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Available in 5 languages" > <label id="p-lang-btn-label" for="p-lang-btn-checkbox" class="vector-dropdown-label cdx-button cdx-button--fake-button cdx-button--fake-button--enabled cdx-button--weight-quiet cdx-button--action-progressive mw-portlet-lang-heading-5" aria-hidden="true" ><span class="vector-icon mw-ui-icon-language-progressive mw-ui-icon-wikimedia-language-progressive"></span> <span class="vector-dropdown-label-text">5 languages</span> </label> <div class="vector-dropdown-content"> <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li class="interlanguage-link interwiki-azb mw-list-item"><a href="https://azb.wikipedia.org/wiki/%D8%A7%D9%88%D9%BE%D8%A7%D9%84%DB%8C%D9%86" title="اوپالین – South Azerbaijani" lang="azb" hreflang="azb" data-title="اوپالین" data-language-autonym="تۆرکجه" data-language-local-name="South Azerbaijani" class="interlanguage-link-target"><span>تۆرکجه</span></a></li><li class="interlanguage-link interwiki-es mw-list-item"><a href="https://es.wikipedia.org/wiki/Eupal%C3%ADn" title="Eupalín – Spanish" lang="es" hreflang="es" data-title="Eupalín" data-language-autonym="Español" data-language-local-name="Spanish" class="interlanguage-link-target"><span>Español</span></a></li><li class="interlanguage-link interwiki-fa mw-list-item"><a href="https://fa.wikipedia.org/wiki/%D8%A7%D9%88%D9%BE%D8%A7%D9%84%DB%8C%D9%86" title="اوپالین – Persian" lang="fa" hreflang="fa" data-title="اوپالین" data-language-autonym="فارسی" data-language-local-name="Persian" class="interlanguage-link-target"><span>فارسی</span></a></li><li class="interlanguage-link interwiki-sr mw-list-item"><a href="https://sr.wikipedia.org/wiki/Eupalin" title="Eupalin – Serbian" lang="sr" hreflang="sr" data-title="Eupalin" data-language-autonym="Српски / srpski" data-language-local-name="Serbian" class="interlanguage-link-target"><span>Српски / srpski</span></a></li><li class="interlanguage-link interwiki-sh mw-list-item"><a href="https://sh.wikipedia.org/wiki/Eupalin" title="Eupalin – Serbo-Croatian" lang="sh" hreflang="sh" data-title="Eupalin" data-language-autonym="Srpskohrvatski / српскохрватски" data-language-local-name="Serbo-Croatian" class="interlanguage-link-target"><span>Srpskohrvatski / српскохрватски</span></a></li> </ul> <div class="after-portlet after-portlet-lang"><span class="wb-langlinks-edit wb-langlinks-link"><a href="https://www.wikidata.org/wiki/Special:EntityPage/Q5409893#sitelinks-wikipedia" title="Edit interlanguage links" class="wbc-editpage">Edit links</a></span></div> </div> </div> </div> </header> <div class="vector-page-toolbar"> <div class="vector-page-toolbar-container"> <div id="left-navigation"> <nav aria-label="Namespaces"> <div id="p-associated-pages" class="vector-menu vector-menu-tabs mw-portlet mw-portlet-associated-pages" > <div class="vector-menu-content"> <ul class="vector-menu-content-list"> <li id="ca-nstab-main" class="selected vector-tab-noicon mw-list-item"><a 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class="mw-content-ltr mw-parser-output" lang="en" dir="ltr"><style data-mw-deduplicate="TemplateStyles:r1268415487">.mw-parser-output .ib-chembox{border-collapse:collapse;text-align:left}.mw-parser-output .ib-chembox td,.mw-parser-output .ib-chembox th{border:1px solid #a2a9b1;width:40%}.mw-parser-output .ib-chembox td+td{width:60%}@media screen{html.skin-theme-clientpref-night .mw-parser-output .ib-chembox figure:not(.skin-invert-image):not(.skin-invert):not(.bg-transparent){background:var(--background-color-inverted,#f8f9fa)}}@media screen and (prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .ib-chembox figure:not(.skin-invert-image):not(.skin-invert):not(.bg-transparent){background:var(--background-color-inverted,#f8f9fa)}}</style> <table class="infobox ib-chembox"> <caption>Eupalin </caption> <tbody><tr> <td colspan="2" style="text-align:center; padding:2px;"><figure class="mw-halign-center" typeof="mw:File"><a href="/wiki/File:Eupalin.svg" class="mw-file-description"><img src="//upload.wikimedia.org/wikipedia/commons/thumb/8/83/Eupalin.svg/220px-Eupalin.svg.png" decoding="async" width="220" height="189" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/83/Eupalin.svg/330px-Eupalin.