification+and+structural+characterization+of+synthetic+cathinones%3A+N-propylcathinone%2C+2%2C4-dimethylmethcathinone%2C+2%2C4-dimethylethcathinone%2C+2%2C4-dimethyl-%CE%B1-pyrrolidinopropiophenone%2C+4-bromo-%CE%B1-pyrrolidinopropiophenone%2C+1-%282%2C3-dihydro-1H-inden-5-yl%29-2-%28pyrrolidin-1-yl%29hexan-1-one+and+2%2C4-dimethylisocathinone.&amp;rft.volume=37&amp;rft.issue=2&amp;rft.pages=288-307&amp;rft.date=2019&amp;rft_id=info%3Adoi%2F10.1007%2Fs11419-018-00463-w&amp;rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A59618061%23id-name%3DS2CID&amp;rft.aulast=B%C5%82a%C5%BCewicz&amp;rft.aufirst=A&amp;rft.au=Bednarek%2C+E&amp;rft.au=Pop%C5%82awska%2C+M&amp;rft.au=Olech%2C+N&amp;rft.au=Sitkowski%2C+J&amp;rft.au=Kozerski%2C+L&amp;rft_id=https%3A%2F%2Fdoi.org%2F10.1007%252Fs11419-018-00463-w&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-31"><span class="mw-cite-backlink"><b><a href="#cite_ref-31">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFWestphalGirreserAngererAuwärter2016" class="citation journal cs1">Westphal F, Girreser U, Angerer V, Auwärter V (January 2016). "Analytische Daten neuer 2-aminosubstituierter Methylendioxyvalerophenonderivate". <i>Toxichem Krimtech</i>. <b>83</b> (1): 3–29.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Toxichem+Krimtech&amp;rft.atitle=Analytische+Daten+neuer+2-aminosubstituierter+Methylendioxyvalerophenonderivate.&amp;rft.volume=83&amp;rft.issue=1&amp;rft.pages=3-29&amp;rft.date=2016-01&amp;rft.aulast=Westphal&amp;rft.aufirst=F&amp;rft.au=Girreser%2C+U&amp;rft.au=Angerer%2C+V&amp;rft.au=Auw%C3%A4rter%2C+V&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-pmid29367861-32"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid29367861_32-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFMajchrzakCelińskiKuśKowalska2018" class="citation journal cs1">Majchrzak M, Celiński R, Kuś P, Kowalska T, Sajewicz M (2018). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754390">"The newest cathinone derivatives as designer drugs: an analytical and toxicological review"</a>. <i>Forensic Toxicology</i>. <b>36</b> (1): 33–50. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1007%2Fs11419-017-0385-6">10.1007/s11419-017-0385-6</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754390">5754390</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/29367861">29367861</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Forensic+Toxicology&amp;rft.atitle=The+newest+cathinone+derivatives+as+designer+drugs%3A+an+analytical+and+toxicological+review&amp;rft.volume=36&amp;rft.issue=1&amp;rft.pages=33-50&amp;rft.date=2018&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC5754390%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F29367861&amp;rft_id=info%3Adoi%2F10.1007%2Fs11419-017-0385-6&amp;rft.aulast=Majchrzak&amp;rft.aufirst=M&amp;rft.au=Celi%C5%84ski%2C+R&amp;rft.au=Ku%C5%9B%2C+P&amp;rft.au=Kowalska%2C+T&amp;rft.au=Sajewicz%2C+M&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC5754390&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-pmid29426062-33"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid29426062_33-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFCarlssonSandgrenSvenssonKonradsson2018" class="citation journal cs1">Carlsson A, Sandgren V, Svensson S, Konradsson P, Dunne S, Josefsson M, Dahlén J (February 2018). "Prediction of designer drugs: Synthesis and spectroscopic analysis of synthetic cathinone analogs that may appear on the Swedish drug market". <i>Drug Testing and Analysis</i>. <b>10</b> (7): 1076–1098. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1002%2Fdta.2366">10.1002/dta.2366</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/29426062">29426062</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Drug+Testing+and+Analysis&amp;rft.atitle=Prediction+of+designer+drugs%3A+Synthesis+and+spectroscopic+analysis+of+synthetic+cathinone+analogs+that+may+appear+on+the+Swedish+drug+market&amp;rft.volume=10&amp;rft.issue=7&amp;rft.pages=1076-1098&amp;rft.date=2018-02&amp;rft_id=info%3Adoi%2F10.1002%2Fdta.2366&amp;rft_id=info%3Apmid%2F29426062&amp;rft.aulast=Carlsson&amp;rft.aufirst=A&amp;rft.au=Sandgren%2C+V&amp;rft.au=Svensson%2C+S&amp;rft.au=Konradsson%2C+P&amp;rft.au=Dunne%2C+S&amp;rft.au=Josefsson%2C+M&amp;rft.au=Dahl%C3%A9n%2C+J&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-pmid30925345-34"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid30925345_34-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFChengWong2019" class="citation journal cs1">Cheng WC, Wong WC (May 2019). "Forensic drug analysis of chloro-N,N-dimethylcathinone (CDC) and chloroethcathinone (CEC): Identification of 4-CDC and 4-CEC in drug seizures and differentiation from their ring-substituted positional isomers". <i>Forensic Science International</i>. <b>298</b>: 268–277. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.forsciint.2019.03.002">10.1016/j.forsciint.2019.03.002</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/30925345">30925345</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a>&#160;<a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:87589412">87589412</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Forensic+Science+International&amp;rft.atitle=Forensic+drug+analysis+of+chloro-N%2CN-dimethylcathinone+%28CDC%29+and+chloroethcathinone+%28CEC%29%3A+Identification+of+4-CDC+and+4-CEC+in+drug+seizures+and+differentiation+from+their+ring-substituted+positional+isomers&amp;rft.volume=298&amp;rft.pages=268-277&amp;rft.date=2019-05&amp;rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A87589412%23id-name%3DS2CID&amp;rft_id=info%3Apmid%2F30925345&amp;rft_id=info%3Adoi%2F10.1016%2Fj.forsciint.2019.03.002&amp;rft.aulast=Cheng&amp;rft.aufirst=WC&amp;rft.au=Wong%2C+WC&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-pmid32882537-35"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid32882537_35-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFLajtaiMayerLakatosKuzma2020" class="citation journal cs1">Lajtai A, Mayer M, Lakatos Á, Kuzma M, Miseta A (November 2020). <a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.legalmed.2020.101780">"New psychoactive versus conventional stimulants - a ten-year review of casework in Hungary"</a>. <i>Legal Medicine</i>. <b>47</b>: 101780. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.legalmed.2020.101780">10.1016/j.legalmed.2020.101780</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/32882537">32882537</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a>&#160;<a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:221496728">221496728</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Legal+Medicine&amp;rft.atitle=New+psychoactive+versus+conventional+stimulants+-+a+ten-year+review+of+casework+in+Hungary&amp;rft.volume=47&amp;rft.pages=101780&amp;rft.date=2020-11&amp;rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A221496728%23id-name%3DS2CID&amp;rft_id=info%3Apmid%2F32882537&amp;rft_id=info%3Adoi%2F10.1016%2Fj.legalmed.2020.101780&amp;rft.aulast=Lajtai&amp;rft.aufirst=A&amp;rft.au=Mayer%2C+M&amp;rft.au=Lakatos%2C+%C3%81&amp;rft.au=Kuzma%2C+M&amp;rft.au=Miseta%2C+A&amp;rft_id=https%3A%2F%2Fdoi.org%2F10.1016%252Fj.legalmed.2020.101780&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-pmid33385148-36"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid33385148_36-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFJonesComparin2020" class="citation journal cs1">Jones NS, Comparin JH (2020). <a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770462">"Interpol review of controlled substances 2016-2019"</a>. <i>Forensic Science International. Synergy</i>. <b>2</b>: 608–669. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1016%2Fj.fsisyn.2020.01.019">10.1016/j.fsisyn.2020.01.019</a>. <a href="/wiki/PMC_(identifier)" class="mw-redirect" title="PMC (identifier)">PMC</a>&#160;<span class="id-lock-free" title="Freely accessible"><a rel="nofollow" class="external text" href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770462">7770462</a></span>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a>&#160;<a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/33385148">33385148</a>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.jtitle=Forensic+Science+International.+Synergy&amp;rft.atitle=Interpol+review+of+controlled+substances+2016-2019&amp;rft.volume=2&amp;rft.pages=608-669&amp;rft.date=2020&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC7770462%23id-name%3DPMC&amp;rft_id=info%3Apmid%2F33385148&amp;rft_id=info%3Adoi%2F10.1016%2Fj.fsisyn.2020.01.019&amp;rft.aulast=Jones&amp;rft.aufirst=NS&amp;rft.au=Comparin%2C+JH&amp;rft_id=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpmc%2Farticles%2FPMC7770462&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-37"><span class="mw-cite-backlink"><b><a href="#cite_ref-37">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1 cs1-prop-foreign-lang-source"><a rel="nofollow" class="external text" href="https://finlex.fi/fi/laki/ajantasa/2014/20141130#a12.11.2020-764">"Valtioneuvoston asetus kuluttajamarkkinoilta kielletyistä psykoaktiivisista aineista"</a> &#91;Government Decree on Psychoactive Substances Banned from the Consumer Market&#93;. <i>Finlex Data Bank</i> (in Finnish).</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=unknown&amp;rft.jtitle=Finlex+Data+Bank&amp;rft.atitle=Valtioneuvoston+asetus+kuluttajamarkkinoilta+kielletyist%C3%A4+psykoaktiivisista+aineista&amp;rft_id=https%3A%2F%2Ffinlex.fi%2Ffi%2Flaki%2Fajantasa%2F2014%2F20141130%23a12.11.2020-764&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-38"><span class="mw-cite-backlink"><b><a href="#cite_ref-38">^</a></b></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://patentscope.wipo.int/search/docs2/pct/WO2022061242/pdf/d-Al9aJlB0RxMhOKRtAmzc0zWYBlQMtlEPPAwrFzVXCP4zVtp32KPFndslDTNmTtm2Yi_eJPREIfizbOW83Rm695cIgRNuOlYvPC5BuGKjEaBMaKSoZVLX0b_NhYEMD2?docId=id00000065267029&amp;filename=WO2022061242-PAMPH-20220324-7029.pdf">Baggott M. Advantageous Tryptamine Compositions For Mental Disorders or Enhancement. Patent WO 2022/061242</a></span> </li> <li id="cite_note-ACMD2010-39"><span class="mw-cite-backlink"><b><a href="#cite_ref-ACMD2010_39-0">^</a></b></span> <span class="reference-text">Advisory Council on the Misuse of Drugs (UK). <a rel="nofollow" class="external text" href="http://www.homeoffice.gov.uk/publications/alcohol-drugs/drugs/acmd1/acmd-cathinodes-report-2010?view=Binary">Consideration of the cathinones. 31 March 2010.</a> <a rel="nofollow" class="external text" href="https://web.archive.org/web/20110922230621/http://www.homeoffice.gov.uk/publications/alcohol-drugs/drugs/acmd1/acmd-cathinodes-report-2010?view=Binary">Archived</a> 22 September 2011 at the <a href="/wiki/Wayback_Machine" title="Wayback Machine">Wayback Machine</a> Retrieved 2011-07-17.</span> </li> <li id="cite_note-40"><span class="mw-cite-backlink"><b><a href="#cite_ref-40">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="http://www.opsi.gov.uk/si/si2010/uksi_20101144_en_1">"The Misuse of Drugs (Amendment) (England, Wales and Scotland) Regulations 2010 No. 1144"</a>. Opsi.gov.uk<span class="reference-accessdate">. Retrieved <span class="nowrap">8 April</span> 2010</span>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&amp;rft.genre=unknown&amp;rft.btitle=The+Misuse+of+Drugs+%28Amendment%29+%28England%2C+Wales+and+Scotland%29+Regulations+2010+No.+1144&amp;rft.pub=Opsi.gov.uk&amp;rft_id=http%3A%2F%2Fwww.opsi.gov.uk%2Fsi%2Fsi2010%2Fuksi_20101144_en_1&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-41"><span class="mw-cite-backlink"><b><a href="#cite_ref-41">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="http://news.bbc.co.uk/1/hi/uk/10602398.stm">"NRG-1 'legal high' drug is banned"</a>. BBC News. 12 July 2010<span class="reference-accessdate">. Retrieved <span class="nowrap">17 July</span> 2010</span>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&amp;rft.genre=unknown&amp;rft.btitle=NRG-1+%27legal+high%27+drug+is+banned&amp;rft.pub=BBC+News&amp;rft.date=2010-07-12&amp;rft_id=http%3A%2F%2Fnews.bbc.co.uk%2F1%2Fhi%2Fuk%2F10602398.stm&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-42"><span class="mw-cite-backlink"><b><a href="#cite_ref-42">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="https://web.archive.org/web/20100717121420/http://www.homeoffice.gov.uk/publications/drugs/acmd1/naphyrone-report">"Advisory Council on the Misuse of Drugs Naphyrone Report (2010)"</a>. Home Office. 7 July 2010. Archived from <a rel="nofollow" class="external text" href="http://www.homeoffice.gov.uk/publications/drugs/acmd1/naphyrone-report">the original</a> on 17 July 2010<span class="reference-accessdate">. Retrieved <span class="nowrap">17 July</span> 2010</span>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&amp;rft.genre=unknown&amp;rft.btitle=Advisory+Council+on+the+Misuse+of+Drugs+Naphyrone+Report+%282010%29&amp;rft.pub=Home+Office&amp;rft.date=2010-07-07&amp;rft_id=http%3A%2F%2Fwww.homeoffice.gov.uk%2Fpublications%2Fdrugs%2Facmd1%2Fnaphyrone-report&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-43"><span class="mw-cite-backlink"><b><a href="#cite_ref-43">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="http://www.opsi.gov.uk/si/si2010/em/uksiem_20101799_en.pdf">"Explanatory Memorandum To The Misuse of Drugs (Amendment No. 2) (England, Wales and Scotland) Regulations 2010 No. 1799"</a> <span class="cs1-format">(PDF)</span>. Opsi.gov.uk<span class="reference-accessdate">. Retrieved <span class="nowrap">18 July</span> 2010</span>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&amp;rft.genre=unknown&amp;rft.btitle=Explanatory+Memorandum+To+The+Misuse+of+Drugs+%28Amendment+No.+2%29+%28England%2C+Wales+and+Scotland%29+Regulations+2010+No.+1799&amp;rft.pub=Opsi.gov.uk&amp;rft_id=http%3A%2F%2Fwww.opsi.gov.uk%2Fsi%2Fsi2010%2Fem%2Fuksiem_20101799_en.pdf&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-44"><span class="mw-cite-backlink"><b><a href="#cite_ref-44">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite class="citation web cs1"><a rel="nofollow" class="external text" href="http://www.opsi.gov.uk/si/si2010/pdf/uksi_20101799_en.pdf">"The Misuse of Drugs (Amendment No. 2) (England, Wales and Scotland) Regulations 2010 No. 1799"</a> <span class="cs1-format">(PDF)</span>. Opsi.gov.uk<span class="reference-accessdate">. Retrieved <span class="nowrap">18 July</span> 2010</span>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&amp;rft.genre=unknown&amp;rft.btitle=The+Misuse+of+Drugs+%28Amendment+No.+2%29+%28England%2C+Wales+and+Scotland%29+Regulations+2010+No.+1799&amp;rft.pub=Opsi.gov.uk&amp;rft_id=http%3A%2F%2Fwww.opsi.gov.uk%2Fsi%2Fsi2010%2Fpdf%2Fuksi_20101799_en.pdf&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> <li id="cite_note-45"><span class="mw-cite-backlink"><b><a href="#cite_ref-45">^</a></b></span> <span class="reference-text">European Monitoring Centre on Drugs and Drug Addiction. <a rel="nofollow" class="external text" href="http://www.emcdda.europa.eu/attachements.cfm/att_132857_EN_EMCDDA-Europol%20Annual%20Report%202010A.pdf">EMCDDA–Europol 2010 Annual Report on the implementation of Council Decision 2005/387/JHA.</a> <a rel="nofollow" class="external text" href="https://web.archive.org/web/20120314043454/http://www.emcdda.europa.eu/attachements.cfm/att_132857_EN_EMCDDA-Europol%20Annual%20Report%202010A.pdf">Archived</a> 14 March 2012 at the <a href="/wiki/Wayback_Machine" title="Wayback Machine">Wayback Machine</a> Retrieved 2011-07-17.</span> </li> <li id="cite_note-46"><span class="mw-cite-backlink"><b><a href="#cite_ref-46">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFGoodnoughZezima2011" class="citation web cs1">Goodnough A, Zezima K (16 July 2011). <a rel="nofollow" class="external text" href="https://www.nytimes.com/2011/07/17/us/17salts.html">"An Alarming New Stimulant, Legal in Many States"</a>. <i><a href="/wiki/The_New_York_Times" title="The New York Times">The New York Times</a></i><span class="reference-accessdate">. Retrieved <span class="nowrap">17 July</span> 2011</span>.</cite><span title="ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=unknown&amp;rft.jtitle=The+New+York+Times&amp;rft.atitle=An+Alarming+New+Stimulant%2C+Legal+in+Many+States.