Spiroindolones, a Potent Compound Class for the Treatment of Malaria

Matthias Rottmann(Swiss Tropical and Public Health Institute), Case W. McNamara(Genomics Institute of the Novartis Research Foundation), Bryan K. S. Yeung(Novartis (Singapore)), Lee M(Columbia University Irving Medical Center), Bin Zou(Novartis (Singapore)), Bruce Russell(National University of Singapore), Patrick Seitz(Swiss Tropical and Public Health Institute), David Plouffe(Genomics Institute of the Novartis Research Foundation), Neekesh V. Dharia(Scripps Research Institute), Jocelyn Tan(Novartis (Singapore)), Steven A. Cohen(Genomics Institute of the Novartis Research Foundation), Kathryn R. Spencer(Scripps Research Institute), Gonzalo E. González‐Páez(Scripps Research Institute), Suresh B. Lakshminarayana(Novartis (Singapore)), Anne Goh(Novartis (Singapore)), Rossarin Suwanarusk(Singapore Immunology Network), Timothy Jegla(Pennsylvania State University), E. Schmitt(Novartis (Switzerland)), Hans‐Peter Beck(Swiss Tropical and Public Health Institute), Reto Brun(Swiss Tropical and Public Health Institute), François Nosten(Mahidol University), Laurent Rénia(Singapore Immunology Network), Véronique Dartois(Novartis (Singapore)), Thomas H. Keller(Novartis (Singapore)), David A. Fidock(Columbia University Irving Medical Center), Elizabeth A. Winzeler(Scripps Research Institute), Thierry T. Diagana(Novartis (Singapore))
Science
September 2, 2010
Cited by 1,210Open Access
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Abstract

Recent reports of increased tolerance to artemisinin derivatives--the most recently adopted class of antimalarials--have prompted a need for new treatments. The spirotetrahydro-beta-carbolines, or spiroindolones, are potent drugs that kill the blood stages of Plasmodium falciparum and Plasmodium vivax clinical isolates at low nanomolar concentration. Spiroindolones rapidly inhibit protein synthesis in P. falciparum, an effect that is ablated in parasites bearing nonsynonymous mutations in the gene encoding the P-type cation-transporter ATPase4 (PfATP4). The optimized spiroindolone NITD609 shows pharmacokinetic properties compatible with once-daily oral dosing and has single-dose efficacy in a rodent malaria model.


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