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List of estrogen esters - Wikipedia
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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-Esters_of_steroidal_estrogens" class="vector-toc-list-item vector-toc-level-1"> <a class="vector-toc-link" href="#Esters_of_steroidal_estrogens"> <div class="vector-toc-text"> <span class="vector-toc-numb">1</span> <span>Esters of steroidal estrogens</span> </div> </a> <button aria-controls="toc-Esters_of_steroidal_estrogens-sublist" class="cdx-button cdx-button--weight-quiet cdx-button--icon-only vector-toc-toggle"> <span class="vector-icon mw-ui-icon-wikimedia-expand"></span> <span>Toggle Esters of steroidal estrogens subsection</span> </button> <ul id="toc-Esters_of_steroidal_estrogens-sublist" class="vector-toc-list"> <li id="toc-Estradiol_esters" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Estradiol_esters"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.1</span> <span>Estradiol esters</span> </div> </a> <ul id="toc-Estradiol_esters-sublist" class="vector-toc-list"> <li id="toc-Marketed" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.1.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Never_marketed" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Never_marketed"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.1.2</span> <span>Never marketed</span> </div> </a> <ul id="toc-Never_marketed-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Estrone_esters" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Estrone_esters"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.2</span> <span>Estrone esters</span> </div> </a> <ul id="toc-Estrone_esters-sublist" class="vector-toc-list"> <li id="toc-Marketed_2" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_2"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.2.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_2-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Never_marketed_2" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Never_marketed_2"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.2.2</span> <span>Never marketed</span> </div> </a> <ul id="toc-Never_marketed_2-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Estriol_esters" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Estriol_esters"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.3</span> <span>Estriol esters</span> </div> </a> <ul id="toc-Estriol_esters-sublist" class="vector-toc-list"> <li id="toc-Marketed_3" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_3"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.3.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_3-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Never_marketed_3" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Never_marketed_3"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.3.2</span> <span>Never marketed</span> </div> </a> <ul id="toc-Never_marketed_3-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Ethinylestradiol_esters" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Ethinylestradiol_esters"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.4</span> <span>Ethinylestradiol esters</span> </div> </a> <ul id="toc-Ethinylestradiol_esters-sublist" class="vector-toc-list"> <li id="toc-Marketed_4" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_4"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.4.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_4-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Never_marketed_4" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Never_marketed_4"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.4.2</span> <span>Never marketed</span> </div> </a> <ul id="toc-Never_marketed_4-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Esters_of_other_steroidal_estrogens" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Esters_of_other_steroidal_estrogens"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.5</span> <span>Esters of other steroidal estrogens</span> </div> </a> <ul id="toc-Esters_of_other_steroidal_estrogens-sublist" class="vector-toc-list"> <li id="toc-Marketed_5" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_5"> <div class="vector-toc-text"> <span class="vector-toc-numb">1.5.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_5-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> </ul> </li> <li id="toc-Ethers_of_steroidal_estrogens" class="vector-toc-list-item vector-toc-level-1"> <a class="vector-toc-link" href="#Ethers_of_steroidal_estrogens"> <div class="vector-toc-text"> <span class="vector-toc-numb">2</span> <span>Ethers of steroidal estrogens</span> </div> </a> <button aria-controls="toc-Ethers_of_steroidal_estrogens-sublist" class="cdx-button cdx-button--weight-quiet cdx-button--icon-only vector-toc-toggle"> <span class="vector-icon mw-ui-icon-wikimedia-expand"></span> <span>Toggle Ethers of steroidal estrogens subsection</span> </button> <ul id="toc-Ethers_of_steroidal_estrogens-sublist" class="vector-toc-list"> <li id="toc-Marketed_6" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Marketed_6"> <div class="vector-toc-text"> <span class="vector-toc-numb">2.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_6-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Never_marketed_5" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Never_marketed_5"> <div class="vector-toc-text"> <span class="vector-toc-numb">2.2</span> <span>Never marketed</span> </div> </a> <ul id="toc-Never_marketed_5-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Esters_of_nonsteroidal_estrogens" class="vector-toc-list-item vector-toc-level-1"> <a class="vector-toc-link" href="#Esters_of_nonsteroidal_estrogens"> <div class="vector-toc-text"> <span class="vector-toc-numb">3</span> <span>Esters of nonsteroidal estrogens</span> </div> </a> <button aria-controls="toc-Esters_of_nonsteroidal_estrogens-sublist" class="cdx-button cdx-button--weight-quiet cdx-button--icon-only vector-toc-toggle"> <span class="vector-icon mw-ui-icon-wikimedia-expand"></span> <span>Toggle Esters of nonsteroidal estrogens subsection</span> </button> <ul id="toc-Esters_of_nonsteroidal_estrogens-sublist" class="vector-toc-list"> <li id="toc-Diethylstilbestrol_esters" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Diethylstilbestrol_esters"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.1</span> <span>Diethylstilbestrol esters</span> </div> </a> <ul id="toc-Diethylstilbestrol_esters-sublist" class="vector-toc-list"> <li id="toc-Marketed_7" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_7"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.1.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_7-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Never_marketed_6" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Never_marketed_6"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.1.2</span> <span>Never marketed</span> </div> </a> <ul id="toc-Never_marketed_6-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Hexestrol_esters" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Hexestrol_esters"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.2</span> <span>Hexestrol esters</span> </div> </a> <ul id="toc-Hexestrol_esters-sublist" class="vector-toc-list"> <li id="toc-Marketed_8" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_8"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.2.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_8-sublist" class="vector-toc-list"> </ul> </li> <li id="toc-Never_marketed_7" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Never_marketed_7"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.2.2</span> <span>Never marketed</span> </div> </a> <ul id="toc-Never_marketed_7-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> <li id="toc-Esters_of_other_nonsteroidal_estrogens" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Esters_of_other_nonsteroidal_estrogens"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.3</span> <span>Esters of other nonsteroidal estrogens</span> </div> </a> <ul id="toc-Esters_of_other_nonsteroidal_estrogens-sublist" class="vector-toc-list"> <li id="toc-Marketed_9" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_9"> <div class="vector-toc-text"> <span class="vector-toc-numb">3.3.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_9-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> </ul> </li> <li id="toc-Ethers_of_nonsteroidal_estrogens" class="vector-toc-list-item vector-toc-level-1"> <a class="vector-toc-link" href="#Ethers_of_nonsteroidal_estrogens"> <div class="vector-toc-text"> <span class="vector-toc-numb">4</span> <span>Ethers of nonsteroidal estrogens</span> </div> </a> <button aria-controls="toc-Ethers_of_nonsteroidal_estrogens-sublist" class="cdx-button cdx-button--weight-quiet cdx-button--icon-only vector-toc-toggle"> <span class="vector-icon mw-ui-icon-wikimedia-expand"></span> <span>Toggle Ethers of nonsteroidal estrogens subsection</span> </button> <ul id="toc-Ethers_of_nonsteroidal_estrogens-sublist" class="vector-toc-list"> <li id="toc-Diethylstilbestrol" class="vector-toc-list-item vector-toc-level-2"> <a class="vector-toc-link" href="#Diethylstilbestrol"> <div class="vector-toc-text"> <span class="vector-toc-numb">4.1</span> <span>Diethylstilbestrol</span> </div> </a> <ul id="toc-Diethylstilbestrol-sublist" class="vector-toc-list"> <li id="toc-Marketed_10" class="vector-toc-list-item vector-toc-level-3"> <a class="vector-toc-link" href="#Marketed_10"> <div class="vector-toc-text"> <span class="vector-toc-numb">4.1.1</span> <span>Marketed</span> </div> </a> <ul id="toc-Marketed_10-sublist" class="vector-toc-list"> </ul> </li> </ul> </li> </ul> </li> <li id="toc-See_also" class="vector-toc-list-item vector-toc-level-1"> <a class="vector-toc-link" href="#See_also"> <div class="vector-toc-text"> <span class="vector-toc-numb">5</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"> <a class="vector-toc-link" href="#References"> <div class="vector-toc-text"> <span class="vector-toc-numb">6</span> <span>References</span> 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class="mw-body-content"><div class="mw-content-ltr mw-parser-output" lang="en" dir="ltr"><p class="mw-empty-elt"> </p> <figure class="mw-halign-right" typeof="mw:File/Thumb"><a href="/wiki/File:Estradiol.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/0/00/Estradiol.svg/200px-Estradiol.svg.png" decoding="async" width="200" height="127" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/0/00/Estradiol.svg/300px-Estradiol.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/0/00/Estradiol.svg/400px-Estradiol.svg.png 2x" data-file-width="512" data-file-height="324" /></a><figcaption><a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">Estradiol</a>, the base estrogen of most estrogen esters.</figcaption></figure> <p>This is a <b>list of <a href="/wiki/Estrogen_ester" title="Estrogen ester">estrogen esters</a></b>, or <a href="/wiki/Ester" title="Ester">ester</a> <a href="/wiki/Prodrug" title="Prodrug">prodrugs</a> of <a href="/wiki/Estrogen_(medication)" title="Estrogen (medication)">estrogens</a>. It includes esters, as well as <a href="/wiki/Ether" title="Ether">ethers</a>, of <a href="/wiki/Steroid" title="Steroid">steroidal</a> <a href="/wiki/Estrogen_(medication)" title="Estrogen (medication)">estrogens</a> like <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">estradiol</a>, <a href="/wiki/Estrone_(medication)" title="Estrone (medication)">estrone</a>, and <a href="/wiki/Estriol_(medication)" title="Estriol (medication)">estriol</a> and of <a href="/wiki/Nonsteroidal_estrogen" title="Nonsteroidal estrogen">nonsteroidal estrogens</a> like the <a href="/wiki/Stilbestrol" title="Stilbestrol">stilbestrols</a> <a href="/wiki/Diethylstilbestrol" title="Diethylstilbestrol">diethylstilbestrol</a> and <a href="/wiki/Hexestrol" title="Hexestrol">hexestrol</a>. </p> <style data-mw-deduplicate="TemplateStyles:r886046785">.mw-parser-output .toclimit-2 .toclevel-1 ul,.mw-parser-output .toclimit-3 .toclevel-2 ul,.mw-parser-output .toclimit-4 .toclevel-3 ul,.mw-parser-output .toclimit-5 .toclevel-4 ul,.mw-parser-output .toclimit-6 .toclevel-5 ul,.mw-parser-output .toclimit-7 .toclevel-6 ul{display:none}</style><div class="toclimit-3"><meta property="mw:PageProp/toc" /></div> <div class="mw-heading mw-heading2"><h2 id="Esters_of_steroidal_estrogens">Esters of steroidal estrogens</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=1" title="Edit section: Esters of steroidal estrogens"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading3"><h3 id="Estradiol_esters">Estradiol esters</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=2" title="Edit section: Estradiol esters"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=3" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Many esters of estradiol have been marketed, including the following major esters:<sup id="cite_ref-IndexNominum2000_1-0" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-Roberts1991_2-0" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Estradiol_acetate" title="Estradiol acetate">Estradiol acetate</a> (Femring, Femtrace, Menoring)</li> <li><a href="/wiki/Estradiol_benzoate" title="Estradiol benzoate">Estradiol benzoate</a> (Agofollin Depot, Progynon-B; Duogynon, Primosiston, Sistocyclin)</li> <li><a href="/wiki/Estradiol_cypionate" title="Estradiol cypionate">Estradiol cypionate</a> (Depo-Estradiol, Depofemin, Estradep; Cyclofem, Lunelle)</li> <li><a href="/wiki/Estradiol_dipropionate" title="Estradiol dipropionate">Estradiol dipropionate</a> (Agofollin, Di-Ovocyclin, Progynon-DP; EP Hormone Depot)</li> <li><a href="/wiki/Estradiol_enantate" title="Estradiol enantate">Estradiol enantate</a> (Perlutal, Topasel, Unalmes, Yectames)</li> <li><a href="/wiki/Estradiol_undecylate" title="Estradiol undecylate">Estradiol undecylate</a> (Delestrec, Progynon Depot)</li> <li><a href="/wiki/Estradiol_valerate" title="Estradiol valerate">Estradiol valerate</a> (Delestrogen, Progynon Depot, Progynova; Gravibinon, Mesigyna, Mesygest)</li> <li><a href="/wiki/Polyestradiol_phosphate" title="Polyestradiol phosphate">Polyestradiol phosphate</a> (Estradurin) (an estradiol ester in <a href="/wiki/Polymer" title="Polymer">polymeric</a> form)</li></ul> <p>And the following less commonly used esters:<sup id="cite_ref-IndexNominum2000_1-1" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-Roberts1991_2-1" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Cloxestradiol_acetate" title="Cloxestradiol acetate">Cloxestradiol acetate</a> (Genovul; diacetate ester of <a href="/wiki/Cloxestradiol" title="Cloxestradiol">cloxestradiol</a>, or estradiol 17β-chloral hemiacetal ether)</li> <li><a href="/wiki/Estradiol_benzoate_butyrate" title="Estradiol benzoate butyrate">Estradiol benzoate butyrate</a> (Redimen, Soluna, Unijab, Unimens)</li> <li><a href="/wiki/Estradiol_butyrylacetate" title="Estradiol butyrylacetate">Estradiol butyrylacetate</a> (Follikoside)</li> <li><a href="/wiki/Estradiol_dibutyrate" title="Estradiol dibutyrate">Estradiol dibutyrate</a> (Triormon Depositum)</li> <li><a href="/wiki/Estradiol_dienantate" title="Estradiol dienantate">Estradiol dienantate</a> (Climacteron, Lactimex, Lactostat)</li> <li><a href="/wiki/Estradiol_diundecylate" title="Estradiol diundecylate">Estradiol diundecylate</a> (Estrolent; Trioestrine Retard)</li> <li><a href="/wiki/Estradiol_diundecylenate" title="Estradiol diundecylenate">Estradiol diundecylenate</a> (Etrosteron)</li> <li><a href="/wiki/Estradiol_furoate" title="Estradiol furoate">Estradiol furoate</a> (Di-Folliculine)</li> <li><a href="/wiki/Estradiol_hemisuccinate" title="Estradiol hemisuccinate">Estradiol hemisuccinate</a> (Eutocol; Hosterona)</li> <li><a href="/wiki/Estradiol_hemihydrate" class="mw-redirect" title="Estradiol hemihydrate">Estradiol hemihydrate</a> (Estrofem)</li> <li><a href="/wiki/Estradiol_hexahydrobenzoate" title="Estradiol hexahydrobenzoate">Estradiol hexahydrobenzoate</a> (Benzo-Ginoestril A.P., BenzoGynoestryl Retard, Ginestryl-15-Depot, Menodin, Tardoginestryl)</li> <li><a href="/wiki/Estradiol_palmitate" title="Estradiol palmitate">Estradiol palmitate</a> (Esmopal)</li> <li><a href="/wiki/Estradiol_phenylpropionate" title="Estradiol phenylpropionate">Estradiol phenylpropionate</a> (Dimenformon Prolongatum; Estandron Prolongatum, Lynandron Prolongatum, Mixogen)</li> <li><a href="/wiki/Estradiol_pivalate" title="Estradiol pivalate">Estradiol pivalate</a> (Estrotate; Estrotate with Progesterone)</li> <li><a href="/wiki/Estradiol_monopropionate" title="Estradiol monopropionate">Estradiol propionate</a> (estradiol 17β-propionate) (Acrofollin, Akrofollin, Follhormon)</li> <li><a href="/wiki/Estradiol_propoxyphenylpropionate" title="Estradiol propoxyphenylpropionate">Estradiol propoxyphenylpropionate</a> (Durovex)</li> <li><a href="/wiki/Estradiol_stearate" title="Estradiol stearate">Estradiol stearate</a> (Depofollan)</li> <li><a href="/wiki/Estradiol_sulfate" title="Estradiol sulfate">Estradiol sulfate</a> (a minor constituent of <a href="/wiki/Conjugated_estrogens" title="Conjugated estrogens">conjugated estrogens</a> (Premarin))</li></ul> <p>The following <a href="/wiki/Nitrogen_mustard" title="Nitrogen mustard">nitrogen mustard</a> ester of estradiol is a <a href="/wiki/Cytostatic_antineoplastic_agent" class="mw-redirect" title="Cytostatic antineoplastic agent">cytostatic antineoplastic agent</a> and has been marketed:<sup id="cite_ref-IndexNominum2000_1-2" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-Roberts1991_2-2" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Estramustine_phosphate" title="Estramustine phosphate">Estramustine phosphate</a> (Emcyt, Estracyt; estradiol 3-normustine 17β-phosphate)</li></ul> <div class="mw-heading mw-heading4"><h4 id="Never_marketed">Never marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=4" title="Edit section: Never marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>A number of other estradiol esters which have not been marketed include:<sup id="cite_ref-Roberts1991_2-3" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/w/index.php?title=Estradiol_3-furoate&action=edit&redlink=1" class="new" title="Estradiol 3-furoate (page does not exist)">Estradiol 3-furoate</a><sup id="cite_ref-Ferin1952_3-0" class="reference"><a href="#cite_note-Ferin1952-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_3-propionate" title="Estradiol 3-propionate">Estradiol 3-propionate</a> (<i>not