Ontology highlight
ABSTRACT:
SUBMITTER: Nilsen A
PROVIDER: S-EPMC4227885 | biostudies-literature | 2013 Mar
REPOSITORIES: biostudies-literature
Nilsen Aaron A LaCrue Alexis N AN White Karen L KL Forquer Isaac P IP Cross Richard M RM Marfurt Jutta J Mather Michael W MW Delves Michael J MJ Shackleford David M DM Saenz Fabian E FE Morrisey Joanne M JM Steuten Jessica J Mutka Tina T Li Yuexin Y Wirjanata Grennady G Ryan Eileen E Duffy Sandra S Kelly Jane Xu JX Sebayang Boni F BF Zeeman Anne-Marie AM Noviyanti Rintis R Sinden Robert E RE Kocken Clemens H M CHM Price Ric N RN Avery Vicky M VM Angulo-Barturen Iñigo I Jiménez-Díaz María Belén MB Ferrer Santiago S Herreros Esperanza E Sanz Laura M LM Gamo Francisco-Javier FJ Bathurst Ian I Burrows Jeremy N JN Siegl Peter P Guy R Kiplin RK Winter Rolf W RW Vaidya Akhil B AB Charman Susan A SA Kyle Dennis E DE Manetsch Roman R Riscoe Michael K MK
Science translational medicine 20130301 177
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 a ...[more]