Centaureidin
From Self-sufficiency
| Centaureidin | |
|---|---|
| Chemical structure of centaureidin | |
| 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,6-dimethoxychromen-4-one | |
| Other names Desmethoxycentaureidine 5,7,3'-Trihydroxy-3,6,4'-trimethoxyflavone | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 17313-52-9 |
| PubChem | 5315773 |
| SMILES | Script error: No such module "collapsible list". |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C18H16O8 |
| Molar mass | 360.31 g/mol |
| Exact mass | 360.084517 u |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Centaureidin is an O-methylated flavonol. It can be isolated from Tanacetum microphyllum, Brickellia veronicaefolia, Bidens pilosa[1] and Polymnia fruticosa[2].
Glycosides
References
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- ↑ Flavonoids, centaurein and centaureidin, from Bidens pilosa, stimulate IFN-γ expression. Shu-Lin Chang, Yi-Ming Chiang, Cicero Lee-Tian Chang, Hsu-Hua Yeh, Lie-Fen Shyur, Yueh-Hsiung Kuo, Tung-Kung Wu and Wen-Chin Yang, Journal of Ethnopharmacology, Volume 112, Issue 2, 13 June 2007, Pages 232-236
- ↑ Centaureidin, a cytotoxic flavone from Polymnia fruticosa, inhibits tubulin polymerization. John A. Beutler, John H. Cardellina, Chii M. Lin, Ernest Hamel, Gordon M. Cragg and Michael R. Boyd, Bioorganic & Medicinal Chemistry Letters, Volume 3, Issue 4, April 1993, Pages 581-584
