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data-pinnable-element-id="vector-appearance" data-pinned-container-id="vector-appearance-pinned-container" data-unpinned-container-id="vector-appearance-unpinned-container" > <div class="vector-pinnable-header-label">Appearance</div> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-pin-button" data-event-name="pinnable-header.vector-appearance.pin">move to sidebar</button> <button class="vector-pinnable-header-toggle-button vector-pinnable-header-unpin-button" data-event-name="pinnable-header.vector-appearance.unpin">hide</button> </div> </div> </div> </nav> </div> </div> <div id="bodyContent" class="vector-body" aria-labelledby="firstHeading" data-mw-ve-target-container> <div class="vector-body-before-content"> <div class="mw-indicators"> </div> <div id="siteSub" class="noprint">From Wikipedia, the free encyclopedia</div> </div> <div id="contentSub"><div id="mw-content-subtitle"></div></div> <div id="mw-content-text" class="mw-body-content"><div class="mw-content-ltr mw-parser-output" lang="en" dir="ltr"><style data-mw-deduplicate="TemplateStyles:r1084375498">.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%}</style> <table class="infobox ib-chembox"> <caption>Plicatin B </caption> <tbody><tr> <td colspan="2" style="text-align:center; padding:2px;"><span typeof="mw:File"><a href="/wiki/File:Plicatin_B.svg" class="mw-file-description" title="Chemical structure of plicatin B"><img alt="Chemical structure of plicatin B" src="//upload.wikimedia.org/wikipedia/commons/thumb/8/80/Plicatin_B.svg/250px-Plicatin_B.svg.png" decoding="async" width="250" height="85" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/8/80/Plicatin_B.svg/375px-Plicatin_B.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/8/80/Plicatin_B.svg/500px-Plicatin_B.svg.png 2x" data-file-width="620" data-file-height="210" /></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/Preferred_IUPAC_name" title="Preferred IUPAC name">Preferred 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;">Methyl (2<i>E</i>)-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-enoate</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=72704-01-9">72704-01-9</a></span><sup> <span typeof="mw:File"><span><img alt="☒" src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png" decoding="async" width="7" height="8" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/11px-X_mark.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/14px-X_mark.svg.png 2x" data-file-width="525" data-file-height="600" /></span></span><span style="display:none">N</span></sup>=</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=O%3DC%28OC%29%5CC%3DC%5Cc1ccc%28O%29c%28c1%29C%2FC%3DC%28%5CC%29C">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/chembldb/index.php/compound/inspect/ChEMBL451699">ChEMBL451699</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><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.4943161.html">4943161</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/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/6438704">6438704</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/DTXSID801029774">DTXSID801029774</a> <span class="mw-valign-text-top noprint" typeof="mw:File/Frameless"><a href="https://www.wikidata.org/wiki/Q7204957#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/C15H18O3/c1-11(2)4-7-13-10-12(5-8-14(13)16)6-9-15(17)18-3/h4-6,8-10,16H,7H2,1-3H3/b9-6+<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></div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: LZEOAWXRNGQEHO-RMKNXTFCSA-N<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></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/C15H18O3/c1-11(2)4-7-13-10-12(5-8-14(13)16)6-9-15(17)18-3/h4-6,8-10,16H,7H2,1-3H3/b9-6+</div><div style="word-wrap:break-word; text-indent:-1.5em; font-size:97%; line-height:120%;">Key: LZEOAWXRNGQEHO-RMKNXTFCBP</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%;">O=C(OC)\C=C\c1ccc(O)c(c1)C/C=C(\C)C</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>18</sub>O<sub>3</sub>  </td></tr> <tr> <td><a href="/wiki/Molar_mass" title="Molar mass">Molar mass</a> </td> <td>246.30 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 style="text-align:center;"><span typeof="mw:File"><span><img alt="☒" src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/12px-X_mark.svg.png" decoding="async" width="12" height="14" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/18px-X_mark.