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Pinocembrin

From Wikipedia, the free encyclopedia
Pinocembrin
Names
IUPAC name
5,7-Dihydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one
Other names
Dihydrochrysin
Galangin flavanone
5,7-Dihydroxyflavanone
5,7-Dihydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-
5,7-Dihydroxy-2-phenyl-chroman-4-one
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
  • InChI=1S/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2 checkY
    Key: URFCJEUYXNAHFI-UHFFFAOYSA-N checkY
  • InChI=1/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2
    Key: URFCJEUYXNAHFI-UHFFFAOYAA
  • O=C2c3c(OC(c1ccccc1)C2)cc(O)cc3O
Properties
C15H12O4
Molar mass256.257 g·mol−1
Density1.386 g/mL
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Pinocembrin is aflavanone, a type offlavonoid. It is anantioxidant found indamiana,[1]honey,fingerroot,[2] andpropolis.[3]

Pinocembrin can be convertedbiosynthetically topinobanksin byhydroxylation.

See also

[edit]

References

[edit]
  1. ^Zhao, J; Dasmahapatra AK; Khan SI; Khan IA (Dec 2008). "Anti-aromatase activity of the constituents from damiana (Turnera diffusa)".J Ethnopharmacol.120 (3):387–393.doi:10.1016/j.jep.2008.09.016.PMID 18948180.
  2. ^Punvittayagul, C; Wongpoomchai R; Taya S; Pompimon W. (January 2011). "Effect of pinocembrin isolated from Boesenbergia pandurata on xenobiotic-metabolizing enzymes in rat liver".Drug Metabolism Letters.5 (1):1–5.doi:10.2174/187231211794455226.PMID 20942797.
  3. ^Bosio K; Avanzini C; D’Avolio A; Ozino O; Savoia D (2000). "In vitro activity of propolis against Streptococcus pyogenes".Letters in Applied Microbiology.31 (2):174–177.doi:10.1046/j.1365-2672.2000.00785.x.PMID 10972723.S2CID 1622868.

External links

[edit]
Flavanones and theirglycosides
Flavanones
O-methylated flavanones
C-methylated flavanones
Glycosides
Acetylated
Acetylated glycosides


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