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/83/Eupalin.svg/440px-Eupalin.svg.png 2x" data-file-width="512" data-file-height="439" /></a><figcaption></figcaption></figure> </td></tr> <tr> <th colspan="2" style="background: #f8eaba;color:inherit; text-align: center;">Names </th></tr> <tr> <td colspan="2" style="text-align:left;"><a href="/wiki/Chemical_nomenclature" title="Chemical nomenclature">IUPAC name</a> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;">5-Hydroxy-2-(4-hydroxyphenyl)-6,7-dimethoxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one</div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba;color:inherit; text-align: center;">Identifiers </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/CAS_Registry_Number" title="CAS Registry Number">CAS Number</a></div> </td> <td><style data-mw-deduplicate="TemplateStyles:r1126788409">.mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}</style><div class="plainlist"><ul><li><span title="commonchemistry.cas.org"><a rel="nofollow" class="external text" href="https://commonchemistry.cas.org/detail?cas_rn=29617-75-2">29617-75-2</a></span></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">3D model (<a href="/wiki/JSmol" class="mw-redirect" title="JSmol">JSmol</a>)</div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409" /><div class="plainlist"><ul><li><span title="chemapps.stolaf.edu (3D interactive model)"><a rel="nofollow" class="external text" href="https://chemapps.stolaf.edu/jmol/jmol.php?model=C%5BC%40H%5D1%5BC%40%40H%5D%28%5BC%40H%5D%28%5BC%40H%5D%28%5BC%40%40H%5D%28O1%29OC2%3DC%28OC3%3DCC%28%3DC%28C%28%3DC3C2%3DO%29O%29OC%29OC%29C4%3DCC%3DC%28C%3DC4%29O%29O%29O%29O">Interactive image</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/ChEMBL" title="ChEMBL">ChEMBL</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409" /><div class="plainlist"><ul><li><span title="www.ebi.ac.uk"><a rel="nofollow" class="external text" href="https://www.ebi.ac.uk/chembl/explore/compound/ChEMBL483203">ChEMBL483203</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/ChemSpider" title="ChemSpider">ChemSpider</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409" /><div class="plainlist"><ul><li><span title="www.chemspider.com"><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.4508995.html">4508995</a></span></li><li><span title="www.chemspider.com"><a rel="nofollow" class="external text" href="https://www.chemspider.com/Chemical-Structure.4572250.html">4572250</a></span></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/PubChem" title="PubChem">PubChem</a> <abbr title="Compound ID">CID</abbr></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409" /><div class="plainlist"><ul><li><span title="pubchem.ncbi.nlm.nih.gov"><a rel="nofollow" class="external text" href="https://pubchem.ncbi.nlm.nih.gov/compound/5458259">5458259</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/Unique_Ingredient_Identifier" title="Unique Ingredient Identifier">UNII</a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409" /><div class="plainlist"><ul><li><span title="precision.fda.gov"><a rel="nofollow" class="external text" href="https://precision.fda.gov/uniisearch/srs/unii/T9YV6RMN56">T9YV6RMN56</a></span><sup> <span typeof="mw:File"><span><img alt="check" src="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png" decoding="async" width="7" height="7" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/11px-Yes_check.