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Chrysoeriol

From Wikipedia, the free encyclopedia
Chrysoeriol
Names
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)
ChemSpider
ECHA InfoCard 100.007.039 Edit this at Wikidata
UNII
  • InChI=1S/C16H12O6/c1-21-14-4-8(2-3-10(14)18)13-7-12(20)16-11(19)5-9(17)6-15(16)22-13/h2-7,17-19H,1H3
    Key: SCZVLDHREVKTSH-UHFFFAOYSA-N
  • InChI=1/C16H12O6/c1-21-14-4-8(2-3-10(14)18)13-7-12(20)16-11(19)5-9(17)6-15(16)22-13/h2-7,17-19H,1H3
    Key: SCZVLDHREVKTSH-UHFFFAOYAS
  • COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O
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).

Chrysoeriol is a flavone, chemically the 3'-methoxy derivative of luteolin.

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Diosmetin is one of three possible regioisomers of chrysoeriol.

Natural sources

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Found in Artemisia.

Pharmacodynamics

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Vasorelaxant and hypotensive activity in vitro and in vivo in a murine model by intravenous infusion.[1]

See also

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References

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  1. ^ Gorzalczany, S; Moscatelli, V; Ferraro, G (2013). "Artemisia copa aqueous extract as vasorelaxant and hypotensive agent". J Ethnopharmacol. 148 (1): 56–61. doi:10.1016/j.jep.2013.03.061. PMID 23588093.
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