Pyrrolidine-5,5-trans-lactams. 5. Pharmacokinetic optimization of inhibitors of hepatitis C virus NS3/4A protease

Org Lett. 2003 Nov 27;5(24):4631-4. doi: 10.1021/ol035827n.

Abstract

[reaction: see text] In this, the second of two Letters, the optimization of the pyrrolidine-5,5-trans-lactam template (exemplified by 1a) as a mechanism-based inhibitor of hepatitis C NS3/4A protease is described. "Right Box" analysis of cassette dosing screening pharmacokinetic data was used to rapidly categorize the compounds. GW0014 (compound 4d) emerged as the compound displaying an optimal balance of biochemical and replicon potency, along with low i.v. clearance in the dog.

MeSH terms

  • Inhibitory Concentration 50
  • Lactams / chemistry*
  • Molecular Structure
  • Protease Inhibitors / chemical synthesis*
  • Protease Inhibitors / chemistry
  • Protease Inhibitors / pharmacokinetics*
  • Pyrrolidines / chemistry*
  • Viral Nonstructural Proteins / antagonists & inhibitors*
  • Viral Nonstructural Proteins / metabolism

Substances

  • Lactams
  • NS3 protein, hepatitis C virus
  • Protease Inhibitors
  • Pyrrolidines
  • Viral Nonstructural Proteins
  • pyrrolidine