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/24px-X_mark.svg.png 2x" data-file-width="525" data-file-height="600" /></span></span><span style="display:none">N</span> <span class="reflink plainlinks nourlexpansion"><a class="external text" href="https://en.wikipedia.org/w/index.php?title=Special:ComparePages&rev1=477512114&page2=Plicatin+B">verify</a></span> (<a href="/wiki/Wikipedia:WikiProject_Chemicals/Chembox_validation" title="Wikipedia:WikiProject Chemicals/Chembox validation">what is</a> <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><span typeof="mw:File"><span><img alt="☒" src="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png" decoding="async" width="7" height="8" class="mw-file-element" srcset="//upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/11px-X_mark.svg.png 1.5x, //upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/14px-X_mark.svg.png 2x" data-file-width="525" data-file-height="600" /></span></span><span style="display:none">N</span></sup> ?) </div></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>Plicatin B</b> is a <a href="/wiki/Hydroxycinnamic_acid" title="Hydroxycinnamic acid">hydroxycinnamic acid</a> found in <i><a href="/wiki/Psoralea_plicata" class="mw-redirect" title="Psoralea plicata">Psoralea plicata</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=Plicatin_B&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">Plicatin A and B, two phenolic cinnamates from Psoralea plicata. Nazli Rasool, Abdul Qasim Khan and Abdul Malik, Phytochemistry, Volume 29, Issue 12, 1990, Pages 3979-3981, <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 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this template">v</abbr></a></li><li class="nv-talk"><a href="/wiki/Template_talk:Hydroxycinnamic_acid" title="Template talk:Hydroxycinnamic acid"><abbr title="Discuss this template">t</abbr></a></li><li class="nv-edit"><a href="/wiki/Special:EditPage/Template:Hydroxycinnamic_acid" title="Special:EditPage/Template:Hydroxycinnamic acid"><abbr title="Edit this template">e</abbr></a></li></ul></div><div id="Types_of_hydroxycinnamic_acids" style="font-size:114%;margin:0 4em">Types of <a href="/wiki/Hydroxycinnamic_acid" title="Hydroxycinnamic acid">hydroxycinnamic acids</a></div></th></tr><tr><th scope="row" class="navbox-group" style="width:1%">Aglycones</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%">Precursor</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/Cinnamic_acid" title="Cinnamic acid">Cinnamic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Monohydroxycinnamic acids<br />(Coumaric acids)</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/P-Coumaric_acid" title="P-Coumaric acid"><i>p</i>-Coumaric acid</a></li> <li><a href="/wiki/O-Coumaric_acid" title="O-Coumaric acid"><i>o</i>-Coumaric acid</a></li> <li><a href="/wiki/M-Coumaric_acid" title="M-Coumaric acid"><i>m</i>-Coumaric acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><a href="/wiki/Dihydroxycinnamic_acid" title="Dihydroxycinnamic acid">Dihydroxycinnamic acids</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/Caffeic_acid" title="Caffeic acid">Caffeic acid</a> (3,4-dihydroxycinnamic acid)</li> <li><a href="/wiki/Umbellic_acid" title="Umbellic acid">Umbellic acid</a> (2,4-dihydroxycinnamic acid)</li> <li><a href="/wiki/2,3-Dihydroxycinnamic_acid" title="2,3-Dihydroxycinnamic acid">2,3-Dihydroxycinnamic acid</a></li> <li><a href="/wiki/2,5-Dihydroxycinnamic_acid" title="2,5-Dihydroxycinnamic acid">2,5-Dihydroxycinnamic acid</a></li> <li><a href="/wiki/3,5-Dihydroxycinnamic_acid" title="3,5-Dihydroxycinnamic acid">3,5-Dihydroxycinnamic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Trihydroxycinnamic acids</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/2,4,5-Trihydroxycinnamic_acid" title="2,4,5-Trihydroxycinnamic acid">2,4,5-Trihydroxycinnamic acid</a></li> <li><a href="/w/index.php?title=3,4,5-Trihydroxycinnamic_acid&action=edit&redlink=1" class="new" title="3,4,5-Trihydroxycinnamic acid (page does not exist)">3,4,5-Trihydroxycinnamic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%"><i>O</i>-methylated forms</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/Ferulic_acid" title="Ferulic acid">Ferulic acid</a></li> <li><a href="/wiki/5-Hydroxyferulic_acid" title="5-Hydroxyferulic acid">5-Hydroxyferulic acid</a></li> <li><a href="/wiki/Isoferulic_acid" title="Isoferulic acid">Isoferulic acid</a></li> <li><a href="/wiki/Sinapinic_acid" title="Sinapinic acid">Sinapinic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">others</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/Plicatin_A" title="Plicatin A">Plicatin A</a></li> <li><a class="mw-selflink selflink">Plicatin