Axillarin
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| Axillarin | |
|---|---|
| Chemical structure of axillarin | |
| 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxychromen-4-one | |
| Other names DMQT 3,6-Dimethoxyquercetagetin Quercetagetin 3,6-dimethyl ether 3',4',5,7-Tetrahydroxy-3,6-dimethoxyflavone | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 5188-73-8 |
| PubChem | 5281603 |
| SMILES | Script error: No such module "collapsible list". |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C17H14O8 |
| Molar mass | 346.28 g/mol |
| Exact mass | 346.068867 u |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Axillarin is an O-methylated flavonol. It can be found in Pulicaria crispa, Filifolium sibiricum, Inula britannica[1], Wyethia bolanderi and in Balsamorhiza macrophylla[2]. It can also be synthetized[3].
Glycosides
Axillarin 7-O-β-D-glucoside can be found in Tagetes mendocina, a medicinal plant widely used in the Andean provinces of Argentina[4].
References
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- ↑ Acylated Flavonol Glycosides from the Flower of Inula britannica. Eun Jung Park, Youngleem Kim, and Jinwoong Kim, J. Nat. Prod., 2000, 63 (1), pp 34–36
- ↑ Methylated flavonols from Wyethia bolanderi and Balsamorhiza macrophylla. Susan McCormick, Kathleen Robson and Bruce Bohm, Phytochemistry, Volume 24, Issue 9, 1985, Page 2133
- ↑ The syntheses of axillarin and its related compounds. K. Fukui, M. Nakayama and T. Horie, Cellular and Molecular Life Sciences, Volume 24, Number 8 / august 1968, Pages 769-770
- ↑ Free Radical Scavengers and Antioxidants from Tagetes mendocina. Guillermo Schmeda-Hirschmann, Alejandro Tapia, Cristina Theoduloz, Jaime Rodrıguez, Susana Lopez and Gabriela Egly Feresin.