to be confused with estradiol monopropionate (estradiol 17β-propionate)</i>)</li> <li><a href="/wiki/Estradiol_17%CE%B2-(1-(4-(aminosulfonyl)benzoyl)-L-proline)" class="mw-redirect" title="Estradiol 17β-(1-(4-(aminosulfonyl)benzoyl)-L-proline)">Estradiol 17β-(1-(4-(aminosulfonyl)benzoyl)-<span style="font-size:85%;">L</span>-proline)</a> (EC508)<sup id="cite_ref-Evestra_4-0" class="reference"><a href="#cite_note-Evestra-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-pmid27449818_5-0" class="reference"><a href="#cite_note-pmid27449818-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-pmid28886996_6-0" class="reference"><a href="#cite_note-pmid28886996-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-NickischSanthamma2017_7-0" class="reference"><a href="#cite_note-NickischSanthamma2017-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup></li> <li><a href="/w/index.php?title=Estradiol_acetate_benzoate&action=edit&redlink=1" class="new" title="Estradiol acetate benzoate (page does not exist)">Estradiol acetate benzoate</a><sup id="cite_ref-HumansOrganization2007_8-0" class="reference"><a href="#cite_note-HumansOrganization2007-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-VizzoneMurari1966_9-0" class="reference"><a href="#cite_note-VizzoneMurari1966-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_17%CE%B2-acetate" title="Estradiol 17β-acetate">Estradiol 17β-acetate</a></li> <li><a href="/wiki/Estradiol_17%CE%B2-benzoate" title="Estradiol 17β-benzoate">Estradiol 17β-benzoate</a></li> <li><a href="/wiki/Estradiol_acetylsalicylate" title="Estradiol acetylsalicylate">Estradiol acetylsalicylate</a> (estradiol 3-acetylsalicylate)<sup id="cite_ref-pmid3244608_10-0" class="reference"><a href="#cite_note-pmid3244608-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-LokindLorenzen1991_11-0" class="reference"><a href="#cite_note-LokindLorenzen1991-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_anthranilate" title="Estradiol anthranilate">Estradiol anthranilate</a> (estradiol 3-anthranilate)<sup id="cite_ref-pmid3244608_10-1" class="reference"><a href="#cite_note-pmid3244608-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-LokindLorenzen1991_11-1" class="reference"><a href="#cite_note-LokindLorenzen1991-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup></li> <li><a href="/w/index.php?title=Estradiol_arachidonate&action=edit&redlink=1" class="new" title="Estradiol arachidonate (page does not exist)">Estradiol arachidonate</a></li> <li><a href="/wiki/Estradiol_benzoate_cyclooctenyl_ether" title="Estradiol benzoate cyclooctenyl ether">Estradiol benzoate cyclooctenyl ether</a> (estradiol 3-benzoate 17β-cyclooctenyl ether; EBCO)<sup id="cite_ref-pmid4654978_12-0" class="reference"><a href="#cite_note-pmid4654978-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-pmid4438394_13-0" class="reference"><a href="#cite_note-pmid4438394-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup></li> <li><a href="/w/index.php?title=Estradiol_caprylate&action=edit&redlink=1" class="new" title="Estradiol caprylate (page does not exist)">Estradiol caprylate</a> (estradiol octanoate)<sup id="cite_ref-Dorfman2016_14-0" class="reference"><a href="#cite_note-Dorfman2016-14"><span class="cite-bracket">[</span>14<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-JanockoLarner1984_15-0" class="reference"><a href="#cite_note-JanockoLarner1984-15"><span class="cite-bracket">[</span>15<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_cyclooctyl_acetate" title="Estradiol cyclooctyl acetate">Estradiol cyclooctyl acetate</a> (E2CoA)<sup id="cite_ref-pmid3932144_16-0" class="reference"><a href="#cite_note-pmid3932144-16"><span class="cite-bracket">[</span>16<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_decanoate" title="Estradiol decanoate">Estradiol decanoate</a> (estradiol 17β-decanoate)<sup id="cite_ref-pmid755846_17-0" class="reference"><a href="#cite_note-pmid755846-17"><span class="cite-bracket">[</span>17<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_diacetate" title="Estradiol diacetate">Estradiol diacetate</a></li> <li><a href="/wiki/Estradiol_dibenzoate" title="Estradiol dibenzoate">Estradiol dibenzoate</a></li> <li><a href="/wiki/Estradiol_dicypionate" title="Estradiol dicypionate">Estradiol dicypionate</a></li> <li><a href="/w/index.php?title=Estradiol_dioleate&action=edit&redlink=1" class="new" title="Estradiol dioleate (page does not exist)">Estradiol dioleate</a></li> <li><a href="/w/index.php?title=Estradiol_dipalmitate&action=edit&redlink=1" class="new" title="Estradiol dipalmitate (page does not exist)">Estradiol dipalmitate</a></li> <li><a href="/wiki/Estradiol_distearate" title="Estradiol distearate">Estradiol distearate</a></li> <li><a href="/wiki/Estradiol_disulfate" title="Estradiol disulfate">Estradiol disulfate</a></li> <li><a href="/wiki/Estradiol_glucuronide" title="Estradiol glucuronide">Estradiol glucuronide</a></li> <li><a href="/wiki/Estradiol_sulfate_glucuronide" class="mw-redirect" title="Estradiol sulfate glucuronide">Estradiol sulfate glucuronide</a></li> <li><a href="/w/index.php?title=Estradiol_linoleate&action=edit&redlink=1" class="new" title="Estradiol linoleate (page does not exist)">Estradiol linoleate</a></li> <li><a href="/w/index.php?title=Estradiol_oleate&action=edit&redlink=1" class="new" title="Estradiol oleate (page does not exist)">Estradiol oleate</a></li> <li><a href="/wiki/Estradiol_phosphate" title="Estradiol phosphate">Estradiol phosphate</a></li> <li><a href="/wiki/Estradiol_salicylate" title="Estradiol salicylate">Estradiol salicylate</a> (estradiol 3-salicylate)<sup id="cite_ref-pmid3244608_10-2" class="reference"><a href="#cite_note-pmid3244608-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-LokindLorenzen1991_11-2" class="reference"><a href="#cite_note-LokindLorenzen1991-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_sulfamate" title="Estradiol sulfamate">Estradiol sulfamate</a> (E2MATE; J995, PGL-2, PGL-2001, ZK-190628; estradiol-3-O-sulfamate)</li> <li><a href="/wiki/Estradiol_undecylenate" title="Estradiol undecylenate">Estradiol undecylenate</a> (SH-368)</li> <li><a href="/wiki/Estrapronicate" title="Estrapronicate">Estrapronicate</a> (estradiol 3-propionate 17β-nicotinate; Trophobolene, Trophoboline)</li> <li><a href="/wiki/Orestrate" title="Orestrate">Orestrate</a> (estradiol 3-propionate 17β-(1-cyclohexenyl) ether)</li></ul> <p>The following cytostatic antineoplastic nitrogen mustard esters of estradiol have not been marketed:<sup id="cite_ref-Roberts1991_2-4" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Alestramustine" title="Alestramustine">Alestramustine</a> (estradiol 3-(bis(2-chloroethyl)carbamate), 17-ester with <small>L</small>-alanine)</li> <li><a href="/wiki/Atrimustine" title="Atrimustine">Atrimustine</a> (KM-2210; bestrabucil, busramustine)</li> <li><a href="/wiki/Estradiol_mustard" title="Estradiol mustard">Estradiol mustard</a> (NSC-112259; chlorphenacyl estradiol diester)</li> <li><a href="/wiki/Estramustine" title="Estramustine">Estramustine</a> (Leo 275; Ro 21-8837)</li> <li><a href="/wiki/Estromustine" title="Estromustine">Estromustine</a> (Leo 271 f; estrone 17β-3-N-bis(2-chloroethyl)carbamate, estrone–cytostatic complex)</li></ul> <div class="mw-heading mw-heading3"><h3 id="Estrone_esters">Estrone esters</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=5" title="Edit section: Estrone esters"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_2">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=6" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Esters of estrone that have been marketed include:<sup id="cite_ref-IndexNominum2000_1-3" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-Roberts1991_2-5" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Estrone_acetate" title="Estrone acetate">Estrone acetate</a> (Hovigal)</li> <li><a href="/wiki/Estrone_sulfate_(medication)" title="Estrone sulfate (medication)">Estrone sulfate</a> (as the primary component of <a href="/wiki/Conjugated_estrogens" title="Conjugated estrogens">conjugated estrogens</a> (Premarin)) <ul><li><a href="/wiki/Estropipate" title="Estropipate">Estropipate</a> (Ogen, Ortho-Est) (a salt of estrone sulfate and <a href="/wiki/Piperazine" title="Piperazine">piperazine</a>)</li></ul></li> <li><a href="/wiki/Estrone_tetraacetylglucoside" title="Estrone tetraacetylglucoside">Estrone tetraacetylglucoside</a> (Glucovex, Glycovex)</li></ul> <div class="mw-heading mw-heading4"><h4 id="Never_marketed_2">Never marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=7" title="Edit section: Never marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Other estrone esters which are notable but have not been marketed include: </p> <ul><li><a href="/wiki/Estrone_benzoate" title="Estrone benzoate">Estrone benzoate</a></li> <li><a href="/wiki/Estrone_cyanate" title="Estrone cyanate">Estrone cyanate</a></li> <li><a href="/w/index.php?title=Estrone_enanthate&action=edit&redlink=1" class="new" title="Estrone enanthate (page does not exist)">Estrone enanthate</a><sup id="cite_ref-pmid13828402_18-0" class="reference"><a href="#cite_note-pmid13828402-18"><span class="cite-bracket">[</span>18<span class="cite-bracket">]</span></a></sup></li> <li><a href="/w/index.php?title=Estrone_enanthate_benzilic_acid_hydrazone&action=edit&redlink=1" class="new" title="Estrone enanthate benzilic acid hydrazone (page does not exist)">Estrone enanthate benzilic acid hydrazone</a><sup id="cite_ref-pmid13828402_18-1" class="reference"><a href="#cite_note-pmid13828402-18"><span class="cite-bracket">[</span>18<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estrone_glucuronide" title="Estrone glucuronide">Estrone glucuronide</a></li> <li><a href="/wiki/Estrone_phosphate" title="Estrone phosphate">Estrone phosphate</a></li> <li><a href="/w/index.php?title=Estrone_propionate&action=edit&redlink=1" class="new" title="Estrone propionate (page does not exist)">Estrone propionate</a><sup id="cite_ref-Milne2018_19-0" class="reference"><a href="#cite_note-Milne2018-19"><span class="cite-bracket">[</span>19<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estrone_sulfamate" title="Estrone sulfamate">Estrone sulfamate</a> (EMATE; J994; estrone-3-O-sulfamate)</li> <li><a href="/wiki/Estrone_oleate" class="mw-redirect" title="Estrone oleate">Estrone oleate</a></li></ul> <div class="mw-heading mw-heading3"><h3 id="Estriol_esters">Estriol esters</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=8" title="Edit section: Estriol esters"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_3">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=9" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Esters of estriol that have been marketed include:<sup id="cite_ref-IndexNominum2000_1-4" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-Roberts1991_2-6" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Estriol_3-glucuronide" title="Estriol 3-glucuronide">Estriol 3-glucuronide</a> (as a component of <a href="/wiki/Conjugated_estriol" title="Conjugated estriol">conjugated estriol</a> (Emmenin, Progynon))</li> <li><a href="/wiki/Estriol_acetate_benzoate" title="Estriol acetate benzoate">Estriol acetate benzoate</a> (Holin-Depot)</li> <li><a href="/wiki/Estriol_glucuronide" title="Estriol glucuronide">Estriol glucuronide</a> (as a component of <a href="/wiki/Conjugated_estriol" title="Conjugated estriol">conjugated estriol</a> (Emmenin, Progynon))</li> <li><a href="/wiki/Estriol_succinate" title="Estriol succinate">Estriol succinate</a> (Sinapause, Styptanon, Synapause) <ul><li><a href="/wiki/Estriol_sodium_succinate" class="mw-redirect" title="Estriol sodium succinate">Estriol sodium succinate</a> (Pausan, Styptanon)</li></ul></li> <li><a href="/wiki/Estriol_sulfate" title="Estriol sulfate">Estriol sulfate</a> (as a component of <a href="/wiki/Conjugated_estriol" title="Conjugated estriol">conjugated estriol</a> (Emmenin, Progynon))</li> <li><a href="/wiki/Estriol_sulfate_glucuronide" title="Estriol sulfate glucuronide">Estriol sulfate glucuronide</a> (as a component of <a href="/wiki/Conjugated_estriol" title="Conjugated estriol">conjugated estriol</a> (Emmenin, Progynon))</li> <li><a href="/wiki/Estriol_tripropionate" title="Estriol tripropionate">Estriol tripropionate</a> (Estriel)</li> <li><a href="/wiki/Polyestriol_phosphate" title="Polyestriol phosphate">Polyestriol phosphate</a> (Gynäsan, Klimadurin, Triodurin) (an estriol ester in <a href="/wiki/Polymer" title="Polymer">polymeric</a> form)</li></ul> <div class="mw-heading mw-heading4"><h4 id="Never_marketed_3">Never marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=10" title="Edit section: Never marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>The following ester of estriol was never marketed: </p> <ul><li><a href="/wiki/Estriol_dihexanoate" title="Estriol dihexanoate">Estriol dihexanoate</a></li> <li><a href="/wiki/Estriol_dipropionate" title="Estriol dipropionate">Estriol dipropionate</a></li> <li><a href="/wiki/Estriol_phosphate" title="Estriol phosphate">Estriol phosphate</a> (E3P)</li> <li><a href="/wiki/Estriol_sulfamate" title="Estriol sulfamate">Estriol sulfamate</a> (E3MATE; J1034; estriol-3-O-sulfamate)</li> <li><a href="/wiki/Estriol_triacetate" title="Estriol triacetate">Estriol triacetate</a></li></ul> <div class="mw-heading mw-heading3"><h3 id="Ethinylestradiol_esters">Ethinylestradiol esters</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=11" title="Edit section: Ethinylestradiol esters"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_4">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=12" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>The following esters of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a> exist and have been marketed:<sup id="cite_ref-IndexNominum2000_1-5" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-Roberts1991_2-7" class="reference"><a href="#cite_note-Roberts1991-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Ethinylestradiol_sulfonate" title="Ethinylestradiol sulfonate">Ethinylestradiol sulfonate</a> (Turisteron; ethinylestradiol 3-isopropylsulfonate)</li></ul> <div class="mw-heading mw-heading4"><h4 id="Never_marketed_4">Never marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=13" title="Edit section: Never marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Ethinylestradiol_benzoate" title="Ethinylestradiol benzoate">Ethinylestradiol benzoate</a> – the 3-benzoate ester of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a></li> <li><a href="/w/index.php?title=Ethinylestradiol_N,N-diethylsulfamate&action=edit&redlink=1" class="new" title="Ethinylestradiol N,N-diethylsulfamate (page does not exist)">Ethinylestradiol <i>N</i>,<i>N</i>-diethylsulfamate</a> (J271) – the 3-(<i>N</i>,<i>N</i>-diethyl)sulfamate ester of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a><sup id="cite_ref-pmid15991994_20-0" class="reference"><a href="#cite_note-pmid15991994-20"><span class="cite-bracket">[</span>20<span class="cite-bracket">]</span></a></sup></li> <li><a href="/w/index.php?title=Ethinylestradiol_pyrrolidinosulfonate&action=edit&redlink=1" class="new" title="Ethinylestradiol pyrrolidinosulfonate (page does not exist)">Ethinylestradiol pyrrolidinosulfonate</a> (J272) – the 3-pyrrolidinosulfonate ester of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a><sup id="cite_ref-pmid15991994_20-1" class="reference"><a href="#cite_note-pmid15991994-20"><span class="cite-bracket">[</span>20<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Ethinylestradiol_sulfamate" title="Ethinylestradiol sulfamate">Ethinylestradiol sulfamate</a> (J1028) – the 3-sulfamate ester of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a><sup id="cite_ref-pmid8541236_21-0" class="reference"><a href="#cite_note-pmid8541236-21"><span class="cite-bracket">[</span>21<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Ethinylestradiol_sulfate" title="Ethinylestradiol sulfate">Ethinylestradiol sulfate</a></li></ul> <div class="mw-heading mw-heading3"><h3 id="Esters_of_other_steroidal_estrogens">Esters of other steroidal estrogens</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=14" title="Edit section: Esters of other steroidal estrogens"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_5">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=15" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>The following esters of other estrogens exist and have been marketed:<sup id="cite_ref-IndexNominum2000_1-6" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Hydroxyestrone_diacetate" title="Hydroxyestrone diacetate">Hydroxyestrone diacetate</a> (Colpoginon, Colpormon, Hormobion, Hormocervix) – the 3,16α-diacetate ester of <a href="/wiki/16%CE%B1-hydroxyestrone" class="mw-redirect" title="16α-hydroxyestrone">16α-hydroxyestrone</a></li></ul> <div class="mw-heading mw-heading2"><h2 id="Ethers_of_steroidal_estrogens">Ethers of steroidal estrogens</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=16" title="Edit section: Ethers of steroidal estrogens"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading3"><h3 id="Marketed_6">Marketed</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=17" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>A number of <b>estrogen <i><a href="/wiki/Ether" title="Ether">ethers</a></i></b> also exist and have been marketed, including:<sup id="cite_ref-Elks2014_22-0" class="reference"><a href="#cite_note-Elks2014-22"><span class="cite-bracket">[</span>22<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-IndexNominum2000_1-7" class="reference"><a href="#cite_note-IndexNominum2000-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Clomestrone" title="Clomestrone">Clomestrone</a> (Arterolo, Atheran, Colesterel, Iposclerone, Liprotene, Persclerol) – the 3-methyl ether of <a href="/w/index.php?title=16%CE%B1-chloroestrone&action=edit&redlink=1" class="new" title="16α-chloroestrone (page does not exist)">16α-chloroestrone</a></li> <li><a href="/wiki/Cloxestradiol_acetate" title="Cloxestradiol acetate">Cloxestradiol acetate</a> (Genovul) – the <i>O</i>,<i>O</i>-diacetate ester of <a href="/wiki/Cloxestradiol" title="Cloxestradiol">cloxestradiol</a> (estradiol 17β-chloral hemiacetal ether)</li> <li><a href="/wiki/Mestranol" title="Mestranol">Mestranol</a> (Devocin, Ovastol, Tranel) (component of Enovid, Enavid, Ortho-Novin, Femigen, Norbiogest) – the 3-methyl ether of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a></li> <li><a href="/wiki/Moxestrol" title="Moxestrol">Moxestrol</a> (Surestryl) – the 11β-methoxy derivative of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a> (and hence the 11β-methyl ether of the 11β-hydroxyl derivative of ethinylestradiol)</li> <li><a href="/wiki/Nilestriol" title="Nilestriol">Nilestriol</a> (Wei Ni An) – the 3-cyclopentyl ether of <a href="/wiki/Ethinylestriol" title="Ethinylestriol">ethinylestriol</a></li> <li><a href="/wiki/Promestriene" title="Promestriene">Promestriene</a> (Colpotrofin, Colpotrophine, Delipoderm) – the 3-propyl and 17β-methyl diether of <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">estradiol</a></li> <li><a href="/wiki/Quinestradol" title="Quinestradol">Quinestradol</a> (Colpovis, Colpovister, Pentovis) – the 3-cyclopentyl ether of <a href="/wiki/Estriol_(medication)" title="Estriol (medication)">estriol</a></li> <li><a href="/wiki/Quinestrol" title="Quinestrol">Quinestrol</a> (Agalacto-Quilea, Basaquines, Eston, Estrovis, Estrovister, Plestrovis, Qui-lea) – the 3-cyclopentyl ether of <a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">ethinylestradiol</a></li></ul> <div class="mw-heading mw-heading3"><h3 id="Never_marketed_5">Never marketed</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=18" title="Edit section: Never marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>A few other estrogen ethers which are notable but have not been marketed include:<sup id="cite_ref-Elks2014_22-1" class="reference"><a href="#cite_note-Elks2014-22"><span class="cite-bracket">[</span>22<span class="cite-bracket">]</span></a></sup> </p> <ul><li><a href="/wiki/Cloxestradiol" title="Cloxestradiol">Cloxestradiol</a> – the 17β-chloral hemiacetal ether of <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">estradiol</a></li> <li><a href="/wiki/Estradiol_benzoate_cyclooctenyl_ether" title="Estradiol benzoate cyclooctenyl ether">Estradiol benzoate cyclooctenyl ether</a> – the 17β-cyclooctenyl ether of <a href="/wiki/Estradiol_3-benzoate" class="mw-redirect" title="Estradiol 3-benzoate">estradiol 3-benzoate</a><sup id="cite_ref-pmid4654978_12-1" class="reference"><a href="#cite_note-pmid4654978-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_3-saccharinylmethyl_ether" title="Estradiol 3-saccharinylmethyl ether">Estradiol 3-saccharinylmethyl ether</a> – the 3-(saccharinylmethyl) ether of <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">estradiol</a><sup id="cite_ref-pmid7884673_23-0" class="reference"><a href="#cite_note-pmid7884673-23"><span class="cite-bracket">[</span>23<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-pmid7738796_24-0" class="reference"><a href="#cite_note-pmid7738796-24"><span class="cite-bracket">[</span>24<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_3-tetrahydropyranyl_ether" title="Estradiol 3-tetrahydropyranyl ether">Estradiol 3-tetrahydropyranyl ether</a> – the 3-(tetrahydropyran-2-yl) ether of <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">estradiol</a><sup id="cite_ref-LemkeWilliams2012_25-0" class="reference"><a href="#cite_note-LemkeWilliams2012-25"><span class="cite-bracket">[</span>25<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estradiol_17%CE%B2-tetrahydropyranyl_ether" title="Estradiol 17β-tetrahydropyranyl ether">Estradiol 17β-tetrahydropyranyl ether</a> – the 17β-(tetrahydropyran-2-yl) ether of <a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">estradiol</a><sup id="cite_ref-LemkeWilliams2012_25-1" class="reference"><a href="#cite_note-LemkeWilliams2012-25"><span class="cite-bracket">[</span>25<span class="cite-bracket">]</span></a></sup></li> <li><a href="/wiki/Estrone_methyl_ether" title="Estrone methyl ether">Estrone methyl ether</a> – the 3-methyl ether of <a href="/wiki/Estrone_(medication)" title="Estrone (medication)">estrone</a></li> <li><a href="/wiki/Mytatrienediol" title="Mytatrienediol">Mytatrienediol</a> – the 3-methyl ether of <a href="/w/index.php?title=16%CE%B1-methyl-16%CE%B2-epiestriol&action=edit&redlink=1" class="new" title="16α-methyl-16β-epiestriol (page does not exist)">16α-methyl-16β-epiestriol</a></li> <li><a href="/wiki/Orestrate" title="Orestrate">Orestrate</a> – the 17β-(1-cyclohexenyl) ether of <a href="/wiki/Estradiol_3-propionate" title="Estradiol 3-propionate">estradiol 3-propionate</a></li></ul> <div class="mw-heading mw-heading2"><h2 id="Esters_of_nonsteroidal_estrogens">Esters of nonsteroidal estrogens</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=19" title="Edit section: Esters of nonsteroidal estrogens"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading3"><h3 id="Diethylstilbestrol_esters">Diethylstilbestrol esters</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=20" title="Edit section: Diethylstilbestrol esters"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_7">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=21" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>Major esters of diethylstilbestrol include: </p> <ul><li><a href="/wiki/Diethylstilbestrol_dipropionate" title="Diethylstilbestrol dipropionate">Diethylstilbestrol dipropionate</a> (Agostilben, Biokeral, Clinestrol, Cyclen, Estilbin, Estril, Neobenzoestrol, Orestol, Oroestrol, Ostregenin, Prostilbene, Stilbestriol DP, Stilboestrolum Dipropionicum, Stilboestrol, Synestrin, Willestrol)</li> <li><a href="/wiki/Fosfestrol" title="Fosfestrol">Fosfestrol</a> (diethylstilbestrol diphosphate) (Honvan, Difostilben, Fosfostilben, Fostrolin, Stilbol, Stilphostrol, Vagestrol)</li></ul> <p>Less commonly used esters of diethylstilbestrol include: </p> <ul><li><a href="/wiki/Diethylstilbestrol_diacetate" title="Diethylstilbestrol diacetate">Diethylstilbestrol diacetate</a> (Hormostilboral Stark)</li> <li><a href="/wiki/Diethylstilbestrol_dilaurate" title="Diethylstilbestrol dilaurate">Diethylstilbestrol dilaurate</a> (Acnestrol-Lotion)</li> <li><a href="/wiki/Diethylstilbestrol_dipalmitate" title="Diethylstilbestrol dipalmitate">Diethylstilbestrol dipalmitate</a> (stilpalmitate) (Palmestril, Stilpalmitate)</li> <li><a href="/wiki/Diethylstilbestrol_disulfate" title="Diethylstilbestrol disulfate">Diethylstilbestrol disulfate</a> (Hydroestryl, Idroestril)</li></ul> <div class="mw-heading mw-heading4"><h4 id="Never_marketed_6">Never marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=22" title="Edit section: Never marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/w/index.php?title=Diethylstilbestrol_sulfate&action=edit&redlink=1" class="new" title="Diethylstilbestrol sulfate (page does not exist)">Diethylstilbestrol sulfate</a></li> <li><a href="/wiki/Furostilbestrol" title="Furostilbestrol">Furostilbestrol</a> (diethylstilbestrol difuroate)</li> <li><a href="/wiki/Polydiethylstilbestrol_phosphate" title="Polydiethylstilbestrol phosphate">Polydiethylstilbestrol phosphate</a></li></ul> <p>As well as the following nitrogen mustard ester: </p> <ul><li><a href="/wiki/ICI-85966" title="ICI-85966">ICI-85966</a> (Stilbostat; diethylstilbestrol bis(di(2-chloroethyl)carbamate))</li></ul> <div class="mw-heading mw-heading3"><h3 id="Hexestrol_esters">Hexestrol esters</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=23" title="Edit section: Hexestrol esters"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_8">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=24" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Hexestrol_diacetate" title="Hexestrol diacetate">Hexestrol diacetate</a> (Retalon Lingual, Robal, Sintestrol, Sintofolin)</li> <li><a href="/wiki/Hexestrol_dicaprylate" title="Hexestrol dicaprylate">Hexestrol dicaprylate</a> (dioctanoylhexestrol) (Taston)</li> <li><a href="/wiki/Hexestrol_diphosphate" title="Hexestrol diphosphate">Hexestrol diphosphate</a> (Cytostesin, Pharmestrin, Retalon Aquosum)</li> <li><a href="/wiki/Hexestrol_dipropionate" title="Hexestrol dipropionate">Hexestrol dipropionate</a> (Hexanoestrol, Retalon Oleosum)</li> <li><a href="/wiki/Hexestrol_phosphate" class="mw-redirect" title="Hexestrol phosphate">Hexestrol phosphate</a> (Retalon Aquosum)</li></ul> <div class="mw-heading mw-heading4"><h4 id="Never_marketed_7">Never marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=25" title="Edit section: Never marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <p>The following nitrogen mustard ester of hexestrol was never marketed: </p> <ul><li><a href="/wiki/Phenestrol" title="Phenestrol">Phenestrol</a> (fenestrol; hexestrol bis[4-[bis(2-chloroethyl)amino]phenylacetate)</li></ul> <div class="mw-heading mw-heading3"><h3 id="Esters_of_other_nonsteroidal_estrogens">Esters of other nonsteroidal estrogens</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=26" title="Edit section: Esters of other nonsteroidal estrogens"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_9">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=27" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Dienestrol_diacetate" title="Dienestrol diacetate">Dienestrol diacetate</a> (Faragynol, Gynocyrol)</li> <li><a href="/wiki/Methestrol_dipropionate" title="Methestrol dipropionate">Methestrol dipropionate</a> (promethestrol dipropionate, dimethylhexestrol dipropionate) (Meprane Dipropionate)</li></ul> <div class="mw-heading mw-heading2"><h2 id="Ethers_of_nonsteroidal_estrogens">Ethers of nonsteroidal estrogens</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=28" title="Edit section: Ethers of nonsteroidal estrogens"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading3"><h3 id="Diethylstilbestrol">Diethylstilbestrol</h3><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=29" title="Edit section: Diethylstilbestrol"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <div class="mw-heading mw-heading4"><h4 id="Marketed_10">Marketed</h4><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=List_of_estrogen_esters&action=edit&section=30" title="Edit section: Marketed"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Diethylstilbestrol_monobenzyl_ether" title="Diethylstilbestrol monobenzyl ether">Diethylstilbestrol monobenzyl ether</a> (benzelstilbestrol) (Monozol, Hypantin, Pituitrope)</li> <li><a href="/wiki/Dimestrol" title="Dimestrol">Dimestrol</a> (dianisylhexene, diethylstilbestrol dimethyl ether, dimethoxydiethylstilbestrol) (Depot-Ostromon, Synthila)</li> <li><a href="/wiki/Mestilbol" title="Mestilbol">Mestilbol</a> (diethylstilbestrol monomethyl ether) (Monomestro or Monomestrol)</li></ul> <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=List_of_estrogen_esters&action=edit&section=31" title="Edit section: See also"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/List_of_estrogens" title="List of estrogens">List of estrogens</a></li> <li><a href="/wiki/List_of_progestogen_esters" title="List of progestogen esters">List of progestogen esters</a></li> <li><a href="/wiki/List_of_androgen_esters" title="List of androgen esters">List of androgen esters</a></li> <li><a href="/wiki/List_of_combined_sex-hormonal_preparations" title="List of combined sex-hormonal preparations">List of combined sex-hormonal preparations</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=List_of_estrogen_esters&action=edit&section=32" 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-IndexNominum2000-1"><span class="mw-cite-backlink">^ <a href="#cite_ref-IndexNominum2000_1-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-IndexNominum2000_1-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-IndexNominum2000_1-2"><sup><i><b>c</b></i></sup></a> <a href="#cite_ref-IndexNominum2000_1-3"><sup><i><b>d</b></i></sup></a> <a href="#cite_ref-IndexNominum2000_1-4"><sup><i><b>e</b></i></sup></a> <a href="#cite_ref-IndexNominum2000_1-5"><sup><i><b>f</b></i></sup></a> <a href="#cite_ref-IndexNominum2000_1-6"><sup><i><b>g</b></i></sup></a> <a href="#cite_ref-IndexNominum2000_1-7"><sup><i><b>h</b></i></sup></a></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 class="citation book cs1"><a rel="nofollow" class="external text" href="https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA404"><i>IndexNominum2000</i></a>. Taylor & Francis US. 2000. p. 404. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-3-88763-075-1" title="Special:BookSources/978-3-88763-075-1"><bdi>978-3-88763-075-1</bdi></a><span class="reference-accessdate">. Retrieved <span class="nowrap">29 May</span> 2012</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=IndexNominum2000&rft.pages=404&rft.pub=Taylor+%26+Francis+US&rft.date=2000&rft.isbn=978-3-88763-075-1&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D5GpcTQD_L2oC%26pg%3DPA404&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-Roberts1991-2"><span class="mw-cite-backlink">^ <a href="#cite_ref-Roberts1991_2-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-Roberts1991_2-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-Roberts1991_2-2"><sup><i><b>c</b></i></sup></a> <a href="#cite_ref-Roberts1991_2-3"><sup><i><b>d</b></i></sup></a> <a href="#cite_ref-Roberts1991_2-4"><sup><i><b>e</b></i></sup></a> <a href="#cite_ref-Roberts1991_2-5"><sup><i><b>f</b></i></sup></a> <a href="#cite_ref-Roberts1991_2-6"><sup><i><b>g</b></i></sup></a> <a href="#cite_ref-Roberts1991_2-7"><sup><i><b>h</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFA._D._Roberts1991" class="citation book cs1">A. D. Roberts (1991). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=qw5X0NK1A90C&pg=PA415"><i>Dictionary of Steroids: Chemical Data, Structures, and Bibliographies</i></a>. CRC Press. p. 415. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-0-412-27060-4" title="Special:BookSources/978-0-412-27060-4"><bdi>978-0-412-27060-4</bdi></a><span class="reference-accessdate">. Retrieved <span class="nowrap">20 May</span> 2012</span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Dictionary+of+Steroids%3A+Chemical+Data%2C+Structures%2C+and+Bibliographies&rft.pages=415&rft.pub=CRC+Press&rft.date=1991&rft.isbn=978-0-412-27060-4&rft.au=A.+D.+Roberts&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3Dqw5X0NK1A90C%26pg%3DPA415&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-Ferin1952-3"><span class="mw-cite-backlink"><b><a href="#cite_ref-Ferin1952_3-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFFerin1952" class="citation journal cs1">Ferin, J. (1952). "Relative duration of action of natural and synthetic estrogens administered parenterally in women with estrogen deficiency". <i>The Journal of Clinical Endocrinology & Metabolism</i>. <b>12</b> (1): 28–35. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1210%2Fjcem-12-1-28">10.1210/jcem-12-1-28</a>. <a href="/wiki/ISSN_(identifier)" class="mw-redirect" title="ISSN (identifier)">ISSN</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/issn/0021-972X">0021-972X</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/14907837">14907837</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=The+Journal+of+Clinical+Endocrinology+%26+Metabolism&rft.atitle=Relative+duration+of+action+of+natural+and+synthetic+estrogens+administered+parenterally+in+women+with+estrogen+deficiency&rft.volume=12&rft.issue=1&rft.pages=28-35&rft.date=1952&rft.issn=0021-972X&rft_id=info%3Apmid%2F14907837&rft_id=info%3Adoi%2F10.1210%2Fjcem-12-1-28&rft.aulast=Ferin&rft.aufirst=J.&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-Evestra-4"><span class="mw-cite-backlink"><b><a href="#cite_ref-Evestra_4-0">^</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/20170929164030/http://www.evestra.com/index-Dateien/Page1242.htm">"R&D Research"</a>. Archived from <a rel="nofollow" class="external text" href="http://www.evestra.com/index-Dateien/Page1242.htm">the original</a> on 2017-09-29<span class="reference-accessdate">. Retrieved <span class="nowrap">2018-06-25</span></span>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=unknown&rft.btitle=R%26D+Research&rft_id=http%3A%2F%2Fwww.evestra.com%2Findex-Dateien%2FPage1242.htm&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid27449818-5"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid27449818_5-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFElgerWyrwaAhmedMeece2017" class="citation journal cs1">Elger W, Wyrwa R, Ahmed G, Meece F, Nair HB, Santhamma B, Killeen Z, Schneider B, Meister R, Schubert H, Nickisch K (January 2017). "Estradiol prodrugs (EP) for efficient oral estrogen treatment and abolished effects on estrogen modulated liver functions". <i>J. Steroid Biochem. Mol. Biol</i>. <b>165</b> (Pt B): 305–311. <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.jsbmb.2016.07.008">10.1016/j.jsbmb.2016.07.008</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/27449818">27449818</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a> <a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:26650319">26650319</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=J.+Steroid+Biochem.+Mol.+Biol.&rft.atitle=Estradiol+prodrugs+%28EP%29+for+efficient+oral+estrogen+treatment+and+abolished+effects+on+estrogen+modulated+liver+functions&rft.volume=165&rft.issue=Pt+B&rft.pages=305-311&rft.date=2017-01&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A26650319%23id-name%3DS2CID&rft_id=info%3Apmid%2F27449818&rft_id=info%3Adoi%2F10.1016%2Fj.jsbmb.2016.07.008&rft.aulast=Elger&rft.aufirst=W&rft.au=Wyrwa%2C+R&rft.au=Ahmed%2C+G&rft.au=Meece%2C+F&rft.au=Nair%2C+HB&rft.au=Santhamma%2C+B&rft.au=Killeen%2C+Z&rft.au=Schneider%2C+B&rft.au=Meister%2C+R&rft.au=Schubert%2C+H&rft.au=Nickisch%2C+K&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid28886996-6"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid28886996_6-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFAhmedElgerMeeceNair2017" class="citation journal cs1">Ahmed G, Elger W, Meece F, Nair HB, Schneider B, Wyrwa R, Nickisch K (October 2017). "A prodrug design for improved oral absorption and reduced hepatic interaction". <i>Bioorg. Med. Chem</i>. <b>25</b> (20): 5569–5575. <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.bmc.2017.08.027">10.1016/j.bmc.2017.08.027</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/28886996">28886996</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Bioorg.+Med.+Chem.&rft.atitle=A+prodrug+design+for+improved+oral+absorption+and+reduced+hepatic+interaction&rft.volume=25&rft.issue=20&rft.pages=5569-5575&rft.date=2017-10&rft_id=info%3Adoi%2F10.1016%2Fj.bmc.2017.08.027&rft_id=info%3Apmid%2F28886996&rft.aulast=Ahmed&rft.aufirst=G&rft.au=Elger%2C+W&rft.au=Meece%2C+F&rft.au=Nair%2C+HB&rft.au=Schneider%2C+B&rft.au=Wyrwa%2C+R&rft.au=Nickisch%2C+K&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-NickischSanthamma2017-7"><span class="mw-cite-backlink"><b><a href="#cite_ref-NickischSanthamma2017_7-0">^</a></b></span> <span class="reference-text">Nickisch, K., Santhamma, B., Ahmed, G., Meece, F., Elger, W., Wyrwa, R., & Nair, H. (2017). <i>U.S. Patent No. 9,745,338.