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data-v-7724c9dd>Simple</li></a><a href="/StructureSearch" class="" id="menu-structure" data-v-7724c9dd><li class="nav-item" data-v-7724c9dd>Structure</li></a><a href="/AdvancedSearch" class="" id="menu-advanced" data-v-7724c9dd><li class="nav-item" data-v-7724c9dd>Advanced</li></a></ul></div></header></div><div class="sidenav-container" data-v-c6aa881c data-v-b3571781></div><div class="all" data-v-c6aa881c><section class="divisor" data-v-c6aa881c><div class="result-sections" data-v-8b58e9d6><div class="result-content" data-v-8b58e9d6><div class="result-item" data-v-8b58e9d6><div class="mobile-block" data-v-8b58e9d6><div class="compound-title" data-v-8b58e9d6><h4 class="ellipsis" id="cmp-title-label" data-v-8b58e9d6>Scilliroside</h4></div></div><div class="item-image" data-v-8b58e9d6><div id="div-svg" data-v-8b58e9d6></div></div><div class="info-buttons-mobile" data-v-8b58e9d6><button id="button-download-mobile" class="button darkblue-button button1" data-v-8b58e9d6>Download .mol <img 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src="/_nuxt/infoDarkBlue140.ea80f8c6.svg" loading="lazy" alt="download-icon" data-v-8b58e9d6></button></span><table class="" data-v-8b58e9d6><tr data-v-8b58e9d6><td class="header" id="molecular-fml-label" data-v-8b58e9d6>Molecular formula:</td><td class="molecular-formula" id="molecular-fml-value" data-v-8b58e9d6>C<span style='vertical-align:sub'>32</span>H<span style='vertical-align:sub'>44</span>O<span style='vertical-align:sub'>12</span></td></tr><tr data-v-8b58e9d6><td class="header" id="avg-mass-label" data-v-8b58e9d6>Average mass:</td><td id="avg-mass-value" data-v-8b58e9d6>620.692</td></tr><tr data-v-8b58e9d6><td class="header" id="monoisotopic-mass-label" data-v-8b58e9d6>Monoisotopic mass:</td><td id="monoisotopic-mass-value" data-v-8b58e9d6>620.283277</td></tr><tr data-v-8b58e9d6><td class="header" id="cmp-id-label" data-v-8b58e9d6>ChemSpider ID:</td><td id="cmp-id-value" data-v-8b58e9d6>390447</td></tr></table><div class="icons-container" data-v-8b58e9d6><div class="icon" data-v-dfbcea86><img src="/_nuxt/search-stereocenter-icon.c5b3e873.svg" alt="stereocenter-icon" style="width:25px;height:25px;" data-v-dfbcea86><p data-v-dfbcea86>13 of 13 defined stereocentres </p></div><div class="icon" data-v-dfbcea86><img src="/_nuxt/search-wikipedia-icon.d29c987d.svg" alt="wikipedia-icon" style="width:25px;height:25px;" data-v-dfbcea86><p data-v-dfbcea86>Wikipedia</p></div></div></div><div class="info-buttons-desktop" data-v-8b58e9d6><button id="button-download" class="button darkblue-button" data-v-8b58e9d6> Download .mol <img class="download-icon" src="/_nuxt/download.18c2a6e1.svg" alt="download-icon" loading="lazy" data-v-8b58e9d6></button><button id="button-cite-record" class="button darkblue-button" data-v-8b58e9d6> Cite this record <img class="download-icon" src="/_nuxt/blankPage.8f22336f.svg" alt="download-icon" loading="lazy" data-v-8b58e9d6></button><a href="https://legacy.chemspider.com/Chemical-Structure.390447.html" target="_blank" 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data-v-79d9d332><div class="v-expansion-panel__shadow"></div><button class="v-expansion-panel-title expansion-panel-title" style="" type="button" aria-expanded="false" id="accordion-structural-identifiers-title" data-v-79d9d332><span class="v-expansion-panel-title__overlay"></span><div class="title disabled-accordion-title" data-v-79d9d332><img class="plus-icon" src="/_nuxt/Plus.fed13eb2.svg" alt="plus-icon" loading="lazy" data-v-79d9d332><img class="less-icon" src="/_nuxt/Less.4b527497.svg" alt="less-icon" loading="lazy" data-v-79d9d332><span data-v-79d9d332>Structural identifiers</span><div class="line" data-v-79d9d332></div></div><span class="v-expansion-panel-title__icon"><i class="none mdi v-icon notranslate v-theme--light v-icon--size-default" style="" aria-hidden="true"></i></span></button><div class="v-expansion-panel-text" style="display:none;" data-v-79d9d332></div></div></div><div data-v-8b58e9d6><div class="item-options" data-v-b98185ac><ul class="options-list" data-v-b98185ac><li class="option-active option" id="tab0" data-v-b98185ac>Names <span data-v-b98185ac><img src="/_nuxt/downArrow.e3348a8d.svg" alt="down_Arrow" loading="lazy" class="drop-down-icon" data-v-b98185ac></span></li></ul></div><div class="selected-component" data-v-b98185ac><section class="names" data-v-b98185ac data-v-3ad33253><div class="accordion-margins" data-v-3ad33253><div class="v-expansion-panels v-theme--light v-expansion-panels--variant-default expansion-panels" id="Names-Accordion-0" data-v-3ad33253 data-v-79d9d332><div class="v-expansion-panel v-expansion-panel--active" style="" aria-expanded="true" data-v-79d9d332><div class="v-expansion-panel__shadow"></div><button class="v-expansion-panel-title v-expansion-panel-title--active expansion-panel-title" style="" type="button" aria-expanded="true" id="accordion-names-and-synonyms-title" data-v-79d9d332><span class="v-expansion-panel-title__overlay"></span><div class="title enabled-accordion-title" data-v-79d9d332><img class="plus-icon" src="/_nuxt/Plus.fed13eb2.svg" alt="plus-icon" loading="lazy" data-v-79d9d332><img class="less-icon" src="/_nuxt/Less.4b527497.svg" alt="less-icon" loading="lazy" data-v-79d9d332><span data-v-79d9d332>Names and synonyms</span><div class="line" data-v-79d9d332></div></div><span class="v-expansion-panel-title__icon"><i class="none mdi v-icon notranslate v-theme--light v-icon--size-default" style="" aria-hidden="true"></i></span></button><div class="v-expansion-panel-text" data-v-79d9d332><div class="v-expansion-panel-text__wrapper"><div class="names-and-synonyms" name="Names and synonyms" data-v-79d9d332 data-v-176fa3f8><h5 id="verified-synonyms-label" data-v-176fa3f8>Verified</h5><p class="result" id="verified-synonym-(3b,6b)-6-(acetyloxy)-3-(b-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide" data-v-176fa3f8>(3b,6b)-6-(Acetyloxy)-3-(b-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide </p><p class="result" id="verified-synonym-(3s,6r,8s,9r,10r,13r,14r,17r)-8,14-dihydroxy-10,13-dimethyl-17-(2-oxo-2h-pyran-5-yl)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl]oxy}-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-6-yl-acetate" data-v-176fa3f8>(3S,6R,8S,9R,10R,13R,14R,17R)-8,14-Dihydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl acetate </p><p class="result" id="verified-synonym-(3尾,6尾)-6-(acetyloxy)-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide-(9ci)" data-v-176fa3f8>(3尾,6尾)-6-(Acetyloxy)-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide (9CI) </p><p class="result" id="verified-synonym-(3尾,6尾)-6-acetoxy-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolid" data-v-176fa3f8>(3尾,6尾)-6-Acetoxy-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolid <span class="flag" data-v-176fa3f8> [German] </span><span class="flag" id="verified-synonym-(3尾,6尾)-6-acetoxy-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolid-ACD/IUPAC Name" data-v-176fa3f8> [ACD/IUPAC Name] </span></p><p class="result" id="verified-synonym-(3尾,6尾)-6-acetoxy-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide" data-v-176fa3f8>(3尾,6尾)-6-Acetoxy-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide <span class="flag" id="verified-synonym-(3尾,6尾)-6-acetoxy-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide-ACD/IUPAC Name" data-v-176fa3f8> [ACD/IUPAC Name] </span></p><p class="result" id="verified-synonym-(3尾,6尾)-6-ac茅toxy-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-tri猫nolide" data-v-176fa3f8>(3尾,6尾)-6-Ac茅toxy-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-tri猫nolide </p><p class="result" id="verified-synonym-(3尾,6尾)-6-ac茅toxy-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-tri茅nolide" data-v-176fa3f8>(3尾,6尾)-6-Ac茅toxy-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-tri茅nolide <span class="flag" data-v-176fa3f8> [French] </span><span class="flag" id="verified-synonym-(3尾,6尾)-6-ac茅toxy-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-tri茅nolide-ACD/IUPAC Name" data-v-176fa3f8> [ACD/IUPAC Name] </span></p><p class="result" id="verified-synonym-208-077-4" data-v-176fa3f8>208-077-4 <span class="flag" id="verified-synonym-208-077-4-EINECS" data-v-176fa3f8> [EINECS] </span></p><p class="result" id="verified-synonym-2815004nho" data-v-176fa3f8>2815004NHO <span class="flag" id="verified-synonym-2815004nho-UNII" data-v-176fa3f8> [UNII] </span></p><p class="result" id="verified-synonym-507-60-8" data-v-176fa3f8>507-60-8 <span class="flag" id="verified-synonym-507-60-8-RN" data-v-176fa3f8> [RN] </span></p><p class="result" id="verified-synonym-6-尾-(acetyloxy)-3-尾-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide" data-v-176fa3f8>6-尾-(Acetyloxy)-3-尾-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide </p><p class="result" id="verified-synonym-6尾-(acetyloxy)-3-尾-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide" data-v-176fa3f8>6尾-(Acetyloxy)-3-尾-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide </p><p class="result" id="verified-synonym-bufa-4,20,22-trienolide,-6--(acetyloxy)-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxy-,-(3尾,6尾)-" data-v-176fa3f8>Bufa-4,20,22-trienolide, 6- (acetyloxy)-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxy-, (3尾,6尾)- </p><p class="result" id="verified-synonym-bufa-4,20,22-trienolide,-6-(acetyloxy)-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxy-,-(3尾,6尾)-" data-v-176fa3f8>Bufa-4,20,22-trienolide, 6-(acetyloxy)-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxy-, (3尾,6尾)- <span class="flag" id="verified-synonym-bufa-4,20,22-trienolide,-6-(acetyloxy)-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxy-,-(3尾,6尾)--ACD/Index Name" data-v-176fa3f8> [ACD/Index Name] </span></p><p class="result" id="verified-synonym-scilliroside" data-v-176fa3f8>Scilliroside <span class="wiki-flag" data-v-176fa3f8><a target="_blank" href="https://en.wikipedia.org/wiki/Scilliroside" id="verified-synonym-scilliroside-Wiki" data-v-176fa3f8> [Wiki] <img src="/_nuxt/search-link.b5935a3d.svg" alt="link-icon" loading="lazy" id="verified-synonym-scilliroside-link-icon" data-v-176fa3f8></a></span></p><h5 id="unverified-synonyms-label" data-v-176fa3f8>Unverified</h5><p class="result" id="unverified-synonym-(3尾,6尾)-6-(acetyloxy)-3-(尾-d-glucopyranosyloxy)-8,14-di--hydroxybufa-4,20,22-trienolide" data-v-176fa3f8>(3尾,6尾)-6-(ACETYLOXY)-3-(尾-D-GLUCOPYRANOSYLOXY)-8,14-DI- HYDROXYBUFA-4,20,22-TRIENOLIDE </p><p class="result" id="unverified-synonym-(3尾,6尾)-6-(acetyloxy)-3-(尾-d-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide" data-v-176fa3f8>(3尾,6尾)-6-(Acetyloxy)-3-(尾-D-glucopyranosyloxy)-8,14-dihydroxybufa-4,20,22-trienolide </p><p class="result" id="unverified-synonym-3-o-(尾-d-glucopyranosyl)-6尾-acetoxy-3尾,8尾,14尾-trihydroxybufa-4,20,22-trienolide" data-v-176fa3f8>3-O-(尾-D-glucopyranosyl)-6尾-acetoxy-3尾,8尾,14尾-trihydroxybufa-4,20,22-trienolide </p><p class="result" id="unverified-synonym-3尾-(尾-d-glucopyranosyloxy)-17尾-(2-oxo-2h-pyran-5-yl)-14尾-androst-4-ene-6尾,8,14-triol-6-acetate" data-v-176fa3f8>3尾-(尾-D-glucopyranosyloxy)-17尾-(2-oxo-2H-pyran-5-yl)-14尾-androst-4-ene-6尾,8,14-triol 6-acetate </p><p class="result" id="unverified-synonym-red-squill" data-v-176fa3f8>Red Squill </p><p class="result" id="unverified-synonym-scillirosidin-3-o-glucoside" data-v-176fa3f8>Scillirosidin 3-O-glucoside </p><p class="result" id="unverified-synonym-scillirosidin-3-o-尾-d-glucoside" data-v-176fa3f8>Scillirosidin 3-O-尾-D-glucoside </p><p class="result" id="unverified-synonym-sea-onion" data-v-176fa3f8>sea onion </p><p class="result" id="unverified-synonym-silliroside" data-v-176fa3f8>Silliroside </p><p class="result" id="unverified-synonym-squill" data-v-176fa3f8>squill </p></div></div></div></div></div></div><div class="accordion-margins" data-v-3ad33253><div class="v-expansion-panels v-theme--light v-expansion-panels--variant-default expansion-panels" id="Names-Accordion-1" data-v-3ad33253 data-v-79d9d332><div class="v-expansion-panel" style="" aria-expanded="false" data-v-79d9d332><div class="v-expansion-panel__shadow"></div><button class="v-expansion-panel-title expansion-panel-title" style="" type="button" aria-expanded="false" id="accordion-database-ids-title" data-v-79d9d332><span class="v-expansion-panel-title__overlay"></span><div class="title disabled-accordion-title" data-v-79d9d332><img class="plus-icon" src="/_nuxt/Plus.fed13eb2.svg" alt="plus-icon" loading="lazy" 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