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/14px-Yes_check.svg.png 2x" data-file-width="600" data-file-height="600" /></span></span><span style="display:none">Y</span></sup></li></ul></div> </td></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/CompTox_Chemicals_Dashboard" title="CompTox Chemicals Dashboard">CompTox Dashboard</a> <span style="font-weight:normal">(<abbr title="U.S. Environmental Protection Agency">EPA</abbr>)</span></div> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409" /><div class="plainlist"><ul><li><span title="comptox.epa.gov"><a rel="nofollow" class="external text" href="https://comptox.epa.gov/dashboard/chemical/details/DTXSID70952087">DTXSID70952087</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q5409893#P3117" title="Edit this at Wikidata"><img alt="Edit this at Wikidata" src="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png" decoding="async" width="10" height="10" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/15px-OOjs_UI_icon_edit-ltr-progressive.svg.png 1.5x, //upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/20px-OOjs_UI_icon_edit-ltr-progressive.svg.png 2x" data-file-width="20" data-file-height="20" /></a></span></span></li></ul></div> </td></tr> <tr> <td colspan="2"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold; text-align:left; font-weight:normal;"><div><a href="/wiki/International_Chemical_Identifier" title="International Chemical Identifier">InChI</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.5em; text-align:left;"><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">InChI=1S/C23H24O11/c1-9-15(25)18(28)19(29)23(32-9)34-22-17(27)14-12(8-13(30-2)21(31-3)16(14)26)33-20(22)10-4-6-11(24)7-5-10/h4-9,15,18-19,23-26,28-29H,1-3H3/t9-,15-,18+,19+,23-/m0/s1</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: CXVSHWFUBVZVSW-YPNBZCAISA-N</div></div></li><li style="line-height: inherit; margin: 0"><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.5em; text-align:left;"><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">InChI=1/C23H24O11/c1-9-15(25)18(28)19(29)23(32-9)34-22-17(27)14-12(8-13(30-2)21(31-3)16(14)26)33-20(22)10-4-6-11(24)7-5-10/h4-9,15,18-19,23-26,28-29H,1-3H3/t9-,15-,18+,19+,23-/m0/s1</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: CXVSHWFUBVZVSW-YPNBZCAIBS</div></div></li></ul> </div> </td></tr> <tr> <td colspan="2"><div class="collapsible-list mw-collapsible mw-collapsed" style="text-align: left;"> <div style="line-height: 1.6em; font-weight: bold; text-align:left; font-weight:normal;"><div><a href="/wiki/Simplified_molecular-input_line-entry_system" class="mw-redirect" title="Simplified molecular-input line-entry system">SMILES</a></div></div> <ul class="mw-collapsible-content" style="margin-top: 0; margin-bottom: 0; line-height: inherit; list-style: none; margin-left: 0; word-break:break-all;"><li style="line-height: inherit; margin: 0"><div style="border-top:1px solid #ccc; padding:0.2em 0 0.2em 1.6em; word-wrap:break-word; text-indent:-1.5em; text-align:left; font-size:97%; line-height:120%;">C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(OC3=CC(=C(C(=C3C2=O)O)OC)OC)C4=CC=C(C=C4)O)O)O)O</div></li></ul> </div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba;color:inherit; text-align: center;">Properties </th></tr> <tr> <td><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;"><a href="/wiki/Chemical_formula" title="Chemical formula">Chemical formula</a></div> </td> <td><span title="Carbon">C</span><sub>23</sub><span title="Hydrogen">H</span><sub>24</sub><span title="Oxygen">O</span><sub>11</sub> </td></tr> <tr> <td><a href="/wiki/Molar_mass" title="Molar mass">Molar mass</a> </td> <td><span class="nowrap"><span data-sort-value="7002476434000000000♠"></span>476.434</span> g·mol<sup>−1</sup>   </td></tr> <tr> <td colspan="2" style="text-align:left; background:#f8eaba; color:inherit; border:1px solid #a2a9b1;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0;">Except where otherwise noted, data are given for materials in their <a href="/wiki/Standard_state" title="Standard state">standard state</a> (at 25 °C [77 °F], 100 kPa).