4.8 Article

Imaging of Plasmodium Liver Stages to Drive Next-Generation Antimalarial Drug Discovery

Journal

SCIENCE
Volume 334, Issue 6061, Pages 1372-1377

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1211936

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Funding

  1. Keck Foundation
  2. NIH [R01AI090141, R01 AI079709]
  3. Deutsche Forschungsgemeinschaft [ME 3528/1-1]
  4. Medicines for Malaria Venture
  5. Wellcome Trust [WT078285]

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Most malaria drug development focuses on parasite stages detected in red blood cells, even though, to achieve eradication, next-generation drugs active against both erythrocytic and exo-erythrocytic forms would be preferable. We applied a multifactorial approach to a set of >4000 commercially available compounds with previously demonstrated blood-stage activity (median inhibitory concentration < 1 micromolar) and identified chemical scaffolds with potent activity against both forms. From this screen, we identified an imidazolopiperazine scaffold series that was highly enriched among compounds active against Plasmodium liver stages. The orally bioavailable lead imidazolopiperazine confers complete causal prophylactic protection (15 milligrams/kilogram) in rodent models of malaria and shows potent in vivo blood-stage therapeutic activity. The open-source chemical tools resulting from our effort provide starting points for future drug discovery programs, as well as opportunities for researchers to investigate the biology of exo-erythrocytic forms.

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