Novel bicyclic lactam inhibitors of thrombin: potency and selectivity optimization through P1 residues

Bioorg Med Chem Lett. 2001 Dec 17;11(24):3161-4. doi: 10.1016/s0960-894x(01)00661-8.

Abstract

Peptidomimetic inhibitors of thrombin lacking the important Ser195-carbonyl interaction have been prepared. The binding energy lost after the removal of the activated carbonyl was recaptured through a series of modifications of the P1 residues of the bicyclic lactam inhibitors. Selected substituted compounds displayed useful pharmacological profiles both in vitro and in vivo.

MeSH terms

  • Animals
  • Antithrombins / chemistry
  • Antithrombins / pharmacology*
  • Arteries / drug effects
  • In Vitro Techniques
  • Lactams / chemistry
  • Lactams / pharmacology*
  • Rats
  • Thrombin / antagonists & inhibitors*

Substances

  • Antithrombins
  • Lactams
  • Thrombin