</div> <div style="margin-top: 0.3em;"></div> <div style="margin-top: 0.3em; text-align: center;"><a href="/wiki/Wikipedia:Chemical_infobox#References" title="Wikipedia:Chemical infobox">Infobox references</a></div> </td></tr> </tbody></table><div class="shortdescription nomobile noexcerpt noprint searchaux" style="display:none">Chemical compound</div> <p><b>Eupalin</b> is a <a href="/wiki/Flavonol" class="mw-redirect" title="Flavonol">flavonol</a>. It is the <a href="/wiki/Eupalitin" title="Eupalitin">eupalitin</a> 3-O-<a href="/wiki/Rhamnoside" class="mw-redirect" title="Rhamnoside">rhamnoside</a>. It can be isolated from <i><a href="/wiki/Eupatorium_ligustrinum" class="mw-redirect" title="Eupatorium ligustrinum">Eupatorium ligustrinum</a></i>.<sup id="cite_ref-1" class="reference"><a href="#cite_note-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup> </p> <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=Eupalin&action=edit&section=1" 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"><ol class="references"> <li id="cite_note-1"><span class="mw-cite-backlink"><b><a href="#cite_ref-1">^</a></b></span> <span class="reference-text">The structures of eupalin and eupatolin. Two new flavonol rhamnosides isolated from Eupatorium ligustrinum D.C. L. Quijano, F. Malanco and Tirso Ríos, Tetrahedron, Volume 26, Issue 12, 1970, pages 2851-2859, <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 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title="3-Hydroxyflavone">3-Hydroxyflavone</a> (synthetic) and derivatives</li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Flavonols" title="Flavonols">Flavonols</a></th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Aglycones</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Fisetin" title="Fisetin">Fisetin</a></li> <li><a href="/wiki/Galangin" title="Galangin">Galangin</a></li> <li><a href="/wiki/Gossypetin" title="Gossypetin">Gossypetin</a></li> <li><a href="/wiki/Herbacetin" title="Herbacetin">Herbacetin</a></li> <li><a href="/wiki/Kaempferol" title="Kaempferol">Kaempferol</a></li> <li><a href="/wiki/Morin_(flavonol)" title="Morin (flavonol)">Morin</a></li> <li><a href="/wiki/Myricetin" title="Myricetin">Myricetin</a></li> <li><a href="/wiki/Quercetagetin" title="Quercetagetin">Quercetagetin</a></li> <li><a href="/wiki/Quercetin" title="Quercetin">Quercetin</a></li> <li><a href="/wiki/Robinetin" title="Robinetin">Robinetin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Conjugates</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides of <a href="/wiki/Herbacetin" title="Herbacetin">herbacetin</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Rhodionin" title="Rhodionin">Rhodionin</a></li> <li><a href="/w/index.php?title=Rhodiosin&action=edit&redlink=1" class="new" title="Rhodiosin (page does not exist)">Rhodiosin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides of <a href="/wiki/Kaempferol" title="Kaempferol">kaempferol</a></th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Afzelin" title="Afzelin">Afzelin</a> (Kaempferol 3-rhamnoside)</li> <li><a href="/wiki/Astragalin" title="Astragalin">Astragalin</a> (kaempferol 3-O-glucoside)</li> <li><a href="/wiki/Kaempferitrin" title="Kaempferitrin">Kaempferitrin</a> (kaempferol 3,7-dirhamnoside)</li> <li><a href="/wiki/Juglanin" title="Juglanin">Juglanin</a> (Kaempferol 3-O-arabinoside)</li> <li><a href="/w/index.php?title=Kaempferol_3-alpha-L-arabinopyranoside&action=edit&redlink=1" class="new" title="Kaempferol 3-alpha-L-arabinopyranoside (page does not exist)">Kaempferol 3-alpha-L-arabinopyranoside</a></li> <li><a href="/w/index.php?title=Kaempferol_3-alpha-D-arabinopyranoside&action=edit&redlink=1" class="new" title="Kaempferol 3-alpha-D-arabinopyranoside (page does not exist)">Kaempferol 3-alpha-D-arabinopyranoside</a></li> <li><a href="/w/index.php?title=Kaempferol_7-alpha-L-arabinoside&action=edit&redlink=1" class="new" title="Kaempferol 7-alpha-L-arabinoside (page does not exist)">Kaempferol 7-alpha-L-arabinoside</a></li> <li><a href="/wiki/Kaempferol_7-O-glucoside" title="Kaempferol 7-O-glucoside">Kaempferol 7-O-glucoside</a></li> <li><a href="/w/index.php?title=Kaempferol_3-lathyroside&action=edit&redlink=1" class="new" title="Kaempferol 3-lathyroside (page does not exist)">Kaempferol 3-lathyroside</a></li> <li><a href="/w/index.php?title=Kaempferol_4%27-rhamnoside&action=edit&redlink=1" class="new" title="Kaempferol 4'-rhamnoside (page does not exist)">Kaempferol 4'-rhamnoside</a></li> <li><a href="/w/index.php?title=Kaempferol_5-rhamnoside&action=edit&redlink=1" class="new" title="Kaempferol 5-rhamnoside (page does not exist)">Kaempferol 5-rhamnoside</a></li> <li><a href="/w/index.php?title=Kaempferol_7-rhamnoside&action=edit&redlink=1" class="new" title="Kaempferol 7-rhamnoside (page does not exist)">Kaempferol 7-rhamnoside</a></li> <li><a href="/w/index.php?title=Kaempferol_7-O-alpha-L-rhamnofuranoside&action=edit&redlink=1" class="new" title="Kaempferol 7-O-alpha-L-rhamnofuranoside (page does not exist)">Kaempferol 7-O-alpha-L-rhamnofuranoside</a></li> <li><a href="/w/index.php?title=Kaempferol_3-xyloside&action=edit&redlink=1" class="new" title="Kaempferol 3-xyloside (page does not exist)">Kaempferol 3-xyloside</a></li> <li><a href="/w/index.php?title=Kaempferol_7-xyloside&action=edit&redlink=1" class="new" title="Kaempferol 7-xyloside (page does not exist)">Kaempferol 7-xyloside</a></li> <li><a href="/wiki/Robinin" title="Robinin">Robinin</a> (kaempferol-3-O-robinoside-7-O-rhamnoside)</li> <li><a href="/wiki/Kaempferol_3-O-rutinoside" title="Kaempferol 3-O-rutinoside">Kaempferol 3-O-rutinoside</a></li> <li><a href="/w/index.php?title=Sophoraflavonoloside&action=edit&redlink=1" class="new" title="Sophoraflavonoloside (page does not exist)">Sophoraflavonoloside</a> (Kaempferol 3-O-sophoroside)</li> <li><a href="/wiki/Trifolin" title="Trifolin">Trifolin</a> (Kaempferol 3-O-beta-D-galactoside)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides of <a href="/wiki/Myricetin" title="Myricetin">myricetin</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/w/index.php?title=Betmidin&action=edit&redlink=1" class="new" title="Betmidin (page does not exist)">Betmidin</a> (<a href="/w/index.php?title=Myricetin_3-O-arabinoside&action=edit&redlink=1" class="new" title="Myricetin 3-O-arabinoside (page does not exist)">Myricetin 3-O-arabinoside</a>)</li> <li><a href="/wiki/Myricetin_3-O-rutinoside" title="Myricetin 3-O-rutinoside">Myricetin 3-O-rutinoside</a></li> <li><a href="/w/index.php?title=Myricetin-3-O-neohesperidoside&action=edit&redlink=1" class="new" title="Myricetin-3-O-neohesperidoside (page does not exist)">Myricetin-3-O-neohesperidoside</a></li> <li><a href="/wiki/Myricitrin" title="Myricitrin">Myricitrin</a> (Myricetin 3-O-rhamnoside)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Conjugates of <a href="/wiki/Quercetin" title="Quercetin">quercetin</a></th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Sulfates</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Quercetin_3-O-sulfate" title="Quercetin 3-O-sulfate">Quercetin 3-O-sulfate</a></li> <li><a href="/w/index.php?title=Quercetin_3,3%27-bissulfate&action=edit&redlink=1" class="new" title="Quercetin 3,3'-bissulfate (page does not exist)">Quercetin 3,3'-bissulfate</a></li> <li><a href="/w/index.php?title=Quercetin_3,4%27-bissulfate&action=edit&redlink=1" class="new" title="Quercetin 3,4'-bissulfate (page does not exist)">Quercetin 3,4'-bissulfate</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Avicularin" title="Avicularin">Avicularin</a> (quercetin-3-O-α-L-arabinofuranoside)</li> <li><a href="/wiki/CTN-986" title="CTN-986">CTN-986</a></li> <li><a href="/wiki/Guaijaverin" title="Guaijaverin">Guaijaverin</a> (quercetin 3-O-<a href="/wiki/Arabinoside" class="mw-redirect" title="Arabinoside">arabinoside</a>)</li> <li><a href="/w/index.php?title=Heliosin&action=edit&redlink=1" class="new" title="Heliosin (page does not exist)">Heliosin</a> (quercetin 3-di<a href="/wiki/Galactoside" title="Galactoside">galactoside</a>)</li> <li><a href="/wiki/Hyperoside" title="Hyperoside">Hyperoside</a> (quercetin 3-O-galactoside)</li> <li><a href="/wiki/Isoquercetin" title="Isoquercetin">Isoquercetin</a> (quercetin 3-O-glucoside)</li> <li><a