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体外活性新青蒿素衍生物对来自加蓬的恶性疟原虫临床分离株。

In vitro activity of new artemisinin derivatives against Plasmodium falciparum clinical isolates from Gabon.

机构信息

Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany.

出版信息

Int J Antimicrob Agents. 2011 May;37(5):485-8. doi: 10.1016/j.ijantimicag.2010.12.022. Epub 2011 Mar 10.

Abstract

Nowadays, artemisinins are the mainstay of malaria treatment, but initial indications of resistance against clinically used derivatives are present. In this study, ten new artemisinin derivatives were tested in vitro against Plasmodium falciparum laboratory strains as well as clinical isolates from Gabon. All derivatives were highly active, with 50% inhibitory concentrations (IC(50) values) <13 nM in the clinical isolates. The activity of one fluoro-containing derivative did not correlate with that of the parent compound, suggesting a different activity profile. New artemisinin derivatives with different activity profiles are of special interest as they represent an important class of candidates for pre-clinical testing in clinical parasite isolates adapted to currently used artemisinins, since derivatisation is one possible strategy to prolong the clinical usefulness of this important class of antimalarials.

摘要

如今,青蒿素类药物是治疗疟疾的主要药物,但已出现对临床应用的青蒿素衍生物有耐药性的初步迹象。在这项研究中,十种新的青蒿素衍生物在体外对疟原虫实验室株以及来自加蓬的临床分离株进行了测试。所有衍生物均具有高度活性,在临床分离株中的 50%抑制浓度(IC50 值)<13 nM。一种含氟衍生物的活性与母体化合物不相关,表明其具有不同的活性谱。具有不同活性谱的新型青蒿素衍生物具有特殊的意义,因为它们是临床寄生虫分离株中临床前测试的重要候选药物,因为衍生化是延长这种重要抗疟药类药物临床应用的一种可能策略。

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