Journal
CHEMMEDCHEM
Volume 12, Issue 24, Pages 2086-2093Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cmdc.201700599
Keywords
artemisinin; azaartemisinin; gametocytes; malaria; transmission
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Funding
- South African Medical Research Council (MRC)
- National Treasury under its Economic Competitiveness and Support Package
- South African National Research Foundation ((NRF) [90682, 98934, 87498]
- North-West University, Potchefstroom Campus
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Dihydroartemisinin (DHA), either used in its own right or as the active drug generated invivo from the other artemisinins in current clinical useartemether and artesunateinduces quiescence in ring-stage parasites of Plasmodium falciparum (Pf). This induction of quiescence is linked to artemisinin resistance. Thus, we have turned to structurally disparate artemisinins that are incapable of providing DHA on metabolism. Accordingly, 11-azaartemisinin 5 and selected N-sulfonyl derivatives were screened against intraerythrocytic asexual stages of drug-sensitive Pf NF54 and drug-resistant K1 and W2 parasites. Most displayed appreciable activities against all three strains, with IC50 values <10.5nm. The p-trifluoromethylbenzenesulfonyl-11-azaartemisinin derivative 11 [(4-trifluoromethyl)benzenesulfonylazaartemisinin] was the most active, with IC50 values between 2 and 3nm. The compounds were screened against Pf NF54 early and transmissible late intraerythrocytic-stage gametocytes using luciferase and parasite lactate dehydrogenase (pLDH) assays. The 2-thienylsulfonyl derivative 16 (2-thiophenesulfonylazaartemisinin) was notably active against late-stage (IV-V) gametocytes with an IC50 value of 8.7nm. All compounds were relatively nontoxic to human fetal lung WI-38 fibroblasts, showing selectivity indices of >2000 toward asexual parasites. Overall, the readily accessible 11-azaartemisinin 5 and the sulfonyl derivatives 11 and 16 represent potential candidates for further development, in particular for transmission blocking of artemisinin-resistant parasites.
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