&amp;rft.date=2011-07-16&amp;rft.aulast=Goodnough&amp;rft.aufirst=A&amp;rft.au=Zezima%2C+K&amp;rft_id=https%3A%2F%2Fwww.nytimes.com%2F2011%2F07%2F17%2Fus%2F17salts.html&amp;rfr_id=info%3Asid%2Fen.wikipedia.org%3ASubstituted+cathinone" class="Z3988"></span></span> </li> </ol></div></div> <div class="navbox-styles"><style data-mw-deduplicate="TemplateStyles:r1129693374">.mw-parser-output .hlist dl,.mw-parser-output .hlist ol,.mw-parser-output .hlist ul{margin:0;padding:0}.mw-parser-output .hlist dd,.mw-parser-output .hlist dt,.mw-parser-output .hlist li{margin:0;display:inline}.mw-parser-output .hlist.inline,.mw-parser-output .hlist.inline dl,.mw-parser-output .hlist.inline ol,.mw-parser-output .hlist.inline ul,.mw-parser-output .hlist dl dl,.mw-parser-output .hlist dl ol,.mw-parser-output .hlist dl ul,.mw-parser-output .hlist ol dl,.mw-parser-output .hlist ol ol,.mw-parser-output .hlist ol ul,.mw-parser-output .hlist ul dl,.mw-parser-output .hlist ul ol,.mw-parser-output .hlist ul ul{display:inline}.mw-parser-output .hlist .mw-empty-li{display:none}.mw-parser-output .hlist dt::after{content:": "}.mw-parser-output .hlist dd::after,.mw-parser-output .hlist li::after{content:" · ";font-weight:bold}.mw-parser-output .hlist dd:last-child::after,.mw-parser-output .hlist dt:last-child::after,.mw-parser-output .hlist li:last-child::after{content:none}.mw-parser-output .hlist dd dd:first-child::before,.mw-parser-output .hlist dd dt:first-child::before,.mw-parser-output .hlist dd li:first-child::before,.mw-parser-output .hlist dt dd:first-child::before,.mw-parser-output .hlist dt dt:first-child::before,.mw-parser-output .hlist dt li:first-child::before,.mw-parser-output .hlist li dd:first-child::before,.mw-parser-output .hlist li dt:first-child::before,.mw-parser-output .hlist li li:first-child::before{content:" (";font-weight:normal}.mw-parser-output .hlist dd dd:last-child::after,.mw-parser-output .hlist dd dt:last-child::after,.mw-parser-output .hlist dd li:last-child::after,.mw-parser-output .hlist dt dd:last-child::after,.mw-parser-output .hlist dt dt:last-child::after,.mw-parser-output .hlist dt li:last-child::after,.mw-parser-output .hlist li dd:last-child::after,.mw-parser-output .hlist li dt:last-child::after,.mw-parser-output .hlist li li:last-child::after{content:")";font-weight:normal}.mw-parser-output .hlist ol{counter-reset:listitem}.mw-parser-output .hlist ol>li{counter-increment:listitem}.mw-parser-output .hlist ol>li::before{content:" "counter(listitem)"\a0 "}.mw-parser-output .hlist dd ol>li:first-child::before,.mw-parser-output .hlist dt ol>li:first-child::before,.mw-parser-output .hlist li ol>li:first-child::before{content:" ("counter(listitem)"\a0 "}</style><style data-mw-deduplicate="TemplateStyles:r1236075235">.mw-parser-output .navbox{box-sizing:border-box;border:1px solid #a2a9b1;width:100%;clear:both;font-size:88%;text-align:center;padding:1px;margin:1em auto 0}.mw-parser-output .navbox .navbox{margin-top:0}.mw-parser-output .navbox+.navbox,.mw-parser-output .navbox+.navbox-styles+.navbox{margin-top:-1px}.mw-parser-output .navbox-inner,.mw-parser-output .navbox-subgroup{width:100%}.mw-parser-output .navbox-group,.mw-parser-output .navbox-title,.mw-parser-output .navbox-abovebelow{padding:0.25em 1em;line-height:1.5em;text-align:center}.mw-parser-output .navbox-group{white-space:nowrap;text-align:right}.mw-parser-output .navbox,.mw-parser-output .navbox-subgroup{background-color:#fdfdfd}.mw-parser-output .navbox-list{line-height:1.5em;border-color:#fdfdfd}.mw-parser-output .navbox-list-with-group{text-align:left;border-left-width:2px;border-left-style:solid}.mw-parser-output tr+tr>.navbox-abovebelow,.mw-parser-output tr+tr>.navbox-group,.mw-parser-output tr+tr>.navbox-image,.mw-parser-output tr+tr>.navbox-list{border-top:2px solid #fdfdfd}.mw-parser-output .navbox-title{background-color:#ccf}.mw-parser-output .navbox-abovebelow,.mw-parser-output .navbox-group,.mw-parser-output .navbox-subgroup .navbox-title{background-color:#ddf}.mw-parser-output .navbox-subgroup .navbox-group,.mw-parser-output .navbox-subgroup .navbox-abovebelow{background-color:#e6e6ff}.mw-parser-output .navbox-even{background-color:#f7f7f7}.mw-parser-output .navbox-odd{background-color:transparent}.mw-parser-output .navbox .hlist td dl,.mw-parser-output .navbox .hlist td ol,.mw-parser-output .navbox .hlist td ul,.mw-parser-output .navbox td.hlist dl,.mw-parser-output .navbox td.hlist ol,.mw-parser-output .navbox td.hlist ul{padding:0.125em 0}.mw-parser-output .navbox .navbar{display:block;font-size:100%}.mw-parser-output .navbox-title .navbar{float:left;text-align:left;margin-right:0.5em}body.skin--responsive .mw-parser-output .navbox-image img{max-width:none!important}@media print{body.ns-0 .mw-parser-output .navbox{display:none!important}}</style></div><div role="navigation" class="navbox" aria-labelledby="Phenethylamines" style="padding:3px"><table class="nowraplinks mw-collapsible autocollapse navbox-inner" style="border-spacing:0;background:transparent;color:inherit"><tbody><tr><th scope="col" class="navbox-title" colspan="2"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><style data-mw-deduplicate="TemplateStyles:r1239400231">.mw-parser-output .navbar{display:inline;font-size:88%;font-weight:normal}.mw-parser-output .navbar-collapse{float:left;text-align:left}.mw-parser-output .navbar-boxtext{word-spacing:0}.mw-parser-output .navbar ul{display:inline-block;white-space:nowrap;line-height:inherit}.mw-parser-output .navbar-brackets::before{margin-right:-0.125em;content:"[ "}.mw-parser-output .navbar-brackets::after{margin-left:-0.125em;content:" ]"}.mw-parser-output .navbar li{word-spacing:-0.125em}.mw-parser-output .navbar a>span,.mw-parser-output .navbar a>abbr{text-decoration:inherit}.mw-parser-output .navbar-mini abbr{font-variant:small-caps;border-bottom:none;text-decoration:none;cursor:inherit}.mw-parser-output .navbar-ct-full{font-size:114%;margin:0 7em}.mw-parser-output .navbar-ct-mini{font-size:114%;margin:0 4em}html.skin-theme-clientpref-night .mw-parser-output .navbar li a abbr{color:var(--color-base)!important}@media(prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .navbar li a abbr{color:var(--color-base)!important}}@media print{.mw-parser-output .navbar{display:none!important}}</style><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Phenethylamines" title="Template:Phenethylamines"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Phenethylamines" title="Template talk:Phenethylamines"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Phenethylamines" title="Special:EditPage/Template:Phenethylamines"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Phenethylamines" style="font-size:114%;margin:0 4em"><a href="/wiki/Substituted_phenethylamine" title="Substituted phenethylamine">Phenethylamines</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Substituted_phenethylamine" title="Substituted phenethylamine">Phenethylamines</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Psychedelics:</i> <a href="/wiki/25B-NBOMe" title="25B-NBOMe">25B-NBOMe</a></li> <li><a href="/wiki/25C-NBOMe" title="25C-NBOMe">25C-NBOMe</a></li> <li><a href="/wiki/25D-NBOMe" title="25D-NBOMe">25D-NBOMe</a></li> <li><a href="/wiki/25I-NBOMe" title="25I-NBOMe">25I-NBOMe</a></li> <li><a href="/wiki/25N-NBOMe" title="25N-NBOMe">25N-NBOMe</a></li></ul> <ul><li><a href="/wiki/2C-B" title="2C-B">2C-B</a></li> <li><a href="/w/index.php?title=2C-B-AN&amp;action=edit&amp;redlink=1" class="new" title="2C-B-AN (page does not exist)">2C-B-AN</a></li> <li><a href="/w/index.php?title=2C-Bn&amp;action=edit&amp;redlink=1" class="new" title="2C-Bn (page does not exist)">2C-Bn</a></li> <li><a href="/w/index.php?title=2C-Bu&amp;action=edit&amp;redlink=1" class="new" title="2C-Bu (page does not exist)">2C-Bu</a></li> <li><a href="/wiki/2C-C" title="2C-C">2C-C</a></li> <li><a href="/w/index.php?title=2C-CN&amp;action=edit&amp;redlink=1" class="new" title="2C-CN (page does not exist)">2C-CN</a></li> <li><a href="/wiki/2C-CP" title="2C-CP">2C-CP</a></li> <li><a href="/wiki/2C-D" title="2C-D">2C-D</a></li> <li><a href="/wiki/2C-E" title="2C-E">2C-E</a></li> <li><a href="/wiki/2C-EF" title="2C-EF">2C-EF</a></li> <li><a href="/wiki/2C-F" title="2C-F">2C-F</a></li> <li><a href="/wiki/2C-G" title="2C-G">2C-G</a></li> <li><a href="/wiki/2C-G-1" class="mw-redirect" title="2C-G-1">2C-G-1</a></li> <li><a href="/wiki/2C-G-2" class="mw-redirect" title="2C-G-2">2C-G-2</a></li> <li><a href="/wiki/2C-G-3" class="mw-redirect" title="2C-G-3">2C-G-3</a></li> <li><a href="/wiki/2C-G-4" class="mw-redirect" title="2C-G-4">2C-G-4</a></li> <li><a href="/wiki/2C-G-5" class="mw-redirect" title="2C-G-5">2C-G-5</a></li> <li><a href="/wiki/2C-G-6" class="mw-redirect" title="2C-G-6">2C-G-6</a></li> <li><a href="/wiki/2C-G-N" class="mw-redirect" title="2C-G-N">2C-G-N</a></li> <li><a href="/wiki/2C-H" title="2C-H">2C-H</a></li> <li><a href="/wiki/2C-I" title="2C-I">2C-I</a></li> <li><a href="/wiki/2C-iP" title="2C-iP">2C-iP</a></li> <li><a href="/wiki/2C-N" title="2C-N">2C-N</a></li> <li><a href="/w/index.php?title=2C-NH2&amp;action=edit&amp;redlink=1" class="new" title="2C-NH2 (page does not exist)">2C-NH2</a></li> <li><a href="/wiki/2C-O" class="mw-redirect" title="2C-O">2C-O</a></li> <li><a href="/wiki/2C-O-4" title="2C-O-4">2C-O-4</a></li> <li><a href="/wiki/2C-P" title="2C-P">2C-P</a></li> <li><a href="/w/index.php?title=2C-Ph&amp;action=edit&amp;redlink=1" class="new" title="2C-Ph (page does not exist)">2C-Ph</a></li> <li><a href="/wiki/2C-SE" class="mw-redirect" title="2C-SE">2C-SE</a></li> <li><a href="/wiki/2C-T" title="2C-T">2C-T</a></li> <li><a href="/wiki/2C-T-2" title="2C-T-2">2C-T-2</a></li> <li><a href="/wiki/2C-T-3" title="2C-T-3">2C-T-3</a></li> <li><a href="/wiki/2C-T-4" title="2C-T-4">2C-T-4</a></li> <li><a href="/w/index.php?title=2C-T-5&amp;action=edit&amp;redlink=1" class="new" title="2C-T-5 (page does not exist)">2C-T-5</a></li> <li><a href="/w/index.php?title=2C-T-6&amp;action=edit&amp;redlink=1" class="new" title="2C-T-6 (page does not exist)">2C-T-6</a></li> <li><a href="/wiki/2C-T-7" title="2C-T-7">2C-T-7</a></li> <li><a href="/wiki/2C-T-8" title="2C-T-8">2C-T-8</a></li> <li><a href="/wiki/2C-T-9" class="mw-redirect" title="2C-T-9">2C-T-9</a></li> <li><a href="/w/index.php?title=2C-T-10&amp;action=edit&amp;redlink=1" class="new" title="2C-T-10 (page does not exist)">2C-T-10</a></li> <li><a href="/w/index.php?title=2C-T-11&amp;action=edit&amp;redlink=1" class="new" title="2C-T-11 (page does not exist)">2C-T-11</a></li> <li><a href="/w/index.php?title=2C-T-12&amp;action=edit&amp;redlink=1" class="new" title="2C-T-12 (page does not exist)">2C-T-12</a></li> <li><a href="/wiki/2C-T-13" title="2C-T-13">2C-T-13</a></li> <li><a href="/w/index.php?title=2C-T-14&amp;action=edit&amp;redlink=1" class="new" title="2C-T-14 (page does not exist)">2C-T-14</a></li> <li><a href="/wiki/2C-T-15" title="2C-T-15">2C-T-15</a></li> <li><a href="/wiki/2C-T-16" title="2C-T-16">2C-T-16</a></li> <li><a href="/wiki/2C-T-17" title="2C-T-17">2C-T-17</a></li> <li><a href="/w/index.php?title=2C-T-18&amp;action=edit&amp;redlink=1" class="new" title="2C-T-18 (page does not exist)">2C-T-18</a></li> <li><a href="/wiki/2C-T-19" title="2C-T-19">2C-T-19</a></li> <li><a href="/w/index.php?title=2C-T-20&amp;action=edit&amp;redlink=1" class="new" title="2C-T-20 (page does not exist)">2C-T-20</a></li> <li><a href="/wiki/2C-T-21" title="2C-T-21">2C-T-21</a></li> <li><a href="/w/index.php?title=2C-T-22&amp;action=edit&amp;redlink=1" class="new" title="2C-T-22 (page does not exist)">2C-T-22</a></li> <li><a href="/w/index.php?title=2C-T-22.5&amp;action=edit&amp;redlink=1" class="new" title="2C-T-22.5 (page does not exist)">2C-T-22.5</a></li> <li><a href="/w/index.php?title=2C-T-23&amp;action=edit&amp;redlink=1" class="new" title="2C-T-23 (page does not exist)">2C-T-23</a></li> <li><a href="/w/index.php?title=2C-T-24&amp;action=edit&amp;redlink=1" class="new" title="2C-T-24 (page does not exist)">2C-T-24</a></li> <li><a href="/w/index.php?title=2C-T-25&amp;action=edit&amp;redlink=1" class="new" title="2C-T-25 (page does not exist)">2C-T-25</a></li> <li><a href="/w/index.php?title=2C-T-27&amp;action=edit&amp;redlink=1" class="new" title="2C-T-27 (page does not exist)">2C-T-27</a></li> <li><a href="/wiki/2C-T-28" title="2C-T-28">2C-T-28</a></li> <li><a href="/w/index.php?title=2C-T-30&amp;action=edit&amp;redlink=1" class="new" title="2C-T-30 (page does not exist)">2C-T-30</a></li> <li><a href="/w/index.php?title=2C-T-31&amp;action=edit&amp;redlink=1" class="new" title="2C-T-31 (page does not exist)">2C-T-31</a></li> <li><a href="/w/index.php?title=2C-T-32&amp;action=edit&amp;redlink=1" class="new" title="2C-T-32 (page does not exist)">2C-T-32</a></li> <li><a href="/w/index.php?title=2C-T-33&amp;action=edit&amp;redlink=1" class="new" title="2C-T-33 (page does not exist)">2C-T-33</a></li> <li><a href="/wiki/2C-TFE" title="2C-TFE">2C-TFE</a></li> <li><a href="/wiki/2C-TFM" title="2C-TFM">2C-TFM</a></li> <li><a href="/wiki/2C-YN" title="2C-YN">2C-YN</a></li> <li><a href="/wiki/2C-V" title="2C-V">2C-V</a></li></ul> <ul><li><a href="/wiki/Allylescaline" title="Allylescaline">Allylescaline</a></li> <li><a href="/wiki/DESOXY" title="DESOXY">DESOXY</a></li> <li><a href="/wiki/Escaline" title="Escaline">Escaline</a></li> <li><a href="/wiki/Isoproscaline" title="Isoproscaline">Isoproscaline</a></li> <li><a href="/wiki/Jimscaline" title="Jimscaline">Jimscaline</a></li> <li><a href="/wiki/Macromerine" title="Macromerine">Macromerine</a></li> <li><a href="/wiki/3-Methoxy-4-ethoxyphenethylamine" title="3-Methoxy-4-ethoxyphenethylamine">MEPEA</a></li> <li><a href="/wiki/Mescaline" title="Mescaline">Mescaline</a></li> <li><a href="/wiki/Metaescaline" title="Metaescaline">Metaescaline</a></li> <li><a href="/wiki/Methallylescaline" title="Methallylescaline">Methallylescaline</a></li> <li><a href="/wiki/Proscaline" title="Proscaline">Proscaline</a></li> <li><a href="/wiki/Psi-2C-T-4" class="mw-redirect" title="Psi-2C-T-4">Psi-2C-T-4</a></li> <li><a href="/wiki/TCB-2" title="TCB-2">TCB-2</a></li></ul> <p><br /><i>Stimulants:</i> <a href="/wiki/Phenylethanolamine" title="Phenylethanolamine">Phenylethanolamine</a> </p> <ul><li><a href="/wiki/Hordenine" title="Hordenine">Hordenine</a></li> <li><a href="/wiki/Phenethylamine" title="Phenethylamine">Phenethylamine</a></li> <li><a href="/wiki/Phenpromethamine" title="Phenpromethamine">Phenpromethamine</a></li> <li><a href="/wiki/Amphetamine" title="Amphetamine">α-Methylphenethylamine</a> (amphetamine)</li> <li><a href="/wiki/%CE%92-Methylphenethylamine" title="Β-Methylphenethylamine">β-Methylphenethylamine</a></li> <li><a href="/wiki/M-Methylphenethylamine" class="mw-redirect" title="M-Methylphenethylamine"><i>m</i>-Methylphenethylamine</a></li> <li><a href="/wiki/N-Methylphenethylamine" title="N-Methylphenethylamine"><i>N</i>-Methylphenethylamine</a></li> <li><a href="/wiki/O-Methylphenethylamine" class="mw-redirect" title="O-Methylphenethylamine"><i>o</i>-Methylphenethylamine</a></li> <li><a href="/wiki/P-Methylphenethylamine" class="mw-redirect" title="P-Methylphenethylamine"><i>p</i>-Methylphenethylamine</a></li> <li><a href="/wiki/Methylphenidate" title="Methylphenidate">Methylphenidate</a></li></ul> <ul><li><i>Entactogens:</i> <a href="/wiki/Lophophine" title="Lophophine">Lophophine</a></li> <li><a href="/wiki/Methylenedioxyphenethylamine" class="mw-redirect" title="Methylenedioxyphenethylamine">MDPEA</a></li> <li><a href="/wiki/Methylenedioxymethylphenethylamine" class="mw-redirect" title="Methylenedioxymethylphenethylamine">MDMPEA</a><br /><i>Others:</i> <a href="/wiki/BOH_(drug)" title="BOH (drug)">BOH</a></li> <li><a href="/wiki/3,4-Dimethoxyphenethylamine" title="3,4-Dimethoxyphenethylamine">DMPEA</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Substituted_amphetamine" title="Substituted amphetamine">Amphetamines</a></th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Psychedelics:</i> <a href="/wiki/3C-AL" title="3C-AL">3C-AL</a></li> <li><a href="/wiki/3C-BZ" title="3C-BZ">3C-BZ</a></li> <li><a href="/wiki/3C-E" title="3C-E">3C-E</a></li> <li><a href="/wiki/3C-MAL" title="3C-MAL">3C-MAL</a></li> <li><a href="/wiki/3C-P" title="3C-P">3C-P</a></li> <li><a href="/wiki/Aleph_(psychedelic)" title="Aleph (psychedelic)">Aleph</a></li> <li><a href="/wiki/Beatrice_(psychedelic)" title="Beatrice (psychedelic)">Beatrice</a></li> <li><a href="/wiki/Bromo-DragonFLY" title="Bromo-DragonFLY">Bromo-DragonFLY</a></li> <li><a href="/wiki/D-Deprenyl" title="D-Deprenyl">D-Deprenyl</a></li> <li><a href="/wiki/Dimethoxyamphetamine" title="Dimethoxyamphetamine">DMA</a></li> <li><a href="/wiki/4-Methyl-2,5-methoxyphenylcyclopropylamine" class="mw-redirect" title="4-Methyl-2,5-methoxyphenylcyclopropylamine">DMCPA</a></li> <li><a href="/wiki/DMMDA" title="DMMDA">DMMDA</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-bromoamphetamine" title="2,5-Dimethoxy-4-bromoamphetamine">DOB</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-chloroamphetamine" title="2,5-Dimethoxy-4-chloroamphetamine">DOC</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-fluoroethylamphetamine" class="mw-redirect" title="2,5-Dimethoxy-4-fluoroethylamphetamine">DOEF</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-ethylamphetamine" title="2,5-Dimethoxy-4-ethylamphetamine">DOET</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-iodoamphetamine" title="2,5-Dimethoxy-4-iodoamphetamine">DOI</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-methylamphetamine" title="2,5-Dimethoxy-4-methylamphetamine">DOM</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-nitroamphetamine" title="2,5-Dimethoxy-4-nitroamphetamine">DON</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-propylamphetamine" title="2,5-Dimethoxy-4-propylamphetamine">DOPR</a></li> <li><a href="/wiki/2,5-Dimethoxy-4-trifluoromethylamphetamine" title="2,5-Dimethoxy-4-trifluoromethylamphetamine">DOTFM</a></li> <li><a href="/wiki/Ganesha_(psychedelic)" title="Ganesha (psychedelic)">Ganesha</a></li> <li><a href="/wiki/MMDA_(drug)" title="MMDA (drug)">MMDA</a></li> <li><a href="/wiki/MMDA-2" title="MMDA-2">MMDA-2</a></li> <li><a href="/wiki/Psi-DOM" class="mw-redirect" title="Psi-DOM">Psi-DOM</a></li> <li><a href="/wiki/Trimethoxyamphetamine" title="Trimethoxyamphetamine">TMA</a></li> <li><a href="/wiki/Tetramethoxyamphetamine" class="mw-redirect" title="Tetramethoxyamphetamine">TeMA</a></li> <li><a href="/wiki/ZDCM-04" title="ZDCM-04">ZDCM-04</a><br /><i>Stimulants:</i> <a href="/wiki/2-Fluoroamphetamine" title="2-Fluoroamphetamine">2-FA</a></li> <li><a href="/wiki/2-Fluoromethamphetamine" title="2-Fluoromethamphetamine">2-FMA</a></li> <li><a href="/wiki/3-Fluoroamphetamine" title="3-Fluoroamphetamine">3-FA</a></li> <li><a href="/wiki/3-Fluoromethamphetamine" title="3-Fluoromethamphetamine">3-FMA</a></li> <li><a href="/wiki/Acridorex" title="Acridorex">Acridorex</a></li> <li><a href="/wiki/Alfetamine" title="Alfetamine">Alfetamine</a></li> <li><a href="/wiki/Amfecloral" title="Amfecloral">Amfecloral</a></li> <li><a href="/wiki/Amfepentorex" title="Amfepentorex">Amfepentorex</a></li> <li><a href="/wiki/Amphetamine" title="Amphetamine">Amphetamine</a> (<a href="/wiki/Dextroamphetamine" title="Dextroamphetamine">Dextroamphetamine</a>, <a href="/wiki/Levoamphetamine" title="Levoamphetamine">Levoamphetamine</a>)</li> <li><a href="/wiki/Amphetaminil" class="mw-redirect" title="Amphetaminil">Amphetaminil</a></li> <li><a href="/wiki/Benfluorex" title="Benfluorex">Benfluorex</a></li> <li><a href="/wiki/Benzphetamine" title="Benzphetamine">Benzphetamine</a></li> <li><a href="/wiki/Cathine" title="Cathine">Cathine</a></li> <li><a href="/wiki/Clobenzorex" title="Clobenzorex">Clobenzorex</a></li> <li><a href="/wiki/Dimethylamphetamine" title="Dimethylamphetamine">Dimethylamphetamine</a></li> <li><a href="/wiki/Ephedrine" title="Ephedrine">Ephedrine</a></li> <li><a href="/wiki/Etilamfetamine" title="Etilamfetamine">Etilamfetamine</a></li> <li><a href="/wiki/Fencamfamin" title="Fencamfamin">Fencamfamin</a></li> <li><a href="/wiki/Fencamine" title="Fencamine">Fencamine</a></li> <li><a href="/wiki/Fenethylline" title="Fenethylline">Fenethylline</a></li> <li><a href="/wiki/Fenfluramine" title="Fenfluramine">Fenfluramine</a> (<a href="/wiki/Dexfenfluramine" title="Dexfenfluramine">Dexfenfluramine</a>, <a href="/wiki/Levofenfluramine" title="Levofenfluramine">Levofenfluramine</a>)</li> <li><a href="/wiki/Fenproporex" title="Fenproporex">Fenproporex</a></li> <li><a href="/wiki/Flucetorex" title="Flucetorex">Flucetorex</a></li> <li><a href="/wiki/Fludorex" title="Fludorex">Fludorex</a></li> <li><a href="/wiki/Formetorex" title="Formetorex">Formetorex</a></li> <li><a href="/wiki/Furfenorex" title="Furfenorex">Furfenorex</a></li> <li><a href="/wiki/Gepefrine" title="Gepefrine">Gepefrine</a></li> <li><a href="/wiki/4-Hydroxyamphetamine" title="4-Hydroxyamphetamine">4-Hydroxyamphetamine</a></li> <li><a href="/wiki/Iofetamine" class="mw-redirect" title="Iofetamine">Iofetamine</a></li> <li><a href="/wiki/Isopropylamphetamine" title="Isopropylamphetamine">Isopropylamphetamine</a></li> <li><a href="/wiki/Lefetamine" title="Lefetamine">Lefetamine</a></li> <li><a href="/wiki/Lisdexamfetamine" title="Lisdexamfetamine">Lisdexamfetamine</a></li> <li><a href="/wiki/Mefenorex" title="Mefenorex">Mefenorex</a></li> <li><a href="/wiki/Metaraminol" title="Metaraminol">Metaraminol</a></li> <li><a href="/wiki/Methamphetamine" title="Methamphetamine">Methamphetamine</a> (Dextromethamphetamine, <a href="/wiki/Levomethamphetamine" class="mw-redirect" title="Levomethamphetamine">Levomethamphetamine</a>)</li> <li><a href="/wiki/Methoxyphenamine" title="Methoxyphenamine">Methoxyphenamine</a></li> <li><a href="/wiki/3-Methoxy-4-methylamphetamine" title="3-Methoxy-4-methylamphetamine">MMA</a></li> <li><a href="/wiki/Morforex" title="Morforex">Morforex</a></li> <li><a href="/wiki/Norfenfluramine" title="Norfenfluramine">Norfenfluramine</a></li> <li><a href="/wiki/L-Norpseudoephedrine" title="L-Norpseudoephedrine"><span style="font-size:85%;">L</span>-Norpseudoephedrine</a></li> <li><a href="/wiki/N,alpha-Diethylphenylethylamine" class="mw-redirect" title="N,alpha-Diethylphenylethylamine">N,alpha-Diethylphenylethylamine</a></li> <li><a href="/wiki/Oxifentorex" title="Oxifentorex">Oxifentorex</a></li> <li><a href="/wiki/Oxilofrine" title="Oxilofrine">Oxilofrine</a></li> <li><a href="/wiki/Ortetamine" title="Ortetamine">Ortetamine</a></li> <li><a href="/wiki/Para-Bromoamphetamine" title="Para-Bromoamphetamine">PBA</a></li> <li><a href="/wiki/Para-Chloroamphetamine" title="Para-Chloroamphetamine">PCA</a></li> <li><a href="/wiki/4-Fluoroamphetamine" title="4-Fluoroamphetamine">PFA</a></li> <li><a href="/wiki/4-Fluoromethamphetamine" title="4-Fluoromethamphetamine">PFMA</a></li> <li><a href="/wiki/Para-Iodoamphetamine" title="Para-Iodoamphetamine">PIA</a></li> <li><a href="/wiki/Para-Methoxyamphetamine" title="Para-Methoxyamphetamine">PMA</a></li> <li><a href="/wiki/Para-Methoxy-N-ethylamphetamine" title="Para-Methoxy-N-ethylamphetamine">PMEA</a></li> <li><a href="/wiki/Para-Methoxy-N-methylamphetamine" title="Para-Methoxy-N-methylamphetamine">PMMA</a></li> <li><a href="/wiki/Phenylpropanolamine" title="Phenylpropanolamine">Phenylpropanolamine</a></li> <li><a href="/wiki/Pholedrine" title="Pholedrine">Pholedrine</a></li> <li><a href="/wiki/Prenylamine" title="Prenylamine">Prenylamine</a></li> <li><a href="/wiki/Propylamphetamine" title="Propylamphetamine">Propylamphetamine</a></li> <li><a href="/wiki/Pseudoephedrine" title="Pseudoephedrine">Pseudoephedrine</a></li> <li><a href="/wiki/Sibutramine" title="Sibutramine">Sibutramine</a></li> <li><a href="/wiki/Tiflorex" title="Tiflorex">Tiflorex</a></li> <li><a href="/wiki/Tranylcypromine" title="Tranylcypromine">Tranylcypromine</a></li> <li><a href="/wiki/Xylopropamine" title="Xylopropamine">Xylopropamine</a></li> <li><a href="/wiki/Zylofuramine" title="Zylofuramine">Zylofuramine</a><br /><i>Entactogens:</i> <a href="/wiki/4-Fluoroamphetamine" title="4-Fluoroamphetamine">4-FA</a></li> <li><a href="/wiki/4-Fluoromethamphetamine" title="4-Fluoromethamphetamine">4-FMA</a></li> <li><a href="/wiki/4-Methylamphetamine" title="4-Methylamphetamine">4-MA</a></li> <li><a href="/wiki/4-Methylmethamphetamine" class="mw-redirect" title="4-Methylmethamphetamine">4-MMA</a></li> <li><a href="/wiki/4-Methylthioamphetamine" title="4-Methylthioamphetamine">4-MTA</a></li> <li><a href="/wiki/5-APB" title="5-APB">5-APB</a></li> <li><a href="/wiki/5-APDB" title="5-APDB">5-APDB</a></li> <li><a href="/wiki/5-EAPB" title="5-EAPB">5-EAPB</a></li> <li><a href="/wiki/5-IT" title="5-IT">5-IT</a></li> <li><a href="/wiki/5-MAPB" title="5-MAPB">5-MAPB</a></li> <li><a href="/wiki/5-MAPDB" title="5-MAPDB">5-MAPDB</a></li> <li><a href="/wiki/6-APB" title="6-APB">6-APB</a></li> <li><a href="/wiki/6-APDB" title="6-APDB">6-APDB</a></li> <li><a href="/wiki/6-Chloro-MDMA" title="6-Chloro-MDMA">6-Chloro-MDMA</a></li> <li><a href="/wiki/6-EAPB" title="6-EAPB">6-EAPB</a></li> <li><a href="/wiki/6-IT" class="mw-redirect" title="6-IT">6-IT</a></li> <li><a href="/wiki/6-MAPB" title="6-MAPB">6-MAPB</a></li> <li><a href="/wiki/6-MAPDB" title="6-MAPDB">6-MAPDB</a></li> <li><a href="/wiki/Ethylidenedioxyamphetamine" class="mw-redirect" title="Ethylidenedioxyamphetamine">EDA</a></li> <li><a href="/wiki/Indanylaminopropane" class="mw-redirect" title="Indanylaminopropane">IAP</a></li> <li><a href="/wiki/2,3-Methylenedioxyamphetamine" title="2,3-Methylenedioxyamphetamine">2,3-MDA</a></li> <li><a href="/wiki/3,4-Methylenedioxyamphetamine" title="3,4-Methylenedioxyamphetamine">3,4-MDA (tenamfetamine)</a></li> <li><a href="/wiki/Methylenedioxyethylamphetamine" class="mw-redirect" title="Methylenedioxyethylamphetamine">MDEA</a></li> <li><a href="/wiki/Methylenedioxyhydroxylmethamphetamine" class="mw-redirect" title="Methylenedioxyhydroxylmethamphetamine">MDHMA</a></li> <li><a href="/wiki/MDMA" title="MDMA">MDMA (midomafetamine)</a></li> <li><a href="/wiki/Methylenedioxyhydroxyamphetamine" class="mw-redirect" title="Methylenedioxyhydroxyamphetamine">MDOH</a></li> <li><a href="/wiki/Methamnetamine" title="Methamnetamine">Methamnetamine</a></li> <li><a href="/wiki/MMDMA" title="MMDMA">MMDMA</a></li> <li><a href="/wiki/Naphthylaminopropane" title="Naphthylaminopropane">Naphthylaminopropane</a></li> <li><a href="/wiki/Tetralinylaminopropane" class="mw-redirect" title="Tetralinylaminopropane">TAP</a><br /><i>Others:</i> <a href="/wiki/3,4-Dichloroamphetamine" title="3,4-Dichloroamphetamine">3,4-DCA</a></li> <li><a href="/wiki/Amiflamine" title="Amiflamine">Amiflamine</a></li> <li><a href="/wiki/DiFMDA" class="mw-redirect" title="DiFMDA">DiFMDA</a></li> <li><a href="/wiki/Selegiline" title="Selegiline">Selegiline</a> (also <a href="/wiki/D-Deprenyl" title="D-Deprenyl"><span style="font-size:85%;">D</span>-Deprenyl</a>)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Phentermine" title="Phentermine">Phentermines</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Stimulants:</i> <a href="/wiki/Chlorphentermine" title="Chlorphentermine">Chlorphentermine</a></li> <li><a href="/wiki/Cloforex" title="Cloforex">Cloforex</a></li> <li><a href="/wiki/Clortermine" title="Clortermine">Clortermine</a></li> <li><a href="/wiki/Etolorex" title="Etolorex">Etolorex</a></li> <li><a href="/wiki/Mephentermine" title="Mephentermine">Mephentermine</a></li> <li><a href="/wiki/Pentorex" title="Pentorex">Pentorex</a></li> <li><a href="/wiki/Phentermine" title="Phentermine">Phentermine</a><br /><i>Entactogens:</i> <a href="/wiki/Methylenedioxyphentermine" class="mw-redirect" title="Methylenedioxyphentermine">MDPH</a></li> <li><a href="/wiki/Methylenedioxymethylphentermine" class="mw-redirect" title="Methylenedioxymethylphentermine">MDMPH</a><br /><i>Others:</i> <a href="/wiki/Cericlamine" title="Cericlamine">Cericlamine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a class="mw-selflink selflink">Cathinones</a></th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Stimulants:</i> <a href="/wiki/3-Fluoromethcathinone" title="3-Fluoromethcathinone">3-FMC</a></li> <li><a href="/wiki/4-Methylcathinone" title="4-Methylcathinone">4-MC</a></li> <li><a href="/wiki/4-Bromomethcathinone" title="4-Bromomethcathinone">4-BMC</a></li> <li><a href="/wiki/4-Chloromethcathinone" title="4-Chloromethcathinone">4-CMC</a></li> <li><a href="/wiki/4-Ethylmethcathinone" title="4-Ethylmethcathinone">4-EMC</a></li> <li><a href="/wiki/Flephedrone" title="Flephedrone">4-FMC</a></li> <li><a href="/wiki/4-Methylethcathinone" title="4-Methylethcathinone">4-MEC</a></li> <li><a href="/wiki/4-Methylbuphedrone" title="4-Methylbuphedrone">4-MeMABP</a></li> <li><a href="/wiki/4-Methylpentedrone" title="4-Methylpentedrone">4-MPD</a></li> <li><a href="/wiki/Amfepramone" title="Amfepramone">Amfepramone</a></li> <li><a href="/wiki/Benzedrone" title="Benzedrone">Benzedrone</a></li> <li><a href="/wiki/Brephedrone" class="mw-redirect" title="Brephedrone">Brephedrone</a></li> <li><a href="/wiki/Buphedrone" title="Buphedrone">Buphedrone</a></li> <li><a href="/wiki/Bupropion" title="Bupropion">Bupropion</a></li> <li><a href="/wiki/Cathinone" title="Cathinone">Cathinone</a></li> <li><a href="/wiki/Dimethylcathinone" class="mw-redirect" title="Dimethylcathinone">Dimethylcathinone</a></li> <li><a href="/wiki/Ethcathinone" title="Ethcathinone">Ethcathinone</a></li> <li><a href="/wiki/Eutylone" title="Eutylone">Eutylone</a></li> <li><a href="/wiki/Hydroxybupropion" title="Hydroxybupropion">Hydroxybupropion</a></li> <li><a href="/wiki/Methcathinone" title="Methcathinone">Methcathinone</a></li> <li><a href="/wiki/Methedrone" title="Methedrone">Methedrone</a></li> <li><a href="/wiki/N-Ethylbuphedrone" title="N-Ethylbuphedrone">NEB</a></li> <li><a href="/wiki/N-Ethylhexedrone" title="N-Ethylhexedrone">N-Ethylhexedrone</a></li> <li><a href="/wiki/N-Ethylpentedrone" title="N-Ethylpentedrone">N-Ethylpentedrone</a></li> <li><a href="/wiki/Pentedrone" title="Pentedrone">Pentedrone</a></li> <li><a href="/wiki/Pentylone" title="Pentylone">Pentylone</a></li> <li><a href="/wiki/Radafaxine" title="Radafaxine">Radafaxine</a><br /><i>Entactogens:</i> <a href="/wiki/3,4-Dimethylmethcathinone" title="3,4-Dimethylmethcathinone">3,4-DMMC</a></li> <li><a href="/wiki/3-Methylmethcathinone" title="3-Methylmethcathinone">3-MMC</a></li> <li><a href="/wiki/Butylone" title="Butylone">Butylone</a></li> <li><a href="/wiki/Ethylone" title="Ethylone">Ethylone</a></li> <li><a href="/wiki/Methylone" title="Methylone">Methylone</a></li> <li><a href="/wiki/Methylenedioxycathinone" title="Methylenedioxycathinone">Methylenedioxycathinone</a></li> <li><a href="/wiki/Mephedrone" title="Mephedrone">Mephedrone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Phenylisobutylamine" title="Phenylisobutylamine">Phenylisobutylamines</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Entactogens:</i> <a href="/wiki/4-Chlorophenylisobutylamine" title="4-Chlorophenylisobutylamine">4-CAB</a></li> <li><a href="/wiki/4-Methylphenylisobutylamine" title="4-Methylphenylisobutylamine">4-MAB</a></li> <li><a href="/wiki/Ariadne_(psychedelic)" class="mw-redirect" title="Ariadne (psychedelic)">Ariadne</a></li> <li><a href="/wiki/Benzodioxolylbutanamine" class="mw-redirect" title="Benzodioxolylbutanamine">BDB</a></li> <li><a href="/wiki/Butylone" title="Butylone">Butylone</a></li> <li><a href="/wiki/Ethylbenzodioxolylbutanamine" class="mw-redirect" title="Ethylbenzodioxolylbutanamine">EBDB</a></li> <li><a href="/wiki/Eutylone" title="Eutylone">Eutylone</a></li> <li><a href="/wiki/MBDB" title="MBDB">MBDB</a><br /><i>Stimulants:</i> <a href="/wiki/Phenylisobutylamine" title="Phenylisobutylamine">Phenylisobutylamine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Phenylethylpyrrolidine" title="Phenylethylpyrrolidine">Phenylalkylpyrrolidines</a></th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Stimulants:</i> <a href="/wiki/Alpha-Pyrrolidinobutiophenone" class="mw-redirect" title="Alpha-Pyrrolidinobutiophenone">α-PBP</a></li> <li><a href="/wiki/Alpha-Pyrrolidinohexiophenone" class="mw-redirect" title="Alpha-Pyrrolidinohexiophenone">α-PHP</a></li> <li><a href="/wiki/Alpha-Pyrrolidinopropiophenone" class="mw-redirect" title="Alpha-Pyrrolidinopropiophenone">α-PPP</a></li> <li><a href="/wiki/Alpha-Pyrrolidinopentiophenone" class="mw-redirect" title="Alpha-Pyrrolidinopentiophenone">α-PVP</a></li> <li><a href="/wiki/3%27,4%27-Methylenedioxy-%CE%B1-pyrrolidinobutiophenone" title="3&#39;,4&#39;-Methylenedioxy-α-pyrrolidinobutiophenone">MDPBP</a></li> <li><a