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The therapeutic potential of semi-synthetic artemisinin and synthetic endoperoxide antimalarial agents

机译:半合成青蒿素和合成内过氧化物抗疟药的治疗潜力

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Artemisinin derivatives such as artesunate,dihydroartemisinin and arte-mether are playing an increasing role in the treatment of drug-resistant malaria.They are the most potent antimalarials available,rapidly killing all asexual stages of the parasite Plasmodium falciparum.This review highlights the recent developments in the area of improved second-generation semi-synthetic artemisinin derivatives and fully synthetic antimalarial endoperoxide drugs.In pursuit of synthetic analogues of the artemisinins,one of the major challenges for chemists in this area has been the non-trivial development of techniques for the introduction of the peroxide bridge into candidate drugs.Although chemical research has enabled chemists to incorporate the endoperoxide 'warhead' into synthetic analogues of artemisinin,significant drawbacks with many candidates have included comparatively poor antimalarial activity,non-stereoselective syntheses and chemical approaches that are not readily amenable to scale up.However,very recent progress with synthetic 1,2,4-trioxolanes provides a new benchmark for future medicinal chemistry efforts in this area.
机译:青蒿素衍生物,如青蒿琥酯,二氢青蒿素和青蒿琥酯在耐药性疟疾的治疗中起着越来越重要的作用。它们是最有效的抗疟疾药物,可迅速杀死寄生虫恶性疟原虫的所有无性阶段。在改进的第二代半合成青蒿素衍生物和完全合成的抗疟疾内过氧化物药物领域。追求青蒿素的合成类似物,该领域化学家面临的主要挑战之一是非常规技术的发展。尽管化学研究使化学家能够将过氧化物过氧化物“战斗部”掺入青蒿素的合成类似物中,但许多候选药物的显着缺点包括抗疟活性相对较差,非立体选择性合成以及化学方法不可行。容易适应规模p。然而,合成1,2,4-三氧戊环酮的最新进展为该领域的未来药物化学研究提供了新的基准。

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