Phellamurin
 | |
| 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 | |
| Identifiers | |
52589-11-4  | |
| 3D model (Jmol) | Interactive image |
| ChEBI | CHEBI:8048  |
| ChemSpider | 168247 |
| KEGG | C09808 |
| MeSH | C016043 |
| PubChem | 193876 |
| |
| |
| 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). | |
| verify (what is ?) | |
| Infobox references | |
Phellamurin is a flavanonol, a type of flavonoid. It can be found in Commiphora africana[1] and in Phellodendron amurense.[2]
Related compounds
6"′-O-acetyl phellamurin is found in the leaves of Phellodendron japonicum.[3]
References
- ↑ A Dihydroflavonol Glucoside from Commiphora africana that Mediates DNA Strand Scission, Ji Ma, Shannon H. Jones, and Sidney M. Hecht, 2005
- ↑ A flavonoid glucoside, phellamurin, regulates differential oviposition on a rutaceous plant, Phellodendron amurense, by two sympatric swallowtail butterflies, Papilio protenor and P. xuthus: The front line of a coevolutionary arms race? Keiichi Honda and Nanao Hayashi, 1995
- ↑ Constituents of Leaves of Phellodendron japonicum MAXIM. and Their Antioxidant Activity, Chih-Yang Chiu, Chia-Ying Li, Chao-Chen Chiu, Masatake Niwa, Susumu Kitanaka, Amooru Gangaiah Damu, E-Jian Lee and Tian-Shung Wu, 2005
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