The aminopeptidase inhibitor CHR-2863 is an orally bioavailable inhibitor of murine malaria

  • Tina S. Skinner-Adams
  • , Christopher L. Peatey
  • , Karen Anderson
  • , Katharine R. Trenholme
  • , David Krige
  • , Christopher L. Brown
  • , Colin Stack
  • , Desire M.M. Nsangou
  • , Rency T. Mathews
  • , Karine Thivierge
  • , John P. Dalton
  • , Donald L. Gardiner

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

41 Citations (Scopus)

Abstract

Malaria remains a significant risk in many areas of the world, with resistance to the current antimalarial pharmacopeia an everincreasing problem. The M1 alanine aminopeptidase (PfM1AAP) and M17 leucine aminopeptidase (PfM17LAP) are believed to play a role in the terminal stages of digestion of host hemoglobin and thereby generate a pool of free amino acids that are essential for parasite growth and development. Here, we show that an orally bioavailable aminopeptidase inhibitor, CHR-2863, is efficacious against murine malaria.

Original languageEnglish
Pages (from-to)3244-3249
Number of pages6
JournalAntimicrobial Agents and Chemotherapy
Volume56
Issue number6
DOIs
Publication statusPublished - Jun 2012
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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