Phellamurin

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search
Phellamurin
Phellamurin.svg
Names
IUPAC name
(2R,3R)-3,5-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one
Other names
Fellavine
8-Prenyldihydrokaempferol 7-glucoside
Epimedoside C
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
MeSH C016043
Properties
C26H30O11
Molar mass 518.52 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is ☑Y☒N ?)
Infobox references

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]


Related compounds[edit]

6"′-O-acetyl phellamurin is found in the leaves of Phellodendron japonicum.[5]


References[edit]

External links[edit]