Identification and initial structure-activity relationships of a novel non-peptide quinolone GnRH receptor antagonist

Bioorg Med Chem Lett. 1999 Sep 6;9(17):2615-20. doi: 10.1016/s0960-894x(99)00446-1.

Abstract

Screening of the Merck sample collection for non-peptide compounds with binding affinity for the rat GnRH receptor led to the identification of the substituted quinolone (1) as a lead compound in the search for a non-peptide GnRH receptor antagonist. Substantial improvements in potency (approximately 300 fold) were achieved by addition of an alkyl amine at the 4-position, a 3,5-dimethylphenyl group at the 3-position and 6-nitro-7-chloro-substitution of the 1 H-quinolone core.

MeSH terms

  • Animals
  • Protein Binding
  • Quinolones / chemistry*
  • Quinolones / metabolism
  • Quinolones / pharmacology*
  • Rats
  • Receptors, LHRH / antagonists & inhibitors*
  • Receptors, LHRH / metabolism
  • Structure-Activity Relationship

Substances

  • Quinolones
  • Receptors, LHRH