</i> Washington, DC: U.S. Patent and Trademark Office. <a rel="nofollow" class="external free" href="https://patents.google.com/patent/US9745338B2/en">https://patents.google.com/patent/US9745338B2/en</a></span> </li> <li id="cite_note-HumansOrganization2007-8"><span class="mw-cite-backlink"><b><a href="#cite_ref-HumansOrganization2007_8-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFIARC_Working_Group_on_the_Evaluation_of_Carcinogenic_Risks_to_HumansWorld_Health_OrganizationInternational_Agency_for_Research_on_Cancer2007" class="citation book cs1">IARC Working Group on the Evaluation of Carcinogenic Risks to Humans; World Health Organization; International Agency for Research on Cancer (2007). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=aGDU5xibtNgC&pg=PA388"><i>Combined Estrogen-progestogen Contraceptives and Combined Estrogen-progestogen Menopausal Therapy</i></a>. World Health Organization. pp. 388–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-92-832-1291-1" title="Special:BookSources/978-92-832-1291-1"><bdi>978-92-832-1291-1</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Combined+Estrogen-progestogen+Contraceptives+and+Combined+Estrogen-progestogen+Menopausal+Therapy&rft.pages=388-&rft.pub=World+Health+Organization&rft.date=2007&rft.isbn=978-92-832-1291-1&rft.au=IARC+Working+Group+on+the+Evaluation+of+Carcinogenic+Risks+to+Humans&rft.au=World+Health+Organization&rft.au=International+Agency+for+Research+on+Cancer&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DaGDU5xibtNgC%26pg%3DPA388&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-VizzoneMurari1966-9"><span class="mw-cite-backlink"><b><a href="#cite_ref-VizzoneMurari1966_9-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFVizzoneMurari1966" class="citation journal cs1">Vizzone, A.; Murari, G. (November 1966). "[Estradiol esters (3-monobenzoate and 3-benzoate-17-beta-acetate) in the therapy of the surgical menopause syndrome. Experimental and clinical results]". <i>Quaderni di Clinica Ostetrica e Ginecologica</i>. <b>21</b> (11): 779–790. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/5999221">5999221</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Quaderni+di+Clinica+Ostetrica+e+Ginecologica&rft.atitle=%5BEstradiol+esters+%283-monobenzoate+and+3-benzoate-17-beta-acetate%29+in+the+therapy+of+the+surgical+menopause+syndrome.+Experimental+and+clinical+results%5D&rft.volume=21&rft.issue=11&rft.pages=779-790&rft.date=1966-11&rft_id=info%3Apmid%2F5999221&rft.aulast=Vizzone&rft.aufirst=A.&rft.au=Murari%2C+G.&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid3244608-10"><span class="mw-cite-backlink">^ <a href="#cite_ref-pmid3244608_10-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-pmid3244608_10-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-pmid3244608_10-2"><sup><i><b>c</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFHussainAungstShefter1988" class="citation journal cs1">Hussain MA, Aungst BJ, Shefter E (January 1988). "Prodrugs for improved oral beta-estradiol bioavailability". <i>Pharm. Res</i>. <b>5</b> (1): 44–7. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1023%2FA%3A1015863412137">10.1023/A:1015863412137</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/3244608">3244608</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a> <a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:7308414">7308414</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Pharm.+Res.&rft.atitle=Prodrugs+for+improved+oral+beta-estradiol+bioavailability&rft.volume=5&rft.issue=1&rft.pages=44-7&rft.date=1988-01&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A7308414%23id-name%3DS2CID&rft_id=info%3Apmid%2F3244608&rft_id=info%3Adoi%2F10.1023%2FA%3A1015863412137&rft.aulast=Hussain&rft.aufirst=MA&rft.au=Aungst%2C+BJ&rft.au=Shefter%2C+E&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-LokindLorenzen1991-11"><span class="mw-cite-backlink">^ <a href="#cite_ref-LokindLorenzen1991_11-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-LokindLorenzen1991_11-1"><sup><i><b>b</b></i></sup></a> <a href="#cite_ref-LokindLorenzen1991_11-2"><sup><i><b>c</b></i></sup></a></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFLokindLorenzenBundgaard1991" class="citation journal cs1">Lokind, Kenneth B.; Lorenzen, Finn Hjort; Bundgaard, Hans (1991). "Oral bioavailability of 17β-estradiol and various ester prodrugs in the rat". <i>International Journal of Pharmaceutics</i>. <b>76</b> (1–2): 177–182. <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%2F0378-5173%2891%2990356-S">10.1016/0378-5173(91)90356-S</a>. <a href="/wiki/ISSN_(identifier)" class="mw-redirect" title="ISSN (identifier)">ISSN</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/issn/0378-5173">0378-5173</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=International+Journal+of+Pharmaceutics&rft.atitle=Oral+bioavailability+of+17%CE%B2-estradiol+and+various+ester+prodrugs+in+the+rat&rft.volume=76&rft.issue=1%E2%80%932&rft.pages=177-182&rft.date=1991&rft_id=info%3Adoi%2F10.1016%2F0378-5173%2891%2990356-S&rft.issn=0378-5173&rft.aulast=Lokind&rft.aufirst=Kenneth+B.&rft.au=Lorenzen%2C+Finn+Hjort&rft.au=Bundgaard%2C+Hans&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid4654978-12"><span class="mw-cite-backlink">^ <a href="#cite_ref-pmid4654978_12-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-pmid4654978_12-1"><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="CITEREFFalconiGallettiCelascoGardi1972" class="citation journal cs1">Falconi G, Galletti F, Celasco G, Gardi R (November 1972). "Oral long-lasting estrogenic activity of estradiol 3-benzoate 17-cyclooctenyl ether". <i>Steroids</i>. <b>20</b> (5): 627–38. <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%2F0039-128X%2872%2990020-7">10.1016/0039-128X(72)90020-7</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/4654978">4654978</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Steroids&rft.atitle=Oral+long-lasting+estrogenic+activity+of+estradiol+3-benzoate+17-cyclooctenyl+ether&rft.volume=20&rft.issue=5&rft.pages=627-38&rft.date=1972-11&rft_id=info%3Adoi%2F10.1016%2F0039-128X%2872%2990020-7&rft_id=info%3Apmid%2F4654978&rft.aulast=Falconi&rft.aufirst=G&rft.au=Galletti%2C+F&rft.au=Celasco%2C+G&rft.au=Gardi%2C+R&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid4438394-13"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid4438394_13-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFGallettiGardi1974" class="citation journal cs1">Galletti F, Gardi R (April 1974). "Effect of two orally active estradiol derivatives on sulfobromphthalein retention in rats". <i>Pharmacol Res Commun</i>. <b>6</b> (2): 135–45. <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%2Fs0031-6989%2874%2980021-4">10.1016/s0031-6989(74)80021-4</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/4438394">4438394</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Pharmacol+Res+Commun&rft.atitle=Effect+of+two+orally+active+estradiol+derivatives+on+sulfobromphthalein+retention+in+rats&rft.volume=6&rft.issue=2&rft.pages=135-45&rft.date=1974-04&rft_id=info%3Adoi%2F10.1016%2Fs0031-6989%2874%2980021-4&rft_id=info%3Apmid%2F4438394&rft.aulast=Galletti&rft.aufirst=F&rft.au=Gardi%2C+R&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-Dorfman2016-14"><span class="mw-cite-backlink"><b><a href="#cite_ref-Dorfman2016_14-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFRalph_I._Dorfman2016" class="citation book cs1">Ralph I. Dorfman (5 December 2016). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=BbLfBAAAQBAJ&pg=PA36"><i>Steroidal Activity in Experimental Animals and Man</i></a>. Elsevier Science. pp. 36–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-1-4832-7299-3" title="Special:BookSources/978-1-4832-7299-3"><bdi>978-1-4832-7299-3</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Steroidal+Activity+in+Experimental+Animals+and+Man&rft.pages=36-&rft.pub=Elsevier+Science&rft.date=2016-12-05&rft.isbn=978-1-4832-7299-3&rft.au=Ralph+I.+Dorfman&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DBbLfBAAAQBAJ%26pg%3DPA36&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-JanockoLarner1984-15"><span class="mw-cite-backlink"><b><a href="#cite_ref-JanockoLarner1984_15-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFJanockoLarnerHochberg1984" class="citation journal cs1">Janocko, Laura; Larner, Janice M.; Hochberg, Richard B. (1984). "The Interaction of C-17 Esters of Estradiol with the Estrogen Receptor*". <i>Endocrinology</i>. <b>114</b> (4): 1180–1186. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1210%2Fendo-114-4-1180">10.1210/endo-114-4-1180</a>. <a href="/wiki/ISSN_(identifier)" class="mw-redirect" title="ISSN (identifier)">ISSN</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/issn/0013-7227">0013-7227</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/6705734">6705734</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Endocrinology&rft.atitle=The+Interaction+of+C-17+Esters+of+Estradiol+with+the+Estrogen+Receptor%2A&rft.volume=114&rft.issue=4&rft.pages=1180-1186&rft.date=1984&rft.issn=0013-7227&rft_id=info%3Apmid%2F6705734&rft_id=info%3Adoi%2F10.1210%2Fendo-114-4-1180&rft.aulast=Janocko&rft.aufirst=Laura&rft.au=Larner%2C+Janice+M.&rft.au=Hochberg%2C+Richard+B.&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid3932144-16"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid3932144_16-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFDahlgrenCronaJansonSamsioe1985" class="citation journal cs1">Dahlgren E, Crona N, Janson PO, Samsioe G (1985). "Oral replacement with estradiol-cyclooctyl acetate: a new estradiol analogue. Effects on serum lipids, proteins, gonadotrophins, estrogens and uterine endometrial morphology". <i>Gynecol. Obstet. Invest</i>. <b>20</b> (2): 84–90. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1159%2F000298978">10.1159/000298978</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/3932144">3932144</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Gynecol.+Obstet.+Invest.&rft.atitle=Oral+replacement+with+estradiol-cyclooctyl+acetate%3A+a+new+estradiol+analogue.+Effects+on+serum+lipids%2C+proteins%2C+gonadotrophins%2C+estrogens+and+uterine+endometrial+morphology&rft.volume=20&rft.issue=2&rft.pages=84-90&rft.date=1985&rft_id=info%3Adoi%2F10.1159%2F000298978&rft_id=info%3Apmid%2F3932144&rft.aulast=Dahlgren&rft.aufirst=E&rft.au=Crona%2C+N&rft.au=Janson%2C+PO&rft.au=Samsioe%2C+G&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid755846-17"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid755846_17-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFLuisiKicovicAliciccoFranchi1978" class="citation journal cs1">Luisi M, Kicovic PM, Alicicco E, Franchi F (1978). "Effects of estradiol decanoate in ovariectomized women". <i>J. Endocrinol. Invest</i>. <b>1</b> (2): 101–6. <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%2FBF03350355">10.1007/BF03350355</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/755846">755846</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a> <a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:38187367">38187367</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=J.+Endocrinol.+Invest.&rft.atitle=Effects+of+estradiol+decanoate+in+ovariectomized+women&rft.volume=1&rft.issue=2&rft.pages=101-6&rft.date=1978&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A38187367%23id-name%3DS2CID&rft_id=info%3Apmid%2F755846&rft_id=info%3Adoi%2F10.1007%2FBF03350355&rft.aulast=Luisi&rft.aufirst=M&rft.au=Kicovic%2C+PM&rft.au=Alicicco%2C+E&rft.au=Franchi%2C+F&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid13828402-18"><span class="mw-cite-backlink">^ <a href="#cite_ref-pmid13828402_18-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-pmid13828402_18-1"><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="CITEREFGleasonParker1959" class="citation journal cs1">Gleason CH, Parker JM (1959). "The duration of activity of the benziloyl hydrazones of testosterone-17-heptanoate, estrone-3-heptanoate and 17α-hydroxy-progesterone-17-heptanoate". <i>Endocrinology</i>. <b>65</b> (3): 508–511. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1210%2Fendo-65-3-508">10.1210/endo-65-3-508</a>. <a href="/wiki/ISSN_(identifier)" class="mw-redirect" title="ISSN (identifier)">ISSN</a> <a rel="nofollow" class="external text" href="https://search.worldcat.org/issn/0013-7227">0013-7227</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/13828402">13828402</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Endocrinology&rft.atitle=The+duration+of+activity+of+the+benziloyl+hydrazones+of+testosterone-17-heptanoate%2C+estrone-3-heptanoate+and+17%CE%B1-hydroxy-progesterone-17-heptanoate&rft.volume=65&rft.issue=3&rft.pages=508-511&rft.date=1959&rft.issn=0013-7227&rft_id=info%3Apmid%2F13828402&rft_id=info%3Adoi%2F10.1210%2Fendo-65-3-508&rft.aulast=Gleason&rft.aufirst=CH&rft.au=Parker%2C+JM&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-Milne2018-19"><span class="mw-cite-backlink"><b><a href="#cite_ref-Milne2018_19-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFGeorge_W.A_Milne2018" class="citation book cs1">George W.A Milne (8 May 2018). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=xUlaDwAAQBAJ&pg=PT1406"><i>Drugs: Synonyms and Properties: Synonyms and Properties</i></a>. Taylor & Francis. pp. 1406–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-1-351-78989-9" title="Special:BookSources/978-1-351-78989-9"><bdi>978-1-351-78989-9</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Drugs%3A+Synonyms+and+Properties%3A+Synonyms+and+Properties&rft.pages=1406-&rft.pub=Taylor+%26+Francis&rft.date=2018-05-08&rft.isbn=978-1-351-78989-9&rft.au=George+W.A+Milne&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DxUlaDwAAQBAJ%26pg%3DPT1406&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid15991994-20"><span class="mw-cite-backlink">^ <a href="#cite_ref-pmid15991994_20-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-pmid15991994_20-1"><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="CITEREFElgerPalmeSchwarz1998" class="citation journal cs1">Elger W, Palme HJ, Schwarz S (April 1998). "Novel oestrogen sulfamates: a new approach to oral hormone therapy". <i>Expert Opin Investig Drugs</i>. <b>7</b> (4): 575–89. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1517%2F13543784.7.4.575">10.1517/13543784.7.4.575</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/15991994">15991994</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=Expert+Opin+Investig+Drugs&rft.atitle=Novel+oestrogen+sulfamates%3A+a+new+approach+to+oral+hormone+therapy&rft.volume=7&rft.issue=4&rft.pages=575-89&rft.date=1998-04&rft_id=info%3Adoi%2F10.1517%2F13543784.7.4.575&rft_id=info%3Apmid%2F15991994&rft.aulast=Elger&rft.aufirst=W&rft.au=Palme%2C+HJ&rft.au=Schwarz%2C+S&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid8541236-21"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid8541236_21-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFElgerSchwarzHeddenReddersen1995" class="citation journal cs1">Elger W, Schwarz S, Hedden A, Reddersen G, Schneider B (December 1995). "Sulfamates of various estrogens are prodrugs with increased systemic and reduced hepatic estrogenicity at oral application". <i>J. Steroid Biochem. Mol. Biol</i>. <b>55</b> (3–4): 395–403. <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%2F0960-0760%2895%2900214-6">10.1016/0960-0760(95)00214-6</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/8541236">8541236</a>. <a href="/wiki/S2CID_(identifier)" class="mw-redirect" title="S2CID (identifier)">S2CID</a> <a rel="nofollow" class="external text" href="https://api.semanticscholar.org/CorpusID:31312">31312</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=J.+Steroid+Biochem.+Mol.+Biol.&rft.atitle=Sulfamates+of+various+estrogens+are+prodrugs+with+increased+systemic+and+reduced+hepatic+estrogenicity+at+oral+application&rft.volume=55&rft.issue=3%E2%80%934&rft.pages=395-403&rft.date=1995-12&rft_id=https%3A%2F%2Fapi.semanticscholar.org%2FCorpusID%3A31312%23id-name%3DS2CID&rft_id=info%3Apmid%2F8541236&rft_id=info%3Adoi%2F10.1016%2F0960-0760%2895%2900214-6&rft.aulast=Elger&rft.aufirst=W&rft.au=Schwarz%2C+S&rft.au=Hedden%2C+A&rft.au=Reddersen%2C+G&rft.au=Schneider%2C+B&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-Elks2014-22"><span class="mw-cite-backlink">^ <a href="#cite_ref-Elks2014_22-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-Elks2014_22-1"><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="CITEREFJ._Elks2014" class="citation book cs1">J. Elks (14 November 2014). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PR2"><i>The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies</i></a>. Springer. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-1-4757-2085-3" title="Special:BookSources/978-1-4757-2085-3"><bdi>978-1-4757-2085-3</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=The+Dictionary+of+Drugs%3A+Chemical+Data%3A+Chemical+Data%2C+Structures+and+Bibliographies&rft.pub=Springer&rft.date=2014-11-14&rft.isbn=978-1-4757-2085-3&rft.au=J.+Elks&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3D0vXTBwAAQBAJ%26pg%3DPR2&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid7884673-23"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid7884673_23-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFPatelPrankerdSloan1994" class="citation journal cs1">Patel JU, Prankerd RJ, Sloan KB (October 1994). "A prodrug approach to increasing the oral potency of a phenolic drug. 1. Synthesis, characterization, and stability of an O-(imidomethyl) derivative of 17 beta-estradiol". <i>J Pharm Sci</i>. <b>83</b> (10): 1477–81. <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%2Fjps.2600831022">10.1002/jps.2600831022</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7884673">7884673</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=J+Pharm+Sci&rft.atitle=A+prodrug+approach+to+increasing+the+oral+potency+of+a+phenolic+drug.+1.