Antimalarial efficacy of MMV390048, an inhibitor of Plasmodium phosphatidylinositol 4-kinase

26 Apr 2017

Tanya Paquet,  Claire Le Manach,  Diego González Cabrera,  Yassir Younis,  Philipp P. Henrich,  Tara S. Abraham,  Marcus C. S. Lee,  Rajshekhar Basak,  Sonja Ghidelli-Disse,  María José Lafuente-Monasterio,  Marcus Bantscheff,  Andrea Ruecker,  Andrew M. Blagborough,  Sara E. Zakutansky,  Anne-Marie Zeeman,  Karen L. White,  David M. Shackleford,  Janne Mannila,  Julia Morizzi,  Christian Scheurer,  Iñigo Angulo-Barturen,  María Santos Martínez,  Santiago Ferrer,  Laura María Sanz,  Francisco Javier Gamo,  Janette Reader,  Mariette Botha,  Koen J. Dechering,  Robert W. Sauerwein,  Anchalee Tungtaeng,  Pattaraporn Vanachayangkul,  Chek Shik Lim,  Jeremy Burrows,  Michael J. Witty,  Kennan C. Marsh,  Christophe Bodenreider,  Rosemary Rochford,  Suresh M. Solapure,  María Belén Jiménez-Díaz,  Sergio Wittlin,  Susan A. Charman,  Cristina Donini,  Brice Campo,  Lyn-Marie Birkholtz,  Kirsten K. Hanson,  Gerard Drewes,  Clemens H. M. Kocken,  Michael J. Delves,  Didier Leroy, David A. Fidock,  David Waterson, 
Leslie J. Street and Kelly Chibale

Science Translational Medicine

DOI: 10.1126/scitranslmed.aad9735

Photo: Prapann/


As part of the global effort toward malaria eradication, phenotypic whole-cell screening revealed the 2-aminopyridine class of small molecules as a good starting point to develop new antimalarial drugs. Stemming from this series, we found that the derivative, MMV390048, lacked cross-resistance with current drugs used to treat malaria.

This compound was efficacious against all Plasmodium life cycle stages, apart from late hypnozoites in the liver. Efficacy was shown in the humanized Plasmodium falciparum mouse model, and modest reductions in mouse-to-mouse transmission were achieved in the Plasmodium berghei mouse model. Experiments in monkeys revealed the ability of MMV390048 to be used for full chemoprotection. Although MMV390048 was not able to eliminate liver hypnozoites, it delayed relapse in a Plasmodium cynomolgi monkey model.

Both genomic and chemoproteomic studies identified a kinase of the Plasmodium parasite, phosphatidylinositol 4-kinase, as the molecular target of MMV390048. The ability of MMV390048 to block all life cycle stages of the malaria parasite suggests that this compound should be further developed and may contribute to malaria control and eradication as part of a single-dose combination treatment.

View the full article on the Science Translational Medicine website.