Eupatolitin
 | |
| Names | |
|---|---|
| IUPAC name 3,3′,4′,5-Tetrahydroxy-6,7-dimethoxyflavone | |
| Systematic IUPAC name 2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-6,7-dimethoxy-4H-1-benzopyran-4-one | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChemSpider | |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C17H14O8 | |
| Molar mass | 346.291 g·mol−1 |
| Density | 1.592 g/mL |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Eupatolitin is a chemical compound. It is an O-methylated flavonol, a type of flavonoid. Eupatolitin can be found in Brickellia veronicaefolia[1] and in Ipomopsis aggregata.[2]
Glycoside
[edit]Eupatolin is a eupatolitin glycoside containing a rhamnose attached at the 3 position. It can be found in Eupatorium ligustrinum.[3]
References
[edit]- ^ Roberts, Margaret F.; Timmermann, Barbara N.; Mabry, Tom J. (1980). "6-Methoxyflavonols from Brickellia veronicaefolia (compositae)". Phytochemistry. 19: 127–129. doi:10.1016/0031-9422(80)85028-X.
- ^ Smith, D.M.; Glennie, C.W.; Harborne, J.B. (1971). "Identification of eupalitin, eupatolitin and patuletin glycosides in Ipomopsis aggregata". Phytochemistry. 10 (12): 3115–3120. doi:10.1016/S0031-9422(00)97361-8.
- ^ Quijano, L.; Malanco, F.; Ríos, Tirso (1970). "The structures of eupalin and eupatolin. Two new flavonol rhamnosides isolated from Eupatorium ligustrinum D.C". Tetrahedron. 26 (12): 2851–2859. doi:10.1016/S0040-4020(01)92863-7.
External links
[edit]- Eupatolotin on www.genome.jp
 | This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |