Initial structure-activity relationship of a novel class of nonpeptidyl GnRH receptor antagonists: 2-arylindoles

Bioorg Med Chem Lett. 2001 Feb 26;11(4):509-13. doi: 10.1016/s0960-894x(00)00707-1.

Abstract

A nonpeptidyl GnRH receptor antagonist (1), with a unique 2-arylindole core, was identified through the Merck in-house screening for binding affinity on the rat GnRH receptor. SAR studies directed toward the alkoxy-ethanolamine and 2-aryl groups resulted in a simpler lead structure with improved activity. This compound 50 exhibits a 60-fold improvement in binding activity over our initial lead 1.

MeSH terms

  • Animals
  • Indoles / pharmacology*
  • Rats
  • Receptors, LHRH / antagonists & inhibitors*
  • Structure-Activity Relationship

Substances

  • Indoles
  • Receptors, LHRH