Estrone and estradiol C-16 derivatives as inhibitors of type 1 17beta-hydroxysteroid dehydrogenase

Mol Cell Endocrinol. 2006 Mar 27;248(1-2):236-8. doi: 10.1016/j.mce.2005.10.017. Epub 2005 Dec 7.

Abstract

Three series of steroid derivatives, enones 1, enols 2 and saturated alcohols 3, were easily synthesized from estrone according to a sequence of three reactions: an aldol condensation with an aromatic aldehyde (R(a-g)CHO) to afford 1, the carbonyl reduction of 1 to obtain the enol 2, and the double bond reduction of 2 to give 3 with the R(a-g) group 16beta-oriented. All compounds were tested as inhibitors of type 1 17beta-HSD. The inhibitory potency increases in the following order 1<2<3, suggesting that the presence of a flexible 16beta-methylene group allows a better positioning of the aryl moiety. With an IC50 of 0.8 microM, the 16beta-benzyl-E2 (3a) is the best inhibitor in this series.

MeSH terms

  • Alcohols / chemical synthesis
  • Alcohols / chemistry
  • Alcohols / pharmacology
  • Cyclohexanones / chemical synthesis
  • Cyclohexanones / chemistry
  • Cyclohexanones / pharmacology
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Estradiol / analogs & derivatives*
  • Estradiol / chemistry
  • Estradiol Dehydrogenases / antagonists & inhibitors*
  • Estradiol Dehydrogenases / chemistry
  • Estrone / analogs & derivatives*
  • Estrone / chemistry
  • Humans
  • Protein Conformation

Substances

  • Alcohols
  • Cyclohexanones
  • Enzyme Inhibitors
  • Estrone
  • Estradiol
  • Estradiol Dehydrogenases