href="/wiki/3%27,4%27-Methylenedioxy-%CE%B1-pyrrolidinopropiophenone" title="3&#39;,4&#39;-Methylenedioxy-α-pyrrolidinopropiophenone">MDPPP</a></li> <li><a href="/wiki/3,4-Methylenedioxypyrovalerone" class="mw-redirect" title="3,4-Methylenedioxypyrovalerone">MDPV</a></li> <li><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinobutiophenone" title="4&#39;-Methyl-α-pyrrolidinobutiophenone">4-MePBP</a></li> <li><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinohexiophenone" title="4&#39;-Methyl-α-pyrrolidinohexiophenone">4-MePHP</a></li> <li><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinopropiophenone" title="4&#39;-Methyl-α-pyrrolidinopropiophenone">4-MePPP</a></li> <li><a href="/wiki/4%27-Methoxy-%CE%B1-pyrrolidinopropiophenone" title="4&#39;-Methoxy-α-pyrrolidinopropiophenone">MOPPP</a></li> <li><a href="/wiki/4%27-Methoxy-%CE%B1-pyrrolidinopentiophenone" title="4&#39;-Methoxy-α-pyrrolidinopentiophenone">MOPVP</a></li> <li><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinobutiophenone" title="4&#39;-Methyl-α-pyrrolidinobutiophenone">MPBP</a></li> <li><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinohexiophenone" title="4&#39;-Methyl-α-pyrrolidinohexiophenone">MPHP</a></li> <li><a href="/wiki/4%27-Methyl-%CE%B1-pyrrolidinopropiophenone" title="4&#39;-Methyl-α-pyrrolidinopropiophenone">MPPP</a></li> <li><a href="/wiki/Naphyrone" title="Naphyrone">Naphyrone</a></li> <li><a href="/wiki/Phenylethylpyrrolidine" title="Phenylethylpyrrolidine">PEP</a></li> <li><a href="/wiki/Prolintane" title="Prolintane">Prolintane</a></li> <li><a href="/wiki/Pyrovalerone" title="Pyrovalerone">Pyrovalerone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Catecholamine" title="Catecholamine">Catecholamines</a><br /><span style="font-size:85%;">(and close relatives)</span></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/6-Fluoronorepinephrine" title="6-Fluoronorepinephrine">6-FNE</a></li> <li><a href="/wiki/6-Hydroxydopamine" class="mw-redirect" title="6-Hydroxydopamine">6-OHDA</a></li> <li><a href="/wiki/Alpha-Methyldopamine" class="mw-redirect" title="Alpha-Methyldopamine">a-Me-DA</a></li> <li><a href="/wiki/Alpha-Methyltyramine" class="mw-redirect" title="Alpha-Methyltyramine">a-Me-TRA</a></li> <li><a href="/wiki/Adrenochrome" title="Adrenochrome">Adrenochrome</a></li> <li><a href="/wiki/Ciladopa" title="Ciladopa">Ciladopa</a></li> <li><a href="/wiki/D-DOPA" title="D-DOPA"><span style="font-size:85%;">D</span>-DOPA</a> (Dextrodopa)</li> <li><a href="/wiki/Dimetofrine" title="Dimetofrine">Dimetofrine</a></li> <li><a href="/wiki/Dopamine" title="Dopamine">Dopamine</a></li> <li><a href="/wiki/Epinephrine_(neurotransmitter)" class="mw-redirect" title="Epinephrine (neurotransmitter)">Epinephrine</a></li> <li><a href="/wiki/Epinine" class="mw-redirect" title="Epinine">Epinine</a></li> <li><a href="/wiki/Etilefrine" title="Etilefrine">Etilefrine</a></li> <li><a href="/wiki/Ethylnorepinephrine" title="Ethylnorepinephrine">Ethylnorepinephrine</a></li> <li><a href="/wiki/Fenclonine" title="Fenclonine">Fenclonine</a></li> <li><a href="/wiki/Ibopamine" title="Ibopamine">Ibopamine</a></li> <li><a href="/wiki/Isoprenaline" title="Isoprenaline">Isoprenaline</a></li> <li><a href="/wiki/Isoetarine" title="Isoetarine">Isoetarine</a></li> <li><a href="/wiki/L-DOPA" title="L-DOPA"><span style="font-size:85%;">L</span>-DOPA</a> (Levodopa)</li> <li><a href="/wiki/L-DOPS" class="mw-redirect" title="L-DOPS"><span style="font-size:85%;">L</span>-DOPS</a> (Droxidopa)</li> <li><a href="/wiki/L-Phenylalanine" class="mw-redirect" title="L-Phenylalanine"><span style="font-size:85%;">L</span>-Phenylalanine</a></li> <li><a href="/wiki/L-Tyrosine" class="mw-redirect" title="L-Tyrosine"><span style="font-size:85%;">L</span>-Tyrosine</a></li> <li><a href="/wiki/Meta-Tyramine" title="Meta-Tyramine"><i>m</i>-Tyramine</a></li> <li><a href="/wiki/Metanephrine" title="Metanephrine">Metanephrine</a></li> <li><a href="/wiki/Metaraminol" title="Metaraminol">Metaraminol</a></li> <li><a href="/wiki/Metaterol" title="Metaterol">Metaterol</a></li> <li><a href="/wiki/Metirosine" class="mw-redirect" title="Metirosine">Metirosine</a></li> <li><a href="/wiki/Methyldopa" title="Methyldopa">Methyldopa</a></li> <li><a href="/wiki/N,N-Dimethyldopamine" title="N,N-Dimethyldopamine">N,N-Dimethyldopamine</a></li> <li><a href="/wiki/Nordefrin" class="mw-redirect" title="Nordefrin">Nordefrin</a> (<a href="/wiki/Levonordefrin" class="mw-redirect" title="Levonordefrin">Levonordefrin</a>)</li> <li><a href="/wiki/Norepinephrine" title="Norepinephrine">Norepinephrine</a></li> <li><a href="/wiki/Norfenefrine" title="Norfenefrine">Norfenefrine</a> (<i>m</i>-Octopamine)</li> <li><a href="/wiki/Normetanephrine" title="Normetanephrine">Normetanephrine</a></li> <li><a href="/wiki/Orciprenaline" title="Orciprenaline">Orciprenaline</a></li> <li><a href="/wiki/Octopamine" title="Octopamine"><i>p</i>-Octopamine</a></li> <li><a href="/wiki/Tyramine" title="Tyramine"><i>p</i>-Tyramine</a></li> <li><a href="/wiki/Phenylephrine" title="Phenylephrine">Phenylephrine</a></li> <li><a href="/wiki/Synephrine" title="Synephrine">Synephrine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Miscellaneous</th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/AL-LAD" title="AL-LAD">AL-LAD</a></li> <li><a href="/wiki/Amidephrine" title="Amidephrine">Amidephrine</a></li> <li><a href="/wiki/Arbutamine" title="Arbutamine">Arbutamine</a></li> <li><a href="/wiki/Cafedrine" title="Cafedrine">Cafedrine</a></li> <li><a href="/wiki/Denopamine" title="Denopamine">Denopamine</a></li> <li><a href="/wiki/Desvenlafaxine" title="Desvenlafaxine">Desvenlafaxine</a></li> <li><a href="/wiki/Diphenidine" title="Diphenidine">Diphenidine</a></li> <li><a href="/wiki/Dizocilpine" title="Dizocilpine">Dizocilpine</a></li> <li><a href="/wiki/Dobutamine" title="Dobutamine">Dobutamine</a></li> <li><a href="/wiki/Dopexamine" title="Dopexamine">Dopexamine</a></li> <li><a href="/wiki/Ephenidine" title="Ephenidine">Ephenidine</a></li> <li><a href="/wiki/Etafedrine" title="Etafedrine">Etafedrine</a></li> <li><a href="/wiki/ETH-LAD" title="ETH-LAD">ETH-LAD</a></li> <li><a href="/wiki/Famprofazone" title="Famprofazone">Famprofazone</a></li> <li><a href="/wiki/Fluorolintane" title="Fluorolintane">Fluorolintane</a></li> <li><a href="/wiki/Hexapradol" title="Hexapradol">Hexapradol</a></li> <li><a href="/wiki/IP-LAD" class="mw-redirect" title="IP-LAD">IP-LAD</a></li> <li><a href="/wiki/Lysergic_acid_amide" class="mw-redirect" title="Lysergic acid amide">Lysergic acid amide</a></li> <li><a href="/wiki/Lysergic_acid_2-butyl_amide" title="Lysergic acid 2-butyl amide">Lysergic acid 2-butyl amide</a></li> <li><a href="/wiki/Lysergic_acid_2,4-dimethylazetidide" title="Lysergic acid 2,4-dimethylazetidide">Lysergic acid 2,4-dimethylazetidide</a></li> <li><a href="/wiki/LSD" title="LSD">Lysergic acid diethylamide</a></li> <li><a href="/wiki/Methoxamine" title="Methoxamine">Methoxamine</a></li> <li><a href="/wiki/Methoxphenidine" title="Methoxphenidine">Methoxphenidine</a></li> <li><a href="/wiki/MT-45" title="MT-45">MT-45</a></li> <li><a href="/wiki/PARGY-LAD" title="PARGY-LAD">PARGY-LAD</a></li> <li><a href="/wiki/Phenibut" title="Phenibut">Phenibut</a></li> <li><a href="/wiki/PRO-LAD" title="PRO-LAD">PRO-LAD</a></li> <li><a href="/wiki/Pronethalol" title="Pronethalol">Pronethalol</a></li> <li><a href="/wiki/Salbutamol" title="Salbutamol">Salbutamol</a> (<a href="/wiki/Levosalbutamol" title="Levosalbutamol">Levosalbutamol</a>)</li> <li><a href="/wiki/Solriamfetol" title="Solriamfetol">Solriamfetol</a></li> <li><a href="/wiki/Theodrenaline" title="Theodrenaline">Theodrenaline</a></li> <li><a href="/wiki/Thiamphenicol" title="Thiamphenicol">Thiamphenicol</a></li> <li><a href="/wiki/UWA-101" title="UWA-101">UWA-101</a></li> <li><a href="/wiki/Venlafaxine" title="Venlafaxine">Venlafaxine</a></li></ul> </div></td></tr></tbody></table></div> <div class="navbox-styles"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1236075235"></div><div role="navigation" class="navbox" aria-labelledby="Adrenergic_receptor_modulators" style="padding:3px"><table class="nowraplinks hlist mw-collapsible mw-collapsed navbox-inner" style="border-spacing:0;background:transparent;color:inherit"><tbody><tr><th scope="col" class="navbox-title" colspan="2"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1239400231"><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Adrenergic_receptor_modulators" title="Template:Adrenergic receptor modulators"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Adrenergic_receptor_modulators" title="Template talk:Adrenergic receptor modulators"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Adrenergic_receptor_modulators" title="Special:EditPage/Template:Adrenergic receptor modulators"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Adrenergic_receptor_modulators" style="font-size:114%;margin:0 4em"><a href="/wiki/Adrenergic_receptor" title="Adrenergic receptor">Adrenergic receptor</a> <a href="/wiki/Receptor_modulator" title="Receptor modulator">modulators</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Alpha-1_adrenergic_receptor" title="Alpha-1 adrenergic receptor">α<sub>1</sub></a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Agonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/6-Fluoronorepinephrine" title="6-Fluoronorepinephrine">6-FNE</a></li> <li><a href="/wiki/Amidephrine" title="Amidephrine">Amidephrine</a></li> <li><a href="/wiki/Buspirone" title="Buspirone">Buspirone</a></li> <li><a href="/wiki/Cirazoline" title="Cirazoline">Cirazoline</a></li> <li><a href="/wiki/Corbadrine" title="Corbadrine">Corbadrine</a></li> <li><a href="/wiki/Deoxyepinephrine" title="Deoxyepinephrine">Deoxyepinephrine (epinine, <i>N</i>-methyldopamine)</a></li> <li><a href="/wiki/Desglymidodrine" title="Desglymidodrine">Desglymidodrine</a></li> <li><a href="/w/index.php?title=Dexisometheptene&amp;action=edit&amp;redlink=1" class="new" title="Dexisometheptene (page does not exist)">Dexisometheptene</a></li> <li><a href="/wiki/Dipivefrine" title="Dipivefrine">Dipivefrine</a></li> <li><a href="/wiki/Dopamine" title="Dopamine">Dopamine</a></li> <li><a href="/wiki/Droxidopa" title="Droxidopa">Droxidopa (L-DOPS)</a></li> <li><a href="/wiki/Epinephrine" class="mw-redirect" title="Epinephrine">Epinephrine</a></li> <li><a href="/wiki/Etilefrine" title="Etilefrine">Etilefrine</a></li> <li><a href="/wiki/Etilevodopa" title="Etilevodopa">Etilevodopa</a></li> <li><a href="/wiki/Ethylnorepinephrine" title="Ethylnorepinephrine">Ethylnorepinephrine</a></li> <li><a href="/wiki/Ibopamine" title="Ibopamine">Ibopamine</a></li> <li><a href="/wiki/Indanidine" title="Indanidine">Indanidine</a></li> <li><a href="/wiki/Isometheptene" title="Isometheptene">Isometheptene</a></li> <li><a href="/wiki/L-DOPA" title="L-DOPA">L-DOPA (levodopa)</a></li> <li><a href="/wiki/Phenylalanine" title="Phenylalanine">L-Phenylalanine</a></li> <li><a href="/wiki/Tyrosine" title="Tyrosine">L-Tyrosine</a></li> <li><a href="/wiki/Melevodopa" title="Melevodopa">Melevodopa</a></li> <li><a href="/wiki/Metaraminol" title="Metaraminol">Metaraminol</a></li> <li><a href="/wiki/Methoxamine" title="Methoxamine">Methoxamine</a></li> <li><a href="/wiki/Methyldopa" title="Methyldopa">Methyldopa</a></li> <li><a href="/wiki/Midodrine" title="Midodrine">Midodrine</a></li> <li><a href="/wiki/Naphazoline" title="Naphazoline">Naphazoline</a></li> <li><a href="/wiki/Norepinephrine" title="Norepinephrine">Norepinephrine</a></li> <li><a href="/wiki/Octopamine" title="Octopamine">Octopamine</a></li> <li><a href="/wiki/Oxymetazoline" title="Oxymetazoline">Oxymetazoline</a></li> <li><a href="/wiki/Phenylephrine" title="Phenylephrine">Phenylephrine</a></li> <li><a href="/wiki/Phenylpropanolamine" title="Phenylpropanolamine">Phenylpropanolamine</a></li> <li><a href="/wiki/Synephrine" title="Synephrine">Synephrine</a></li> <li><a href="/wiki/Tetryzoline" title="Tetryzoline">Tetryzoline</a></li> <li><a href="/wiki/Tiamenidine" title="Tiamenidine">Tiamenidine</a></li> <li><a href="/wiki/XP21279" class="mw-redirect" title="XP21279">XP21279</a></li> <li><a href="/wiki/Xylometazoline" title="Xylometazoline">Xylometazoline</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Abanoquil" title="Abanoquil">Abanoquil</a></li> <li><a href="/wiki/Ajmalicine" title="Ajmalicine">Ajmalicine</a></li> <li><a href="/wiki/Alfuzosin" title="Alfuzosin">Alfuzosin</a></li> <li><a href="/wiki/Anisodamine" title="Anisodamine">Anisodamine</a></li> <li><a href="/wiki/Anisodine" title="Anisodine">Anisodine</a></li> <li><a href="/wiki/Atiprosin" title="Atiprosin">Atiprosin</a></li> <li><a href="/wiki/Atypical_antipsychotic" title="Atypical antipsychotic">Atypical antipsychotics</a> (e.g., <a href="/wiki/Brexpiprazole" title="Brexpiprazole">brexpiprazole</a>, <a href="/wiki/Clozapine" title="Clozapine">clozapine</a>, <a href="/wiki/Olanzapine" title="Olanzapine">olanzapine</a>, <a href="/wiki/Quetiapine" title="Quetiapine">quetiapine</a>, <a href="/wiki/Risperidone" title="Risperidone">risperidone</a>)</li> <li><a href="/wiki/Benoxathian" title="Benoxathian">Benoxathian</a></li> <li><a href="/wiki/Beta_blocker" title="Beta blocker">Beta blockers</a> (e.g., <a href="/wiki/Adimolol" title="Adimolol">adimolol</a>, <a href="/wiki/Amosulalol" title="Amosulalol">amosulalol</a>, <a href="/wiki/Arotinolol" title="Arotinolol">arotinolol</a>, <a href="/wiki/Carvedilol" title="Carvedilol">carvedilol</a>, <a href="/wiki/Eugenodilol" title="Eugenodilol">eugenodilol</a>, <a href="/wiki/Labetalol" title="Labetalol">labetalol</a>)</li> <li><a href="/wiki/Buflomedil" title="Buflomedil">Buflomedil</a></li> <li><a href="/wiki/Bunazosin" title="Bunazosin">Bunazosin</a></li> <li><a href="/wiki/Corynanthine" title="Corynanthine">Corynanthine</a></li> <li><a href="/wiki/Dapiprazole" title="Dapiprazole">Dapiprazole</a></li> <li><a href="/wiki/Domesticine" title="Domesticine">Domesticine</a></li> <li><a href="/wiki/Doxazosin" title="Doxazosin">Doxazosin</a></li> <li><a href="/wiki/Ergoline" title="Ergoline">Ergolines</a> (e.g., <a href="/wiki/Acetergamine" title="Acetergamine">acetergamine</a>, <a href="/wiki/Ergotamine" title="Ergotamine">ergotamine</a>, <a href="/wiki/Dihydroergotamine" title="Dihydroergotamine">dihydroergotamine</a>, <a href="/wiki/Lisuride" title="Lisuride">lisuride</a>, <a href="/wiki/Nicergoline" title="Nicergoline">nicergoline</a>, <a href="/wiki/Terguride" title="Terguride">terguride</a>)</li> <li><a href="/wiki/Etoperidone" title="Etoperidone">Etoperidone</a></li> <li><a href="/wiki/Fenspiride" title="Fenspiride">Fenspiride</a></li> <li><a href="/wiki/Hydroxyzine" title="Hydroxyzine">Hydroxyzine</a></li> <li><a href="/wiki/Indoramin" title="Indoramin">Indoramin</a></li> <li><a href="/wiki/Ketanserin" title="Ketanserin">Ketanserin</a></li> <li><a href="/wiki/L-765,314" title="L-765,314">L-765,314</a></li> <li><a href="/wiki/Meta-Chlorophenylpiperazine" title="Meta-Chlorophenylpiperazine">mCPP</a></li> <li><a href="/wiki/Mepiprazole" title="Mepiprazole">Mepiprazole</a></li> <li><a href="/wiki/Metazosin" title="Metazosin">Metazosin</a></li> <li><a href="/wiki/Monatepil" title="Monatepil">Monatepil</a></li> <li><a href="/wiki/Moxisylyte" title="Moxisylyte">Moxisylyte</a></li> <li><a href="/wiki/Naftopidil" title="Naftopidil">Naftopidil</a></li> <li><a href="/wiki/Nantenine" title="Nantenine">Nantenine</a></li> <li><a href="/wiki/Neldazosin" title="Neldazosin">Neldazosin</a></li> <li><a href="/wiki/Niaprazine" title="Niaprazine">Niaprazine</a></li> <li><a href="/wiki/Niguldipine" title="Niguldipine">Niguldipine</a></li> <li><a href="/wiki/Pardoprunox" title="Pardoprunox">Pardoprunox</a></li> <li><a href="/wiki/Pelanserin" title="Pelanserin">Pelanserin</a></li> <li><a href="/wiki/Perlapine" title="Perlapine">Perlapine</a></li> <li><a href="/wiki/Phendioxan" title="Phendioxan">Phendioxan</a></li> <li><a href="/wiki/Phenoxybenzamine" title="Phenoxybenzamine">Phenoxybenzamine</a></li> <li><a href="/wiki/Phentolamine" title="Phentolamine">Phentolamine</a></li> <li><a href="/wiki/Phenylpiperazine" title="Phenylpiperazine">Phenylpiperazine</a> <a href="/wiki/Antidepressant" title="Antidepressant">antidepressants</a> (e.g., <a