4.7 Article

The Aminopeptidase Inhibitor CHR-2863 Is an Orally Bioavailable Inhibitor of Murine Malaria

Journal

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 56, Issue 6, Pages 3244-3249

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.06245-11

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Funding

  1. Australian Postgraduate award
  2. NHMRC [571917]
  3. Australian NHMRC
  4. Canada Institute of Health Research (CIHR)

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Malaria remains a significant risk in many areas of the world, with resistance to the current antimalarial pharmacopeia an ever-increasing problem. The M1 alanine aminopeptidase (PfM1AAP) and M17 leucine atninopeptidase (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.

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