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typeof="mw:File"><a href="/wiki/File:Norartocarpetin.svg" class="mw-file-description"><img alt="Chemical structure of norartocarpetin." src="//upload.wikimedia.org/wikipedia/commons/thumb/c/cf/Norartocarpetin.svg/250px-Norartocarpetin.svg.png" decoding="async" width="250" height="140" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/c/cf/Norartocarpetin.svg/375px-Norartocarpetin.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/c/cf/Norartocarpetin.svg/500px-Norartocarpetin.svg.png 2x" data-file-width="620" data-file-height="348" /></a></span> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; 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;">2′,4′,5,7-Tetrahydroxyflavone</div> </td></tr> <tr> <td colspan="2" style="text-align:left;"><a href="/wiki/Chemical_nomenclature#Systematic_name" title="Chemical nomenclature">Systematic IUPAC name</a> <div style="max-width:22em; word-wrap:break-word; padding-left:1.7em;"><div style="display: inline-block; line-height: 1.2em; padding: .1em 0; max-width:22em;">2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-4<i>H</i>-1-benzopyran-4-one</div></div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; 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=520-30-9">520-30-9</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=C1%3DCC%28%3DC%28C%3DC1O%29O%29C2%3DCC%28%3DO%29C3%3DC%28C%3DC%28C%3DC3O2%29O%29O">Interactive image</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.4587698.html">4587698</a></span></li></ul></div> </td></tr> <tr> <td><a href="/wiki/European_Community_number" title="European Community number"><span title="European Community number (chemical identifier)">EC Number</span></a> </td> <td><link rel="mw-deduplicated-inline-style" href="mw-data:TemplateStyles:r1126788409"><div class="plainlist"><ul><li>208-287-6</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/5481970">5481970</a></span></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/DTXSID00199963">DTXSID00199963</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q15425765#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; background:transparent;"><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/C15H10O6/c16-7-1-2-9(10(18)3-7)13-6-12(20)15-11(19)4-8(17)5-14(15)21-13/h1-6,16-19H</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: ZSYPIPFQOQGYHH-UHFFFAOYSA-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/C15H10O6/c16-7-1-2-9(10(18)3-7)13-6-12(20)15-11(19)4-8(17)5-14(15)21-13/h1-6,16-19H</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: ZSYPIPFQOQGYHH-UHFFFAOYAJ</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; background:transparent;"><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%;">C1=CC(=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O</div></li></ul> </div> </td></tr> <tr> <th colspan="2" style="background: #f8eaba; 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>C<sub>15</sub>H<sub>10</sub>O<sub>6</sub>  </td></tr> <tr> <td><a href="/wiki/Molar_mass" title="Molar mass">Molar mass</a> </td> <td>286.23 g/mol    </td></tr> <tr> <td colspan="2" style="text-align:left; background:#f8eaba; 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>Norartocarpetin</b> is a flavone. It is found in <i><a href="/wiki/Artocarpus_dadah" title="Artocarpus dadah">Artocarpus dadah</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="See_also">See also</h2><span class="mw-editsection"><span class="mw-editsection-bracket">[</span><a href="/w/index.php?title=Norartocarpetin&action=edit&section=1" title="Edit section: See also"><span>edit</span></a><span class="mw-editsection-bracket">]</span></span></div> <ul><li><a href="/wiki/Dihydromorin" title="Dihydromorin">Dihydromorin</a>, the corresponding <a href="/wiki/Flavanonol" title="Flavanonol">flavanonol</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=Norartocarpetin&action=edit&section=2" 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"><style data-mw-deduplicate="TemplateStyles:r1238218222">.mw-parser-output cite.citation{font-style:inherit;word-wrap:break-word}.mw-parser-output .citation q{quotes:"\"""\"""'""'"}.mw-parser-output .citation:target{background-color:rgba(0,127,255,0.133)}.mw-parser-output .id-lock-free.id-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/6/65/Lock-green.