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Pratensein

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Pratensein
Chemical structure of pratensein
Pratensein molecule
Names
IUPAC name 3′,5,7-Trihydroxy-4′-methoxyisoflavone
Systematic IUPAC name 5,7-Dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one
Other names 4′-Methoxy-3′,5,7-trihydroxyisoflavone
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.347.521 Edit this at Wikidata
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C16H12O6/c1-21-13-3-2-8(4-11(13)18)10-7-22-14-6-9(17)5-12(19)15(14)16(10)20/h2-7,17-19H,1H3Key: FPIOBTBNRZPWJW-UHFFFAOYSA-N
  • InChI=1/C16H12O6/c1-21-13-3-2-8(4-11(13)18)10-7-22-14-6-9(17)5-12(19)15(14)16(10)20/h2-7,17-19H,1H3Key: FPIOBTBNRZPWJW-UHFFFAOYAF
SMILES
  • COC1=C(C=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O
Properties
Chemical formula C16H12O6
Molar mass 300.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Pratensein is an O-methylated isoflavone, a type of flavonoid. It can be found in Trifolium pratense (red clover) and can have effects for the prevention of atherosclerosis.

References

  1. Isoflavone contents of red and subterranean clovers. E. Wong, Journal of the Science of Food and Agriculture, Volume 14 Issue 6, Pages 376-379
  2. Characterization of the Isoflavone Pratensein as a Novel Transcriptional Up-Regulator of Scavenger Receptor Class B Type I in HepG2 Cells. Yang Yuan, JIiang Wei, Wang Li, Hang Zhong-Bing, Si Shu-Yi and Hong Bin, Biological & pharmaceutical bulletin, 2009, vol. 32, no7, pp. 1289-1294
Isoflavones and their glycosides
Isoflavones
O-methylated isoflavones
Glycosides
Prenylated isoflavones
Pyranoisoflavones
Derivatives
Synthetic
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