Protease inhibitors in the clinic

Med Chem. 2005 Jan;1(1):71-104. doi: 10.2174/1573406053402569.

Abstract

This review describes the clinical status (based on available information) of experimental drugs that inhibit enzymes called proteases, or more precisely a sub-class of proteases called peptidases that catalyse the hydrolysis of polypeptide main chain amide bonds. These peptidases are classified by the key catalytic residue in the active site of the enzyme that effects hydrolysis, namely aspartic, serine, cysteine, metallo or threonine proteases. In this review we show structures for 108 inhibitors of these enzymes and update the clinical disposition of over 100 inhibitors that have been considered worthy enough by pharmaceutical, biotechnology or academic researchers and their financial backers to be trialed in humans as prospective medicines. We outline some of their chemical and pharmacological characteristics and compare the current status of protease inhibitors in the clinic with what was observed about 5 years ago (Leung et al, J. Med. Chem. 2000, 43, 305-341). We assess the progress of protease inhibitors into man, predict their futures, and outline some of the hurdles that have been overcome and that still remain for this promising class of new therapeutic agents.

Publication types

  • Review

MeSH terms

  • Aspartic Acid Endopeptidases / chemistry
  • Aspartic Acid Endopeptidases / pharmacology
  • Clinical Trials as Topic*
  • Cysteine Proteinase Inhibitors / chemistry
  • Cysteine Proteinase Inhibitors / pharmacology
  • Databases as Topic*
  • Humans
  • Molecular Structure
  • Protease Inhibitors*
  • Serine Proteinase Inhibitors / chemistry
  • Serine Proteinase Inhibitors / pharmacology
  • Tissue Inhibitor of Metalloproteinases / chemistry
  • Tissue Inhibitor of Metalloproteinases / pharmacology

Substances

  • Cysteine Proteinase Inhibitors
  • Protease Inhibitors
  • Serine Proteinase Inhibitors
  • Tissue Inhibitor of Metalloproteinases
  • Aspartic Acid Endopeptidases