+Synthesis%2C+characterization%2C+and+stability+of+an+O-%28imidomethyl%29+derivative+of+17+beta-estradiol&rft.volume=83&rft.issue=10&rft.pages=1477-81&rft.date=1994-10&rft_id=info%3Adoi%2F10.1002%2Fjps.2600831022&rft_id=info%3Apmid%2F7884673&rft.aulast=Patel&rft.aufirst=JU&rft.au=Prankerd%2C+RJ&rft.au=Sloan%2C+KB&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-pmid7738796-24"><span class="mw-cite-backlink"><b><a href="#cite_ref-pmid7738796_24-0">^</a></b></span> <span class="reference-text"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1238218222"><cite id="CITEREFPatelKatovichSloanCurry1995" class="citation journal cs1">Patel J, Katovich MJ, Sloan KB, Curry SH, Prankerd RJ (February 1995). "A prodrug approach to increasing the oral potency of a phenolic drug. Part 2. Pharmacodynamics and preliminary bioavailability of an orally administered O-(imidomethyl) derivative of 17 beta-estradiol". <i>J Pharm Sci</i>. <b>84</b> (2): 174–8. <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%2Fjps.2600840210">10.1002/jps.2600840210</a>. <a href="/wiki/PMID_(identifier)" class="mw-redirect" title="PMID (identifier)">PMID</a> <a rel="nofollow" class="external text" href="https://pubmed.ncbi.nlm.nih.gov/7738796">7738796</a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.jtitle=J+Pharm+Sci&rft.atitle=A+prodrug+approach+to+increasing+the+oral+potency+of+a+phenolic+drug.+Part+2.+Pharmacodynamics+and+preliminary+bioavailability+of+an+orally+administered+O-%28imidomethyl%29+derivative+of+17+beta-estradiol&rft.volume=84&rft.issue=2&rft.pages=174-8&rft.date=1995-02&rft_id=info%3Adoi%2F10.1002%2Fjps.2600840210&rft_id=info%3Apmid%2F7738796&rft.aulast=Patel&rft.aufirst=J&rft.au=Katovich%2C+MJ&rft.au=Sloan%2C+KB&rft.au=Curry%2C+SH&rft.au=Prankerd%2C+RJ&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" class="Z3988"></span></span> </li> <li id="cite_note-LemkeWilliams2012-25"><span class="mw-cite-backlink">^ <a href="#cite_ref-LemkeWilliams2012_25-0"><sup><i><b>a</b></i></sup></a> <a href="#cite_ref-LemkeWilliams2012_25-1"><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="CITEREFThomas_L._LemkeDavid_A._Williams2012" class="citation book cs1">Thomas L. Lemke; David A. Williams (24 January 2012). <a rel="nofollow" class="external text" href="https://books.google.com/books?id=Sd6ot9ul-bUC&pg=PA1395"><i>Foye's Principles of Medicinal Chemistry</i></a>. Lippincott Williams & Wilkins. pp. 1395–. <a href="/wiki/ISBN_(identifier)" class="mw-redirect" title="ISBN (identifier)">ISBN</a> <a href="/wiki/Special:BookSources/978-1-60913-345-0" title="Special:BookSources/978-1-60913-345-0"><bdi>978-1-60913-345-0</bdi></a>.</cite><span title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rft.genre=book&rft.btitle=Foye%27s+Principles+of+Medicinal+Chemistry&rft.pages=1395-&rft.pub=Lippincott+Williams+%26+Wilkins&rft.date=2012-01-24&rft.isbn=978-1-60913-345-0&rft.au=Thomas+L.+Lemke&rft.au=David+A.+Williams&rft_id=https%3A%2F%2Fbooks.google.com%2Fbooks%3Fid%3DSd6ot9ul-bUC%26pg%3DPA1395&rfr_id=info%3Asid%2Fen.wikipedia.org%3AList+of+estrogen+esters" 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 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navbar-mini"><ul><li class="nv-view"><a href="/w/index.php?title=Template:Estradiol_inorganic_esters_and_salts&action=edit&redlink=1" class="new" title="Template:Estradiol inorganic esters and salts (page does not exist)"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/w/index.php?title=Template_talk:Estradiol_inorganic_esters_and_salts&action=edit&redlink=1" class="new" title="Template talk:Estradiol inorganic esters and salts (page does not exist)"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Estradiol_inorganic_esters_and_salts" title="Special:EditPage/Template:Estradiol inorganic esters and salts"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Salts_and_covalent_derivatives_of_the_estradiol_ion" style="font-size:114%;margin:0 4em">Salts and covalent derivatives of the <a href="/wiki/Estradiol" title="Estradiol">estradiol</a> ion</div></th></tr><tr><td colspan="2" class="navbox-list navbox-odd" style="width:100%;padding:0;border-width:0;"><div style="padding:0"><div class="mw-collapsible-content" style="overflow-x:auto"> <table class="center"> <tbody><tr style="background-color:mistyrose"> <td><a href="/wiki/Estradiol" title="Estradiol">HO<i>E2</i>OH</a><br /> </td> <td style="background-color:white;border:none"> </td> <td style="background-color:white;border:none" colspan="11" rowspan="3"> </td> <td style="background-color:white;border:none" colspan="5"> </td> <td>He </td></tr> <tr style="background-color:mistyrose"> <td>Li </td> <td>Be </td> <td>B </td> <td><a class="mw-selflink-fragment" href="#Estradiol_esters"><i>various</i></a> </td> <td>N </td> <td>O </td> <td>F </td> <td>Ne </td></tr> <tr style="background-color:mistyrose"> <td><a href="/w/index.php?title=Sodium_estradiolate&action=edit&redlink=1" class="new" title="Sodium estradiolate (page does not exist)">NaO<i>E2</i>OH</a> </td> <td>Mg </td> <td>Al </td> <td>Si </td> <td><a href="/wiki/Estradiol_phosphate" title="Estradiol phosphate">HO<i>E2</i>O<sub>4</sub>PH<sub>2</sub></a><br /><a href="/w/index.php?title=Estradiol_diphosphate&action=edit&redlink=1" class="new" title="Estradiol diphosphate (page does not exist)">H<sub>2</sub>PO<sub>4</sub><i>E2</i>O<sub>4</sub>PH<sub>2</sub></a>?<br /><a href="/wiki/Polyestradiol_phosphate" title="Polyestradiol phosphate">(O<i>E2</i>O<sub>3</sub>PH)<sub><i>n</i></sub></a> </td> <td><a href="/wiki/Estradiol_sulfate" title="Estradiol sulfate">HSO<sub>4</sub><i>E2</i>OH</a><br /><a href="/wiki/Estradiol_disulfate" title="Estradiol disulfate">HSO<sub>4</sub><i>E2</i>O<sub>4</sub>SH</a> </td> <td><a href="/w/index.php?title=Estradiyl_chloride&action=edit&redlink=1" class="new" title="Estradiyl chloride (page does not exist)">Cl<i>E2</i>OH</a><br />Cl<i>E2</i>Cl? </td> <td>Ar </td></tr> <tr style="background-color:mistyrose"> <td><a href="/w/index.php?title=Potassium_estradiolate&action=edit&redlink=1" class="new" title="Potassium estradiolate (page does not exist)">KO<i>E2</i>OH</a>? </td> <td>Ca </td> <td style="background-color:white;border:none"> </td> <td>Sc </td> <td>Ti </td> <td>V </td> <td>Cr </td> <td><a href="/w/index.php?title=Estradiol_Permanganate&action=edit&redlink=1" class="new" title="Estradiol Permanganate (page does not exist)">MnO<sub>4</sub><i>E2</i>OH</a> </td> <td>Fe </td> <td>Co </td> <td>Ni </td> <td>Cu </td> <td>Zn </td> <td>Ga </td> <td>Ge </td> <td>As </td> <td><a href="/w/index.php?title=Estradiol_Selenate&action=edit&redlink=1" class="new" title="Estradiol Selenate (page does not exist)">HSeO<sub>4</sub><i>E2</i>OH</a> </td> <td>Br </td> <td>Kr </td></tr> <tr style="background-color:mistyrose"> <td><a href="/w/index.php?title=Rubidium_estradiolate&action=edit&redlink=1" class="new" title="Rubidium estradiolate (page does not exist)">RbO<i>E2</i>OH</a>? </td> <td>Sr </td> <td style="background-color:white;border:none"> </td> <td>Y </td> <td>Zr </td> <td>Nb </td> <td><a href="/w/index.php?title=Estradiol_Molybdate&action=edit&redlink=1" class="new" title="Estradiol Molybdate (page does not exist)">HMoO<sub>4</sub><i>E2</i>OH</a> </td> <td>Tc </td> <td>Ru </td> <td>Rh </td> <td>Pd </td> <td>Ag </td> <td>Cd </td> <td>In </td> <td>Sn </td> <td>Sb </td> <td>Te </td> <td>I </td> <td>Xe </td></tr> <tr style="background-color:mistyrose"> <td>Cs </td> <td>Ba </td> <td style="background-color:white;border:none">* </td> <td>Lu </td> <td>Hf </td> <td>Ta </td> <td>W </td> <td>Re </td> <td>Os </td> <td>Ir </td> <td>Pt </td> <td>Au </td> <td>Hg </td> <td>Tl </td> <td>Pb </td> <td>Bi </td> <td>Po </td> <td>At </td> <td>Rn </td></tr> <tr style="background-color:mistyrose"> <td>Fr </td> <td>Ra </td> <td style="background-color:white;border:none">** </td> <td>Lr </td> <td>Rf </td> <td>Db </td> <td>Sg </td> <td>Bh </td> <td>Hs </td> <td>Mt </td> <td>Ds </td> <td>Rg </td> <td>Cn </td> <td>Nh </td> <td>Fl </td> <td>Mc </td> <td>Lv </td> <td>Ts </td> <td>Og </td></tr> <tr> <td style="background-color:white;border:none" colspan="2" rowspan="3"> </td> <td style="background-color:white;border:none" colspan="20">  </td></tr> <tr style="background-color:mistyrose"> <td style="background-color:white;border:none">* </td> <td>La </td> <td>Ce </td> <td>Pr </td> <td>Nd </td> <td>Pm </td> <td>Sm </td> <td>Eu </td> <td>Gd </td> <td>Tb </td> <td>Dy </td> <td>Ho </td> <td>Er </td> <td>Tm </td> <td>Yb </td></tr> <tr style="background-color:mistyrose"> <td style="background-color:white;border:none">** </td> <td>Ac </td> <td>Th </td> <td>Pa </td> <td>U </td> <td>Np </td> <td>Pu </td> <td>Am </td> <td>Cm </td> <td>Bk </td> <td>Cf </td> <td>Es </td> <td>Fm </td> <td>Md </td> <td>No </td></tr></tbody></table></div> </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="Estradiol" style="padding:3px"><table class="nowraplinks mw-collapsible expanded 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:Estradiol" title="Template:Estradiol"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Estradiol" title="Template talk:Estradiol"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Estradiol" title="Special:EditPage/Template:Estradiol"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Estradiol" style="font-size:114%;margin:0 4em"><a href="/wiki/Estradiol" title="Estradiol">Estradiol</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;">Topics</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/Estradiol" title="Estradiol">Estradiol (as a hormone)</a></li> <li><a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">Estradiol (as a medication)</a></li> <li><a href="/wiki/Pharmacodynamics_of_estradiol" title="Pharmacodynamics of estradiol">Pharmacodynamics of estradiol</a></li> <li><a href="/wiki/Pharmacokinetics_of_estradiol" title="Pharmacokinetics of estradiol">Pharmacokinetics of estradiol</a></li> <li><a href="/wiki/Estrogen" title="Estrogen">Estrogen (as a hormone)</a></li> <li><a href="/wiki/Estrogen_(medication)" title="Estrogen (medication)">Estrogen (as a medication)</a></li> <li><a href="/wiki/Hormone_replacement_therapy" title="Hormone replacement therapy">Menopausal hormone therapy</a></li> <li><a href="/wiki/Feminizing_hormone_therapy" title="Feminizing hormone therapy">Feminizing hormone therapy</a></li> <li><a href="/wiki/Estradiol-containing_birth_control_pill" title="Estradiol-containing birth control pill">Estradiol-containing birth control pill</a></li> <li><a href="/wiki/Combined_injectable_birth_control" title="Combined injectable birth control">Combined injectable birth control</a></li> <li><a href="/wiki/High-dose_estrogen" class="mw-redirect" title="High-dose estrogen">High-dose estrogen</a></li> <li><a href="/wiki/Hydroxylation_of_estradiol" title="Hydroxylation of estradiol">Hydroxylation of estradiol</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/Estrogen_ester" title="Estrogen ester">Esters</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><a href="/wiki/Estradiol_acetate" title="Estradiol acetate">Estradiol acetate</a></li> <li><a href="/wiki/Estradiol_acetylsalicylate" title="Estradiol acetylsalicylate">Estradiol acetylsalicylate</a></li> <li><a href="/wiki/Estradiol_anthranilate" title="Estradiol anthranilate">Estradiol anthranilate</a></li> <li><a href="/wiki/Estradiol_benzoate_butyrate" title="Estradiol benzoate butyrate">Estradiol benzoate butyrate</a></li> <li><a href="/wiki/Estradiol_benzoate_cyclooctenyl_ether" title="Estradiol benzoate cyclooctenyl ether">Estradiol benzoate cyclooctenyl ether</a></li> <li><a href="/wiki/Estradiol_benzoate" title="Estradiol benzoate">Estradiol benzoate</a></li> <li><a href="/wiki/Estradiol_butyrylacetate" title="Estradiol butyrylacetate">Estradiol butyrylacetate</a></li> <li><a href="/wiki/Estradiol_cyclooctyl_acetate" title="Estradiol cyclooctyl acetate">Estradiol cyclooctyl acetate</a></li> <li><a href="/wiki/Estradiol_cypionate" title="Estradiol cypionate">Estradiol cypionate</a></li> <li><a href="/wiki/Estradiol_decanoate" title="Estradiol decanoate">Estradiol decanoate</a></li> <li><a href="/wiki/Estradiol_diacetate" title="Estradiol diacetate">Estradiol diacetate</a></li> <li><a href="/wiki/Estradiol_dibutyrate" title="Estradiol dibutyrate">Estradiol dibutyrate</a></li> <li><a href="/wiki/Estradiol_dienantate" title="Estradiol dienantate">Estradiol dienantate</a></li> <li><a href="/wiki/Estradiol_dipropionate" title="Estradiol dipropionate">Estradiol dipropionate</a></li> <li><a href="/wiki/Estradiol_distearate" title="Estradiol distearate">Estradiol distearate</a></li> <li><a href="/wiki/Estradiol_disulfate" title="Estradiol disulfate">Estradiol disulfate</a></li> <li><a href="/wiki/Estradiol_diundecylate" title="Estradiol diundecylate">Estradiol diundecylate</a></li> <li><a href="/wiki/Estradiol_diundecylenate" title="Estradiol diundecylenate">Estradiol diundecylenate</a></li> <li><a href="/wiki/Estradiol_enantate" title="Estradiol enantate">Estradiol enantate</a></li> <li><a href="/wiki/Estradiol_furoate" title="Estradiol furoate">Estradiol furoate</a></li> <li><a href="/wiki/Estradiol_glucuronide" title="Estradiol glucuronide">Estradiol glucuronide</a></li> <li><a href="/wiki/Estradiol_hemisuccinate" title="Estradiol hemisuccinate">Estradiol hemisuccinate</a></li> <li><a href="/wiki/Estradiol_hexahydrobenzoate" title="Estradiol hexahydrobenzoate">Estradiol hexahydrobenzoate</a></li> <li><a href="/wiki/Estradiol_monopropionate" title="Estradiol monopropionate">Estradiol monopropionate</a></li> <li><a href="/wiki/Estradiol_mustard" title="Estradiol mustard">Estradiol mustard</a></li> <li><a href="/wiki/Estradiol_palmitate" title="Estradiol palmitate">Estradiol palmitate</a></li> <li><a href="/wiki/Estradiol_phenylpropionate" title="Estradiol phenylpropionate">Estradiol phenylpropionate</a></li> <li><a href="/wiki/Estradiol_phosphate" title="Estradiol phosphate">Estradiol phosphate</a></li> <li><a href="/wiki/Estradiol_pivalate" title="Estradiol pivalate">Estradiol pivalate</a></li> <li><a href="/wiki/Estradiol_propoxyphenylpropionate" title="Estradiol propoxyphenylpropionate">Estradiol propoxyphenylpropionate</a></li> <li><a href="/wiki/Estradiol_salicylate" title="Estradiol salicylate">Estradiol salicylate</a></li> <li><a href="/wiki/Estradiol_stearate" title="Estradiol stearate">Estradiol stearate</a></li> <li><a href="/wiki/Estradiol_sulfamate" title="Estradiol sulfamate">Estradiol sulfamate</a></li> <li><a href="/wiki/Estradiol_sulfate" title="Estradiol sulfate">Estradiol sulfate</a></li> <li><a href="/wiki/Estradiol_undecylate" title="Estradiol undecylate">Estradiol undecylate</a></li> <li><a href="/wiki/Estradiol_undecylenate" title="Estradiol undecylenate">Estradiol undecylenate</a></li> <li><a href="/wiki/Estradiol_valerate" title="Estradiol valerate">Estradiol valerate</a></li> <li><a href="/wiki/Estramustine_phosphate" title="Estramustine phosphate">Estramustine phosphate (estradiol normustine phosphate)</a></li> <li><a href="/wiki/Estrogen_ester" title="Estrogen ester">Estrogen ester</a></li> <li><a href="/wiki/Polyestradiol_phosphate" title="Polyestradiol phosphate">Polyestradiol phosphate</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;">Related</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/Estrone_(medication)" title="Estrone (medication)">Estrone</a></li> <li><a href="/wiki/Estriol_(medication)" title="Estriol (medication)">Estriol</a></li> <li><a href="/wiki/Estetrol_(medication)" title="Estetrol (medication)">Estetrol</a></li> <li><a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">Ethinylestradiol</a></li> <li><a href="/wiki/Conjugated_estrogens" title="Conjugated estrogens">Conjugated estrogens</a></li> <li><a href="/wiki/Esterified_estrogens" title="Esterified estrogens">Esterified estrogens</a></li> <li><a href="/wiki/Estrone_sulfate_(medication)" title="Estrone sulfate (medication)">Estrone sulfate</a></li> <li><a href="/wiki/Estropipate" title="Estropipate">Estropipate (piperazine estrone sulfate)</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"><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1129693374"></div><div role="navigation" class="navbox" aria-labelledby="Estrogens_and_antiestrogens" style="padding:3px"><table class="nowraplinks 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:Estrogens_and_antiestrogens" title="Template:Estrogens and antiestrogens"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Estrogens_and_antiestrogens" title="Template talk:Estrogens and antiestrogens"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Estrogens_and_antiestrogens" title="Special:EditPage/Template:Estrogens and antiestrogens"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Estrogens_and_antiestrogens" style="font-size:114%;margin:0 4em"><a href="/wiki/Estrogen_(medication)" title="Estrogen (medication)">Estrogens</a> and <a href="/wiki/Antiestrogen" title="Antiestrogen">antiestrogens</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%;text-align:center;"><a href="/wiki/Estrogen_(medication)" title="Estrogen (medication)">Estrogens</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0;background:#DDDDFF;"><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:10em;;text-align:center;"><a href="/wiki/Estrogen_receptor" title="Estrogen receptor"><abbr title="Estrogen receptor">ER</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Estrogen receptor</span> agonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><i>Steroidal:</i> <a href="/wiki/Alfatradiol" title="Alfatradiol">Alfatradiol</a></li> <li>Certain <a href="/wiki/Androgen" title="Androgen">androgens</a>/<a href="/wiki/Anabolic_steroid" title="Anabolic steroid">anabolic steroids</a> (e.g., <a href="/wiki/Testosterone_(medication)" title="Testosterone (medication)">testosterone</a>, <a href="/wiki/List_of_androgen_esters#Testosterone_esters" title="List of androgen esters">testosterone esters</a>, <a href="/wiki/Methyltestosterone" title="Methyltestosterone">methyltestosterone</a>, <a href="/wiki/Metandienone" title="Metandienone">metandienone</a>, <a href="/wiki/List_of_androgen_esters#Nandrolone_esters" title="List of androgen esters">nandrolone esters</a>) (via estrogenic metabolites)</li> <li>Certain <a href="/wiki/Progestin" class="mw-redirect" title="Progestin">progestins</a> (e.g., <a href="/wiki/Norethisterone" title="Norethisterone">norethisterone</a>, <a href="/wiki/Noretynodrel" title="Noretynodrel">noretynodrel</a>, <a href="/wiki/Etynodiol_diacetate" title="Etynodiol diacetate">etynodiol diacetate</a>, <a href="/wiki/Tibolone" title="Tibolone">tibolone</a>)</li> <li><a href="/wiki/Clomestrone" title="Clomestrone">Clomestrone</a></li> <li><a href="/wiki/Cloxestradiol_acetate" title="Cloxestradiol acetate">Cloxestradiol