href="/wiki/Hydroxynefazodone" title="Hydroxynefazodone">hydroxynefazodone</a>, <a href="/wiki/Nefazodone" title="Nefazodone">nefazodone</a>, <a href="/wiki/Trazodone" title="Trazodone">trazodone</a>, <a href="/wiki/Triazoledione" title="Triazoledione">triazoledione</a>)</li> <li><a href="/wiki/Piperoxan" title="Piperoxan">Piperoxan</a></li> <li><a href="/wiki/Prazosin" title="Prazosin">Prazosin</a></li> <li><a href="/wiki/Quinazosin" title="Quinazosin">Quinazosin</a></li> <li><a href="/wiki/Quinidine" title="Quinidine">Quinidine</a></li> <li><a href="/wiki/Silodosin" title="Silodosin">Silodosin</a></li> <li><a href="/wiki/Spegatrine" title="Spegatrine">Spegatrine</a></li> <li><a href="/wiki/Spiperone" title="Spiperone">Spiperone</a></li> <li><a href="/wiki/Talipexole" title="Talipexole">Talipexole</a></li> <li><a href="/wiki/Tamsulosin" title="Tamsulosin">Tamsulosin</a></li> <li><a href="/wiki/Terazosin" title="Terazosin">Terazosin</a></li> <li><a href="/wiki/Tiodazosin" title="Tiodazosin">Tiodazosin</a></li> <li><a href="/wiki/Tolazoline" title="Tolazoline">Tolazoline</a></li> <li><a href="/wiki/Tetracyclic_antidepressant" title="Tetracyclic antidepressant">Tetracyclic antidepressants</a> (e.g., <a href="/wiki/Amoxapine" title="Amoxapine">amoxapine</a>, <a href="/wiki/Maprotiline" title="Maprotiline">maprotiline</a>, <a href="/wiki/Mianserin" title="Mianserin">mianserin</a>)</li> <li><a href="/wiki/Tricyclic_antidepressant" title="Tricyclic antidepressant">Tricyclic antidepressants</a> (e.g., <a href="/wiki/Amitriptyline" title="Amitriptyline">amitriptyline</a>, <a href="/wiki/Clomipramine" title="Clomipramine">clomipramine</a>, <a href="/wiki/Doxepin" title="Doxepin">doxepin</a>, <a href="/wiki/Imipramine" title="Imipramine">imipramine</a>, <a href="/wiki/Trimipramine" title="Trimipramine">trimipramine</a>)</li> <li><a href="/wiki/Trimazosin" title="Trimazosin">Trimazosin</a></li> <li><a href="/wiki/Typical_antipsychotic" title="Typical antipsychotic">Typical antipsychotics</a> (e.g., <a href="/wiki/Chlorpromazine" title="Chlorpromazine">chlorpromazine</a>, <a href="/wiki/Fluphenazine" title="Fluphenazine">fluphenazine</a>, <a href="/wiki/Loxapine" title="Loxapine">loxapine</a>, <a href="/wiki/Thioridazine" title="Thioridazine">thioridazine</a>)</li> <li><a href="/wiki/Urapidil" title="Urapidil">Urapidil</a></li> <li><a href="/wiki/WB-4101" title="WB-4101">WB-4101</a></li> <li><a href="/wiki/Zolertine" title="Zolertine">Zolertine</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Alpha-2_adrenergic_receptor" title="Alpha-2 adrenergic receptor">α<sub>2</sub></a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Agonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/(R)-3-Nitrobiphenyline" title="(R)-3-Nitrobiphenyline">(R)-3-Nitrobiphenyline</a></li> <li><a href="/wiki/4-NEMD" title="4-NEMD">4-NEMD</a></li> <li><a href="/wiki/6-Fluoronorepinephrine" title="6-Fluoronorepinephrine">6-FNE</a></li> <li><a href="/wiki/Amitraz" title="Amitraz">Amitraz</a></li> <li><a href="/wiki/Apraclonidine" title="Apraclonidine">Apraclonidine</a></li> <li><a href="/wiki/Brimonidine" title="Brimonidine">Brimonidine</a></li> <li><a href="/wiki/Clonidine" title="Clonidine">Clonidine</a></li> <li><a href="/wiki/Corbadrine" title="Corbadrine">Corbadrine</a></li> <li><a href="/wiki/Deoxyepinephrine" title="Deoxyepinephrine">Deoxyepinephrine (epinine, <i>N</i>-methyldopamine)</a></li> <li><a href="/wiki/Detomidine" title="Detomidine">Detomidine</a></li> <li><a href="/wiki/Dexmedetomidine" title="Dexmedetomidine">Dexmedetomidine</a></li> <li><a href="/wiki/Dihydroergotamine" title="Dihydroergotamine">Dihydroergotamine</a></li> <li><a href="/wiki/Dipivefrine" title="Dipivefrine">Dipivefrine</a></li> <li><a href="/wiki/Dopamine" title="Dopamine">Dopamine</a></li> <li><a href="/wiki/Droxidopa" title="Droxidopa">Droxidopa (L-DOPS)</a></li> <li><a href="/wiki/Etilevodopa" title="Etilevodopa">Etilevodopa</a></li> <li><a href="/wiki/Ergotamine" title="Ergotamine">Ergotamine</a></li> <li><a href="/wiki/Epinephrine" class="mw-redirect" title="Epinephrine">Epinephrine</a></li> <li><a href="/wiki/Etilefrine" title="Etilefrine">Etilefrine</a></li> <li><a href="/wiki/Ethylnorepinephrine" title="Ethylnorepinephrine">Ethylnorepinephrine</a></li> <li><a href="/wiki/Guanabenz" title="Guanabenz">Guanabenz</a></li> <li><a href="/wiki/Guanfacine" title="Guanfacine">Guanfacine</a></li> <li><a href="/wiki/Guanoxabenz" title="Guanoxabenz">Guanoxabenz</a></li> <li><a href="/wiki/L-DOPA" title="L-DOPA">L-DOPA (levodopa)</a></li> <li><a href="/wiki/Phenylalanine" title="Phenylalanine">L-Phenylalanine</a></li> <li><a href="/wiki/Tyrosine" title="Tyrosine">L-Tyrosine</a></li> <li><a href="/wiki/Ibopamine" title="Ibopamine">Ibopamine</a></li> <li><a href="/wiki/Lofexidine" title="Lofexidine">Lofexidine</a></li> <li><a href="/wiki/Medetomidine" title="Medetomidine">Medetomidine</a></li> <li><a href="/wiki/Melevodopa" title="Melevodopa">Melevodopa</a></li> <li><a href="/wiki/Methyldopa" title="Methyldopa">Methyldopa</a></li> <li><a href="/wiki/Mivazerol" title="Mivazerol">Mivazerol</a></li> <li><a href="/wiki/Moxonidine" title="Moxonidine">Moxonidine</a></li> <li><a href="/wiki/Naphazoline" title="Naphazoline">Naphazoline</a></li> <li><a href="/wiki/Norepinephrine" title="Norepinephrine">Norepinephrine</a></li> <li><a href="/wiki/Oxymetazoline" title="Oxymetazoline">Oxymetazoline</a></li> <li><a href="/wiki/Phenylpropanolamine" title="Phenylpropanolamine">Phenylpropanolamine</a></li> <li><a href="/wiki/Piperoxan" title="Piperoxan">Piperoxan</a></li> <li><a href="/wiki/PS75" title="PS75">PS75</a></li> <li><a href="/w/index.php?title=Rezatomidine&amp;action=edit&amp;redlink=1" class="new" title="Rezatomidine (page does not exist)">Rezatomidine</a></li> <li><a href="/wiki/Rilmenidine" title="Rilmenidine">Rilmenidine</a></li> <li><a href="/wiki/Romifidine" title="Romifidine">Romifidine</a></li> <li><a href="/wiki/Talipexole" title="Talipexole">Talipexole</a></li> <li><a href="/w/index.php?title=Tasipimidine&amp;action=edit&amp;redlink=1" class="new" title="Tasipimidine (page does not exist)">Tasipimidine</a></li> <li><a href="/wiki/Tetryzoline" title="Tetryzoline">Tetryzoline</a></li> <li><a href="/wiki/Tiamenidine" title="Tiamenidine">Tiamenidine</a></li> <li><a href="/wiki/Tizanidine" title="Tizanidine">Tizanidine</a></li> <li><a href="/wiki/Tolonidine" title="Tolonidine">Tolonidine</a></li> <li><a href="/wiki/Urapidil" title="Urapidil">Urapidil</a></li> <li><a href="/wiki/Vatinoxan" class="mw-redirect" title="Vatinoxan">Vatinoxan</a></li> <li><a href="/wiki/XP21279" class="mw-redirect" title="XP21279">XP21279</a></li> <li><a href="/wiki/Xylazine" title="Xylazine">Xylazine</a></li> <li><a href="/wiki/Xylometazoline" title="Xylometazoline">Xylometazoline</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Pyrimidinylpiperazine" title="Pyrimidinylpiperazine">1-PP</a></li> <li><a href="/wiki/Adimolol" title="Adimolol">Adimolol</a></li> <li><a href="/wiki/Amesergide" title="Amesergide">Amesergide</a></li> <li><a href="/wiki/Aptazapine" title="Aptazapine">Aptazapine</a></li> <li><a href="/wiki/Atipamezole" title="Atipamezole">Atipamezole</a></li> <li><a href="/wiki/Atypical_antipsychotic" title="Atypical antipsychotic">Atypical antipsychotics</a> (e.g., <a href="/wiki/Asenapine" title="Asenapine">asenapine</a>, <a href="/wiki/Brexpiprazole" title="Brexpiprazole">brexpiprazole</a>, <a href="/wiki/Clozapine" title="Clozapine">clozapine</a>, <a href="/wiki/Lurasidone" title="Lurasidone">lurasidone</a>, <a href="/wiki/Olanzapine" title="Olanzapine">olanzapine</a>, <a href="/wiki/Paliperidone" title="Paliperidone">paliperidone</a>, <a href="/wiki/Quetiapine" title="Quetiapine">quetiapine</a>, <a href="/wiki/Risperidone" title="Risperidone">risperidone</a>, <a href="/wiki/Zotepine" title="Zotepine">zotepine</a>)</li> <li><a href="/wiki/Azapirone" title="Azapirone">Azapirones</a> (e.g., <a href="/wiki/Buspirone" title="Buspirone">buspirone</a>, <a href="/wiki/Gepirone" title="Gepirone">gepirone</a>, <a href="/wiki/Ipsapirone" title="Ipsapirone">ipsapirone</a>, <a href="/wiki/Tandospirone" title="Tandospirone">tandospirone</a>)</li> <li><a href="/wiki/BRL-44408" title="BRL-44408">BRL-44408</a></li> <li><a href="/wiki/Buflomedil" title="Buflomedil">Buflomedil</a></li> <li><a href="/wiki/Cirazoline" title="Cirazoline">Cirazoline</a></li> <li><a href="/wiki/Efaroxan" title="Efaroxan">Efaroxan</a></li> <li><a href="/wiki/Esmirtazapine" title="Esmirtazapine">Esmirtazapine</a></li> <li><a href="/wiki/Fenmetozole" title="Fenmetozole">Fenmetozole</a></li> <li><a href="/wiki/Fluparoxan" title="Fluparoxan">Fluparoxan</a></li> <li><a href="/wiki/Idazoxan" title="Idazoxan">Idazoxan</a></li> <li><a href="/wiki/Ketanserin" title="Ketanserin">Ketanserin</a></li> <li><a href="/wiki/Lisuride" title="Lisuride">Lisuride</a></li> <li><a href="/wiki/Meta-Chlorophenylpiperazine" title="Meta-Chlorophenylpiperazine">mCPP</a></li> <li><a href="/wiki/Mianserin" title="Mianserin">Mianserin</a></li> <li><a href="/wiki/Mirtazapine" title="Mirtazapine">Mirtazapine</a></li> <li><a href="/wiki/NAN-190" title="NAN-190">NAN-190</a></li> <li><a href="/wiki/Pardoprunox" title="Pardoprunox">Pardoprunox</a></li> <li><a href="/wiki/Phentolamine" title="Phentolamine">Phentolamine</a></li> <li><a href="/wiki/Phenoxybenzamine" title="Phenoxybenzamine">Phenoxybenzamine</a></li> <li><a href="/wiki/Piperoxan" title="Piperoxan">Piperoxan</a></li> <li><a href="/wiki/Piribedil" title="Piribedil">Piribedil</a></li> <li><a href="/wiki/Rauwolscine" title="Rauwolscine">Rauwolscine</a></li> <li><a href="/wiki/Rotigotine" title="Rotigotine">Rotigotine</a></li> <li><a href="/wiki/Setiptiline" title="Setiptiline">Setiptiline</a></li> <li><a href="/wiki/Spegatrine" title="Spegatrine">Spegatrine</a></li> <li><a href="/wiki/Spiroxatrine" title="Spiroxatrine">Spiroxatrine</a></li> <li><a href="/wiki/Sunepitron" title="Sunepitron">Sunepitron</a></li> <li><a href="/wiki/Terguride" title="Terguride">Terguride</a></li> <li><a href="/wiki/Tolazoline" title="Tolazoline">Tolazoline</a></li> <li><a href="/wiki/Typical_antipsychotic" title="Typical antipsychotic">Typical antipsychotics</a> (e.g., <a href="/wiki/Chlorpromazine" title="Chlorpromazine">chlorpromazine</a>, <a href="/wiki/Fluphenazine" title="Fluphenazine">fluphenazine</a>, <a href="/wiki/Loxapine" title="Loxapine">loxapine</a>, <a href="/wiki/Thioridazine" title="Thioridazine">thioridazine</a>)</li> <li><a href="/wiki/Yohimbine" title="Yohimbine">Yohimbine</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/%CE%92-adrenergic_receptor" class="mw-redirect" title="Β-adrenergic receptor">β</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Agonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Abediterol" title="Abediterol">Abediterol</a></li> <li><a href="/wiki/Alifedrine" title="Alifedrine">Alifedrine</a></li> <li><a href="/wiki/Amibegron" title="Amibegron">Amibegron</a></li> <li><a href="/wiki/Arbutamine" title="Arbutamine">Arbutamine</a></li> <li><a href="/wiki/Arformoterol" title="Arformoterol">Arformoterol</a></li> <li><a href="/wiki/Arotinolol" title="Arotinolol">Arotinolol</a></li> <li><a href="/wiki/Bromoacetylalprenololmenthane" title="Bromoacetylalprenololmenthane">BAAM</a></li> <li><a href="/wiki/Bambuterol" title="Bambuterol">Bambuterol</a></li> <li><a href="/wiki/Befunolol" title="Befunolol">Befunolol</a></li> <li><a href="/wiki/Bitolterol" title="Bitolterol">Bitolterol</a></li> <li><a href="/wiki/Broxaterol" title="Broxaterol">Broxaterol</a></li> <li><a href="/wiki/Buphenine" title="Buphenine">Buphenine</a></li> <li><a href="/wiki/Carbuterol" title="Carbuterol">Carbuterol</a></li> <li><a href="/wiki/Carmoterol" title="Carmoterol">Carmoterol</a></li> <li><a href="/wiki/Cimaterol" title="Cimaterol">Cimaterol</a></li> <li><a href="/wiki/Clenbuterol" title="Clenbuterol">Clenbuterol</a></li> <li><a href="/wiki/Colterol" title="Colterol">Colterol</a></li> <li><a href="/wiki/Corbadrine" title="Corbadrine">Corbadrine</a></li> <li><a href="/wiki/Denopamine" title="Denopamine">Denopamine</a></li> <li><a href="/wiki/Deoxyepinephrine" title="Deoxyepinephrine">Deoxyepinephrine (epinine, <i>N</i>-methyldopamine)</a></li> <li><a href="/wiki/Dipivefrine" title="Dipivefrine">Dipivefrine</a></li> <li><a href="/wiki/Dobutamine" title="Dobutamine">Dobutamine</a></li> <li><a href="/wiki/Dopamine" title="Dopamine">Dopamine</a></li> <li><a href="/wiki/Dopexamine" title="Dopexamine">Dopexamine</a></li> <li><a href="/wiki/Droxidopa" title="Droxidopa">Droxidopa (L-DOPS)</a></li> <li><a href="/wiki/Epinephrine" class="mw-redirect" title="Epinephrine">Epinephrine</a></li> <li><a href="/wiki/Etafedrine" title="Etafedrine">Etafedrine</a></li> <li><a href="/wiki/Etilefrine" title="Etilefrine">Etilefrine</a></li> <li><a href="/wiki/Etilevodopa" title="Etilevodopa">Etilevodopa</a></li> <li><a href="/wiki/Ethylnorepinephrine" title="Ethylnorepinephrine">Ethylnorepinephrine</a></li> <li><a href="/wiki/Eugenodilol" title="Eugenodilol">Eugenodilol</a></li> <li><a href="/wiki/Fenoterol" title="Fenoterol">Fenoterol</a></li> <li><a href="/wiki/Formoterol" title="Formoterol">Formoterol</a></li> <li><a href="/wiki/Hexoprenaline" title="Hexoprenaline">Hexoprenaline</a></li> <li><a href="/wiki/Higenamine" title="Higenamine">Higenamine</a></li> <li><a href="/wiki/Ibopamine" title="Ibopamine">Ibopamine</a></li> <li><a href="/wiki/Indacaterol" title="Indacaterol">Indacaterol</a></li> <li><a href="/wiki/Isoetarine" title="Isoetarine">Isoetarine</a></li> <li><a href="/wiki/Isoprenaline" title="Isoprenaline">Isoprenaline</a></li> <li><a href="/wiki/Isoxsuprine" title="Isoxsuprine">Isoxsuprine</a></li> <li><a href="/wiki/L-DOPA" title="L-DOPA">L-DOPA (levodopa)</a></li> <li><a href="/wiki/Phenylalanine" title="Phenylalanine">L-Phenylalanine</a></li> <li><a href="/wiki/Tyrosine" title="Tyrosine">L-Tyrosine</a></li> <li><a href="/wiki/Levosalbutamol" title="Levosalbutamol">Levosalbutamol</a></li> <li><a href="/wiki/Lubabegron" title="Lubabegron">Lubabegron</a></li> <li><a href="/wiki/Mabuterol" title="Mabuterol">Mabuterol</a></li> <li><a href="/wiki/Melevodopa" title="Melevodopa">Melevodopa</a></li> <li><a href="/wiki/Methoxyphenamine" title="Methoxyphenamine">Methoxyphenamine</a></li> <li><a href="/wiki/Methyldopa" title="Methyldopa">Methyldopa</a></li> <li><a href="/wiki/Mirabegron" title="Mirabegron">Mirabegron</a></li> <li><a href="/wiki/Norepinephrine" title="Norepinephrine">Norepinephrine</a></li> <li><a href="/wiki/Orciprenaline" title="Orciprenaline">Orciprenaline</a></li> <li><a href="/wiki/Oxyfedrine" title="Oxyfedrine">Oxyfedrine</a></li> <li><a href="/wiki/PF-610355" title="PF-610355">PF-610355</a></li> <li><a href="/wiki/Phenylpropanolamine" title="Phenylpropanolamine">Phenylpropanolamine</a></li> <li><a href="/wiki/Pirbuterol" title="Pirbuterol">Pirbuterol</a></li> <li><a href="/wiki/Prenalterol" title="Prenalterol">Prenalterol</a></li> <li><a href="/wiki/Ractopamine" title="Ractopamine">Ractopamine</a></li> <li><a href="/wiki/Procaterol" title="Procaterol">Procaterol</a></li> <li><a href="/wiki/Reproterol" title="Reproterol">Reproterol</a></li> <li><a href="/wiki/Rimiterol" title="Rimiterol">Rimiterol</a></li> <li><a href="/wiki/Ritodrine" title="Ritodrine">Ritodrine</a></li> <li><a href="/wiki/Salbutamol" title="Salbutamol">Salbutamol</a></li> <li><a href="/wiki/Salmeterol" title="Salmeterol">Salmeterol</a></li> <li><a href="/wiki/Solabegron" title="Solabegron">Solabegron</a></li> <li><a href="/wiki/Terbutaline" title="Terbutaline">Terbutaline</a></li> <li><a href="/wiki/Tretoquinol" title="Tretoquinol">Tretoquinol</a></li> <li><a href="/wiki/Tulobuterol" title="Tulobuterol">Tulobuterol</a></li> <li><a href="/wiki/Vibegron" title="Vibegron">Vibegron</a></li> <li><a href="/wiki/Vilanterol" title="Vilanterol">Vilanterol</a></li> <li><a href="/wiki/Xamoterol" title="Xamoterol">Xamoterol</a></li> <li><a href="/wiki/XP21279" class="mw-redirect" title="XP21279">XP21279</a></li> <li><a href="/wiki/Zilpaterol" title="Zilpaterol">Zilpaterol</a></li> <li><a href="/wiki/Zinterol" title="Zinterol">Zinterol</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Acebutolol" title="Acebutolol">Acebutolol</a></li> <li><a href="/wiki/Adaprolol" title="Adaprolol">Adaprolol</a></li> <li><a