6-Hydroxyflavone
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IUPAC name 6-Hydroxyflavone | |
Systematic IUPAC name 6-Hydroxy-2-phenyl-4H-1-benzopyran-4-one | |
Other names 6-Monohydroxyflavone; 6-Hydroxy-2-phenyl-4-benzopyrone | |
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ECHA InfoCard | 100.027.005 |
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Properties | |
Chemical formula | C15H10O3 |
Molar mass | 238.242 g·mol−1 |
Melting point | 234 to 236 °C (453 to 457 °F; 507 to 509 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
6-Hydroxyflavone is a flavone, a type of chemical compound. It is one of the noncompetitive inhibitors of cytochrome P450 2C9. It is reported in Crocus and leaves of Barleria prionitis Linn. (a common Acanthaceae from India).[1] 6-Hydroxyflavone shows anxiolytic activity in a mouse model.[2] Compared to the full agonist diazepam, 6-hydroxyflavone was approximately 200 times less potent.[2]
References
- ^ M Daniel (2006). Medicinal Plants: Chemistry and Properties. Science Publishers. p. 78. ISBN 978-1-57808-395-4.
- ^ a b Ren, Lihuan; Wang, Feng; Xu, Zhiwen; Chan, Wing Man; Zhao, Cunyou; Xue, Hong (2010), "GABAA receptor subtype selectivity underlying anxiolytic effect of 6-hydroxyflavone", Biochemical Pharmacology, 79 (9): 1337–1344, doi:10.1016/j.bcp.2009.12.024, PMID 20067772
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Flavones and their conjugates
Monohydroxyflavone |
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Dihydroxyflavones | |
Trihydroxyflavones | |
Tetrahydroxyflavones | |
Pentahydroxyflavones |
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O-methylated flavones |
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of apigenin | |
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of baicalein | |
of hypolaetin |
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of luteolin |
- Giraldiin A and B
- Nepitrin
- Oroxindin
- Scutellarin
Theograndin I and II
This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
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