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Novel 3-trifluoromethyl-1,2,4-oxadiazole analogues of astemizole with multi-stage antiplasmodium activity and; in vivo; efficacy in a; Plasmodium berghei; mouse malaria infection model
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
ID
4657557
Author(s)
Mambwe, D.; Korkor, CM.; Mabhula, A.; Ngqumba, Z.; Cloete, C.; Kumar, M.; Barros, PL.; Leshabane, M.; Coertzen, D.; Taylor, D.; Gibhard, L.; Njoroge, M.; Lawrence, N.; Reader, J.; Moreira, DR.; Birkholtz, LM.; Wittlin, S.; Egan, TJ.; Chibale, K.
Novel 3-trifluoromethyl-1,2,4-oxadiazole analogues of astemizole with multi-stage antiplasmodium activity and; in vivo; efficacy in a; Plasmodium berghei; mouse malaria infection model
Journal
Journal of medicinal chemistry
Volume
65
Number
24
Pages / Article-Number
16695-16715
Abstract
Iterative medicinal chemistry optimization of an ester-containing astemizole (AST) analogue 1 with an associated metabolic instability liability led to the identification of a highly potent 3-trifluoromethyl-1,2,4-oxadiazole analogue 23 (PfNF54 IC(50) = 0.012 muM; PfK1 IC(50) = 0.040 muM) displaying high microsomal metabolic stability (HLM CL(int) 1000-fold higher selectivity over hERG compared to AST. In addition to asexual blood stage activity, the compound also shows activity against liver and gametocyte life cycle stages and demonstrates in vivo efficacy in Plasmodium berghei-infected mice at 4 x 50 mg.kg(-1) oral dose. Preliminary interrogation of the mode of action using live-cell microscopy and cellular heme speciation revealed that 23 could be affecting multiple processes in the parasitic digestive vacuole, with the possibility of a novel target at play in the organelles associated with it.
