Axillarin
Names | |
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IUPAC name
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 | |
Identifiers | |
5188-73-8 = | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:2941 |
ChEMBL | ChEMBL487810 |
ChemSpider | 4444922 |
PubChem | 5281603 |
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Properties | |
C17H14O8 | |
Molar mass | 346.28 g/mol |
Density | 1.659 g/mL |
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 | |
Axillarin is an O-methylated flavonol. It can be found in Pulicaria crispa, Filifolium sibiricum, Inula britannica,[1] Wyethia bolanderi in Balsamorhiza macrophylla[2] and in Tanacetum vulgare.[3] It can also be synthetized.[4]
Glycosides
Axillarin 7-O-β-D-glucoside can be found in Tagetes mendocina, a medicinal plant widely used in the Andean provinces of Argentina.[5]
References
- ↑ 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
- ↑ Álvarez, Ángel L.; Habtemariam Solomon; Juan-Badaturuge Malindra; Jackson Caroline; Parra Francisco (2011). "In vitro anti HSV-1 and HSV-2 activity of Tanacetum vulgare extracts and isolated compounds: An approach to their mechanisms of action". Phytotherapy Research. 25 (2): 296–301. doi:10.1002/ptr.3382. PMID 21171142.
- ↑ 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.
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