Nonpeptide endothelin antagonists: from lower affinity pyrazol-5-ols to higher affinity pyrazole-5-carboxylic acids

Bioorg Med Chem Lett. 2000 Jun 19;10(12):1351-5. doi: 10.1016/s0960-894x(00)00232-8.

Abstract

Random screening of compounds in endothelin receptor (ET(A) and ET(B)) binding assays led to the discovery of a new class of pyrazol-5-ol ligands. Characterization of structural features crucial for binding activities of these pyrazol-5-ols, by structure activity-relationship (SAR) studies, allowed us to design a novel class of pyrazole-5-carboxylic acids as more potent ET antagonists.

MeSH terms

  • Carboxylic Acids / metabolism*
  • Endothelins / antagonists & inhibitors*
  • Endothelins / metabolism
  • Pyrazoles / metabolism*
  • Structure-Activity Relationship

Substances

  • Carboxylic Acids
  • Endothelins
  • Pyrazoles