Names | |
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IUPAC name
(2R,3R)-7-(β-D-Glucopyranosyloxy)-3,4′,5-trihydroxy-8-(3-methylbut-2-en-1-yl)flavan-4-one
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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)
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ChEBI | |
ChemSpider | |
KEGG | |
MeSH | C016043 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C26H30O11 | |
Molar mass | 518.515 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Phellamurin, a flavonoid, is the 7-O-β-D-glucopyranoside, 8-C-prenyl derivative of the flavan-on-ol Aromadendrin,[1] and may be seen as the 7-O-glucoside of noricaritin.[2] Being a flavanonol, it has two stereocenters on the C-ring, so four stereoisomers of phellamurin are possible.
It can be found in Commiphora africana[3] and in Phellodendron amurense.[4]
6"′-O-acetyl phellamurin is found in the leaves of Phellodendron japonicum.[5]
Flavanonols and their glycosides | |
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3-Hydroxyflavanones: |
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O-methylated flavanonols | |
dihydroflavonol 3-O-glycosides |
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Glycosides |
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Acetylated glycosides |