Synthesis and aromatase inhibitory activity of some new 16E-arylidenosteroids

Bioorg Chem. 2012 Dec:45:36-40. doi: 10.1016/j.bioorg.2012.08.005. Epub 2012 Sep 12.

Abstract

A new series of 16E-arylidene androstene derivatives has been synthesized and evaluated for aromatase inhibitory activity. The impact of various aryl substituents at 16 position of the steroid skeleton on aromatase inhibitory activity has been observed. The 16E-arylidenosteroids 6, 10 and 11 exhibited significant inhibition of the aromatase enzyme. 16-(4-Pyridylmethylene)-4-androstene-3,17-dione (6, IC(50): 5.2 μM) and 16-(benzo-[1,3]dioxol-5-ylmethylene)androsta-1,4-diene-3,17-dione (11, IC(50): 6.4 μM) were found to be approximately five times more potent in comparison to aminoglutethimide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminoglutethimide / chemistry
  • Aminoglutethimide / metabolism
  • Aminoglutethimide / pharmacology
  • Androstenes / chemistry
  • Aromatase / chemistry*
  • Aromatase / metabolism
  • Aromatase Inhibitors / chemical synthesis*
  • Aromatase Inhibitors / chemistry
  • Protein Binding
  • Steroids / chemical synthesis
  • Steroids / chemistry*
  • Steroids / metabolism

Substances

  • Androstenes
  • Aromatase Inhibitors
  • Steroids
  • Aminoglutethimide
  • Aromatase