acetate</a></li> <li><a href="/wiki/Conjugated_estriol" title="Conjugated estriol">Conjugated estriol</a></li> <li><a href="/wiki/Conjugated_estrogens" title="Conjugated estrogens">Conjugated estrogens</a></li> <li><a href="/wiki/Epiestriol" title="Epiestriol">Epiestriol</a></li> <li><a href="/wiki/Epimestrol" title="Epimestrol">Epimestrol</a></li> <li><a href="/wiki/Esterified_estrogens" title="Esterified estrogens">Esterified estrogens</a></li> <li><a href="/wiki/Estetrol_(medication)" title="Estetrol (medication)">Estetrol</a><sup>†</sup></li> <li><a href="/wiki/Estradiol_(medication)" title="Estradiol (medication)">Estradiol</a></li> <li><a class="mw-selflink-fragment" href="#Estradiol_esters">Estradiol esters</a> (e.g., <a href="/wiki/Estradiol_acetate" title="Estradiol acetate">estradiol acetate</a>, <a href="/wiki/Estradiol_benzoate" title="Estradiol benzoate">estradiol benzoate</a>, <a href="/wiki/Estradiol_cypionate" title="Estradiol cypionate">estradiol cypionate</a>, <a href="/wiki/Estradiol_enanthate" class="mw-redirect" title="Estradiol enanthate">estradiol enanthate</a>, <a href="/wiki/Estradiol_undecylate" title="Estradiol undecylate">estradiol undecylate</a>, <a href="/wiki/Estradiol_valerate" title="Estradiol valerate">estradiol valerate</a>, <a href="/wiki/Polyestradiol_phosphate" title="Polyestradiol phosphate">polyestradiol phosphate</a>, <a href="/wiki/Estradiol_ester_mixture" class="mw-redirect" title="Estradiol ester mixture">estradiol ester mixtures</a> (<a href="/wiki/Climacteron" class="mw-redirect" title="Climacteron">Climacteron</a>))</li> <li><a href="/wiki/Estramustine_phosphate" title="Estramustine phosphate">Estramustine phosphate</a></li> <li><a href="/wiki/Estriol_(medication)" title="Estriol (medication)">Estriol</a></li> <li><a class="mw-selflink-fragment" href="#Estriol_esters">Estriol esters</a> (e.g., <a href="/wiki/Estriol_succinate" title="Estriol succinate">estriol succinate</a>, <a href="/wiki/Polyestriol_phosphate" title="Polyestriol phosphate">polyestriol phosphate</a>)</li> <li><a href="/wiki/Estrogenic_substances" title="Estrogenic substances">Estrogenic substances</a></li> <li><a href="/wiki/Estrone_(medication)" title="Estrone (medication)">Estrone</a></li> <li><a class="mw-selflink-fragment" href="#Estrone_esters">Estrone esters</a> <ul><li><a href="/wiki/Estrone_sulfate_(medication)" title="Estrone sulfate (medication)">Estrone sulfate</a></li> <li><a href="/wiki/Estropipate" title="Estropipate">Estropipate (piperazine estrone sulfate)</a></li></ul></li> <li><a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">Ethinylestradiol</a><sup>#</sup> <ul><li><a href="/wiki/Ethinylestradiol_sulfonate" title="Ethinylestradiol sulfonate">Ethinylestradiol sulfonate</a></li></ul></li> <li><a href="/wiki/Hydroxyestrone_diacetate" title="Hydroxyestrone diacetate">Hydroxyestrone diacetate</a></li> <li><a href="/wiki/Mestranol" title="Mestranol">Mestranol</a></li> <li><a href="/wiki/Methylestradiol" title="Methylestradiol">Methylestradiol</a></li> <li><a href="/wiki/Moxestrol" title="Moxestrol">Moxestrol</a></li> <li><a href="/wiki/Nilestriol" title="Nilestriol">Nilestriol</a></li> <li><a href="/wiki/Prasterone" title="Prasterone">Prasterone (dehydroepiandrosterone; DHEA)</a> <ul><li><a href="/wiki/Prasterone_enanthate" title="Prasterone enanthate">Prasterone enanthate</a></li> <li><a href="/wiki/Prasterone_sulfate" title="Prasterone sulfate">Prasterone sulfate</a></li></ul></li> <li><a href="/wiki/Promestriene" title="Promestriene">Promestriene</a></li> <li><a href="/wiki/Quinestradol" title="Quinestradol">Quinestradol</a></li> <li><a href="/wiki/Quinestrol" title="Quinestrol">Quinestrol</a></li></ul> <ul><li><i>Nonsteroidal:</i> <a href="/wiki/Benzestrol" title="Benzestrol">Benzestrol</a></li> <li><a href="/wiki/Bifluranol" title="Bifluranol">Bifluranol</a></li> <li><a href="/wiki/Chlorotrianisene" title="Chlorotrianisene">Chlorotrianisene</a></li> <li><a href="/wiki/Dienestrol" title="Dienestrol">Dienestrol</a> <ul><li><a href="/wiki/Dienestrol_diacetate" title="Dienestrol diacetate">Dienestrol diacetate</a></li></ul></li> <li><a href="/wiki/Diethylstilbestrol" title="Diethylstilbestrol">Diethylstilbestrol (stilbestrol)</a></li> <li><a class="mw-selflink-fragment" href="#Diethylstilbestrol_esters">Diethylstilbestrol esters/ethers</a> <ul><li><a href="/wiki/Dimestrol" title="Dimestrol">Dimestrol (diethylstilbestrol dimethyl ether)</a></li> <li><a href="/wiki/Fosfestrol" title="Fosfestrol">Fosfestrol (diethylstilbestrol diphosphate)</a></li> <li><a href="/wiki/Mestilbol" title="Mestilbol">Mestilbol (diethylstilbestrol monomethyl ether)</a></li></ul></li> <li><a href="/wiki/Doisynoestrol" title="Doisynoestrol">Doisynoestrol (fenocycline)</a></li> <li><a href="/wiki/Hexestrol" title="Hexestrol">Hexestrol</a> <ul><li><a class="mw-selflink-fragment" href="#Hexestrol_esters">Hexestrol esters</a></li></ul></li> <li><a href="/wiki/Methallenestril" title="Methallenestril">Methallenestril</a></li> <li><a href="/wiki/Methestrol" title="Methestrol">Methestrol (promethestrol)</a> <ul><li><a href="/wiki/Methestrol_dipropionate" title="Methestrol dipropionate">Methestrol dipropionate (promethestrol dipropionate)</a></li></ul></li> <li><a href="/wiki/Paroxypropione" title="Paroxypropione">Paroxypropione</a></li> <li><a href="/wiki/Quadrosilan" title="Quadrosilan">Quadrosilan</a></li> <li><a href="/wiki/Triphenylbromoethylene" title="Triphenylbromoethylene">Triphenylbromoethylene</a></li> <li><a href="/wiki/Triphenylchloroethylene" title="Triphenylchloroethylene">Triphenylchloroethylene</a></li> <li><a href="/wiki/Zeranol" title="Zeranol">Zeranol</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:10em;;text-align:center;"><a href="/wiki/Progonadotropin" title="Progonadotropin">Progonadotropins</a></th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Antiandrogen" title="Antiandrogen">Antiandrogens</a> (e.g., <a href="/wiki/Bicalutamide" title="Bicalutamide">bicalutamide</a>)</li> <li><a href="/wiki/GnRH_agonist" class="mw-redirect" title="GnRH agonist"><abbr title="gonadotropin-releasing hormone">GnRH</abbr> agonists</a> (e.g., <a href="/wiki/Gonadotropin-releasing_hormone" title="Gonadotropin-releasing hormone"><abbr title="gonadotropin-releasing hormone">GnRH</abbr> (gonadorelin)</a>, <a href="/wiki/Leuprorelin" title="Leuprorelin">leuprorelin</a>)</li> <li><a href="/wiki/Gonadotropin" title="Gonadotropin">Gonadotropins</a> (e.g., <a href="/wiki/Follicle-stimulating_hormone" title="Follicle-stimulating hormone"><abbr title="follicle-stimulating hormone">FSH</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip follicle-stimulating hormone</span>, <a href="/wiki/Luteinizing_hormone" title="Luteinizing hormone"><abbr title="luteinizing hormone">LH</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip luteinizing hormone</span>)</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/Antiestrogen" title="Antiestrogen">Antiestrogens</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0;background:#DDDDFF;"><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:10em;;text-align:center;"><a href="/wiki/Estrogen_receptor" title="Estrogen receptor"><abbr title="Estrogen receptor">ER</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Estrogen receptor</span> antagonists<br />(incl. <a href="/wiki/Selective_estrogen_receptor_modulators" class="mw-redirect" title="Selective estrogen receptor modulators"><abbr title="selective estrogen receptor modulators">SERMs</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip selective estrogen receptor modulators</span>/<a href="/wiki/Selective_estrogen_receptor_downregulators" class="mw-redirect" title="Selective estrogen receptor downregulators"><abbr title="selective estrogen receptor downregulators">SERDs</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip selective estrogen receptor downregulators</span>)</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Acolbifene" title="Acolbifene">Acolbifene</a><sup>†</sup></li> <li><a href="/wiki/Anordrin" title="Anordrin">Anordrin</a></li> <li><a href="/wiki/Bazedoxifene" title="Bazedoxifene">Bazedoxifene</a></li> <li><a href="/wiki/Broparestrol" title="Broparestrol">Broparestrol</a></li> <li><a href="/wiki/Clomifene" title="Clomifene">Clomifene</a><sup>#</sup></li> <li><a href="/wiki/Cyclofenil" title="Cyclofenil">Cyclofenil</a></li> <li><a href="/wiki/Enclomifene" title="Enclomifene">Enclomifene</a><sup>†</sup></li> <li><a href="/wiki/Epitiostanol" title="Epitiostanol">Epitiostanol</a></li> <li><a href="/wiki/Lasofoxifene" title="Lasofoxifene">Lasofoxifene</a></li> <li><a href="/wiki/Mepitiostane" title="Mepitiostane">Mepitiostane</a></li> <li><a href="/wiki/Ormeloxifene" title="Ormeloxifene">Ormeloxifene</a></li> <li><a href="/wiki/Ospemifene" title="Ospemifene">Ospemifene</a></li> <li><a href="/wiki/Raloxifene" title="Raloxifene">Raloxifene</a></li> <li><a href="/wiki/Tamoxifen" title="Tamoxifen">Tamoxifen</a><sup>#</sup></li> <li><a href="/wiki/Toremifene" title="Toremifene">Toremifene</a></li></ul> <ul><li><i>Exclusively antagonistic:</i> <a href="/wiki/Elacestrant" title="Elacestrant">Elacestrant</a></li> <li><a href="/wiki/Fulvestrant" title="Fulvestrant">Fulvestrant</a></li></ul> <ul><li><i>Noncompetitive inhibitors:</i> <a href="/wiki/Trilostane" title="Trilostane">Trilostane</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:10em;;text-align:center;"><a href="/wiki/Aromatase_inhibitor" title="Aromatase inhibitor">Aromatase inhibitors</a></th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><i>First-generation:</i> <a href="/wiki/Aminoglutethimide" title="Aminoglutethimide">Aminoglutethimide</a></li> <li><a href="/wiki/Testolactone" title="Testolactone">Testolactone</a></li></ul> <ul><li><i>Second-generation:</i> <a href="/wiki/Fadrozole" title="Fadrozole">Fadrozole</a></li> <li><a href="/wiki/Formestane" title="Formestane">Formestane</a></li></ul> <ul><li><i>Third-generation:</i> <a href="/wiki/Anastrozole" title="Anastrozole">Anastrozole</a></li> <li><a href="/wiki/Exemestane" title="Exemestane">Exemestane</a></li> <li><a href="/wiki/Letrozole" title="Letrozole">Letrozole</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:10em;;text-align:center;"><a href="/wiki/Antigonadotropin" title="Antigonadotropin">Antigonadotropins</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Androgen" title="Androgen">Androgens</a>/<a href="/wiki/Anabolic_steroid" title="Anabolic steroid">anabolic steroids</a> (e.g., <a href="/wiki/Testosterone" title="Testosterone">testosterone</a>, <a href="/wiki/List_of_androgen_esters#Testosterone_esters" title="List of androgen esters">testosterone esters</a>, <a href="/wiki/List_of_androgen_esters#Nandrolone_esters" title="List of androgen esters">nandrolone esters</a>, <a href="/wiki/Oxandrolone" title="Oxandrolone">oxandrolone</a>, <a href="/wiki/Fluoxymesterone" title="Fluoxymesterone">fluoxymesterone</a>)</li> <li><a href="/wiki/D2_receptor" class="mw-redirect" title="D2 receptor">D<sub>2</sub> receptor</a> <a href="/wiki/Dopamine_antagonist" title="Dopamine antagonist">antagonists</a> (<a href="/wiki/Prolactin" title="Prolactin">prolactin</a> releasers) (e.g., <a href="/wiki/Domperidone" title="Domperidone">domperidone</a>, <a href="/wiki/Metoclopramide" title="Metoclopramide">metoclopramide</a>, <a href="/wiki/Risperidone" title="Risperidone">risperidone</a>, <a href="/wiki/Haloperidol" title="Haloperidol">haloperidol</a>, <a href="/wiki/Chlorpromazine" title="Chlorpromazine">chlorpromazine</a>, <a href="/wiki/Sulpiride" title="Sulpiride">sulpiride</a>)</li> <li><a href="/wiki/GnRH_agonist" class="mw-redirect" title="GnRH agonist"><abbr title="gonadotropin-releasing hormone">GnRH</abbr> agonists</a> (e.g., <a href="/wiki/Leuprorelin" title="Leuprorelin">leuprorelin</a>, <a href="/wiki/Goserelin" title="Goserelin">goserelin</a>)</li> <li><a href="/wiki/GnRH_antagonist" class="mw-redirect" title="GnRH antagonist"><abbr title="gonadotropin-releasing hormone">GnRH</abbr> antagonists</a> (e.g., <a href="/wiki/Cetrorelix" title="Cetrorelix">cetrorelix</a>, <a href="/wiki/Elagolix" title="Elagolix">elagolix</a>)</li> <li><a href="/wiki/Progestogen" title="Progestogen">Progestogens</a> (e.g., <a href="/wiki/Chlormadinone_acetate" title="Chlormadinone acetate">chlormadinone acetate</a>, <a href="/wiki/Cyproterone_acetate" title="Cyproterone acetate">cyproterone acetate</a>, <a href="/wiki/Gestonorone_caproate" title="Gestonorone caproate">gestonorone caproate</a>, <a href="/wiki/Hydroxyprogesterone_caproate" title="Hydroxyprogesterone caproate">hydroxyprogesterone caproate</a>, <a href="/wiki/Medroxyprogesterone_acetate" title="Medroxyprogesterone acetate">medroxyprogesterone acetate</a>, <a href="/wiki/Megestrol_acetate" title="Megestrol acetate">megestrol acetate</a>)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:10em;;text-align:center;">Others</th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><i>Mixed mechanism of action:</i> <a href="/wiki/Danazol" title="Danazol">Danazol</a></li> <li><a href="/wiki/Gestrinone" title="Gestrinone">Gestrinone</a></li></ul> <ul><li><i>Androstenedione immunogens:</i> <a href="/wiki/Androvax" title="Androvax">Androvax (androstenedione albumin)</a></li> <li><a href="/wiki/Ovandrotone_albumin" title="Ovandrotone albumin">Ovandrotone albumin (Fecundin)</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><td colspan="2" class="navbox-list navbox-odd hlist" style="width:100%;padding:0;background:#DDDDFF;"><div style="padding:0 0.25em"><div class="hlist"> <ul><li><sup>#</sup><a href="/wiki/WHO_Model_List_of_Essential_Medicines" title="WHO Model List of Essential Medicines">WHO-EM</a></li> <li><sup>‡</sup><a href="/wiki/List_of_withdrawn_drugs" title="List of withdrawn drugs">Withdrawn</a> from market</li> <li><a href="/wiki/Clinical_trial" title="Clinical trial">Clinical trials</a>: <ul><li><sup>†</sup><a href="/wiki/Phases_of_clinical_research#Phase_III" title="Phases of clinical research">Phase III</a></li> <li><sup>§</sup>Never to phase III</li></ul></li></ul> </div> <dl><dt>See also</dt> <dd><a href="/wiki/Template:Estrogen_receptor_modulators" title="Template:Estrogen receptor modulators">Estrogen receptor modulators</a></dd> <dd><a href="/wiki/Template:Androgens_and_antiandrogens" title="Template:Androgens and antiandrogens">Androgens and antiandrogens</a></dd> <dd><a href="/wiki/Template:Progestogens_and_antiprogestogens" title="Template:Progestogens and antiprogestogens">Progestogens and antiprogestogens</a></dd> <dd><a href="/wiki/List_of_steroidal_estrogens" class="mw-redirect" title="List of steroidal estrogens">List of estrogens</a></dd></dl></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="Estrogen_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:Estrogen_receptor_modulators" title="Template:Estrogen receptor modulators"><abbr title="View this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Estrogen_receptor_modulators" title="Template talk:Estrogen receptor modulators"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Estrogen_receptor_modulators" title="Special:EditPage/Template:Estrogen receptor modulators"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Estrogen_receptor_modulators" style="font-size:114%;margin:0 4em"><a href="/wiki/Estrogen_receptor" title="Estrogen receptor">Estrogen 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/Estrogen_receptor" title="Estrogen receptor"><abbr title="Estrogen receptor">ER</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Estrogen receptor</span></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:6em;;text-align:center">Agonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><i>Steroidal:</i> <a href="/wiki/2-Hydroxyestradiol" title="2-Hydroxyestradiol">2-Hydroxyestradiol</a></li> <li><a href="/wiki/2-Hydroxyestrone" title="2-Hydroxyestrone">2-Hydroxyestrone</a></li> <li><a href="/wiki/3-Methyl-19-methyleneandrosta-3,5-dien-17%CE%B2-ol" title="3-Methyl-19-methyleneandrosta-3,5-dien-17β-ol">3-Methyl-19-methyleneandrosta-3,5-dien-17β-ol</a></li> <li><a href="/wiki/3%CE%B1-Androstanediol" title="3α-Androstanediol">3α-Androstanediol</a></li> <li><a href="/w/index.php?title=3%CE%B1,5%CE%B1-Dihydrolevonorgestrel&action=edit&redlink=1" class="new" title="3α,5α-Dihydrolevonorgestrel (page does not exist)">3α,5α-Dihydrolevonorgestrel</a></li> <li><a href="/w/index.php?title=3%CE%B2,5%CE%B1-Dihydrolevonorgestrel&action=edit&redlink=1" class="new" title="3β,5α-Dihydrolevonorgestrel (page does not exist)">3β,5α-Dihydrolevonorgestrel</a></li> <li><a href="/wiki/3%CE%B1-Hydroxytibolone" title="3α-Hydroxytibolone">3α-Hydroxytibolone</a></li> <li><a href="/wiki/3%CE%B2-Hydroxytibolone" title="3β-Hydroxytibolone">3β-Hydroxytibolone</a></li> <li><a href="/wiki/3%CE%B2-Androstanediol" title="3β-Androstanediol">3β-Androstanediol</a></li> <li><a href="/wiki/4-Androstenediol" title="4-Androstenediol">4-Androstenediol</a></li> <li><a href="/wiki/4-Androstenedione" class="mw-redirect" title="4-Androstenedione">4-Androstenedione</a></li> <li><a href="/wiki/4-Fluoroestradiol" title="4-Fluoroestradiol">4-Fluoroestradiol</a></li> <li><a href="/wiki/4-Hydroxyestradiol" title="4-Hydroxyestradiol">4-Hydroxyestradiol</a></li> <li><a href="/wiki/4-Hydroxyestrone" title="4-Hydroxyestrone">4-Hydroxyestrone</a></li> <li><a href="/wiki/4-Methoxyestradiol" title="4-Methoxyestradiol">4-Methoxyestradiol</a></li> <li><a href="/wiki/4-Methoxyestrone" title="4-Methoxyestrone">4-Methoxyestrone</a></li> <li><a href="/wiki/5-Androstenediol" class="mw-redirect" title="5-Androstenediol">5-Androstenediol</a></li> <li><a href="/wiki/7-Keto-DHEA" title="7-Keto-DHEA">7-Oxo-DHEA</a></li> <li><a href="/wiki/7%CE%B1-Hydroxy-DHEA" title="7α-Hydroxy-DHEA">7α-Hydroxy-DHEA</a></li> <li><a href="/wiki/7%CE%B1-Methylestradiol" title="7α-Methylestradiol">7α-Methylestradiol</a></li> <li><a href="/wiki/7%CE%B2-Hydroxyepiandrosterone" title="7β-Hydroxyepiandrosterone">7β-Hydroxyepiandrosterone</a></li> <li><a href="/wiki/8,9-Dehydroestradiol" title="8,9-Dehydroestradiol">8,9-Dehydroestradiol</a></li> <li><a href="/wiki/8,9-Dehydroestrone" title="8,9-Dehydroestrone">8,9-Dehydroestrone</a></li> <li><a href="/wiki/8%CE%B2-VE2" title="8β-VE2">8β-VE2</a></li> <li><a href="/wiki/10%CE%B2,17%CE%B2-Dihydroxyestra-1,4-dien-3-one" title="10β,17β-Dihydroxyestra-1,4-dien-3-one">10β,17β-Dihydroxyestra-1,4-dien-3-one (DHED)</a></li> <li><a href="/wiki/11%CE%B2-Chloromethylestradiol" title="11β-Chloromethylestradiol">11β-Chloromethylestradiol</a></li> <li><a