N-substituted 4-(5-indolyl)benzoic acids. Synthesis and evaluation of steroid 5alpha-reductase type I and II inhibitory activity

Bioorg Med Chem Lett. 1999 Jun 7;9(11):1601-6. doi: 10.1016/s0960-894x(99)00234-6.

Abstract

The synthesis of N-alkyl and N-arylalkyl substituted 4-(5-indolyl)benzoic acid derivatives as inhibitors of steroid 5alpha-reductases is described. For the human type II isozyme a benzyl substituent (IC50 6.20 microM) and for the human type I isozyme a cyclohexanemethyl substituent (IC50 2.10 microM) on the indole nitrogen proved to be most efficacious, thus providing interesting leads for the development of drugs for the treatment of benign prostatic hyperplasia (BPH).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Benzoates / chemical synthesis*
  • Benzoates / pharmacology*
  • Cell Line
  • Cells, Cultured
  • Cholestenone 5 alpha-Reductase
  • Humans
  • Inhibitory Concentration 50
  • Male
  • Models, Chemical
  • Oxidoreductases / antagonists & inhibitors*
  • Prostatic Hyperplasia / drug therapy
  • Rats

Substances

  • Benzoates
  • Oxidoreductases
  • Cholestenone 5 alpha-Reductase