Nature Communications (May 2017)

A tetraoxane-based antimalarial drug candidate that overcomes PfK13-C580Y dependent artemisinin resistance

  • Paul M. O’Neill,
  • Richard K. Amewu,
  • Susan A. Charman,
  • Sunil Sabbani,
  • Nina F. Gnädig,
  • Judith Straimer,
  • David A. Fidock,
  • Emma R. Shore,
  • Natalie L. Roberts,
  • Michael H.-L. Wong,
  • W. David Hong,
  • Chandrakala Pidathala,
  • Chris Riley,
  • Ben Murphy,
  • Ghaith Aljayyoussi,
  • Francisco Javier Gamo,
  • Laura Sanz,
  • Janneth Rodrigues,
  • Carolina Gonzalez Cortes,
  • Esperanza Herreros,
  • Iñigo Angulo-Barturén,
  • María Belén Jiménez-Díaz,
  • Santiago Ferrer Bazaga,
  • María Santos Martínez-Martínez,
  • Brice Campo,
  • Raman Sharma,
  • Eileen Ryan,
  • David M. Shackleford,
  • Simon Campbell,
  • Dennis A. Smith,
  • Grennady Wirjanata,
  • Rintis Noviyanti,
  • Ric N. Price,
  • Jutta Marfurt,
  • Michael J. Palmer,
  • Ian M. Copple,
  • Amy E. Mercer,
  • Andrea Ruecker,
  • Michael J. Delves,
  • Robert E. Sinden,
  • Peter Siegl,
  • Jill Davies,
  • Rosemary Rochford,
  • Clemens H. M. Kocken,
  • Anne-Marie Zeeman,
  • Gemma L. Nixon,
  • Giancarlo A. Biagini,
  • Stephen A. Ward

DOI
https://doi.org/10.1038/ncomms15159
Journal volume & issue
Vol. 8, no. 1
pp. 1 – 10

Abstract

Read online

Artemisinin-resistantPlasmodium is an increasing problem. Here, using a medicinal chemistry programme, the authors identify a tetraoxane-based drug candidate that shows no cross-resistance with an artemisinin-resistant strain (PfK13-C580Y) and is efficient in Plasmodiummouse models.