Chrysoeriol
Chemical compound From Wikipedia, the free encyclopedia
Chrysoeriol is a flavone, chemically the 3'-methoxy derivative of luteolin.
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Names | |
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IUPAC name
4′,5,7-Trihydroxy-3′-methoxyflavone | |
Systematic IUPAC name
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
ECHA InfoCard | 100.007.039 |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C16H12O6 | |
Molar mass | 300.266 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Related compounds
Diosmetin is one of three possible regioisomers of chrysoeriol.
Natural sources
Found in Artemisia.
Pharmacodynamics
Vasorelaxant and hypotensive activity in vitro and in vivo in a murine model by intravenous infusion.[1]
See also
- Cannflavins, prenylated derivatives of chrysoeriol
References
External links
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