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| Names | |
|---|---|
| IUPAC name (2R,3R)-7-(β-D-Glucopyranosyloxy)-3,4′,5-trihydroxy-8-(3-methylbut-2-en-1-yl)flavan-4-one | |
| Systematic IUPAC name (2R,3R)-3,5-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-en-1-yl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-4H-1-benzopyran-4-one | |
| Other names | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChemSpider |
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| KEGG |
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| MeSH | C016043 |
| UNII | |
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| Properties | |
| C26H30O11 | |
| Molar mass | 518.515 g·mol−1 |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Phellamurin, a flavonoid, is the 7-O-β-D-glucopyranoside, 8-C-prenyl derivative of theflavan-on-olAromadendrin,[1] and may be seen as the 7-O-glucoside ofnoricaritin.[2] Being a flavanonol, it has two stereocenters on the C-ring, so four stereoisomers of phellamurin are possible.
It can be found inCommiphora africana[3] and inPhellodendron amurense.[4]
6"′-O-acetyl phellamurin is found in the leaves ofPhellodendron japonicum.[5]
Media related toPhellamurin at Wikimedia Commons
