"The 4(1H)-quinolone-3- diarylethers are selective potent inhibitors of the parasite mitochondrial cytochrome bc1 complex," Professor Avery said.
"These compounds are highly active against the types of malaria parasites which infect humans, Plasmodium falciparum and Plasmodium vivax," she said.
"What is really exciting about this study is that a new class of drugs based on the 4(1H)-quinolone-3- diarylethers would target the malaria parasite at different stages of its lifecycle."