href="/wiki/Miquelianin" title="Miquelianin">Miquelianin</a> (quercetin 3-O-glucuronide)</li> <li><a href="/wiki/Quercetin_3,4%27-diglucoside" title="Quercetin 3,4'-diglucoside">Quercetin 3,4'-diglucoside</a></li> <li><a href="/w/index.php?title=Quercetin-3-sophorodide&action=edit&redlink=1" class="new" title="Quercetin-3-sophorodide (page does not exist)">Quercetin-3-sophorodide</a></li> <li><a href="/wiki/Quercitrin" title="Quercitrin">Quercitrin</a> (quercetin 3-O-rhamnoside)</li> <li><a href="/wiki/Rutin" title="Rutin">Rutin</a> (quercetin rutinoside)</li> <li><a href="/w/index.php?title=Reinutrin&action=edit&redlink=1" class="new" title="Reinutrin (page does not exist)">Reinutrin</a> (quercetin-3-D-xyloside)</li> <li><a href="/wiki/Spiraeoside" title="Spiraeoside">Spiraeoside</a> (quercetin 4'-O-glucoside)</li> <li><a href="/wiki/Taxillusin" title="Taxillusin">Taxillusin</a> (galloylated 3-O-glucoside of quercetin°</li></ul> </div></td></tr></tbody></table><div></div></td></tr></tbody></table><div></div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><i>O</i>-Methylated flavonols</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Aglycones</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/5-O-Methylmyricetin" title="5-O-Methylmyricetin">5-O-methylmyricetin</a></li> <li><a href="/wiki/Annulatin" title="Annulatin">Annulatin</a></li> <li><a href="/wiki/Ayanin" title="Ayanin">Ayanin</a></li> <li><a href="/wiki/Axillarin" title="Axillarin">Axillarin</a></li> <li><a href="/wiki/Azaleatin" title="Azaleatin">Azaleatin</a></li> <li><a href="/wiki/Brickellin" title="Brickellin">Brickellin</a></li> <li><a href="/wiki/Centaureidin" title="Centaureidin">Centaureidin</a></li> <li><a href="/wiki/Chrysosplenetin" title="Chrysosplenetin">Chrysosplenetin</a></li> <li><a href="/wiki/Combretol" title="Combretol">Combretol</a></li> <li><a href="/wiki/Ermanin" title="Ermanin">Ermanin</a></li> <li><a href="/wiki/Eupatolitin" title="Eupatolitin">Eupatolitin</a></li> <li><a href="/wiki/Eupalitin" title="Eupalitin">Eupalitin</a></li> <li><a href="/wiki/Europetin" title="Europetin">Europetin</a></li> <li><a href="/wiki/Isorhamnetin" title="Isorhamnetin">Isorhamnetin</a></li> <li><a href="/wiki/Jaceidin" title="Jaceidin">Jaceidin</a></li> <li><a href="/wiki/Kaempferide" title="Kaempferide">Kaempferide</a></li> <li><a href="/wiki/Kumatakenin" title="Kumatakenin">Kumatakenin</a></li> <li><a href="/wiki/Laricitrin" title="Laricitrin">Laricitrin</a></li> <li><a href="/wiki/Natsudaidain" title="Natsudaidain">Natsudaidain</a></li> <li><a href="/wiki/Ombuin" title="Ombuin">Ombuin</a></li> <li><a href="/wiki/Pachypodol" title="Pachypodol">Pachypodol</a></li> <li><a href="/wiki/Patuletin" title="Patuletin">Patuletin</a></li> <li><a href="/wiki/Retusin_(flavonol)" title="Retusin (flavonol)">Retusin</a></li> <li><a href="/wiki/Mearnsetin" title="Mearnsetin">Mearnsetin</a></li> <li><a href="/wiki/Rhamnazin" title="Rhamnazin">Rhamnazin</a></li> <li><a href="/wiki/Rhamnetin" title="Rhamnetin">Rhamnetin</a></li> <li><a href="/wiki/Santin_(flavonol)" title="Santin (flavonol)">Santin</a></li> <li><a href="/wiki/Spinacetin" title="Spinacetin">Spinacetin</a></li> <li><a href="/wiki/Syringetin" title="Syringetin">Syringetin</a></li> <li><a href="/wiki/Isorhamnetin" title="Isorhamnetin">Tamarixetin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">of isorhamnetin</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/w/index.php?title=Narcissin&action=edit&redlink=1" class="new" title="Narcissin (page does not exist)">Narcissin</a> (<a href="/w/index.php?title=Isorhamnetin_3-O-rutinoside&action=edit&redlink=1" class="new" title="Isorhamnetin 3-O-rutinoside (page does not exist)">Isorhamnetin 3-O-rutinoside</a>)</li> <li><a href="/w/index.php?title=Isorhamnetin_3-O-glucoside&action=edit&redlink=1" class="new" title="Isorhamnetin 3-O-glucoside (page does not exist)">Isorhamnetin 3-O-glucoside</a></li> <li><a href="/w/index.php?title=Tamarixetin_7-rutinoside&action=edit&redlink=1" class="new" title="Tamarixetin 