Curcumin derivatives inhibit testicular 17beta-hydroxysteroid dehydrogenase 3

Bioorg Med Chem Lett. 2010 Apr 15;20(8):2549-51. doi: 10.1016/j.bmcl.2010.02.089. Epub 2010 Mar 1.

Abstract

Non-steroidal compounds that inhibit 17beta-hydroxysteroid dehydrogenase isoform 3 (17beta-HSD3), an enzyme catalyzing the final step in testosterone biosynthesis in Leydig cells, are under development for male contraceptive or treatment of androgen dependent diseases including prostate cancer. A series of curcumin analogues with more stable chemical structures were compared to curcumin as inhibitors of 17beta-HSD3 in rat intact Leydig cells as well as rat and human testis microsomes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 17-Hydroxysteroid Dehydrogenases / antagonists & inhibitors*
  • Animals
  • Curcumin / analogs & derivatives*
  • Curcumin / pharmacology
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Male
  • Rats
  • Testis / drug effects*
  • Testis / enzymology

Substances

  • Enzyme Inhibitors
  • 17-Hydroxysteroid Dehydrogenases
  • 17beta-hydroxysteroid dehydrogenase type 3
  • Curcumin