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-limited.id-lock-limited a,.mw-parser-output .id-lock-registration.id-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/d/d6/Lock-gray-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .id-lock-subscription.id-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/a/aa/Lock-red-alt-2.svg")right 0.1em center/9px no-repeat}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/4/4c/Wikisource-logo.svg")right 0.1em center/12px no-repeat}body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-free a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-limited a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-registration a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .id-lock-subscription a,body:not(.skin-timeless):not(.skin-minerva) .mw-parser-output .cs1-ws-icon a{background-size:contain;padding:0 1em 0 0}.mw-parser-output .cs1-code{color:inherit;background:inherit;border:none;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;color:var(--color-error,#d33)}.mw-parser-output .cs1-visible-error{color:var(--color-error,#d33)}.mw-parser-output .cs1-maint{display:none;color:#085;margin-left:0.3em}.mw-parser-output .cs1-kern-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right{padding-right:0.2em}.mw-parser-output .citation .mw-selflink{font-weight:inherit}@media screen{.mw-parser-output .cs1-format{font-size:95%}html.skin-theme-clientpref-night .mw-parser-output .cs1-maint{color:#18911f}}@media screen and (prefers-color-scheme:dark){html.skin-theme-clientpref-os .mw-parser-output .cs1-maint{color:#18911f}}</style><cite id="CITEREFSuCuendetHawthorneKardono2002" class="citation journal cs1">Su, BN; Cuendet, M; Hawthorne, ME; Kardono, LB; Riswan, S; Fong, HH; Mehta, RG; Pezzuto, JM; Kinghorn, AD (2002). "Constituents of the bark and twigs of Artocarpus dadah with cyclooxygenase inhibitory activity". <i>Journal of Natural Products</i>. <b>65</b> (2): 163–9. <a href="/wiki/Doi_(identifier)" class="mw-redirect" title="Doi (identifier)">doi</a>:<a rel="nofollow" class="external text" href="https://doi.org/10.1021%2Fnp010451c">10.1021/np010451c</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/11858749">11858749</a>.</cite><span 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navbox-odd" style="width:100%;padding:0"><div style="padding:0 0.25em"> <ul><li><a href="/wiki/3-Hydroxyflavone" title="3-Hydroxyflavone">3-Hydroxyflavone</a></li> <li><a href="/wiki/6-Hydroxyflavone" title="6-Hydroxyflavone">6-Hydroxyflavone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Dihydroxyflavones</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/Chrysin" title="Chrysin">Chrysin</a></li> <li><a href="/wiki/4%27,7-Dihydroxyflavone" title="4',7-Dihydroxyflavone">4',7-Dihydroxyflavone</a></li> <li><a href="/wiki/7,8-Dihydroxyflavone" class="mw-redirect" title="7,8-Dihydroxyflavone">7,8-Dihydroxyflavone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Trihydroxyflavones</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/Apigenin" title="Apigenin">Apigenin</a></li> <li><a href="/wiki/Baicalein" title="Baicalein">Baicalein</a></li> <li><a href="/wiki/Galangin" title="Galangin">Galangin</a></li> <li><a href="/wiki/Norwogonin" title="Norwogonin">Norwogonin</a></li> <li><a href="/wiki/7,8,3%27-Trihydroxyflavone" title="7,8,3'-Trihydroxyflavone">7,8,3'-Trihydroxyflavone</a></li> <li><a