Dibasic benzo[b]thiophene derivatives as a novel class of active site directed thrombin inhibitors: 2. Sidechain optimization and demonstration of in vivo efficacy

Bioorg Med Chem Lett. 1999 Mar 8;9(5):775-80. doi: 10.1016/s0960-894x(99)00074-8.

Abstract

Potent, subnanomolar thrombin inhibitors 4, 5, and 6 are developed through side chain optimization of novel, benzo[b]thiophene-based small organic entities 2 and 3 and through SAR additivity studies of the new structural elements identified. X-ray crystallographic studies of 4b-thrombin complex revealed a hydrophobic and an electrostatic interaction of these new elements with thrombin at the S2 and S3 binding sites. In vitro and in vivo pharmacological studies showed that 4, 5, and 6 are potent anticoagulants in human plasma with demonstrated antithrombotic efficacy in a rat model of thrombosis.

MeSH terms

  • Animals
  • Anticoagulants / chemistry
  • Anticoagulants / pharmacology
  • Anticoagulants / therapeutic use
  • Binding Sites
  • Crystallography, X-Ray
  • Disease Models, Animal
  • Humans
  • Models, Molecular
  • Rats
  • Structure-Activity Relationship
  • Thiophenes / chemistry*
  • Thiophenes / pharmacology
  • Thiophenes / therapeutic use
  • Thrombin / antagonists & inhibitors*
  • Thrombin / chemistry
  • Thrombosis / drug therapy

Substances

  • Anticoagulants
  • Thiophenes
  • benzothiophene
  • Thrombin