Screening of protease inhibitors as antiplasmodial agents. Part I: Aziridines and epoxides

ChemMedChem. 2007 Aug;2(8):1214-24. doi: 10.1002/cmdc.200700070.

Abstract

A broad protease-based and cell-based screening of protease inhibitors yielded the aziridine-2-carboxylic acid derivative 2 a and the N-acylated aziridine-2,3-dicarboxylic acid derivatives 32 a and 34 b as the most potent inhibitors of falcipain-2 and falcipain-3 (IC(50) falcipain-2: 0.079-5.4 microM, falcipain-3: 0.25-39.8 microM). As the compounds also display in vitro activity against the P. falciparum parasite in the submicromolar and low micromolar range, these compound classes are leads for new antiplasmodial falcipain inhibitors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimalarials / chemistry
  • Antimalarials / pharmacology*
  • Aziridines / pharmacology*
  • Epoxy Compounds / pharmacology*
  • Plasmodium falciparum / drug effects*
  • Protease Inhibitors / chemistry
  • Protease Inhibitors / pharmacology*
  • Stereoisomerism

Substances

  • Antimalarials
  • Aziridines
  • Epoxy Compounds
  • Protease Inhibitors