href="/wiki/6,7,4%27-Trihydroxyflavone" title="6,7,4'-Trihydroxyflavone">6,7,4'-Trihydroxyflavone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Tetrahydroxyflavones</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/Kaempferol" title="Kaempferol">Kaempferol</a></li> <li><a href="/wiki/Isoscutellarein" title="Isoscutellarein">Isoscutellarein</a></li> <li><a href="/wiki/Luteolin" title="Luteolin">Luteolin</a></li> <li><a class="mw-selflink selflink">Norartocarpetin</a></li> <li><a href="/wiki/Scutellarein" title="Scutellarein">Scutellarein</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Pentahydroxyflavones</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/Herbacetin" title="Herbacetin">Herbacetin</a></li> <li><a href="/wiki/Morin_(molecule)" class="mw-redirect" title="Morin (molecule)">Morin</a></li> <li><a href="/wiki/Quercetin" title="Quercetin">Quercetin</a></li> <li><a href="/w/index.php?title=Nortangeretin&action=edit&redlink=1" class="new" title="Nortangeretin (page does not exist)">Nortangeretin</a></li> <li><a href="/w/index.php?title=6-Hydroxyluteolin&action=edit&redlink=1" class="new" title="6-Hydroxyluteolin (page does not exist)">6-Hydroxyluteolin</a></li> <li><a href="/w/index.php?title=Norwightin&action=edit&redlink=1" class="new" title="Norwightin (page does not exist)">Norwightin</a></li> <li><a href="/wiki/Hypolaetin" title="Hypolaetin">Hypolaetin</a></li> <li><a href="/wiki/Tricetin" title="Tricetin">Tricetin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">O-methylated flavones</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/4%27,7-Dihydroxy-6-methoxyflavone" title="4',7-Dihydroxy-6-methoxyflavone">4',7-Dihydroxy-6-methoxyflavone</a></li> <li><a href="/wiki/Acacetin" title="Acacetin">Acacetin</a></li> <li><a href="/wiki/Alnetin" title="Alnetin">Alnetin</a></li> <li><a href="/w/index.php?title=Artocarpetin&action=edit&redlink=1" class="new" title="Artocarpetin (page does not exist)">Artocarpetin</a></li> <li><a href="/wiki/Chrysoeriol" title="Chrysoeriol">Chrysoeriol</a></li> <li><a href="/wiki/Cirsilineol" title="Cirsilineol">Cirsilineol</a></li> <li><a href="/w/index.php?title=Cirsiliol&action=edit&redlink=1" class="new" title="Cirsiliol (page does not exist)">Cirsiliol</a></li> <li><a href="/w/index.php?title=Cirsimaritin&action=edit&redlink=1" class="new" title="Cirsimaritin (page does not exist)">Cirsimaritin</a></li> <li><a href="/wiki/Diosmetin" title="Diosmetin">Diosmetin</a></li> <li><a href="/wiki/Eupatilin" title="Eupatilin">Eupatilin</a></li> <li><a href="/wiki/Genkwanin" title="Genkwanin">Genkwanin</a></li> <li><a href="/wiki/Hispidulin" title="Hispidulin">Hispidulin</a></li> <li><a href="/wiki/Nepetin" title="Nepetin">Nepetin</a></li> <li><a href="/wiki/Nobiletin" title="Nobiletin">Nobiletin</a></li> <li><a href="/wiki/Oroxylin_A" title="Oroxylin A">Oroxylin A</a></li> <li><a href="/wiki/Pratol" title="Pratol">Pratol</a></li> <li><a href="/w/index.php?title=Salvigenin&action=edit&redlink=1" class="new" title="Salvigenin (page does not exist)">Salvigenin</a></li> <li><a href="/wiki/Sinensetin" title="Sinensetin">Sinensetin</a></li> <li><a href="/wiki/Tangeretin" title="Tangeretin">Tangeretin</a></li> <li><a href="/wiki/Techtochrysin" title="Techtochrysin">Techtochrysin</a></li> <li><a href="/wiki/Tricin" title="Tricin">Tricin</a></li> <li><a href="/wiki/Wogonin" title="Wogonin">Wogonin</a></li> <li><a href="/wiki/Zapotin" title="Zapotin">Zapotin</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Glycoside" title="Glycoside">Glycosides</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%">of apigenin</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/Apiin" title="Apiin">Apiin</a></li> <li><a href="/wiki/Apigetrin" title="Apigetrin">Apigetrin</a></li> <li><a href="/wiki/Isovitexin" title="Isovitexin">Isovitexin</a></li> <li><a href="/wiki/Rhoifolin" title="Rhoifolin">Rhoifolin</a></li> <li><a href="/wiki/Saponarin" title="Saponarin">Saponarin</a></li> <li><a href="/w/index.php?title=Schaftoside&action=edit&redlink=1" class="new" title="Schaftoside (page does not exist)">Schaftoside</a></li> <li><a href="/w/index.php?title=Vicenin-2&action=edit&redlink=1" class="new" title="Vicenin-2 (page does not exist)">Vicenin-2</a></li> <li><a href="/wiki/Vitexin" title="Vitexin">Vitexin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">of baicalein</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/Baicalin" title="Baicalin">Baicalin</a></li> <li><a href="/wiki/Tetuin" title="Tetuin">Tetuin</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">of hypolaetin</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=Hypolaetin_8-glucoside&action=edit&redlink=1" class="new" title="Hypolaetin 8-glucoside (page does not exist)">Hypolaetin 8-glucoside</a></li> <li><a href="/w/index.php?title=Hypolaetin_8-glucuronide&action=edit&redlink=1" class="new" title="Hypolaetin 8-glucuronide (page does not exist)">Hypolaetin 8-glucuronide</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">of luteolin</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/Cynaroside" title="Cynaroside">Cynaroside</a></li> <li><a href="/wiki/Isoorientin" title="Isoorientin">Isoorientin</a></li> <li><a href="/wiki/Orientin" title="Orientin">Orientin</a></li> <li><a href="/wiki/Veronicastroside" title="Veronicastroside">Veronicastroside</a></li> <li><a href="/wiki/Luteolin-7-O-glucuronide" title="Luteolin-7-O-glucuronide">Luteolin-7-O-glucuronide</a></li></ul> </div></td></tr></tbody></table><div> <ul><li><a href="/w/index.php?title=Giraldiin_A&action=edit&redlink=1" class="new" title="Giraldiin A (page does not exist)">Giraldiin A</a> and <a href="/w/index.php?title=Giraldiin_B&action=edit&redlink=1" class="new" title="Giraldiin B (page does not exist)">B</a></li> <li><a href="/w/index.php?title=Nepitrin&action=edit&redlink=1" class="new" title="Nepitrin (page does not exist)">Nepitrin</a></li> <li><a href="/wiki/Oroxindin" title="Oroxindin">Oroxindin</a></li> <li><a href="/wiki/Scutellarin" title="Scutellarin">Scutellarin</a></li></ul></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Acetylated</th><td class="navbox-list-with-group navbox-list navbox-odd hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"> <li><a href="/w/index.php?title=Artocarpetin_A&action=edit&redlink=1" class="new" title="Artocarpetin A (page does not exist)">Artocarpetin A</a></li> <li><a href="/w/index.php?title=Artoindonesianin_P&action=edit&redlink=1" class="new" title="Artoindonesianin P (page does not exist)">Artoindonesianin P</a></li> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Sulfated glycosides</th><td class="navbox-list-with-group navbox-list navbox-even hlist" style="width:100%;padding:0"><div style="padding:0 0.25em"><a href="/wiki/Theograndin_I" title="Theograndin I">Theograndin I</a> and <a href="/w/index.php?title=Theograndin_II&action=edit&redlink=1" class="new" title="Theograndin II (page does not exist)">II</a></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Polymers</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/Amentoflavone" title="Amentoflavone">Amentoflavone</a></li> <li><a href="/wiki/Ochnaflavone" title="Ochnaflavone">Ochnaflavone</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Drugs</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/Diosmin" title="Diosmin">Diosmin</a></li> <li><a href="/wiki/Hidrosmin" title="Hidrosmin">Hidrosmin</a></li></ul> </div></td></tr></tbody></table></div> <p><br /> </p> <style data-mw-deduplicate="TemplateStyles:r1012311289">.mw-parser-output .asbox{position:relative;overflow:hidden}.mw-parser-output .asbox table{background:transparent}.mw-parser-output .asbox p{margin:0}.mw-parser-output .asbox p+p{margin-top:0.25em}.mw-parser-output .asbox-body{font-style:italic}.mw-parser-output .asbox-note{font-size:smaller}.mw-parser-output .asbox .navbar{position:absolute;top:-0.75em;right:1em;display:none}</style><div role="note" class="metadata 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