Chalcones are potent inhibitors of aromatase and 17beta-hydroxysteroid dehydrogenase activities

Life Sci. 2001 Jan 5;68(7):751-61. doi: 10.1016/s0024-3205(00)00974-7.

Abstract

Chalcones were tested for estimating anti-aromatase, anti-3beta-hydroxysteroid dehydrogenase delta5/delta4 isomerase (3beta-HSD) and anti-17beta-hydroxysteroid dehydrogenase (17beta-HSD) activities in human placental microsomes. In the present study, we have demonstrated for the first time that chalcones are potent inhibitors of aromatase and 17beta-hydroxysteroid dehydrogenase activities: these enzymes being considered as important targets in the metabolic pathways of human mammary hormone-dependent cells. Our results showed that naringenin chalcone and 4-hydroxychalcone were the most effective aromatase and 17beta-hydroxysteroid dehydrogenase inhibitors with IC50 values of 2.6 and 16 microM respectively. In addition, inhibitory effects of some flavones and flavanones were compared to those of the corresponding chalcones. A structure-activity relationship was established and regions or/and substituents essential for these inhibitory activities were determined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 17-Hydroxysteroid Dehydrogenases / antagonists & inhibitors*
  • 3-Hydroxysteroid Dehydrogenases / antagonists & inhibitors
  • Androstenedione / metabolism
  • Aromatase Inhibitors*
  • Chalcone / chemistry
  • Chalcone / pharmacology*
  • Chromatography, High Pressure Liquid
  • Dehydroepiandrosterone / metabolism
  • Enzyme Inhibitors / pharmacology*
  • Estradiol / metabolism
  • Estrone / metabolism
  • Humans
  • In Vitro Techniques
  • Microsomes / drug effects
  • Microsomes / enzymology

Substances

  • Aromatase Inhibitors
  • Enzyme Inhibitors
  • Estrone
  • Androstenedione
  • Dehydroepiandrosterone
  • Estradiol
  • Chalcone
  • 17-Hydroxysteroid Dehydrogenases
  • 3-Hydroxysteroid Dehydrogenases