Prenylated flavonoids as tyrosinase inhibitors

Arch Pharm Res. 2004 Nov;27(11):1132-5. doi: 10.1007/BF02975118.

Abstract

In order to find new tyrosinase inhibitors and the effects of prenyl residue on flavonoid molecules, eight prenylated and three synthetic vinylated flavonoids were examined on their inhibitory effect against tyrosinase activity. From the results, kuwanon C, papyriflavonol A, sanggenon D and sophoflavescenol were found to possess the considerable inhibitory activity. Especially, sanggenon D is revealed as a potent inhibitor (IC50 = 7.3 microM), compared to the reference compound, kojic acid (IC50 = 24.8 microM). However, the prenylation with isoprenyl group or the vinylation to flavonoid molecules did not enhance tyrosinase inhibitory activity.

Publication types

  • Comparative Study

MeSH terms

  • Agaricales / enzymology
  • Dose-Response Relationship, Drug
  • Fabaceae / chemistry
  • Flavonoids / chemistry
  • Flavonoids / pharmacology*
  • Kinetics
  • Monophenol Monooxygenase / antagonists & inhibitors
  • Monophenol Monooxygenase / metabolism
  • Moraceae / chemistry
  • Peptides / chemistry
  • Peptides / pharmacology*
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Protein Prenylation

Substances

  • Flavonoids
  • Peptides
  • Plant Extracts
  • sophoflavescenol
  • Monophenol Monooxygenase