href="/wiki/11%CE%B2-Methoxyestradiol" title="11β-Methoxyestradiol">11β-Methoxyestradiol</a></li> <li><a href="/wiki/15%CE%B1-Hydroxyestradiol" title="15α-Hydroxyestradiol">15α-Hydroxyestradiol</a></li> <li><a href="/wiki/16-Ketoestradiol" title="16-Ketoestradiol">16-Ketoestradiol</a></li> <li><a href="/wiki/16-Ketoestrone" title="16-Ketoestrone">16-Ketoestrone</a></li> <li><a href="/wiki/16%CE%B1-Fluoroestradiol" class="mw-redirect" title="16α-Fluoroestradiol">16α-Fluoroestradiol</a></li> <li><a href="/wiki/16%CE%B1-Hydroxy-DHEA" title="16α-Hydroxy-DHEA">16α-Hydroxy-DHEA</a></li> <li><a href="/wiki/16%CE%B1-Hydroxyestrone" title="16α-Hydroxyestrone">16α-Hydroxyestrone</a></li> <li><a href="/wiki/16%CE%B1-Iodoestradiol" class="mw-redirect" title="16α-Iodoestradiol">16α-Iodoestradiol</a></li> <li><a href="/wiki/16%CE%B1-LE2" title="16α-LE2">16α-LE2</a></li> <li><a href="/wiki/16%CE%B2-Hydroxyestrone" title="16β-Hydroxyestrone">16β-Hydroxyestrone</a></li> <li><a href="/wiki/16%CE%B2,17%CE%B1-Epiestriol" title="16β,17α-Epiestriol">16β,17α-Epiestriol (16β-hydroxy-17α-estradiol)</a></li> <li><a href="/wiki/17%CE%B1-Estradiol" title="17α-Estradiol">17α-Estradiol</a> (<a href="/wiki/Alfatradiol" title="Alfatradiol">alfatradiol</a>)</li> <li><a href="/wiki/17%CE%B1-Dihydroequilenin" title="17α-Dihydroequilenin">17α-Dihydroequilenin</a></li> <li><a href="/wiki/17%CE%B1-Dihydroequilin" title="17α-Dihydroequilin">17α-Dihydroequilin</a></li> <li><a href="/wiki/17%CE%B1-Epiestriol" title="17α-Epiestriol">17α-Epiestriol (16α-hydroxy-17α-estradiol)</a></li> <li><a href="/wiki/17%CE%B1-Ethynyl-3%CE%B1-androstanediol" title="17α-Ethynyl-3α-androstanediol">17α-Ethynyl-3α-androstanediol</a></li> <li><a href="/wiki/17%CE%B1-Ethynyl-3%CE%B2-androstanediol" title="17α-Ethynyl-3β-androstanediol">17α-Ethynyl-3β-androstanediol</a></li> <li><a href="/wiki/17%CE%B2-Dihydroequilenin" title="17β-Dihydroequilenin">17β-Dihydroequilenin</a></li> <li><a href="/wiki/17%CE%B2-Dihydroequilin" title="17β-Dihydroequilin">17β-Dihydroequilin</a></li> <li><a href="/wiki/17%CE%B2-Methyl-17%CE%B1-dihydroequilenin" title="17β-Methyl-17α-dihydroequilenin">17β-Methyl-17α-dihydroequilenin</a></li> <li><a href="/wiki/Abiraterone" class="mw-redirect" title="Abiraterone">Abiraterone</a></li> <li><a href="/wiki/Abiraterone_acetate" title="Abiraterone acetate">Abiraterone acetate</a></li> <li><a href="/wiki/Alestramustine" title="Alestramustine">Alestramustine</a></li> <li><a href="/wiki/Almestrone" title="Almestrone">Almestrone</a></li> <li><a href="/wiki/Anabolic_steroid" title="Anabolic steroid">Anabolic steroids</a> (e.g., <a href="/wiki/Testosterone" title="Testosterone">testosterone</a> and <a href="/wiki/List_of_androgen_esters#Testosterone_esters" title="List of androgen esters">esters</a>, <a href="/wiki/Methyltestosterone" title="Methyltestosterone">methyltestosterone</a>, <a href="/wiki/Metandienone" title="Metandienone">metandienone (methandrostenolone)</a>, <a href="/wiki/Nandrolone" title="Nandrolone">nandrolone</a> and <a href="/wiki/List_of_androgen_esters#Nandrolone_esters" title="List of androgen esters">esters</a>, many others; via estrogenic metabolites)</li> <li><a href="/wiki/Atrimustine" title="Atrimustine">Atrimustine</a></li> <li><a href="/wiki/Bolandiol" title="Bolandiol">Bolandiol</a></li> <li><a href="/wiki/Bolandiol_dipropionate" title="Bolandiol dipropionate">Bolandiol dipropionate</a></li> <li><a href="/wiki/Butolame" title="Butolame">Butolame</a></li> <li><a href="/wiki/Clomestrone" title="Clomestrone">Clomestrone</a></li> <li><a href="/wiki/Cloxestradiol" title="Cloxestradiol">Cloxestradiol</a> <ul><li><a href="/wiki/Cloxestradiol_acetate" title="Cloxestradiol acetate">Cloxestradiol acetate</a></li></ul></li> <li><a href="/wiki/Conjugated_estriol" title="Conjugated estriol">Conjugated estriol</a></li> <li><a href="/wiki/Conjugated_estrogens" title="Conjugated estrogens">Conjugated estrogens</a></li> <li><a href="/wiki/Cyclodiol" title="Cyclodiol">Cyclodiol</a></li> <li><a href="/wiki/Cyclotriol" title="Cyclotriol">Cyclotriol</a></li> <li><a href="/wiki/Dehydroepiandrosterone" title="Dehydroepiandrosterone">DHEA</a></li> <li><a href="/wiki/Dehydroepiandrosterone" title="Dehydroepiandrosterone">DHEA-S</a></li> <li><a href="/wiki/Ent-Estradiol" title="Ent-Estradiol"><i>ent</i>-Estradiol</a></li> <li><a href="/wiki/Epiestriol" title="Epiestriol">Epiestriol (16β-epiestriol, 16β-hydroxy-17β-estradiol)</a></li> <li><a href="/wiki/Epimestrol" title="Epimestrol">Epimestrol</a></li> <li><a href="/wiki/Equilenin" title="Equilenin">Equilenin</a></li> <li><a href="/wiki/Equilin" title="Equilin">Equilin</a></li> <li><a href="/wiki/ERA-63" title="ERA-63">ERA-63 (ORG-37663)</a></li> <li><a href="/wiki/Esterified_estrogens" title="Esterified estrogens">Esterified estrogens</a></li> <li><a href="/wiki/Estetrol" title="Estetrol">Estetrol</a></li> <li><a href="/wiki/Estradiol" title="Estradiol">Estradiol</a> <ul><li><a class="mw-selflink-fragment" href="#Estradiol_esters">Estradiol esters</a></li> <li><a href="/wiki/Lipoidal_estradiol" title="Lipoidal estradiol">Lipoidal estradiol</a></li> <li><a href="/wiki/Polyestradiol_phosphate" title="Polyestradiol phosphate">Polyestradiol phosphate</a></li></ul></li> <li><a href="/wiki/Estramustine" title="Estramustine">Estramustine</a></li> <li><a href="/wiki/Estramustine_phosphate" title="Estramustine phosphate">Estramustine phosphate</a></li> <li><a href="/wiki/Estrapronicate" title="Estrapronicate">Estrapronicate</a></li> <li><a href="/wiki/Estrazinol" title="Estrazinol">Estrazinol</a></li> <li><a href="/wiki/Estriol" title="Estriol">Estriol</a> <ul><li><a class="mw-selflink-fragment" href="#Estriol_esters">Estriol esters</a></li> <li><a href="/wiki/Polyestriol_phosphate" title="Polyestriol phosphate">Polyestriol phosphate</a></li></ul></li> <li><a href="/wiki/Estrofurate" title="Estrofurate">Estrofurate</a></li> <li><a href="/wiki/Estrogenic_substances" title="Estrogenic substances">Estrogenic substances</a></li> <li><a href="/wiki/Estromustine" title="Estromustine">Estromustine</a></li> <li><a href="/wiki/Estrone" title="Estrone">Estrone</a> <ul><li><a class="mw-selflink-fragment" href="#Estrone_esters">Estrone esters</a></li> <li><a href="/wiki/Estrone_methyl_ether" title="Estrone methyl ether">Estrone methyl ether</a></li> <li><a href="/wiki/Estropipate" title="Estropipate">Estropipate</a></li></ul></li> <li><a href="/wiki/Etamestrol" title="Etamestrol">Etamestrol (eptamestrol)</a></li> <li><a href="/wiki/Ethinylandrostenediol" title="Ethinylandrostenediol">Ethinylandrostenediol</a> <ul><li><a href="/wiki/Ethandrostate" title="Ethandrostate">Ethandrostate</a></li></ul></li> <li><a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">Ethinylestradiol</a> <ul><li><a href="/wiki/Ethinylestradiol_3-benzoate" class="mw-redirect" title="Ethinylestradiol 3-benzoate">Ethinylestradiol 3-benzoate</a></li> <li><a href="/wiki/Ethinylestradiol_sulfonate" title="Ethinylestradiol sulfonate">Ethinylestradiol sulfonate</a></li></ul></li> <li><a href="/wiki/Ethinylestriol" title="Ethinylestriol">Ethinylestriol</a></li> <li><a href="/wiki/Ethylestradiol" title="Ethylestradiol">Ethylestradiol</a></li> <li><a href="/wiki/Etynodiol" title="Etynodiol">Etynodiol</a></li> <li><a href="/wiki/Etynodiol_diacetate" title="Etynodiol diacetate">Etynodiol diacetate</a></li> <li><a href="/wiki/Hexolame" title="Hexolame">Hexolame</a></li> <li><a href="/wiki/Hippulin" title="Hippulin">Hippulin</a></li> <li><a href="/wiki/Hydroxyestrone_diacetate" title="Hydroxyestrone diacetate">Hydroxyestrone diacetate</a></li> <li><a href="/wiki/Lynestrenol" title="Lynestrenol">Lynestrenol</a></li> <li><a href="/wiki/Lynestrenol_phenylpropionate" title="Lynestrenol phenylpropionate">Lynestrenol phenylpropionate</a></li> <li><a href="/wiki/Mestranol" title="Mestranol">Mestranol</a></li> <li><a href="/wiki/Methylestradiol" title="Methylestradiol">Methylestradiol</a></li> <li><a href="/wiki/Moxestrol" title="Moxestrol">Moxestrol</a></li> <li><a href="/wiki/Mytatrienediol" title="Mytatrienediol">Mytatrienediol</a></li> <li><a href="/wiki/Nilestriol" title="Nilestriol">Nilestriol</a></li> <li><a href="/wiki/Norethisterone" title="Norethisterone">Norethisterone</a></li> <li><a href="/wiki/Noretynodrel" title="Noretynodrel">Noretynodrel</a></li> <li><a href="/wiki/Orestrate" title="Orestrate">Orestrate</a></li> <li><a href="/wiki/Pentolame" title="Pentolame">Pentolame</a></li> <li><a href="/wiki/Prodiame" title="Prodiame">Prodiame</a></li> <li><a href="/wiki/Prolame" title="Prolame">Prolame</a></li> <li><a href="/wiki/Promestriene" title="Promestriene">Promestriene</a></li> <li><a href="/wiki/RU-16117" title="RU-16117">RU-16117</a></li> <li><a href="/wiki/Quinestradol" title="Quinestradol">Quinestradol</a></li> <li><a href="/wiki/Quinestrol" title="Quinestrol">Quinestrol</a></li> <li><a href="/wiki/Tibolone" title="Tibolone">Tibolone</a></li></ul> <ul><li><i>Nonsteroidal:</i> <a href="/wiki/(R,R)-Tetrahydrochrysene" title="(R,R)-Tetrahydrochrysene">(R,R)-THC</a></li> <li><a href="/wiki/(S,S)-Tetrahydrochrysene" title="(S,S)-Tetrahydrochrysene">(S,S)-THC</a></li> <li><a href="/wiki/2,8-Dihydroxyhexahydrochrysene" title="2,8-Dihydroxyhexahydrochrysene">2,8-DHHHC</a></li> <li><a href="/w/index.php?title=%CE%92-LGND1&action=edit&redlink=1" class="new" title="Β-LGND1 (page does not exist)">β-LGND1</a></li> <li><a href="/wiki/%CE%92-LGND2" title="Β-LGND2">β-LGND2 (GTx-878)</a></li> <li><a href="/w/index.php?title=AC-186&action=edit&redlink=1" class="new" title="AC-186 (page does not exist)">AC-186</a></li> <li><a href="/wiki/Allenestrol" title="Allenestrol">Allenestrol</a></li> <li><a href="/wiki/Allenolic_acid" title="Allenolic acid">Allenolic acid</a></li> <li><a href="/wiki/Benzestrol" title="Benzestrol">Benzestrol</a></li> <li><a href="/wiki/Bifluranol" title="Bifluranol">Bifluranol</a></li> <li><a href="/wiki/Bisdehydrodoisynolic_acid" title="Bisdehydrodoisynolic acid">Bisdehydrodoisynolic acid</a></li> <li><a href="/wiki/Butestrol" title="Butestrol">Butestrol</a></li> <li><a href="/wiki/Carbestrol" title="Carbestrol">Carbestrol</a></li> <li><a href="/wiki/D-15414" title="D-15414">D-15414</a></li> <li><a href="/wiki/DCW234" title="DCW234">DCW234</a></li> <li><a href="/wiki/Diarylpropionitrile" title="Diarylpropionitrile">Diarylpropionitrile</a></li> <li><a href="/wiki/Dienestrol" title="Dienestrol">Dienestrol</a> <ul><li><a href="/wiki/Dienestrol_diacetate" title="Dienestrol diacetate">Dienestrol diacetate</a></li></ul></li> <li><a href="/wiki/Diethylstilbestrol" title="Diethylstilbestrol">Diethylstilbestrol</a> <ul><li><a class="mw-selflink-fragment" href="#Diethylstilbestrol_esters">Diethylstilbestrol esters</a></li></ul></li> <li><a href="/wiki/Dimestrol" title="Dimestrol">Dimestrol (dianisylhexene)</a></li> <li><a href="/wiki/Dimethylstilbestrol" title="Dimethylstilbestrol">Dimethylstilbestrol</a></li> <li><a href="/wiki/Doisynoestrol" title="Doisynoestrol">Doisynoestrol (fenocycline)</a></li> <li><a href="/wiki/Doisynolic_acid" title="Doisynolic acid">Doisynolic acid</a></li> <li><a href="/wiki/Efavirenz" title="Efavirenz">Efavirenz</a></li> <li><a href="/wiki/Elacestrant" title="Elacestrant">Elacestrant</a></li> <li><a href="/wiki/ERB-196" title="ERB-196">ERB-196 (WAY-202196)</a></li> <li><a href="/wiki/Erteberel" title="Erteberel">Erteberel (SERBA-1, LY-500307)</a></li> <li><a href="/wiki/Estrobin" title="Estrobin">Estrobin (DBE)</a></li> <li><a href="/wiki/Fenestrel" title="Fenestrel">Fenestrel</a></li> <li><a href="/wiki/FERb_033" title="FERb 033">FERb 033</a></li> <li><a href="/wiki/Fosfestrol" title="Fosfestrol">Fosfestrol (diethylstilbestrol diphosphate)</a></li> <li><a href="/wiki/Furostilbestrol" title="Furostilbestrol">Furostilbestrol (diethylstilbestrol difuroate)</a></li> <li><a href="/wiki/GTx-758" title="GTx-758">GTx-758</a></li> <li><a href="/wiki/Hexestrol" title="Hexestrol">Hexestrol</a> <ul><li><a class="mw-selflink-fragment" href="#Hexestrol_esters">Hexestrol esters</a></li></ul></li> <li><a href="/wiki/ICI-85966" title="ICI-85966">ICI-85966 (Stilbostat)</a></li> <li><a href="/wiki/M2613" title="M2613">M2613</a></li> <li><a href="/wiki/Meso-Butestrol" title="Meso-Butestrol"><i>meso</i>-Butestrol</a></li> <li><a href="/wiki/Meso-Hexestrol" class="mw-redirect" title="Meso-Hexestrol"><i>meso</i>-Hexestrol</a></li> <li><a href="/wiki/Mestilbol" title="Mestilbol">Mestilbol</a></li> <li><a href="/wiki/Methallenestril" title="Methallenestril">Methallenestril</a></li> <li><a href="/wiki/Methestrol" title="Methestrol">Methestrol</a></li> <li><a href="/wiki/Methestrol_dipropionate" title="Methestrol dipropionate">Methestrol dipropionate</a></li> <li><a href="/wiki/Paroxypropione" title="Paroxypropione">Paroxypropione</a></li> <li><a href="/wiki/Pentafluranol" title="Pentafluranol">Pentafluranol</a></li> <li><a href="/wiki/Phenestrol" title="Phenestrol">Phenestrol</a></li> <li><a href="/wiki/Prinaberel" title="Prinaberel">Prinaberel (ERB-041, WAY-202041)</a></li> <li><a href="/wiki/Propylpyrazoletriol" title="Propylpyrazoletriol">Propylpyrazoletriol</a></li> <li><a href="/wiki/Quadrosilan" title="Quadrosilan">Quadrosilan</a></li> <li><a href="/w/index.php?title=SC-3296&action=edit&redlink=1" class="new" title="SC-3296 (page does not exist)">SC-3296</a></li> <li><a href="/wiki/SC-4289" title="SC-4289">SC-4289</a></li> <li><a href="/wiki/SERBA-2" title="SERBA-2">SERBA-2</a></li> <li><a href="/wiki/SKF-82,958" title="SKF-82,958">SKF-82,958</a></li> <li><a href="/wiki/Terfluranol" title="Terfluranol">Terfluranol</a></li> <li><a href="/wiki/Triphenylbromoethylene" title="Triphenylbromoethylene">Triphenylbromoethylene</a></li> <li><a href="/wiki/Triphenylchloroethylene" title="Triphenylchloroethylene">Triphenylchloroethylene</a></li> <li><a href="/wiki/Triphenyliodoethylene" title="Triphenyliodoethylene">Triphenyliodoethylene</a></li> <li><a href="/wiki/Triphenylmethylethylene" title="Triphenylmethylethylene">Triphenylmethylethylene (triphenylpropene)</a></li> <li><a href="/wiki/WAY-166818" title="WAY-166818">WAY-166818</a></li> <li><a href="/w/index.php?title=WAY-169916&action=edit&redlink=1" class="new" title="WAY-169916 (page does not exist)">WAY-169916</a></li> <li><a href="/wiki/WAY-200070" title="WAY-200070">WAY-200070</a></li> <li><a href="/wiki/WAY-204688" title="WAY-204688">WAY-204688 (SIM-688)</a></li> <li><a href="/wiki/WAY-214156" title="WAY-214156">WAY-214156</a></li></ul> <ul><li><i>Unknown/unsorted:</i> <a href="/wiki/ERB-26" title="ERB-26">ERB-26</a></li> <li><a href="/wiki/ERA-45" title="ERA-45">ERA-45</a></li> <li><a href="/wiki/ERB-79" title="ERB-79">ERB-79</a></li> <li><a href="/wiki/ZK-283197" title="ZK-283197">ZK-283197</a></li></ul> <ul><li><i>Xenoestrogens:</i> <a href="/wiki/Anise" title="Anise">Anise</a>-related (e.g., <a href="/wiki/Anethole" title="Anethole">anethole</a>, <a href="/wiki/Anol" title="Anol">anol</a>, <a href="/wiki/Dianethole" title="Dianethole">dianethole</a>, <a href="/wiki/Dianol" title="Dianol">dianol</a>, <a href="/wiki/Photoanethole" title="Photoanethole">photoanethole</a>)</li> <li><a href="/wiki/Chalconoid" title="Chalconoid">Chalconoids</a> (e.g., <a href="/wiki/Isoliquiritigenin" title="Isoliquiritigenin">isoliquiritigenin</a>, <a href="/wiki/Phloretin" title="Phloretin">phloretin</a>, <a href="/wiki/Phlorizin" title="Phlorizin">phlorizin (phloridzin)</a>, <a href="/wiki/Wedelolactone" title="Wedelolactone">wedelolactone</a>)</li> <li><a href="/wiki/Coumestan" title="Coumestan">Coumestans</a> (e.g., <a href="/wiki/Coumestrol" title="Coumestrol">coumestrol</a>, <a href="/wiki/Psoralidin" title="Psoralidin">psoralidin</a>)</li> <li><a href="/wiki/Flavonoid" title="Flavonoid">Flavonoids</a> (incl. <a href="/wiki/7,8-Dihydroxyflavone" class="mw-redirect" title="7,8-Dihydroxyflavone">7,8-DHF</a>, <a href="/wiki/8-Prenylnaringenin" title="8-Prenylnaringenin">8-prenylnaringenin</a>, <a href="/wiki/Apigenin" title="Apigenin">apigenin</a>, <a href="/wiki/Baicalein" title="Baicalein">baicalein</a>, <a href="/wiki/Baicalin" title="Baicalin">baicalin</a>, <a href="/wiki/Biochanin_A" title="Biochanin A">biochanin A</a>, <a href="/wiki/Calycosin" title="Calycosin">calycosin</a>, <a href="/wiki/Catechin" title="Catechin">catechin</a>, <a href="/wiki/Daidzein" title="Daidzein">daidzein</a>, <a href="/wiki/Daidzin" title="Daidzin">daidzin</a>, <a href="/wiki/Epicatechin_gallate" title="Epicatechin gallate">ECG</a>, <a href="/wiki/Epigallocatechin_gallate" title="Epigallocatechin gallate">EGCG</a>, <a href="/wiki/Epicatechin" class="mw-redirect" title="Epicatechin">epicatechin</a>, <a href="/wiki/Equol" title="Equol">equol</a>, <a href="/wiki/Formononetin" title="Formononetin">formononetin</a>, <a href="/wiki/Glabrene" title="Glabrene">glabrene</a>, <a href="/wiki/Glabridin" title="Glabridin">glabridin</a>, <a href="/wiki/Genistein" title="Genistein">genistein</a>, <a href="/wiki/Genistin" title="Genistin">genistin</a>, <a href="/wiki/Glycitein" title="Glycitein">glycitein</a>, <a href="/wiki/Kaempferol" title="Kaempferol">kaempferol</a>, <a href="/wiki/Liquiritigenin" title="Liquiritigenin">liquiritigenin</a>, <a href="/wiki/Mirificin" title="Mirificin">mirificin</a>, <a href="/wiki/Myricetin" title="Myricetin">myricetin</a>, <a href="/wiki/Naringenin" title="Naringenin">naringenin</a>, <a href="/w/index.php?title=Penduletin&action=edit&redlink=1" class="new" title="Penduletin (page does not exist)">penduletin</a>, <a href="/wiki/Pinocembrin" title="Pinocembrin">pinocembrin</a>, <a href="/wiki/Prunetin" title="Prunetin">prunetin</a>, <a href="/wiki/Puerarin" title="Puerarin">puerarin</a>, <a href="/wiki/Quercetin" title="Quercetin">quercetin</a>, <a href="/wiki/Tectoridin" title="Tectoridin">tectoridin</a>, <a href="/wiki/Tectorigenin" title="Tectorigenin">tectorigenin</a>)</li> <li><a href="/wiki/Lavender_oil" title="Lavender oil">Lavender oil</a></li> <li><a href="/wiki/Lignan" title="Lignan">Lignans</a> (e.g., <a href="/wiki/Enterodiol" title="Enterodiol">enterodiol</a>, <a href="/wiki/Enterolactone" title="Enterolactone">enterolactone</a>, <a href="/wiki/Nyasol" title="Nyasol">nyasol (<i>cis</i>-hinokiresinol)</a>)</li> <li><a href="/wiki/Metalloestrogen" title="Metalloestrogen">Metalloestrogens</a> (e.g., <a href="/wiki/Cadmium" title="Cadmium">cadmium</a>)</li> <li><a href="/wiki/Pesticide" title="Pesticide">Pesticides</a> (e.g., <a href="/wiki/Alternariol" title="Alternariol">alternariol</a>, <a href="/wiki/Dieldrin" title="Dieldrin">dieldrin</a>, <a href="/wiki/Endosulfan" title="Endosulfan">endosulfan</a>, <a