Ombuin
From Self-sufficiency
Ombuin | |
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Chemical structure of ombuin | |
3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxychromen-4-one | |
Other names 4',7-Dimethylquercetin 7,4'-Di-O-methylquercetin 4',7-Dimethoxy-3,3',5-trihydroxyflavone | |
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
CAS number | 529-40-8 |
PubChem | 5320287 |
SMILES | Script error: No such module "collapsible list". |
style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
Molecular formula | C17H14O7 |
Molar mass | 330.29 g/mol |
Exact mass | 330.073953 u |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Infobox references |
Ombuin is an O-methylated flavonol, a type of flavonoid. It is the 4',7-O-methyl derivative of quercetin.
Ombuin can be found in species of the genus Erythroxylum. It can also be synthetized[1]. Ombuin 3-sulfate can be isolated from Flaveria chloraefolia[2].
Glycosides
Ombuin-3-rutinoside can be isolated from Phytolacca dioica, the ombu tree[3]. Ombuin-3-O-rhamnosylglucoside can be found in Erythroxylum rufum[4].
Other glycosides (ombuosides) :
- Ombuin 3-galactoside (C23H24O12, CAS number 69168-13-4)
- Ombuin 3-glucoside (C23H24O12, CAS number 158642-42-3)
References
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- ↑ Partial methylation of quercetin: Direct synthesis of tamarixetin, ombuin and ayanin. Koppaka V. Rao, Jacob A. Owoyale, Journal of Heterocyclic Chemistry, Volume 13 Issue 6, Pages 1293 - 1295
- ↑ Ombuin 3-sulphate from Flaveria chloraefolia. Phytochemistry, Volume 27, Issue 7, 1988, Pages 2362-2363, Denis Barron, Ragai K. Ibrahim
- ↑ Über die Synthese von Quercetin-3-glykosiden, II. Synthese des Ombuosids und eine rationelle Synthese von Rutin. Ludwig Hörhammer, Hildebert Wagner, Hans-Günther Arndt, Gustav Hitzler, Lorand Farkas, Chemische Berichte, Volume 101 Issue 4, Pp 1183-1185, 1968 (German)
- ↑ flavonoids of Erythroxylum rufum and Erythroxylum ulei. Bruce A. Bohm, David W. Phillips and Fred R. Gander, J. Nat. Prod., 1981, 44 (6), pp 676–679