href="/wiki/Adimolol" title="Adimolol">Adimolol</a></li> <li><a href="/wiki/Afurolol" title="Afurolol">Afurolol</a></li> <li><a href="/wiki/Alprenolol" title="Alprenolol">Alprenolol</a></li> <li><a href="/wiki/Alprenoxime" title="Alprenoxime">Alprenoxime</a></li> <li><a href="/wiki/Amosulalol" title="Amosulalol">Amosulalol</a></li> <li><a href="/wiki/Ancarolol" title="Ancarolol">Ancarolol</a></li> <li><a href="/wiki/Arnolol" title="Arnolol">Arnolol</a></li> <li><a href="/wiki/Arotinolol" title="Arotinolol">Arotinolol</a></li> <li><a href="/wiki/Atenolol" title="Atenolol">Atenolol</a></li> <li><a href="/wiki/Befunolol" title="Befunolol">Befunolol</a></li> <li><a href="/wiki/Betaxolol" title="Betaxolol">Betaxolol</a></li> <li><a href="/wiki/Bevantolol" title="Bevantolol">Bevantolol</a></li> <li><a href="/wiki/Bisoprolol" title="Bisoprolol">Bisoprolol</a></li> <li><a href="/wiki/Bopindolol" title="Bopindolol">Bopindolol</a></li> <li><a href="/wiki/Bornaprolol" title="Bornaprolol">Bornaprolol</a></li> <li><a href="/wiki/Brefonalol" title="Brefonalol">Brefonalol</a></li> <li><a href="/wiki/Bucindolol" title="Bucindolol">Bucindolol</a></li> <li><a href="/wiki/Bucumolol" title="Bucumolol">Bucumolol</a></li> <li><a href="/wiki/Bufetolol" title="Bufetolol">Bufetolol</a></li> <li><a href="/wiki/Bufuralol" title="Bufuralol">Bufuralol</a></li> <li><a href="/wiki/Bunitrolol" title="Bunitrolol">Bunitrolol</a></li> <li><a href="/wiki/Bunolol" class="mw-redirect" title="Bunolol">Bunolol</a></li> <li><a href="/wiki/Bupranolol" title="Bupranolol">Bupranolol</a></li> <li><a href="/wiki/Butaxamine" title="Butaxamine">Butaxamine</a></li> <li><a href="/wiki/Butidrine" title="Butidrine">Butidrine</a></li> <li><a href="/wiki/Butofilolol" title="Butofilolol">Butofilolol</a></li> <li><a href="/wiki/Capsinolol" title="Capsinolol">Capsinolol</a></li> <li><a href="/wiki/Carazolol" title="Carazolol">Carazolol</a></li> <li><a href="/wiki/Carpindolol" title="Carpindolol">Carpindolol</a></li> <li><a href="/wiki/Carteolol" title="Carteolol">Carteolol</a></li> <li><a href="/wiki/Carvedilol" title="Carvedilol">Carvedilol</a></li> <li><a href="/wiki/Celiprolol" title="Celiprolol">Celiprolol</a></li> <li><a href="/wiki/Cetamolol" title="Cetamolol">Cetamolol</a></li> <li><a href="/wiki/Cicloprolol" title="Cicloprolol">Cicloprolol</a></li> <li><a href="/wiki/Cinamolol" title="Cinamolol">Cinamolol</a></li> <li><a href="/wiki/Cloranolol" title="Cloranolol">Cloranolol</a></li> <li><a href="/wiki/Cyanopindolol" title="Cyanopindolol">Cyanopindolol</a></li> <li><a href="/wiki/Dalbraminol" title="Dalbraminol">Dalbraminol</a></li> <li><a href="/wiki/Dexpropranolol" class="mw-redirect" title="Dexpropranolol">Dexpropranolol</a></li> <li><a href="/wiki/Diacetolol" title="Diacetolol">Diacetolol</a></li> <li><a href="/wiki/Dichloroisoprenaline" title="Dichloroisoprenaline">Dichloroisoprenaline</a></li> <li><a href="/wiki/Dihydroalprenolol" title="Dihydroalprenolol">Dihydroalprenolol</a></li> <li><a href="/wiki/Dilevalol" class="mw-redirect" title="Dilevalol">Dilevalol</a></li> <li><a href="/wiki/Diprafenone" title="Diprafenone">Diprafenone</a></li> <li><a href="/wiki/Draquinolol" title="Draquinolol">Draquinolol</a></li> <li><a href="/wiki/Ecastolol" title="Ecastolol">Ecastolol</a></li> <li><a href="/wiki/Epanolol" title="Epanolol">Epanolol</a></li> <li><a href="/wiki/Ericolol" title="Ericolol">Ericolol</a></li> <li><a href="/wiki/Ersentilide" title="Ersentilide">Ersentilide</a></li> <li><a href="/wiki/Esatenolol" class="mw-redirect" title="Esatenolol">Esatenolol</a></li> <li><a href="/wiki/Esprolol" class="mw-redirect" title="Esprolol">Esprolol</a></li> <li><a href="/wiki/Eugenodilol" title="Eugenodilol">Eugenodilol</a></li> <li><a href="/wiki/Exaprolol" title="Exaprolol">Exaprolol</a></li> <li><a href="/wiki/Falintolol" title="Falintolol">Falintolol</a></li> <li><a href="/wiki/Flestolol" title="Flestolol">Flestolol</a></li> <li><a href="/wiki/Flusoxolol" title="Flusoxolol">Flusoxolol</a></li> <li><a href="/wiki/Hydroxycarteolol" title="Hydroxycarteolol">Hydroxycarteolol</a></li> <li><a href="/wiki/Hydroxytertatolol" title="Hydroxytertatolol">Hydroxytertatolol</a></li> <li><a href="/wiki/ICI-118,551" title="ICI-118,551">ICI-118,551</a></li> <li><a href="/wiki/Idropranolol" class="mw-redirect" title="Idropranolol">Idropranolol</a></li> <li><a href="/wiki/Indenolol" title="Indenolol">Indenolol</a></li> <li><a href="/wiki/Indopanolol" title="Indopanolol">Indopanolol</a></li> <li><a href="/wiki/Iodocyanopindolol" title="Iodocyanopindolol">Iodocyanopindolol</a></li> <li><a href="/wiki/Iprocrolol" title="Iprocrolol">Iprocrolol</a></li> <li><a href="/wiki/Isoxaprolol" title="Isoxaprolol">Isoxaprolol</a></li> <li><a href="/wiki/Isamoltane" title="Isamoltane">Isamoltane</a></li> <li><a href="/wiki/Labetalol" title="Labetalol">Labetalol</a></li> <li><a href="/wiki/Landiolol" title="Landiolol">Landiolol</a></li> <li><a href="/wiki/Levobetaxolol" title="Levobetaxolol">Levobetaxolol</a></li> <li><a href="/wiki/Levobunolol" title="Levobunolol">Levobunolol</a></li> <li><a href="/wiki/Levomoprolol" title="Levomoprolol">Levomoprolol</a></li> <li><a href="/wiki/Medroxalol" title="Medroxalol">Medroxalol</a></li> <li><a href="/wiki/Mepindolol" title="Mepindolol">Mepindolol</a></li> <li><a href="/wiki/Metipranolol" title="Metipranolol">Metipranolol</a></li> <li><a href="/wiki/Metoprolol" title="Metoprolol">Metoprolol</a></li> <li><a href="/wiki/Moprolol" title="Moprolol">Moprolol</a></li> <li><a href="/wiki/Nadolol" title="Nadolol">Nadolol</a></li> <li><a href="/wiki/Nadoxolol" title="Nadoxolol">Nadoxolol</a></li> <li><a href="/wiki/Nebivolol" title="Nebivolol">Nebivolol</a></li> <li><a href="/wiki/Nifenalol" title="Nifenalol">Nifenalol</a></li> <li><a href="/wiki/Nipradilol" title="Nipradilol">Nipradilol</a></li> <li><a href="/wiki/Oxprenolol" title="Oxprenolol">Oxprenolol</a></li> <li><a href="/wiki/Pacrinolol" title="Pacrinolol">Pacrinolol</a></li> <li><a href="/wiki/Pafenolol" title="Pafenolol">Pafenolol</a></li> <li><a href="/wiki/Pamatolol" title="Pamatolol">Pamatolol</a></li> <li><a href="/wiki/Pargolol" title="Pargolol">Pargolol</a></li> <li><a href="/wiki/Penbutolol" title="Penbutolol">Penbutolol</a></li> <li><a href="/wiki/Pindolol" title="Pindolol">Pindolol</a></li> <li><a href="/wiki/Practolol" title="Practolol">Practolol</a></li> <li><a href="/wiki/Primidolol" title="Primidolol">Primidolol</a></li> <li><a href="/wiki/Procinolol" title="Procinolol">Procinolol</a></li> <li><a href="/wiki/Pronethalol" title="Pronethalol">Pronethalol</a></li> <li><a href="/wiki/Propafenone" title="Propafenone">Propafenone</a></li> <li><a href="/wiki/Propranolol" title="Propranolol">Propranolol</a></li> <li><a href="/wiki/Ridazolol" title="Ridazolol">Ridazolol</a></li> <li><a href="/wiki/Ronactolol" title="Ronactolol">Ronactolol</a></li> <li><a href="/wiki/Soquinolol" title="Soquinolol">Soquinolol</a></li> <li><a href="/wiki/Sotalol" title="Sotalol">Sotalol</a></li> <li><a href="/wiki/Spirendolol" title="Spirendolol">Spirendolol</a></li> <li><a href="/wiki/SR_59230A" title="SR 59230A">SR 59230A</a></li> <li><a href="/wiki/Sulfinalol" title="Sulfinalol">Sulfinalol</a></li> <li><a href="/wiki/Talinolol" title="Talinolol">Talinolol</a></li> <li><a href="/wiki/Tazolol" title="Tazolol">Tazolol</a></li> <li><a href="/wiki/Tertatolol" title="Tertatolol">Tertatolol</a></li> <li><a href="/wiki/Tienoxolol" title="Tienoxolol">Tienoxolol</a></li> <li><a href="/wiki/Tilisolol" title="Tilisolol">Tilisolol</a></li> <li><a href="/wiki/Timolol" title="Timolol">Timolol</a></li> <li><a href="/wiki/Tiprenolol" title="Tiprenolol">Tiprenolol</a></li> <li><a href="/wiki/Tolamolol" title="Tolamolol">Tolamolol</a></li> <li><a href="/wiki/Toliprolol" title="Toliprolol">Toliprolol</a></li> <li><a href="/wiki/Xibenolol" title="Xibenolol">Xibenolol</a></li> <li><a href="/wiki/Xipranolol" title="Xipranolol">Xipranolol</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><td class="navbox-abovebelow" colspan="2"><div> <ul><li><i><b>See also:</b> <a href="/wiki/Template:Receptor_modulators" title="Template:Receptor modulators">Receptor/signaling modulators</a></i></li> <li><i><a href="/wiki/Template:Dopamine_receptor_modulators" title="Template:Dopamine receptor modulators">Dopaminergics</a></i></li> <li><i><a href="/wiki/Template:Serotonin_receptor_modulators" title="Template:Serotonin receptor modulators">Serotonergics</a></i></li> <li><i><a href="/wiki/Template:Monoamine_reuptake_inhibitors" title="Template:Monoamine reuptake inhibitors">Monoamine reuptake inhibitors</a></i></li> <li><i><a href="/wiki/Template:Monoamine_releasing_agents" title="Template:Monoamine releasing agents">Monoamine releasing agents</a></i></li> <li><i><a href="/wiki/Template:Monoamine_metabolism_modulators" title="Template:Monoamine metabolism modulators">Monoamine metabolism modulators</a></i></li> <li><i><a href="/wiki/Template:Monoamine_neurotoxins" title="Template:Monoamine neurotoxins">Monoamine neurotoxins</a></i></li></ul> </div></td></tr></tbody></table></div> <div class="navbox-styles"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1236075235"></div><div role="navigation" class="navbox" aria-labelledby="Dopamine_receptor_modulators" style="padding:3px"><table class="nowraplinks hlist mw-collapsible mw-collapsed navbox-inner" style="border-spacing:0;background:transparent;color:inherit"><tbody><tr><th scope="col" class="navbox-title" colspan="2"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1239400231"><div class="navbar plainlinks hlist navbar-mini"><ul><li class="nv-view"><a href="/wiki/Template:Dopamine_receptor_modulators" title="Template:Dopamine receptor modulators"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Dopamine_receptor_modulators" title="Template talk:Dopamine receptor modulators"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Dopamine_receptor_modulators" title="Special:EditPage/Template:Dopamine receptor modulators"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Dopamine_receptor_modulators" style="font-size:114%;margin:0 4em"><a href="/wiki/Dopamine_receptor" title="Dopamine receptor">Dopamine receptor</a> <a href="/wiki/Receptor_modulator" title="Receptor modulator">modulators</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/D1-like_receptor" title="D1-like receptor">D<sub>1</sub>-like</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;">Agonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Benzazepines</i>: <a href="/wiki/6-Br-APB" title="6-Br-APB">6-Br-APB</a></li> <li><a href="/wiki/Fenoldopam" title="Fenoldopam">Fenoldopam</a></li> <li><a href="/wiki/SKF-38,393" title="SKF-38,393">SKF-38,393</a></li> <li><a href="/wiki/SKF-77,434" title="SKF-77,434">SKF-77,434</a></li> <li><a href="/wiki/SKF-81,297" title="SKF-81,297">SKF-81,297</a></li> <li><a href="/wiki/SKF-82,958" title="SKF-82,958">SKF-82,958</a></li> <li><a href="/wiki/SKF-83,959" title="SKF-83,959">SKF-83,959</a></li> <li><a href="/wiki/Trepipam" title="Trepipam">Trepipam</a></li> <li><a href="/wiki/Zelandopam" title="Zelandopam">Zelandopam</a></li></ul> <ul><li><i>Ergolines</i>: <a href="/wiki/Cabergoline" title="Cabergoline">Cabergoline</a></li> <li><a href="/wiki/CY-208,243" title="CY-208,243">CY-208,243</a></li> <li><a href="/wiki/Dihydroergocryptine" title="Dihydroergocryptine">Dihydroergocryptine</a></li> <li><a href="/w/index.php?title=LEK-8829&amp;action=edit&amp;redlink=1" class="new" title="LEK-8829 (page does not exist)">LEK-8829</a></li> <li><a href="/wiki/Lisuride" title="Lisuride">Lisuride</a></li> <li><a href="/wiki/Pergolide" title="Pergolide">Pergolide</a></li> <li><a href="/wiki/Terguride" title="Terguride">Terguride</a></li></ul> <ul><li><i>Dihydrexidine derivatives</i>: <a href="/wiki/A-77636" title="A-77636">A-77636</a></li> <li><a href="/wiki/A-86929" title="A-86929">A-86929</a></li> <li><a href="/wiki/Adrogolide" class="mw-redirect" title="Adrogolide">Adrogolide (ABT-431, DAS-431)</a></li> <li><a href="/wiki/Dihydrexidine" title="Dihydrexidine">Dihydrexidine</a></li> <li><a href="/wiki/Dinapsoline" title="Dinapsoline">Dinapsoline</a></li> <li><a href="/wiki/Dinoxyline" title="Dinoxyline">Dinoxyline</a></li> <li><a href="/wiki/Doxanthrine" title="Doxanthrine">Doxanthrine</a></li></ul> <ul><li><i>Phenethylamines</i>: <a href="/w/index.php?title=BCO-001&amp;action=edit&amp;redlink=1" class="new" title="BCO-001 (page does not exist)">BCO-001</a></li> <li><a href="/wiki/Deoxyepinephrine" title="Deoxyepinephrine">Deoxyepinephrine (N-methyldopamine, epinine)</a></li> <li><a href="/wiki/Dopexamine" title="Dopexamine">Dopexamine</a></li> <li><a href="/wiki/Etilevodopa" title="Etilevodopa">Etilevodopa</a></li> <li><a href="/wiki/Ibopamine" title="Ibopamine">Ibopamine</a></li> <li><a href="/wiki/L-DOPA" title="L-DOPA"><small>L</small>-DOPA (levodopa)</a></li> <li><a href="/wiki/Melevodopa" title="Melevodopa">Melevodopa</a></li> <li><a href="/wiki/Phenylalanine" title="Phenylalanine"><small>L</small>-Phenylalanine</a></li> <li><a href="/wiki/Tyrosine" title="Tyrosine"><small>L</small>-Tyrosine</a></li> <li><a href="/wiki/XP21279" class="mw-redirect" title="XP21279">XP21279</a></li></ul> <ul><li><i>Others</i>: <a href="/wiki/A-68930" title="A-68930">A-68930</a></li> <li><a href="/wiki/Apomorphine" title="Apomorphine">Apomorphine</a></li> <li><a href="/w/index.php?title=Isocorypalmine&amp;action=edit&amp;redlink=1" class="new" title="Isocorypalmine (page does not exist)">Isocorypalmine</a></li> <li><a href="/wiki/Nuciferine" title="Nuciferine">Nuciferine</a></li> <li><a href="/wiki/PF-6649751" class="mw-redirect" title="PF-6649751">PF-6649751</a></li> <li><a href="/w/index.php?title=PF_6669571&amp;action=edit&amp;redlink=1" class="new" title="PF 6669571 (page does not exist)">PF 6669571</a></li> <li><a href="/wiki/Propylnorapomorphine" title="Propylnorapomorphine">Propylnorapomorphine</a></li> <li><a href="/wiki/Rotigotine" title="Rotigotine">Rotigotine</a></li> <li><a href="/wiki/SKF-89,145" title="SKF-89,145">SKF-89,145</a></li> <li><a href="/w/index.php?title=SKF-89,626&amp;action=edit&amp;redlink=1" class="new" title="SKF-89,626 (page does not exist)">SKF-89,626</a></li> <li><a href="/wiki/Stepholidine" title="Stepholidine">Stepholidine</a></li> <li><a href="/wiki/Tavapadon" title="Tavapadon">Tavapadon</a></li> <li><a href="/wiki/Tetrahydropalmatine" title="Tetrahydropalmatine">Tetrahydropalmatine</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;">PAMs<sup class="noprint Inline-Template" style="margin-left:0.1em; white-space:nowrap;">&#91;<i><a href="/wiki/Wikipedia:Please_clarify" title="Wikipedia:Please clarify"><span title="The text near this tag may need clarification or removal of jargon. (September 2024)">clarification needed</span></a></i>&#93;</sup></th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Tetrahydroisoquinolines</i>: <a href="/w/index.php?title=DETQ&amp;action=edit&amp;redlink=1" class="new" title="DETQ (page does not exist)">DETQ</a></li> <li><a href="/w/index.php?title=DPTQ&amp;action=edit&amp;redlink=1" class="new" title="DPTQ (page does not exist)">DPTQ</a></li> <li><a href="/wiki/Mevidalen" title="Mevidalen">Mevidalen</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Typical antipsychotics</i>: <a href="/wiki/Butaclamol" title="Butaclamol">Butaclamol</a></li> <li><a href="/wiki/Chlorpromazine" title="Chlorpromazine">Chlorpromazine</a></li> <li><a href="/wiki/Chlorprothixene" title="Chlorprothixene">Chlorprothixene</a></li> <li><a href="/wiki/Flupentixol" title="Flupentixol">Flupentixol (flupenthixol)</a> (<a href="/wiki/Flupentixol/melitracen" title="Flupentixol/melitracen">+melitracen</a>)</li> <li><a href="/wiki/Fluphenazine" title="Fluphenazine">Fluphenazine</a></li> <li><a href="/wiki/Loxapine" title="Loxapine">Loxapine</a></li> <li><a href="/wiki/Perphenazine" title="Perphenazine">Perphenazine</a> (<a href="/wiki/Amitriptyline/perphenazine" title="Amitriptyline/perphenazine">+amitriptyline</a>)</li> <li><a href="/w/index.php?title=Pifluthixol&amp;action=edit&amp;redlink=1" class="new" title="Pifluthixol (page does not exist)">Pifluthixol</a></li> <li><a href="/wiki/Thioridazine" title="Thioridazine">Thioridazine</a></li> <li><a href="/wiki/Thiothixene" class="mw-redirect" title="Thiothixene">Thiothixene</a></li> <li><a