B</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Esters</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%">glycoside-likes</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%">Esters of<br />caffeic acid<br />with cyclitols</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%">esters of<br /><a href="/wiki/Quinic_acid" title="Quinic acid">quinic acid</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/Chlorogenic_acid" title="Chlorogenic acid">Chlorogenic acid</a> (3-caffeoylquinic acid)</li> <li><a href="/w/index.php?title=Cryptochlorogenic_acid&action=edit&redlink=1" class="new" title="Cryptochlorogenic acid (page does not exist)">Cryptochlorogenic acid</a> (4-<i>O</i>-caffeoylquinic acid)</li> <li><a href="/wiki/Neochlorogenic_acid" title="Neochlorogenic acid">Neochlorogenic acid</a> (5-<i>O</i>-Caffeoylquinic acid)</li> <li><a href="/wiki/Cynarine" title="Cynarine">Cynarine</a> (1,5-dicaffeoylquinic acid)</li> <li><a href="/w/index.php?title=3,4-dicaffeoylquinic_acid&action=edit&redlink=1" class="new" title="3,4-dicaffeoylquinic acid (page does not exist)">3,4-dicaffeoylquinic acid</a></li> <li><a href="/w/index.php?title=3,5-dicaffeoylquinic_acid&action=edit&redlink=1" class="new" title="3,5-dicaffeoylquinic acid (page does not exist)">3,5-dicaffeoylquinic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">esters of<br /><a href="/wiki/Shikimic_acid" title="Shikimic acid">shikimic acid</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/Dactylifric_acid" title="Dactylifric acid">Dactylifric acid</a> (3-<i>O</i>-caffeoylshikimic acid)</li></ul> </div></td></tr></tbody></table><div></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=Ferulic_acid_glucoside&action=edit&redlink=1" class="new" title="Ferulic acid glucoside (page does not exist)">Ferulic acid glucoside</a></li> <li><a href="/wiki/P-Coumaric_acid_glucoside" title="P-Coumaric acid glucoside"><i>p</i>-Coumaric acid glucoside</a></li> <li><a href="/w/index.php?title=1-Sinapoyl-D-glucose&action=edit&redlink=1" class="new" title="1-Sinapoyl-D-glucose (page does not exist)">1-Sinapoyl-<small>D</small>-glucose</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/Tartaric_acid" title="Tartaric acid">Tartaric acid</a> esters</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/Caftaric_acid" title="Caftaric acid">Caftaric acid</a></li> <li><a href="/wiki/Chicoric_acid" title="Chicoric acid">Chicoric acid</a> (dicaffeoyltartaric acid)</li> <li><a href="/wiki/Coutaric_acid" title="Coutaric acid">Coutaric acid</a></li> <li><a href="/wiki/Fertaric_acid" title="Fertaric acid">Fertaric acid</a></li> <li><a href="/wiki/Grape_reaction_product" title="Grape reaction product">Grape reaction product</a> (caftaric acid conjugated with glutathione)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Other esters<br />with caffeic acid</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/Caffeoylmalic_acid" title="Caffeoylmalic acid">Caffeoylmalic acid</a></li> <li><a href="/wiki/Ethyl_caffeate" title="Ethyl caffeate">Ethyl caffeate</a></li> <li><a href="/wiki/Methyl_caffeate" title="Methyl caffeate">Methyl caffeate</a></li> <li><a href="/wiki/Caffeic_acid_phenethyl_ester" title="Caffeic acid phenethyl ester">Caffeic acid phenethyl ester</a> (CAPE)</li> <li><a href="/wiki/Rosmarinic_acid" title="Rosmarinic acid">Rosmarinic acid</a> (ester with 3,4-dihydroxyphenyllactic acid)</li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Caffeoyl phenylethanoid<br /> glycoside (CPG)</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/Echinacoside" title="Echinacoside">Echinacoside</a></li> <li><a href="/w/index.php?title=Calceolarioside_A&action=edit&redlink=1" class="new" title="Calceolarioside A (page does not exist)">Calceolarioside A</a>, <a href="/w/index.php?title=Calceolarioside_B&action=edit&redlink=1" class="new" title="Calceolarioside B (page does not exist)">B</a>, <a href="/w/index.php?title=Calceolarioside_C&action=edit&redlink=1" class="new" title="Calceolarioside C (page does not exist)">C</a>, <a href="/w/index.php?title=Calceolarioside_F&action=edit&redlink=1" class="new" title="Calceolarioside F (page does not exist)">F</a></li> <li><a href="/w/index.php?title=Chiritoside_A&action=edit&redlink=1" class="new" title="Chiritoside A (page does not exist)">Chiritoside A</a>, <a href="/w/index.php?title=Chiritoside_B&action=edit&redlink=1" class="new" title="Chiritoside B (page does not exist)">B</a>, <a href="/w/index.php?title=Chiritoside_C&action=edit&redlink=1" class="new" title="Chiritoside C (page does not exist)">C</a></li> <li><a href="/w/index.php?title=Cistanoside_A&action=edit&redlink=1" class="new" title="Cistanoside A (page does not exist)">Cistanoside A</a>, <a href="/w/index.php?title=Cistanoside_B&action=edit&redlink=1" class="new" title="Cistanoside B (page does not exist)">B</a>, <a href="/w/index.php?title=Cistanoside_C&action=edit&redlink=1" class="new" title="Cistanoside C (page does not exist)">C</a>, <a href="/w/index.php?title=Cistanoside_D&action=edit&redlink=1" class="new" title="Cistanoside D (page does not exist)">D</a>, <a href="/w/index.php?title=Cistanoside_E&action=edit&redlink=1" class="new" title="Cistanoside E (page does not exist)">E</a>, <a href="/w/index.php?title=Cistanoside_F&action=edit&redlink=1" class="new" title="Cistanoside F (page does not exist)">F</a>, <a href="/w/index.php?title=Cistanoside_G&action=edit&redlink=1" class="new" title="Cistanoside G (page does not exist)">G</a>, <a href="/w/index.php?title=Cistanoside_H&action=edit&redlink=1" class="new" title="Cistanoside H (page does not exist)">H</a></li> <li><a href="/w/index.php?title=Conandroside&action=edit&redlink=1" class="new" title="Conandroside (page does not exist)">Conandroside</a></li> <li><a href="/w/index.php?title=Myconoside&action=edit&redlink=1" class="new" title="Myconoside (page does not exist)">Myconoside</a></li> <li><a href="/w/index.php?title=Pauoifloside&action=edit&redlink=1" class="new" title="Pauoifloside (page does not exist)">Pauoifloside</a></li> <li><a href="/w/index.php?title=Plantainoside_A&action=edit&redlink=1" class="new" title="Plantainoside A (page does not exist)">Plantainoside A</a></li> <li><a href="/w/index.php?title=Plantamajoside&action=edit&redlink=1" class="new" title="Plantamajoside (page does not exist)">Plantamajoside</a></li> <li><a href="/w/index.php?title=Tubuloside_B&action=edit&redlink=1" class="new" title="Tubuloside B (page does not exist)">Tubuloside B</a></li> <li><a href="/wiki/Verbascoside" title="Verbascoside">Verbascoside</a> (<a href="/w/index.php?title=Isoverbascoside&action=edit&redlink=1" class="new" title="Isoverbascoside (page does not exist)">Isoverbascoside</a>, <a href="/w/index.php?title=2%27-Acetylverbascoside&action=edit&redlink=1" class="new" title="2'-Acetylverbascoside (page does not exist)">2′-Acetylverbascoside</a>)</li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Oligomeric forms</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%">Dimers</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/Diferulic_acids" title="Diferulic acids">Diferulic acids</a> (DiFA) : <a href="/w/index.php?title=5,5%27-Diferulic_acid&action=edit&redlink=1" class="new" title="5,5'-Diferulic acid (page does not exist)">5,5′-Diferulic acid</a>, <a href="/w/index.php?title=8-O-4%27-Diferulic_acid&action=edit&redlink=1" class="new" title="8-O-4'-Diferulic acid (page does not exist)">8-<i>O</i>-4′-Diferulic acid</a>, <a href="/wiki/8,5%27-Diferulic_acid" title="8,5'-Diferulic acid">8,5′-Diferulic acid</a>, <a href="/wiki/8,5%27-DiFA_(DC)" class="mw-redirect" title="8,5'-DiFA (DC)">8,5′-DiFA (DC)</a>, <a href="/w/index.php?title=8,5%27-DiFA_(BF)&action=edit&redlink=1" class="new" title="8,5'-DiFA (BF) (page does not exist)">8,5′-DiFA (BF)</a>, <a href="/w/index.php?title=8,8%27-Diferulic_acid&action=edit&redlink=1" class="new" title="8,8'-Diferulic acid (page does not exist)">8,8′-Diferulic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Trimers</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/Triferulic_acid" title="Triferulic acid">Triferulic acids</a> : <a href="/w/index.php?title=5-5%27,8%27-O-4%22-Triferulic_acid&action=edit&redlink=1" class="new" title="5-5',8'-O-4"-Triferulic acid (page does not exist)">5-5′,8′-<i>O</i>-4″-Triferulic acid</a></li></ul> </div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Tetramers</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=Tetraferulic_acid&action=edit&redlink=1" class="new" title="Tetraferulic acid (page does not exist)">Tetraferulic acids</a></li></ul> </div></td></tr></tbody></table><div></div></td></tr><tr><th scope="row" class="navbox-group" style="width:1%">Conjugates with<br /><a href="/wiki/Coenzyme_A" title="Coenzyme A">coenzyme A</a> (CoA)</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="/w/index.php?title=Caffeoyl-CoA&action=edit&redlink=1" class="new" title="Caffeoyl-CoA (page does not exist)">Caffeoyl-CoA</a></li> <li><a href="/wiki/Cinnamoyl-CoA" title="Cinnamoyl-CoA">Cinnamoyl-CoA</a></li> <li><a href="/wiki/Coumaroyl-CoA" title="Coumaroyl-CoA">Coumaroyl-CoA</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 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