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Quinolone-3-diarylethers: A new class of antimalarial drug

  • Aaron Nilsen
  • , Alexis N. LaCrue
  • , Karen L. White
  • , Isaac P. Forquer
  • , R. Matthew Cross
  • , Jutta Marfurt
  • , Michael W. Mather
  • , Michael J. Delves
  • , David M. Shackleford
  • , Fabian E. Saenz
  • , Joanne M. Morrisey
  • , Jessica Steuten
  • , Tina Mutka
  • , Yuexin Li
  • , Grennady Wirjanata
  • , Eileen Ryan
  • , Sandra Duffy
  • , Jane Xu Kelly
  • , Boni F. Sebayang
  • , Anne Marie Zeeman
  • Rintis Noviyanti, Robert E. Sinden, Clemens H.M. Kocken, Ric N. Price, Vicky M. Avery, Iñigo Angulo-Barturen, María Belén Jiménez-Díaz, Santiago Ferrer, Esperanza Herreros, Laura M. Sanz, Francisco Javier Gamo, Ian Bathurst, Jeremy N. Burrows, Peter Siegl, R. Kiplin Guy, Rolf W. Winter, Akhil B. Vaidya, Susan A. Charman, Dennis E. Kyle, Roman Manetsch, Michael K. Riscoe
  • Portland VA Medical Center
  • College of Public Health
  • Monash University
  • University of South Florida
  • Charles Darwin University
  • Drexel University
  • Imperial College London
  • Pontificia Universidad Católica del Ecuador
  • Griffith University Queensland
  • Eijkman Institute for Molecular Biology
  • Biomedical Primate Research Centre
  • University of Oxford
  • GlaxoSmithKline
  • Medicines for Malaria Venture
  • Siegl Pharma Consulting LLC
  • St. Jude Children Research Hospital

Research output: Contribution to journalArticlepeer-review

Abstract

The goal for developing new antimalarial drugs is to find a molecule that can target multiple stages of the parasite's life cycle, thus impacting prevention, treatment, and transmission of the disease. The 4(1H)-quinolone-3- diarylethers are selective potent inhibitors of the parasite's mitochondrial cytochrome bc1 complex. These compounds are highly active against the human malaria parasites Plasmodium falciparum and Plasmodium vivax. They target both the liver and blood stages of the parasite as well as the forms that are crucial for disease transmission, that is, the gametocytes, the zygote, the ookinete, and the oocyst. Selected as a preclinical candidate, ELQ-300 has good oral bioavailability at efficacious doses in mice, is metabolically stable, and is highly active in blocking transmission in rodent models of malaria. Given its predicted low dose in patients and its predicted long half-life, ELQ-300 has potential as a new drug for the treatment, prevention, and, ultimately, eradication of human malaria.

Original languageEnglish
Article number177ra37
JournalScience Translational Medicine
Volume5
Issue number177
DOIs
Publication statusPublished - 20 Mar 2013
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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