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Chrysoeriol

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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
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.039 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • 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,1H3Key: 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,1H3Key: SCZVLDHREVKTSH-UHFFFAOYAS
SMILES
  • COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O
Properties
Chemical formula C16H12O6
Molar mass 300.266 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

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

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.

See also

References

  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.

External links

Flavones and their conjugates
Aglycones
Monohydroxyflavone
Dihydroxyflavones
Trihydroxyflavones
Tetrahydroxyflavones
Pentahydroxyflavones
O-methylated flavones
Glycosides
of apigenin
of baicalein
of hypolaetin
of luteolin
Acetylated
  • Artocarpetin A
  • Artoindonesianin P
  • Sulfated glycosidesTheograndin I and II
    Polymers
    Drugs


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