Abstract
Artemisinins show the potential for neurotoxicity in preclinical studies. Artemisone is a leading candidate of second-generation semi-synthetic artemisinin derivatives for antimalarial therapy devoid of neurotoxicity. Artemisone showed 3-5-fold higher in vitro activity (50% effective concentration (EC50) = 0.14 nmol/L, EC90 = 2.55 nmol/L) than artesunate against fresh Plasmodium falciparum isolates from Gabon and a high-activity correlation indicates a shared drug target. Copyright ©2006 by The American Society of Tropical Medicine and Hygiene.
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CITATION STYLE
Ramharter, M., Burkhardt, D., Nemeth, J., Adegnika, A. A., & Kremsner, P. G. (2006). Short report: In vitro activity of artemisone compared with artesunate against Plasmodium falciparum. American Journal of Tropical Medicine and Hygiene, 75(4), 637–639. https://doi.org/10.4269/ajtmh.2006.75.637
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