href="/wiki/Fenarimol" title="Fenarimol">fenarimol</a>, <a href="/wiki/HPTE" title="HPTE">HPTE</a>, <a href="/wiki/Methiocarb" title="Methiocarb">methiocarb</a>, <a href="/wiki/Methoxychlor" title="Methoxychlor">methoxychlor</a>, <a href="/wiki/Triclocarban" title="Triclocarban">triclocarban</a>, <a href="/wiki/Triclosan" title="Triclosan">triclosan</a>)</li> <li><a href="/wiki/Phytosteroid" title="Phytosteroid">Phytosteroids</a> (e.g., <a href="/wiki/Digitoxin" title="Digitoxin">digitoxin</a> (<a href="/wiki/Digitalis" title="Digitalis">digitalis</a>), <a href="/wiki/Diosgenin" title="Diosgenin">diosgenin</a>, <a href="/wiki/Guggulsterone" title="Guggulsterone">guggulsterone</a>)</li> <li><a href="/wiki/Phytosterol" title="Phytosterol">Phytosterols</a> (e.g., <a href="/wiki/%CE%92-sitosterol" class="mw-redirect" title="Β-sitosterol">β-sitosterol</a>, <a href="/wiki/Campesterol" title="Campesterol">campesterol</a>, <a href="/wiki/Stigmasterol" title="Stigmasterol">stigmasterol</a>)</li> <li><a href="/wiki/Resorcylic_acid_lactone" title="Resorcylic acid lactone">Resorcylic acid lactones</a> (e.g., <a href="/wiki/Zearalanone" title="Zearalanone">zearalanone</a>, <a href="/wiki/%CE%91-zearalenol" class="mw-redirect" title="Α-zearalenol">α-zearalenol</a>, <a href="/wiki/%CE%92-zearalenol" class="mw-redirect" title="Β-zearalenol">β-zearalenol</a>, <a href="/wiki/Zearalenone" title="Zearalenone">zearalenone</a>, <a href="/wiki/Zeranol" title="Zeranol">zeranol (α-zearalanol)</a>, <a href="/wiki/Taleranol" title="Taleranol">taleranol (teranol, β-zearalanol)</a>)</li> <li><a href="/wiki/Steroid" title="Steroid">Steroid</a>-like (e.g., <a href="/wiki/Deoxymiroestrol" class="mw-redirect" title="Deoxymiroestrol">deoxymiroestrol</a>, <a href="/wiki/Miroestrol" title="Miroestrol">miroestrol</a>)</li> <li><a href="/wiki/Stilbenoid" title="Stilbenoid">Stilbenoids</a> (e.g., <a href="/wiki/Resveratrol" title="Resveratrol">resveratrol</a>, <a href="/wiki/Rhaponticin" title="Rhaponticin">rhaponticin</a>)</li> <li><a href="/wiki/Synthetic_xenoestrogen" class="mw-redirect" title="Synthetic xenoestrogen">Synthetic xenoestrogens</a> (e.g., <a href="/wiki/Alkylphenol" title="Alkylphenol">alkylphenols</a>, <a href="/wiki/Bisphenol" title="Bisphenol">bisphenols</a> (e.g., <a href="/wiki/Bisphenol_A" title="Bisphenol A">BPA</a>, <a href="/wiki/Bisphenol_F" title="Bisphenol F">BPF</a>, <a href="/wiki/Bisphenol_S" title="Bisphenol S">BPS</a>), <a href="/wiki/Dichlorodiphenyltrichloroethane" class="mw-redirect" title="Dichlorodiphenyltrichloroethane">DDT</a>, <a href="/wiki/Paraben" title="Paraben">parabens</a>, <a href="/wiki/Polybrominated_biphenyl" title="Polybrominated biphenyl">PBBs</a>, <a href="/wiki/4-hydroxybenzoic_acid" class="mw-redirect" title="4-hydroxybenzoic acid">PHBA</a>, <a href="/wiki/Phthalate" class="mw-redirect" title="Phthalate">phthalates</a>, <a href="/wiki/Polychlorinated_biphenyl" title="Polychlorinated biphenyl">PCBs</a>)</li> <li>Others (e.g., <a href="/wiki/Agnuside" title="Agnuside">agnuside</a>, <a href="/w/index.php?title=Rotundifuran&action=edit&redlink=1" class="new" title="Rotundifuran (page does not exist)">rotundifuran</a>)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Mixed<br />(<a href="/wiki/Selective_estrogen_receptor_modulators" class="mw-redirect" title="Selective estrogen receptor modulators"><abbr title="Selective estrogen receptor modulators">SERMs</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip Selective estrogen receptor modulators</span>)</th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/2-Phenylbenzofuran" title="2-Phenylbenzofuran">2-Phenylbenzofuran</a></li> <li><a href="/w/index.php?title=2-Phenylbenzothiophene&action=edit&redlink=1" class="new" title="2-Phenylbenzothiophene (page does not exist)">2-Phenylbenzothiophene</a></li> <li><a href="/wiki/4%27-Hydroxynorendoxifen" title="4'-Hydroxynorendoxifen">4'-Hydroxynorendoxifen</a></li> <li><a href="/wiki/27-Hydroxycholesterol" title="27-Hydroxycholesterol">27-Hydroxycholesterol</a></li> <li><a href="/wiki/Acefluranol" title="Acefluranol">Acefluranol</a></li> <li><a href="/wiki/Acolbifene" title="Acolbifene">Acolbifene</a></li> <li><a href="/wiki/Afimoxifene" title="Afimoxifene">Afimoxifene</a></li> <li><a href="/wiki/Anordiol" title="Anordiol">Anordiol</a></li> <li><a href="/wiki/Anordrin" title="Anordrin">Anordrin</a></li> <li><a href="/wiki/Arzoxifene" title="Arzoxifene">Arzoxifene</a></li> <li><a href="/wiki/Bazedoxifene" title="Bazedoxifene">Bazedoxifene</a></li> <li><a href="/wiki/Brilanestrant" title="Brilanestrant">Brilanestrant</a></li> <li><a href="/wiki/Broparestrol" title="Broparestrol">Broparestrol</a></li> <li><a href="/wiki/Camizestrant" title="Camizestrant">Camizestrant</a></li> <li><a href="/wiki/Chlorotrianisene" title="Chlorotrianisene">Chlorotrianisene</a></li> <li><a href="/wiki/Clomifene" title="Clomifene">Clomifene</a></li> <li><a href="/wiki/Clomifenoxide" title="Clomifenoxide">Clomifenoxide</a></li> <li><a href="/w/index.php?title=CN-55945-27&action=edit&redlink=1" class="new" title="CN-55945-27 (page does not exist)">CN-55945-27</a></li> <li><a href="/wiki/Cyclofenil" title="Cyclofenil">Cyclofenil</a></li> <li><a href="/w/index.php?title=D-15413&action=edit&redlink=1" class="new" title="D-15413 (page does not exist)">D-15413</a></li> <li><a href="/wiki/Desmethylchlorotrianisene" title="Desmethylchlorotrianisene">Desmethylchlorotrianisene</a></li> <li><a href="/wiki/Droloxifene" title="Droloxifene">Droloxifene</a></li> <li><a href="/wiki/Enclomifene" title="Enclomifene">Enclomifene</a></li> <li><a href="/wiki/Endoxifen" title="Endoxifen">Endoxifen</a></li> <li><a href="/wiki/Etacstil" title="Etacstil">Etacstil (GW-5638, DPC-974)</a></li> <li><a href="/wiki/Ethamoxytriphetol" title="Ethamoxytriphetol">Ethamoxytriphetol (MER-25)</a></li> <li><a href="/wiki/Femarelle" title="Femarelle">Femarelle</a></li> <li><a href="/wiki/Fispemifene" title="Fispemifene">Fispemifene</a></li> <li><a href="/w/index.php?title=GW-7604&action=edit&redlink=1" class="new" title="GW-7604 (page does not exist)">GW-7604</a></li> <li><a href="/wiki/ICI-55548" class="mw-redirect" title="ICI-55548">ICI-55548</a></li> <li><a href="/wiki/Idoxifene" title="Idoxifene">Idoxifene</a></li> <li><a href="/wiki/Lasofoxifene" title="Lasofoxifene">Lasofoxifene</a></li> <li><a href="/wiki/Levormeloxifene" title="Levormeloxifene">Levormeloxifene</a></li> <li><a href="/wiki/LN-1643" class="mw-redirect" title="LN-1643">LN-1643</a></li> <li><a href="/wiki/LN-2299" class="mw-redirect" title="LN-2299">LN-2299</a></li> <li><a href="/w/index.php?title=LY-117018&action=edit&redlink=1" class="new" title="LY-117018 (page does not exist)">LY-117018</a></li> <li><a href="/wiki/Menerba" title="Menerba">Menerba</a></li> <li><a href="/wiki/Miproxifene" title="Miproxifene">Miproxifene</a></li> <li><a href="/wiki/Miproxifene_phosphate" title="Miproxifene phosphate">Miproxifene phosphate</a></li> <li><a href="/w/index.php?title=MRL-37&action=edit&redlink=1" class="new" title="MRL-37 (page does not exist)">MRL-37</a></li> <li><a href="/wiki/Nafoxidine" title="Nafoxidine">Nafoxidine</a></li> <li><a href="/wiki/Nitromifene" title="Nitromifene">Nitromifene</a></li> <li><a href="/wiki/NNC_45-0095" title="NNC 45-0095">NNC 45-0095</a></li> <li><a href="/w/index.php?title=NNC_45-0320&action=edit&redlink=1" class="new" title="NNC 45-0320 (page does not exist)">NNC 45-0320</a></li> <li><a href="/w/index.php?title=NNC_45-0781&action=edit&redlink=1" class="new" title="NNC 45-0781 (page does not exist)">NNC 45-0781</a></li> <li><a href="/w/index.php?title=NNC_45-1506&action=edit&redlink=1" class="new" title="NNC 45-1506 (page does not exist)">NNC 45-1506</a></li> <li><a href="/wiki/Ormeloxifene" title="Ormeloxifene">Ormeloxifene</a></li> <li><a href="/wiki/Ospemifene" title="Ospemifene">Ospemifene</a></li> <li><a href="/wiki/Panomifene" title="Panomifene">Panomifene</a></li> <li><a href="/wiki/Pipendoxifene" title="Pipendoxifene">Pipendoxifene</a></li> <li><a href="/w/index.php?title=Promensil&action=edit&redlink=1" class="new" title="Promensil (page does not exist)">Promensil</a></li> <li><a href="/wiki/Raloxifene" title="Raloxifene">Raloxifene</a></li> <li><a href="/wiki/Rimostil" title="Rimostil">Rimostil (P-081)</a></li> <li><a href="/wiki/Spironolactone" title="Spironolactone">Spironolactone</a></li> <li><a href="/w/index.php?title=SS1010&action=edit&redlink=1" class="new" title="SS1010 (page does not exist)">SS1010</a></li> <li><a href="/wiki/Tamoxifen" title="Tamoxifen">Tamoxifen</a></li> <li><a href="/wiki/TAS-108" title="TAS-108">TAS-108 (SR-16234)</a></li> <li><a href="/wiki/Toremifene" title="Toremifene">Toremifene</a></li> <li><a href="/wiki/Trioxifene" title="Trioxifene">Trioxifene</a></li> <li><a href="/w/index.php?title=TZE-5323&action=edit&redlink=1" class="new" title="TZE-5323 (page does not exist)">TZE-5323</a></li> <li><a href="/w/index.php?title=U-11555A&action=edit&redlink=1" class="new" title="U-11555A (page does not exist)">U-11555A</a></li> <li><a href="/w/index.php?title=U-11634&action=edit&redlink=1" class="new" title="U-11634 (page does not exist)">U-11634</a></li> <li><a href="/w/index.php?title=Y-134&action=edit&redlink=1" class="new" title="Y-134 (page does not exist)">Y-134</a></li> <li><a href="/wiki/Zindoxifene" title="Zindoxifene">Zindoxifene</a></li> <li><a href="/wiki/Zuclomifene" title="Zuclomifene">Zuclomifene</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/(R,R)-Tetrahydrochrysene" title="(R,R)-Tetrahydrochrysene">(R,R)-THC</a></li> <li><a href="/wiki/7%CE%B2-Hydroxy-DHEA" title="7β-Hydroxy-DHEA">7β-Hydroxy-DHEA</a></li> <li><a href="/w/index.php?title=Chloroindazole&action=edit&redlink=1" class="new" title="Chloroindazole (page does not exist)">Chloroindazole</a></li> <li><a href="/wiki/Cytestrol_acetate" title="Cytestrol acetate">Cytestrol acetate</a></li> <li><a href="/w/index.php?title=EM-800&action=edit&redlink=1" class="new" title="EM-800 (page does not exist)">EM-800 (SCH-57050)</a></li> <li><a href="/wiki/Epitiostanol" title="Epitiostanol">Epitiostanol</a></li> <li><a href="/w/index.php?title=ERA-90&action=edit&redlink=1" class="new" title="ERA-90 (page does not exist)">ERA-90</a></li> <li><a href="/w/index.php?title=ERB-88&action=edit&redlink=1" class="new" title="ERB-88 (page does not exist)">ERB-88</a></li> <li><a href="/wiki/Fulvestrant" title="Fulvestrant">Fulvestrant (ICI-182780)</a></li> <li><a href="/wiki/Glyceollin" title="Glyceollin">Glyceollins</a> (<a href="/wiki/Glyceollin_I" title="Glyceollin I">I</a>, <a href="/w/index.php?title=Glyceollin_II&action=edit&redlink=1" class="new" title="Glyceollin II (page does not exist)">II</a>, <a href="/wiki/Glyceollin_III" title="Glyceollin III">III</a>, <a href="/w/index.php?title=Glyceollin_IV&action=edit&redlink=1" class="new" title="Glyceollin IV (page does not exist)">IV</a>)</li> <li><a href="/wiki/ICI-164384" title="ICI-164384">ICI-164384</a></li> <li><a href="/w/index.php?title=MDL-101906&action=edit&redlink=1" class="new" title="MDL-101906 (page does not exist)">MDL-101906</a></li> <li><a href="/wiki/Mepitiostane" title="Mepitiostane">Mepitiostane</a></li> <li><a href="/wiki/Methylepitiostanol" title="Methylepitiostanol">Methylepitiostanol</a></li> <li><a href="/wiki/Methylpiperidinopyrazole" title="Methylpiperidinopyrazole">Methylpiperidinopyrazole</a></li> <li><a href="/wiki/MIBE" title="MIBE">MIBE</a></li> <li><a href="/w/index.php?title=Oxabicycloheptene_sulfonate&action=edit&redlink=1" class="new" title="Oxabicycloheptene sulfonate (page does not exist)">Oxabicycloheptene sulfonate</a></li> <li><a href="/wiki/Phenytoin" title="Phenytoin">Phenytoin</a></li> <li><a href="/wiki/PHTPP" title="PHTPP">PHTPP</a></li> <li><a href="/wiki/Prochloraz" title="Prochloraz">Prochloraz</a></li> <li><a href="/w/index.php?title=RU-39411&action=edit&redlink=1" class="new" title="RU-39411 (page does not exist)">RU-39411</a></li> <li><a href="/w/index.php?title=RU-58668&action=edit&redlink=1" class="new" title="RU-58668 (page does not exist)">RU-58668</a></li> <li><a href="/w/index.php?title=SS1020&action=edit&redlink=1" class="new" title="SS1020 (page does not exist)">SS1020</a></li> <li><a href="/wiki/TAS-108" title="TAS-108">TAS-108 (SR-16234)</a></li> <li><a href="/wiki/ZB716" title="ZB716">ZB716</a></li> <li><a href="/w/index.php?title=ZK-164015&action=edit&redlink=1" class="new" title="ZK-164015 (page does not exist)">ZK-164015</a></li> <li><a href="/w/index.php?title=ZK-191703&action=edit&redlink=1" class="new" title="ZK-191703 (page does not exist)">ZK-191703</a></li></ul> <ul><li><i>Coregulator-binding modulators:</i> <a href="/wiki/ERX-11" title="ERX-11">ERX-11</a></li></ul> <ul><li><i>Noncompetitive inhibitors:</i> <a href="/wiki/Trilostane" title="Trilostane">Trilostane</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/G_protein-coupled_estrogen_receptor" class="mw-redirect" title="G protein-coupled estrogen receptor"><abbr title="G protein-coupled estrogen receptor">GPER</abbr></a><span class="sr-only" style="border: 0; clip: rect(0, 0, 0, 0); clip-path: polygon(0px 0px, 0px 0px, 0px 0px); height: 1px; margin: -1px; overflow: hidden; padding: 0; position: absolute; width: 1px; white-space: nowrap;">Tooltip G protein-coupled estrogen receptor</span></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:6em;;text-align:center">Agonists</th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/2-Methoxyestradiol" title="2-Methoxyestradiol">2-Methoxyestradiol</a></li> <li><a href="/wiki/7%CE%B2-Hydroxyepiandrosterone" title="7β-Hydroxyepiandrosterone">7β-Hydroxyepiandrosterone</a></li> <li><a href="/wiki/Afimoxifene" title="Afimoxifene">Afimoxifene (4-hydroxytamoxifen)</a></li> <li><a href="/wiki/Aldosterone" title="Aldosterone">Aldosterone</a></li> <li><a href="/wiki/Atrazine" title="Atrazine">Atrazine</a></li> <li><a href="/wiki/Bisphenol_A" title="Bisphenol A">Bisphenol A</a></li> <li><a href="/wiki/Daidzein" title="Daidzein">Daidzein</a></li> <li><a href="/wiki/DDT" title="DDT">DDT</a> (<a href="/wiki/P,p%27-DDT" class="mw-redirect" title="P,p'-DDT">p,p'-DDT</a>, <a href="/w/index.php?title=O%27,p%27-DDE&action=edit&redlink=1" class="new" title="O',p'-DDE (page does not exist)">o',p'-DDE</a>)</li> <li><a href="/wiki/Diarylpropionitrile" title="Diarylpropionitrile">Diarylpropionitrile</a></li> <li><a href="/wiki/Equol" title="Equol">Equol</a></li> <li><a href="/wiki/Estradiol" title="Estradiol">Estradiol</a></li> <li><a href="/wiki/Ethinylestradiol" title="Ethinylestradiol">Ethinylestradiol</a></li> <li><a href="/wiki/Fulvestrant" title="Fulvestrant">Fulvestrant (ICI-182780)</a></li> <li><a href="/w/index.php?title=G-1_(drug)&action=edit&redlink=1" class="new" title="G-1 (drug) (page does not exist)">G-1</a></li> <li><a href="/wiki/Genistein" title="Genistein">Genistein</a></li> <li><a href="/w/index.php?title=GPER-L1&action=edit&redlink=1" class="new" title="GPER-L1 (page does not exist)">GPER-L1</a></li> <li><a href="/w/index.php?title=GPER-L2&action=edit&redlink=1" class="new" title="GPER-L2 (page does not exist)">GPER-L2</a></li> <li><a href="/wiki/Hydroxytyrosol" title="Hydroxytyrosol">Hydroxytyrosol</a></li> <li><a href="/wiki/Kepone" class="mw-redirect" title="Kepone">Kepone</a></li> <li><a href="/wiki/Niacin" title="Niacin">Niacin</a></li> <li><a href="/wiki/Niacinamide" class="mw-redirect" title="Niacinamide">Niacinamide</a></li> <li><a href="/wiki/Nonylphenol" title="Nonylphenol">Nonylphenol</a></li> <li><a href="/wiki/Oleuropein" title="Oleuropein">Oleuropein</a></li> <li><a href="/wiki/Polychlorinated_biphenyl" title="Polychlorinated biphenyl">PCBs</a> (<a href="/w/index.php?title=2,2%27,5%27-PCB-4-OH&action=edit&redlink=1" class="new" title="2,2',5'-PCB-4-OH (page does not exist)">2,2',5'-PCB-4-OH</a>)</li> <li><a href="/wiki/Propylpyrazoletriol" title="Propylpyrazoletriol">Propylpyrazoletriol</a></li> <li><a href="/wiki/Quercetin" title="Quercetin">Quercetin</a></li> <li><a href="/wiki/Raloxifene" title="Raloxifene">Raloxifene</a></li> <li><a href="/wiki/Resveratrol" title="Resveratrol">Resveratrol</a></li> <li><a href="/w/index.php?title=STX_(drug)&action=edit&redlink=1" class="new" title="STX (drug) (page does not exist)">STX</a></li> <li><a href="/wiki/Tamoxifen" title="Tamoxifen">Tamoxifen</a></li> <li><a href="/wiki/Tectoridin" title="Tectoridin">Tectoridin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Antagonists</th><td class="navbox-list-with-group navbox-list navbox-odd" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/CCL18" title="CCL18">CCL18</a></li> <li><a href="/wiki/Estriol" title="Estriol">Estriol</a></li> <li><a href="/w/index.php?title=G-15_(drug)&action=edit&redlink=1" class="new" title="G-15 (drug) (page does not exist)">G-15</a></li> <li><a href="/w/index.php?title=G-36_(drug)&action=edit&redlink=1" class="new" title="G-36 (drug) (page does not exist)">G-36</a></li> <li><a href="/wiki/MIBE" title="MIBE">MIBE</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:6em;;text-align:center">Unknown</th><td class="navbox-list-with-group navbox-list navbox-even" style="padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Diethylstilbestrol" title="Diethylstilbestrol">Diethylstilbestrol</a></li> <li><a href="/wiki/Zearalenone" title="Zearalenone">Zearalenone</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><td class="navbox-abovebelow" colspan="2"><div> <dl><dt>See also</dt> <dd><a href="/wiki/Template:Receptor_modulators" title="Template:Receptor modulators">Receptor/signaling modulators</a></dd> <dd><a href="/wiki/Template:Estrogens_and_antiestrogens" title="Template:Estrogens and antiestrogens">Estrogens and antiestrogens</a></dd> <dd><a href="/wiki/Template:Androgen_receptor_modulators" title="Template:Androgen receptor modulators">Androgen receptor modulators</a></dd> <dd><a href="/wiki/Template:Progesterone_receptor_modulators" title="Template:Progesterone receptor modulators">Progesterone receptor modulators</a></dd> <dd><a href="/wiki/List_of_steroidal_estrogens" class="mw-redirect" title="List of steroidal estrogens">List of estrogens</a></dd></dl> </div></td></tr></tbody></table></div> <!-- NewPP limit report Parsed by mw‐web.eqiad.main‐5dc468848‐n5x4g Cached time: 20241122153159 Cache expiry: 2592000 Reduced expiry: false Complications: [vary‐revision‐sha1, show‐toc] CPU time usage: 0.609 seconds Real time usage: 0.800 seconds Preprocessor visited node count: 2666/1000000 Post‐expand include 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