Resveratroloside
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Names
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IUPAC name
4-[(E)-2-(3,5-Dihydroxyphenyl)ethen-1-yl]phenyl β-D-glucopyranoside
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Systematic IUPAC name
(2S,3R,4S,5S,6R)-2-{4-[(E)-2-(3,5-Dihydroxyphenyl)ethen-1-yl]phenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol
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Other names
trans-Resveratrol-4'-O-beta-D-glucopyranoside (E)-Resveratroloside; 3,5,4'-Trihydroxystilbene-4'-glucoside
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Identifiers
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ChemSpider
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UNII
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InChI=1S/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-5-3-11(4-6-15)1-2-12-7-13(22)9-14(23)8-12/h1-9,16-26H,10H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1 Key: RUOKEYJFAJITAG-CUYWLFDKSA-N InChI=1/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-5-3-11(4-6-15)1-2-12-7-13(22)9-14(23)8-12/h1-9,16-26H,10H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1 Key: RUOKEYJFAJITAG-CUYWLFDKBI
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C1=CC(=CC=C1/C=C/C2=CC(=CC(=C2)O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
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Properties
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C20H22O8
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Molar mass
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390.388 g·mol−1
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Resveratroloside is a stilbenoid glucoside. It can be found in Paeonia lactiflora.[1]
References
External links
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Dihydroxylated | |
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Trihydroxylated | |
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Tetrahydroxylated | |
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O-methylated | |
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carboxylated | |
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other acylations | |
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Glycosides | | of resveratrol | |
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of rhapontigenin | |
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Oligomeric forms | |
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