7-rutinoside (page does not exist)">Tamarixetin 7-rutinoside</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">other</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Azalein" title="Azalein">Azalein</a> (Azaleatin 3-O-α-L-rhamnoside)</li> <li><a href="/w/index.php?title=Centaurein&action=edit&redlink=1" class="new" title="Centaurein (page does not exist)">Centaurein</a> (<a href="/w/index.php?title=Centaureidin_7-O-glucoside&action=edit&redlink=1" class="new" title="Centaureidin 7-O-glucoside (page does not exist)">Centaureidin 7-O-glucoside</a>)</li> <li><a class="mw-selflink selflink">Eupalin</a> (Eupalitin 3-0-rhamnoside)</li> <li><a href="/wiki/Eupatolin" title="Eupatolin">Eupatolin</a> (Eupatolitin 3-O-rhamnoside)</li> <li><a href="/w/index.php?title=Jacein&action=edit&redlink=1" class="new" title="Jacein (page does not exist)">Jacein</a> (<a href="/w/index.php?title=Jaceidin_7-O-glucoside&action=edit&redlink=1" class="new" title="Jaceidin 7-O-glucoside (page does not exist)">Jaceidin 7-O-glucoside</a>)</li> <li><a href="/w/index.php?title=Patulitrin&action=edit&redlink=1" class="new" title="Patulitrin (page does not exist)">Patulitrin</a> (<a href="/w/index.php?title=Patuletin_7-O-glucoside&action=edit&redlink=1" class="new" title="Patuletin 7-O-glucoside (page does not exist)">Patuletin 7-O-glucoside</a></li> <li><a href="/wiki/Xanthorhamnin" title="Xanthorhamnin">Xanthorhamnin</a> (Rhamnetin glycoside)</li></ul> </div></td></tr></tbody></table><div></div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Derivative flavonols</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Aglycones</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/w/index.php?title=Noricaritin&action=edit&redlink=1" class="new" title="Noricaritin (page does not exist)">Noricaritin</a></li> <li><a href="/w/index.php?title=Dihydronoricaritin&action=edit&redlink=1" class="new" title="Dihydronoricaritin (page does not exist)">Dihydronoricaritin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Amurensin_(flavonol)" title="Amurensin (flavonol)">Amurensin</a></li> <li><a href="/wiki/Icariin" title="Icariin">Icariin</a></li> <li><a href="/w/index.php?title=Phelloside&action=edit&redlink=1" class="new" title="Phelloside (page does not exist)">Phelloside</a></li> <li><a href="/w/index.php?title=Dihydrophelloside&action=edit&redlink=1" class="new" title="Dihydrophelloside (page does not exist)">Dihydrophelloside</a></li> <li><a href="/w/index.php?title=Rutin_S&action=edit&redlink=1" class="new" title="Rutin S (page does not exist)">Rutin S</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pyranoflavonols</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Aglycones</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Karanjachromene" title="Karanjachromene">Karanjachromene</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Furanoflavonols</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Aglycones</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/Karanjin" title="Karanjin">Karanjin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides</th><td class="navbox-list-with-group navbox-list navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/w/index.php?title=Pongamoside_A&action=edit&redlink=1" class="new" title="Pongamoside A (page does not exist)">Pongamoside A</a>, <a href="/w/index.php?title=Pongamoside_B&action=edit&redlink=1" class="new" title="Pongamoside B (page does not exist)">B</a> and <a href="/w/index.php?title=Pongamoside_C&action=edit&redlink=1" class="new" title="Pongamoside C (page does not exist)">C</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Semisynthetic</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"></div><table class="nowraplinks navbox-subgroup" style="border-spacing:0"><tbody><tr><th scope="row" class="navbox-group" style="width:1%">Glycosides</th><td class="navbox-list-with-group navbox-list navbox-even" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a 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