href="/wiki/Trifluoperazine" title="Trifluoperazine">Trifluoperazine</a> (<a href="/wiki/Tranylcypromine/trifluoperazine" title="Tranylcypromine/trifluoperazine">+tranylcypromine</a>)</li> <li><a href="/wiki/Zuclopenthixol" title="Zuclopenthixol">Zuclopenthixol</a></li></ul> <ul><li><i>Atypical antipsychotics</i>: <a href="/wiki/Asenapine" title="Asenapine">Asenapine</a></li> <li><a href="/wiki/Clorotepine" title="Clorotepine">Clorotepine</a></li> <li><a href="/wiki/Clotiapine" title="Clotiapine">Clotiapine</a></li> <li><a href="/wiki/Clozapine" title="Clozapine">Clozapine</a></li> <li><a href="/wiki/DHA-clozapine" title="DHA-clozapine">DHA-clozapine</a></li> <li><a href="/wiki/Fluperlapine" title="Fluperlapine">Fluperlapine</a></li> <li><a href="/wiki/Iloperidone" title="Iloperidone">Iloperidone</a></li> <li><a href="/wiki/Norclozapine" class="mw-redirect" title="Norclozapine">Norclozapine</a></li> <li><a href="/w/index.php?title=Norquetiapine&amp;action=edit&amp;redlink=1" class="new" title="Norquetiapine (page does not exist)">Norquetiapine</a></li> <li><a href="/wiki/Olanzapine" title="Olanzapine">Olanzapine</a> (<a href="/wiki/Olanzapine/fluoxetine" title="Olanzapine/fluoxetine">+fluoxetine</a>)</li> <li><a href="/wiki/Paliperidone" title="Paliperidone">Paliperidone</a></li> <li><a href="/wiki/Quetiapine" title="Quetiapine">Quetiapine</a></li> <li><a href="/wiki/Risperidone" title="Risperidone">Risperidone</a></li> <li><a href="/w/index.php?title=Tefludazine&amp;action=edit&amp;redlink=1" class="new" title="Tefludazine (page does not exist)">Tefludazine</a></li> <li><a href="/wiki/Zicronapine" title="Zicronapine">Zicronapine</a></li> <li><a href="/wiki/Ziprasidone" title="Ziprasidone">Ziprasidone</a></li> <li><a href="/wiki/Zotepine" title="Zotepine">Zotepine</a></li></ul> <ul><li><i>Others</i>: <a href="/wiki/Berupipam" title="Berupipam">Berupipam</a></li> <li><a href="/wiki/Ecopipam" title="Ecopipam">Ecopipam</a></li> <li><a href="/wiki/N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline" title="N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline">EEDQ</a></li> <li><a href="/wiki/Metitepine" title="Metitepine">Metitepine (methiothepin)</a></li> <li><a href="/wiki/Odapipam" title="Odapipam">Odapipam</a></li> <li><a href="/wiki/Perlapine" title="Perlapine">Perlapine</a></li> <li><a href="/wiki/SCH-23390" title="SCH-23390">SCH-23390</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/D2-like_receptor" title="D2-like receptor">D<sub>2</sub>-like</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;">Agonists</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Adamantanes</i>: <a href="/wiki/Amantadine" title="Amantadine">Amantadine</a></li> <li><a href="/wiki/Memantine" title="Memantine">Memantine</a></li> <li><a href="/wiki/Rimantadine" title="Rimantadine">Rimantadine</a></li></ul> <ul><li><i>Aminotetralins</i>: <a href="/wiki/5-OH-DPAT" title="5-OH-DPAT">5-OH-DPAT</a></li> <li><a href="/wiki/7-OH-DPAT" title="7-OH-DPAT">7-OH-DPAT</a></li> <li><a href="/wiki/8-OH-PBZI" title="8-OH-PBZI">8-OH-PBZI</a></li> <li><a href="/wiki/Rotigotine" title="Rotigotine">Rotigotine</a></li> <li><a href="/wiki/UH-232" title="UH-232">UH-232</a></li></ul> <ul><li><i>Ergolines</i>: <a href="/wiki/Bromocriptine" title="Bromocriptine">Bromocriptine</a></li> <li><a href="/wiki/Cabergoline" title="Cabergoline">Cabergoline</a></li> <li><a href="/wiki/Chanoclavine" title="Chanoclavine">Chanoclavine</a></li> <li><a href="/wiki/Dihydroergocryptine" title="Dihydroergocryptine">Dihydroergocryptine</a></li> <li><a href="/wiki/Epicriptine" title="Epicriptine">Epicriptine</a></li> <li><a href="/wiki/Ergocornine" title="Ergocornine">Ergocornine</a></li> <li><a href="/wiki/Lergotrile" title="Lergotrile">Lergotrile</a></li> <li><a href="/wiki/Lisuride" title="Lisuride">Lisuride</a></li> <li><a href="/wiki/LSD" title="LSD">LSD</a></li> <li><a href="/wiki/Pergolide" title="Pergolide">Pergolide</a></li> <li><a href="/wiki/Terguride" title="Terguride">Terguride</a></li></ul> <ul><li><i>Dihydrexidine derivatives</i>: <a href="/wiki/2-OH-NPA" title="2-OH-NPA">2-OH-NPA</a></li> <li><a href="/wiki/Ciladopa" title="Ciladopa">Ciladopa</a></li> <li><a href="/wiki/Dihydrexidine" title="Dihydrexidine">Dihydrexidine</a></li> <li><a href="/wiki/Dinoxyline" title="Dinoxyline">Dinoxyline</a></li> <li><a href="/w/index.php?title=N,N-Propyldihydrexidine&amp;action=edit&amp;redlink=1" class="new" title="N,N-Propyldihydrexidine (page does not exist)">N,N-Propyldihydrexidine</a></li></ul> <ul><li><i>Phenethylamines</i>: <a href="/wiki/Deoxyepinephrine" title="Deoxyepinephrine">Deoxyepinephrine (N-methyldopamine, epinine)</a></li> <li><a href="/wiki/Dopexamine" title="Dopexamine">Dopexamine</a></li> <li><a href="/wiki/Etilevodopa" title="Etilevodopa">Etilevodopa</a></li> <li><a href="/wiki/Ibopamine" title="Ibopamine">Ibopamine</a></li> <li><a href="/wiki/L-DOPA" title="L-DOPA"><small>L</small>-DOPA (levodopa)</a></li> <li><a href="/wiki/Phenylalanine" title="Phenylalanine"><small>L</small>-Phenylalanine</a></li> <li><a href="/wiki/Tyrosine" title="Tyrosine"><small>L</small>-Tyrosine</a></li> <li><a href="/wiki/Melevodopa" title="Melevodopa">Melevodopa</a></li> <li><a href="/wiki/XP21279" class="mw-redirect" title="XP21279">XP21279</a></li></ul> <ul><li><i>Atypical antipsychotics</i>: <a href="/wiki/Alentemol" title="Alentemol">Alentemol (U-66444B)</a></li> <li><a href="/wiki/Aripiprazole" title="Aripiprazole">Aripiprazole</a> (<a href="/wiki/Aripiprazole/sertraline" title="Aripiprazole/sertraline">+sertraline</a>)</li> <li><a href="/wiki/Aripiprazole_lauroxil" title="Aripiprazole lauroxil">Aripiprazole lauroxil</a></li> <li><a href="/wiki/Bifeprunox" title="Bifeprunox">Bifeprunox</a></li> <li><a href="/wiki/Brexpiprazole" title="Brexpiprazole">Brexpiprazole</a></li> <li><a href="/wiki/Brilaroxazine" title="Brilaroxazine">Brilaroxazine</a></li> <li><a href="/wiki/Cariprazine" title="Cariprazine">Cariprazine</a></li> <li><a href="/wiki/F-15063" title="F-15063">F-15063</a></li> <li><a href="/wiki/Lumateperone" title="Lumateperone">Lumateperone</a></li> <li><a href="/wiki/Norclozapine" class="mw-redirect" title="Norclozapine">Norclozapine</a></li></ul> <ul><li><i>Others</i>: <a href="/wiki/3-PPP" title="3-PPP">3-PPP</a></li> <li><a href="/wiki/A-412997" title="A-412997">A-412997</a></li> <li><a href="/wiki/ABT-670" title="ABT-670">ABT-670</a></li> <li><a href="/wiki/ABT-724" title="ABT-724">ABT-724</a></li> <li><a href="/wiki/Adrafinil" title="Adrafinil">Adrafinil</a></li> <li><a href="/wiki/Aplindore" title="Aplindore">Aplindore</a></li> <li><a href="/wiki/Apomorphine" title="Apomorphine">Apomorphine</a></li> <li><a href="/wiki/Arketamine" title="Arketamine">Arketamine</a></li> <li><a href="/wiki/Armodafinil" title="Armodafinil">Armodafinil</a></li> <li><a href="/wiki/BP-897" title="BP-897">BP-897</a></li> <li><a href="/wiki/Captodiame" title="Captodiame">Captodiame</a></li> <li><a href="/wiki/CP-226,269" title="CP-226,269">CP-226,269</a></li> <li><a href="/wiki/Dizocilpine" title="Dizocilpine">Dizocilpine</a></li> <li><a href="/wiki/Esketamine" title="Esketamine">Esketamine</a></li> <li><a href="/wiki/Flibanserin" title="Flibanserin">Flibanserin</a></li> <li><a href="/wiki/Ketamine" title="Ketamine">Ketamine</a></li> <li><a href="/wiki/Mesulergine" title="Mesulergine">Mesulergine</a></li> <li><a href="/wiki/Modafinil" title="Modafinil">Modafinil</a></li> <li><a href="/wiki/OSU-6162" title="OSU-6162">OSU-6162</a></li> <li><a href="/wiki/Pardoprunox" title="Pardoprunox">Pardoprunox</a></li> <li><a href="/wiki/PD-128,907" title="PD-128,907">PD-128,907</a></li> <li><a href="/wiki/PD-168,077" title="PD-168,077">PD-168,077</a></li> <li><a href="/wiki/PF-219,061" title="PF-219,061">PF-219,061</a></li> <li><a href="/wiki/PF-592,379" title="PF-592,379">PF-592,379</a></li> <li><a href="/wiki/Phencyclidine" title="Phencyclidine">Phencyclidine</a></li> <li><a href="/wiki/Piribedil" title="Piribedil">Piribedil</a></li> <li><a href="/wiki/Pramipexole" title="Pramipexole">Pramipexole</a></li> <li><a href="/wiki/Preclamol" class="mw-redirect" title="Preclamol">Preclamol</a></li> <li><a href="/wiki/Propylnorapomorphine" title="Propylnorapomorphine">Propylnorapomorphine</a></li> <li><a href="/wiki/Pukateine" title="Pukateine">Pukateine</a></li> <li><a href="/wiki/Quinagolide" title="Quinagolide">Quinagolide</a></li> <li><a href="/wiki/Quinelorane" title="Quinelorane">Quinelorane</a></li> <li><a href="/wiki/Quinpirole" title="Quinpirole">Quinpirole</a></li> <li><a href="/wiki/RDS-127" title="RDS-127">RDS-127</a></li> <li><a href="/wiki/Ro10-5824" title="Ro10-5824">Ro10-5824</a></li> <li><a href="/wiki/Ropinirole" title="Ropinirole">Ropinirole</a></li> <li><a href="/wiki/Roxindole" title="Roxindole">Roxindole</a></li> <li><a href="/wiki/Salvinorin_A" title="Salvinorin A">Salvinorin A</a></li> <li><a href="/wiki/SKF-83,959" title="SKF-83,959">SKF-83,959</a></li> <li><a href="/wiki/Sumanirole" title="Sumanirole">Sumanirole</a></li> <li><a href="/wiki/Talipexole" title="Talipexole">Talipexole</a></li> <li><a href="/wiki/Umespirone" title="Umespirone">Umespirone</a></li> <li><a href="/wiki/WAY-100,635" class="mw-redirect" title="WAY-100,635">WAY-100,635</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><i>Typical antipsychotics</i>: <a href="/wiki/Acepromazine" title="Acepromazine">Acepromazine</a></li> <li><a href="/wiki/Acetophenazine" title="Acetophenazine">Acetophenazine</a></li> <li><a href="/wiki/Azaperone" title="Azaperone">Azaperone</a></li> <li><a href="/wiki/Benperidol" title="Benperidol">Benperidol</a></li> <li><a href="/wiki/Bromperidol" title="Bromperidol">Bromperidol</a></li> <li><a href="/wiki/Butaclamol" title="Butaclamol">Butaclamol</a></li> <li><a href="/wiki/Butaperazine" title="Butaperazine">Butaperazine</a></li> <li><a href="/wiki/Chloracizine" class="mw-redirect" title="Chloracizine">Chloracizine</a></li> <li><a href="/wiki/Chlorproethazine" title="Chlorproethazine">Chlorproethazine</a></li> <li><a href="/wiki/Chlorpromazine" title="Chlorpromazine">Chlorpromazine</a></li> <li><a href="/wiki/Chlorprothixene" title="Chlorprothixene">Chlorprothixene</a></li> <li><a href="/wiki/Ciclindole" title="Ciclindole">Ciclindole</a></li> <li><a href="/wiki/Clopenthixol" title="Clopenthixol">Clopenthixol</a></li> <li><a href="/w/index.php?title=Clothixamide&amp;action=edit&amp;redlink=1" class="new" title="Clothixamide (page does not exist)">Clothixamide</a></li> <li><a href="/wiki/Clopimozide" title="Clopimozide">Clopimozide</a></li> <li><a href="/wiki/Droperidol" title="Droperidol">Droperidol</a></li> <li><a href="/wiki/Fluacizine" title="Fluacizine">Fluacizine</a></li> <li><a href="/wiki/Fluanisone" title="Fluanisone">Fluanisone</a></li> <li><a href="/wiki/Flucindole" title="Flucindole">Flucindole</a></li> <li><a href="/wiki/Fluotracen" title="Fluotracen">Fluotracen</a></li> <li><a href="/wiki/Flupentixol" title="Flupentixol">Flupentixol (flupenthixol)</a> (<a href="/wiki/Flupentixol/melitracen" title="Flupentixol/melitracen">+melitracen</a>)</li> <li><a href="/wiki/Fluphenazine" title="Fluphenazine">Fluphenazine</a></li> <li><a href="/w/index.php?title=Fluprothixene&amp;action=edit&amp;redlink=1" class="new" title="Fluprothixene (page does not exist)">Fluprothixene</a></li> <li><a href="/wiki/Fluspirilene" title="Fluspirilene">Fluspirilene</a></li> <li><a href="/wiki/Haloperidol" title="Haloperidol">Haloperidol</a></li> <li><a href="/wiki/Homopipramol" title="Homopipramol">Homopipramol</a></li> <li><a href="/wiki/Lenperone" title="Lenperone">Lenperone</a></li> <li><a href="/wiki/Levomepromazine" title="Levomepromazine">Levomepromazine (methotrimeprazine)</a></li> <li><a href="/wiki/Levosulpiride" title="Levosulpiride">Levosulpiride</a></li> <li><a href="/wiki/Loxapine" title="Loxapine">Loxapine</a></li> <li><a href="/wiki/Mesoridazine" title="Mesoridazine">Mesoridazine</a></li> <li><a href="/wiki/Moperone" title="Moperone">Moperone</a></li> <li><a href="/wiki/Naranol" title="Naranol">Naranol</a></li> <li><a href="/wiki/Nemonapride" title="Nemonapride">Nemonapride</a></li> <li><a href="/wiki/Penfluridol" title="Penfluridol">Penfluridol</a></li> <li><a href="/wiki/Perathiepin" title="Perathiepin">Perathiepin</a></li> <li><a href="/wiki/Perazine" title="Perazine">Perazine</a></li> <li><a href="/wiki/Periciazine" title="Periciazine">Pericyazine (periciazine)</a></li> <li><a href="/wiki/Perphenazine" title="Perphenazine">Perphenazine</a> (<a href="/wiki/Amitriptyline/perphenazine" title="Amitriptyline/perphenazine">+amitriptyline</a>)</li> <li><a href="/w/index.php?title=Piflutixol&amp;action=edit&amp;redlink=1" class="new" title="Piflutixol (page does not exist)">Piflutixol (pifluthixol)</a></li> <li><a href="/wiki/Pimozide" title="Pimozide">Pimozide</a></li> <li><a href="/wiki/Pipamperone" title="Pipamperone">Pipamperone</a></li> <li><a href="/wiki/Preclamol" class="mw-redirect" title="Preclamol">Preclamol</a></li> <li><a href="/wiki/Prochlorperazine" title="Prochlorperazine">Prochlorperazine</a></li> <li><a href="/wiki/Promazine" title="Promazine">Promazine</a></li> <li><a href="/wiki/Prothipendyl" title="Prothipendyl">Prothipendyl</a></li> <li><a href="/wiki/Spiperone" title="Spiperone">Spiperone (spiroperidol)</a></li> <li><a href="/wiki/Sulforidazine" title="Sulforidazine">Sulforidazine</a></li> <li><a href="/wiki/Sulpiride" title="Sulpiride">Sulpiride</a></li> <li><a href="/wiki/Sultopride" title="Sultopride">Sultopride</a></li> <li><a href="/w/index.php?title=Teflutixol&amp;action=edit&amp;redlink=1" class="new" title="Teflutixol (page does not exist)">Teflutixol</a></li> <li><a href="/wiki/Thiopropazate" title="Thiopropazate">Thiopropazate</a></li> <li><a href="/wiki/Thioproperazine" title="Thioproperazine">Thioproperazine</a></li> <li><a href="/wiki/Thioridazine" title="Thioridazine">Thioridazine</a></li> <li><a href="/wiki/Thiothixene" class="mw-redirect" title="Thiothixene">Thiothixene</a></li> <li><a href="/wiki/Timiperone" title="Timiperone">Timiperone</a></li> <li><a href="/wiki/Trifluoperazine" title="Trifluoperazine">Trifluoperazine</a> (<a href="/wiki/Tranylcypromine/trifluoperazine" title="Tranylcypromine/trifluoperazine">+tranylcypromine</a>)</li> <li><a href="/wiki/Triflupromazine" title="Triflupromazine">Triflupromazine</a></li> <li><a href="/wiki/Trifluperidol" title="Trifluperidol">Trifluperidol</a></li> <li><a href="/w/index.php?title=Zetidoline&amp;action=edit&amp;redlink=1" class="new" title="Zetidoline (page does not exist)">Zetidoline</a></li> <li><a href="/wiki/Zuclopenthixol" title="Zuclopenthixol">Zuclopenthixol</a></li></ul> <ul><li><i>Atypical antipsychotics</i>: <a href="/wiki/Amisulpride" title="Amisulpride">Amisulpride</a></li> <li><a href="/wiki/Asenapine" title="Asenapine">Asenapine</a></li> <li><a href="/wiki/BL-1020" title="BL-1020">BL-1020</a></li> <li><a href="/wiki/Blonanserin" title="Blonanserin">Blonanserin</a></li> <li><a href="/wiki/Carpipramine" title="Carpipramine">Carpipramine</a></li> <li><a href="/w/index.php?title=Cinuperone&amp;action=edit&amp;redlink=1" class="new" title="Cinuperone (page does not exist)">Cinuperone</a></li> <li><a href="/wiki/Clocapramine" title="Clocapramine">Clocapramine</a></li> <li><a href="/wiki/Clorotepine" title="Clorotepine">Clorotepine</a></li> <li><a href="/wiki/Clotiapine" title="Clotiapine">Clotiapine (clothiapine)</a></li> <li><a href="/wiki/Clozapine" title="Clozapine">Clozapine</a></li> <li><a href="/wiki/Cyamemazine" title="Cyamemazine">Cyamemazine</a></li> <li><a href="/wiki/DHA-clozapine" title="DHA-clozapine">DHA-clozapine</a></li> <li><a href="/wiki/Dixyrazine" title="Dixyrazine">Dixyrazine</a></li> <li><a href="/wiki/Elopiprazole" title="Elopiprazole">Elopiprazole</a></li> <li><a href="/wiki/Flumezapine" title="Flumezapine">Flumezapine</a></li> <li><a href="/wiki/Fluperlapine" title="Fluperlapine">Fluperlapine</a></li> <li><a href="/wiki/Gevotroline" title="Gevotroline">Gevotroline</a></li> <li><a href="/wiki/Iloperidone" title="Iloperidone">Iloperidone</a></li> <li><a href="/wiki/Lurasidone" title="Lurasidone">Lurasidone</a></li> <li><a href="/wiki/Mazapertine" title="Mazapertine">Mazapertine</a></li> <li><a href="/wiki/Melperone" title="Melperone">Melperone</a></li> <li><a href="/wiki/Molindone" title="Molindone">Molindone</a></li> <li><a href="/wiki/Mosapramine" title="Mosapramine">Mosapramine</a></li> <li><a href="/wiki/Ocaperidone" title="Ocaperidone">Ocaperidone</a></li> <li><a href="/wiki/Olanzapine" title="Olanzapine">Olanzapine</a> (<a href="/wiki/Olanzapine/fluoxetine" title="Olanzapine/fluoxetine">+fluoxetine</a>)</li> <li><a href="/wiki/Paliperidone" title="Paliperidone">Paliperidone</a></li> <li><a href="/wiki/Perospirone" title="Perospirone">Perospirone</a></li> <li><a href="/wiki/Piperacetazine" title="Piperacetazine">Piperacetazine</a></li> <li><a href="/wiki/Pipotiazine" title="Pipotiazine">Pipotiazine</a></li> <li><a href="/wiki/Piquindone" title="Piquindone">Piquindone</a></li> <li><a href="/wiki/Quetiapine" title="Quetiapine">Quetiapine</a></li> <li><a href="/wiki/Remoxipride" title="Remoxipride">Remoxipride</a></li> <li><a href="/wiki/Risperidone" title="Risperidone">Risperidone</a></li> <li><a href="/wiki/Sertindole" title="Sertindole">Sertindole</a></li> <li><a href="/w/index.php?title=Tefludazine&amp;action=edit&amp;redlink=1" class="new" title="Tefludazine (page does not exist)">Tefludazine</a></li> <li><a href="/wiki/Tenilapine" title="Tenilapine">Tenilapine</a></li> <li><a href="/wiki/Tiospirone" title="Tiospirone">Tiospirone</a></li> <li><a href="/wiki/Veralipride" title="Veralipride">Veralipride</a></li> <li><a href="/wiki/Zicronapine" title="Zicronapine">Zicronapine</a></li> <li><a href="/wiki/Ziprasidone" title="Ziprasidone">Ziprasidone</a></li> <li><a href="/wiki/Zotepine" title="Zotepine">Zotepine</a></li></ul> <ul><li><i>Antiemetics/gastroprokinetics/sedatives</i>: <a href="/wiki/Aceprometazine" title="Aceprometazine">Aceprometazine</a></li> <li><a href="/wiki/AS-8112" title="AS-8112">AS-8112</a></li> <li><a href="/wiki/Alimemazine" title="Alimemazine">Alimemazine</a></li> <li><a href="/wiki/Alizapride" title="Alizapride">Alizapride</a></li> <li><a href="/wiki/Benzquinamide" title="Benzquinamide">Benzquinamide</a></li> <li><a href="/wiki/Bromopride" title="Bromopride">Bromopride</a></li> <li><a href="/wiki/Clebopride" title="Clebopride">Clebopride</a></li> <li><a href="/wiki/Deudomperidone" title="Deudomperidone">Deudomperidone</a></li> <li><a href="/wiki/Domperidone" title="Domperidone">Domperidone</a></li> <li><a href="/wiki/Eticlopride" title="Eticlopride">Eticlopride</a></li> <li><a href="/wiki/Hydroxyzine" title="Hydroxyzine">Hydroxyzine</a></li> <li><a href="/wiki/Itopride" title="Itopride">Itopride</a></li> <li><a href="/wiki/Metoclopramide" title="Metoclopramide">Metoclopramide</a></li> <li><a href="/wiki/Metopimazine" title="Metopimazine">Metopimazine</a></li> <li><a href="/wiki/Promethazine" title="Promethazine">Promethazine</a></li> <li><a href="/wiki/Thiethylperazine" title="Thiethylperazine">Thiethylperazine</a></li> <li><a href="/wiki/Trazpiroben" title="Trazpiroben">Trazpiroben</a></li> <li><a href="/wiki/Trimethobenzamide" title="Trimethobenzamide">Trimethobenzamide</a></li></ul> <ul><li><i>Antidepressants</i>: <a href="/wiki/Amoxapine" title="Amoxapine">Amoxapine</a></li> <li><a href="/wiki/Nefazodone" title="Nefazodone">Nefazodone</a></li> <li><a href="/wiki/Opipramol" title="Opipramol">Opipramol</a></li> <li><a href="/wiki/Propiomazine" title="Propiomazine">Propiomazine</a></li> <li><a href="/wiki/Trimipramine" title="Trimipramine">Trimipramine</a></li></ul> <ul><li><i>Others</i>: <a href="/wiki/3-PPP" title="3-PPP">3-PPP</a></li> <li><a href="/wiki/Alpiropride" title="Alpiropride">Alpiropride</a></li> <li><a href="/wiki/Azapride" title="Azapride">Azapride</a></li> <li><a href="/wiki/Bromerguride" title="Bromerguride">Bromerguride</a></li> <li><a href="/wiki/Bromocriptine" title="Bromocriptine">Bromocriptine</a></li> <li><a href="/wiki/Buspirone" title="Buspirone">Buspirone</a></li> <li><a href="/wiki/Desmethoxyfallypride" title="Desmethoxyfallypride">Desmethoxyfallypride</a></li> <li><a href="/wiki/N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline" title="N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline">EEDQ</a></li> <li><a href="/wiki/F-15063" title="F-15063">F-15063</a></li> <li><a href="/wiki/Fallypride" title="Fallypride">Fallypride</a></li> <li><a href="/wiki/Fananserin" title="Fananserin">Fananserin</a></li> <li><a href="/wiki/Fenfluramine" title="Fenfluramine">Fenfluramine</a></li> <li><a href="/wiki/Iodobenzamide" title="Iodobenzamide">Iodobenzamide</a></li> <li><a href="/w/index.php?title=Isocorypalmine&amp;action=edit&amp;redlink=1" class="new" title="Isocorypalmine (page does not exist)">Isocorypalmine</a></li> <li><a href="/wiki/L-741,626" title="L-741,626">L-741,626</a></li> <li><a href="/wiki/L-745,870" title="L-745,870">L-745,870</a></li> <li><a href="/wiki/Levofenfluramine" title="Levofenfluramine">Levofenfluramine</a></li> <li><a href="/w/index.php?title=LEK-8829&amp;action=edit&amp;redlink=1" class="new" title="LEK-8829 (page does not exist)">LEK-8829</a></li> <li><a href="/wiki/Metergoline" title="Metergoline">Metergoline</a></li> <li><a href="/wiki/Metitepine" title="Metitepine">Metitepine (methiothepin)</a></li> <li><a href="/wiki/N-Methylspiperone" title="N-Methylspiperone">N-Methylspiperone</a></li> <li><a href="/wiki/Nafadotride" title="Nafadotride">Nafadotride</a></li> <li><a href="/wiki/Nuciferine" title="Nuciferine">Nuciferine</a></li> <li><a href="/wiki/PNU-99,194" title="PNU-99,194">PNU-99,194</a></li> <li><a href="/wiki/Pridopidine" title="Pridopidine">Pridopidine</a></li> <li><a href="/wiki/Raclopride" title="Raclopride">Raclopride</a></li> <li><a href="/wiki/Sarizotan" title="Sarizotan">Sarizotan</a></li> <li><a href="/wiki/SB-277,011-A" title="SB-277,011-A">SB-277,011-A</a></li> <li><a href="/w/index.php?title=Seridopidine&amp;action=edit&amp;redlink=1" class="new" title="Seridopidine (page does not exist)">Seridopidine</a></li> <li><a href="/wiki/Sonepiprazole" title="Sonepiprazole">Sonepiprazole</a></li> <li><a href="/wiki/Spiroxatrine" title="Spiroxatrine">Spiroxatrine</a></li> <li><a href="/wiki/Stepholidine" title="Stepholidine">Stepholidine</a></li> <li><a href="/w/index.php?title=SV-293&amp;action=edit&amp;redlink=1" class="new" title="SV-293 (page does not exist)">SV-293</a></li> <li><a href="/wiki/Terguride" title="Terguride">Terguride</a></li> <li><a href="/wiki/Tetrahydropalmatine" title="Tetrahydropalmatine">Tetrahydropalmatine</a></li> <li><a href="/wiki/Tiapride" title="Tiapride">Tiapride</a></li> <li><a href="/wiki/UH-232" title="UH-232">UH-232</a></li> <li><a href="/wiki/Yohimbine" title="Yohimbine">Yohimbine</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><td class="navbox-abovebelow" colspan="2"><div> <ul><li><small><i><b>See also:</b> <a href="/wiki/Template:Receptor_modulators" title="Template:Receptor modulators">Receptor/signaling modulators</a></i></small></li> <li><small><i><a href="/wiki/Template:Adrenergic_receptor_modulators" title="Template:Adrenergic receptor modulators">Adrenergics</a></i></small></li> <li><small><i><a href="/wiki/Template:Serotonin_receptor_modulators" title="Template:Serotonin receptor modulators">Serotonergics</a></i></small></li> <li><small><i><a href="/wiki/Template:Monoamine_reuptake_inhibitors" title="Template:Monoamine reuptake inhibitors">Monoamine reuptake inhibitors</a></i></small></li> <li><small><i><a href="/wiki/Template:Monoamine_releasing_agents" title="Template:Monoamine releasing agents">Monoamine releasing agents</a></i></small></li> <li><small><i><a href="/wiki/Template:Monoamine_metabolism_modulators" title="Template:Monoamine metabolism modulators">Monoamine metabolism modulators</a></i></small></li> <li><small><i><a href="/wiki/Template:Monoamine_neurotoxins" title="Template:Monoamine neurotoxins">Monoamine neurotoxins</a></i></small></li></ul> </div></td></tr></tbody></table></div> <!-- NewPP limit report Parsed by mw‐web.eqiad.main‐5dc468848‐5hg4f Cached time: 20241122144213 Cache expiry: 2592000 Reduced expiry: false Complications: [vary‐revision‐sha1, show‐toc] CPU time usage: 1.274 seconds Real time usage: 2.895 seconds Preprocessor visited node count: 3183/1000000 Post‐expand include size: 234014/2097152 bytes Template argument size: 2789/2097152 bytes Highest expansion depth: 17/100 Expensive parser function count: 3/500 Unstrip recursion depth: 1/20 Unstrip post‐expand size: 164844/5000000 bytes Lua time usage: 0.358/10.000 seconds Lua memory usage: 5614309/52428800 bytes Number of Wikibase entities loaded: 0/400 --> <!-- Transclusion expansion time report (%,ms,calls,template) 100.00% 857.440 1 -total 40.38% 346.210 1 Template:Reflist 37.12% 318.292 8 Template:Navbox 26.49% 227.128 25 Template:Cite_journal 16.30% 139.798 1 Template:Phenethylamines 14.38% 123.325 1 Template:Short_description 11.93% 102.260 1 Template:Dopaminergics 8.99% 77.073 1 Template:Clarify 8.86% 75.989 2 Template:Pagetype 8.26% 70.848 1 Template:Fix-span --> <!-- Saved in parser cache with key enwiki:pcache:idhash:25835853-0!canonical and timestamp 20241122144213 and revision id 1256601547. Rendering was triggered because: page-view --> </div><!--esi <esi:include src="/esitest-fa8a495983347898/content" /> --><noscript><img src="https://login.wikimedia.org/wiki/Special:CentralAutoLogin/start?type=1x1" alt="" width="1" height="1" style="border: none; position: absolute;"></noscript> <div class="printfooter" data-nosnippet="">Retrieved from "<a dir="ltr" href="https://en.wikipedia.org/w/index.php?title=Substituted_cathinone&amp;oldid=1256601547">https://en.wikipedia.org/w/index.php?title=Substituted_cathinone&amp;oldid=1256601547</a>"</div></div> <div id="catlinks" class="catlinks" data-mw="interface"><div id="mw-normal-catlinks" class="mw-normal-catlinks"><a href="/wiki/Help:Category" title="Help:Category">Categories</a>: <ul><li><a href="/wiki/Category:Chemical_classes_of_psychoactive_drugs" title="Category:Chemical classes of psychoactive drugs">Chemical classes of psychoactive drugs</a></li><li><a href="/wiki/Category:Cathinones" title="Category:Cathinones">Cathinones</a></li></ul></div><div id="mw-hidden-catlinks" class="mw-hidden-catlinks mw-hidden-cats-hidden">Hidden categories: <ul><li><a href="/wiki/Category:CS1_Finnish-language_sources_(fi)" title="Category:CS1 Finnish-language sources (fi)">CS1 Finnish-language sources (fi)</a></li><li><a href="/wiki/Category:Webarchive_template_wayback_links" title="Category:Webarchive template wayback links">Webarchive template wayback links</a></li><li><a href="/wiki/Category:Articles_with_short_description" title="Category:Articles with short description">Articles with short description</a></li><li><a href="/wiki/Category:Short_description_matches_Wikidata" title="Category:Short description matches Wikidata">Short description matches Wikidata</a></li><li><a href="/wiki/Category:Use_dmy_dates_from_October_2021" title="Category:Use dmy dates from October 2021">Use dmy dates from October 2021</a></li><li><a href="/wiki/Category:Wikipedia_articles_needing_clarification_from_September_2024" title="Category:Wikipedia articles needing clarification from September 2024">Wikipedia articles needing clarification from September 2024</a></li></ul></div></div> </div> </main> </div> <div class="mw-footer-container"> <footer id="footer" class="mw-footer" > <ul id="footer-info"> <li id="footer-info-lastmod"> This page was last edited on 10 November 2024, at 18:51<span class="anonymous-show">&#160;(UTC)</span>.</li> <li id="footer-info-copyright">Text is available under the <a href="/wiki/Wikipedia:Text_of_the_Creative_Commons_Attribution-ShareAlike_4.0_International_License" title="Wikipedia:Text of the Creative Commons Attribution-ShareAlike 4.0 International License">Creative Commons Attribution-ShareAlike 4.0 License</a>; additional terms may apply. By using this site, you agree to the <a href="https://foundation.wikimedia.org/wiki/Special:MyLanguage/Policy:Terms_of_Use" class="extiw" title="foundation:Special:MyLanguage/Policy:Terms of Use">Terms of Use</a> and <a href="https://foundation.wikimedia.org/wiki/Special:MyLanguage/Policy:Privacy_policy" class="extiw" title="foundation:Special:MyLanguage/Policy:Privacy policy">Privacy Policy</a>. Wikipedia® is a registered trademark of the <a rel="nofollow" class="external text" href="https://wikimediafoundation.org/">Wikimedia Foundation, Inc.</a>, a non-profit organization.</li> </ul> <ul id="footer-places"> <li id="footer-places-privacy"><a href="https://foundation.wikimedia.org/wiki/Special:MyLanguage/Policy:Privacy_policy">Privacy policy</a></li> <li id="footer-places-about"><a href="/wiki/Wikipedia:About">About Wikipedia</a></li> <li id="footer-places-disclaimers"><a href="/wiki/Wikipedia:General_disclaimer">Disclaimers</a></li> <li id="footer-places-contact"><a href="//en.wikipedia.org/wiki/Wikipedia:Contact_us">Contact Wikipedia</a></li> <li id="footer-places-wm-codeofconduct"><a href="https://foundation.wikimedia.org/wiki/Special:MyLanguage/Policy:Universal_Code_of_Conduct">Code of Conduct</a></li> <li id="footer-places-developers"><a href="https://developer.wikimedia.org">Developers</a></li> <li id="footer-places-statslink"><a href="https://stats.wikimedia.org/#/en.wikipedia.org">Statistics</a></li> <li id="footer-places-cookiestatement"><a href="https://foundation.wikimedia.org/wiki/Special:MyLanguage/Policy:Cookie_statement">Cookie statement</a></li> <li id="footer-places-mobileview"><a href="//en.m.wikipedia.org/w/index.php?title=Substituted_cathinone&amp;mobileaction=toggle_view_mobile" class="noprint stopMobileRedirectToggle">Mobile view</a></li> </ul> <ul id="footer-icons" class="noprint"> <li id="footer-copyrightico"><a href="https://wikimediafoundation.org/" class="cdx-button cdx-button--fake-button cdx-button--size-large cdx-button--fake-button--enabled"><img src="/static/images/footer/wikimedia-button.svg" width="84" height="29" alt="Wikimedia Foundation" loading="lazy"></a></li> <li id="footer-poweredbyico"><a href="https://www.mediawiki.org/" class="cdx-button cdx-button--fake-button cdx-button--size-large cdx-button--fake-button--enabled"><img src="/w/resources/assets/poweredby_mediawiki.svg" alt="Powered by MediaWiki" width="88" height="31" loading="lazy"></a></li> </ul> </footer> </div> </div> </div> <div class="vector-settings" id="p-dock-bottom"> <ul></ul> </div><script>(RLQ=window.RLQ||[]).push(function(){mw.config.set({"wgHostname":"mw-web.codfw.main-f69cdc8f6-2c6ql","wgBackendResponseTime":139,"wgPageParseReport":{"limitreport":{"cputime":"1.274","walltime":"2.895","ppvisitednodes":{"value":3183,"limit":1000000},"postexpandincludesize":{"value":234014,"limit":2097152},"templateargumentsize":{"value":2789,"limit":2097152},"expansiondepth":{"value":17,"limit":100},"expensivefunctioncount":{"value":3,"limit":500},"unstrip-depth":{"value":1,"limit":20},"unstrip-size":{"value":164844,"limit":5000000},"entityaccesscount":{"value":0,"limit":400},"timingprofile":["100.00% 857.440 1 -total"," 40.38% 346.210 1 Template:Reflist"," 37.12% 318.292 8 Template:Navbox"," 26.49% 227.128 25 Template:Cite_journal"," 16.30% 139.798 1 Template:Phenethylamines"," 14.38% 123.325 1 Template:Short_description"," 11.93% 102.260 1 Template:Dopaminergics"," 8.99% 77.073 1 Template:Clarify"," 8.86% 75.989 2 Template:Pagetype"," 8.26% 70.848 1 Template:Fix-span"]},"scribunto":{"limitreport-timeusage":{"value":"0.358","limit":"10.000"},"limitreport-memusage":{"value":5614309,"limit":52428800}},"cachereport":{"origin":"mw-web.eqiad.main-5dc468848-5hg4f","timestamp":"20241122144213","ttl":2592000,"transientcontent":false}}});});</script> <script type="application/ld+json">{"@context":"https:\/\/schema.org","@type":"Article","name":"Substituted cathinone","url":"https:\/\/en.wikipedia.org\/wiki\/Substituted_cathinone","sameAs":"http:\/\/www.wikidata.org\/entity\/Q7632116","mainEntity":"http:\/\/www.wikidata.org\/entity\/Q7632116","author":{"@type":"Organization","name":"Contributors to Wikimedia projects"},"publisher":{"@type":"Organization","name":"Wikimedia Foundation, Inc.","logo":{"@type":"ImageObject","url":"https:\/\/www.wikimedia.org\/static\/images\/wmf-hor-googpub.png"}},"datePublished":"2010-01-17T06:54:33Z","dateModified":"2024-11-10T18:51:56Z","image":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/3\/33\/Cathinone.svg","headline":"class of chemical compounds"}</script> </body> </html>

Pages: 1 2 3 4 5 6 7 8 9 10