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Synthesis and evaluation of antimalarial activity of curcumin derivatives

机译:姜黄素衍生物抗疟活性的合成与评价

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One of the main challenges in the development of new antimalarial drugs is to achieve a viable lead candidate with good pharmacokinetic properties. Curcumin has a broad range of biological activities, including antimalarial activity. Herein, we report the antimalarial activity of six curcumin derivatives (6-12) and an initial analysis of their pharmacokinetic properties. Five compounds have demonstrated potent activity against the P. falciparum in vitro (IC50 values ranging from 1.7 to 15.2 µg mL-1), with moderate or low cytotoxicity against the HeLa cell line. The substitution of the carbonyl group in 6 by a 2,4-dinitrophenylhydrazone group (to afford 11) increases the Selective Index. These preliminary results indicate curcumin derivatives as potential antimalarial compounds.
机译:新的抗疟疾药物发展的主要挑战之一是实现具有良好药代动力学性质的可行的候选者。姜黄素具有广泛的生物活性,包括抗疟疾活动。在此,我们报告了六种姜黄素衍生物(6-12)的抗疟疾活性以及其药代动力学性质的初步分析。在体外(IC 50值范围为1.7至15.2μgmL-1)的P. falciparum,五种化合物已经证明了有效的活性,对Hela细胞系具有中度或低细胞毒性。通过2,4-二硝基苯基腙基团(支付11)在6中取代羰基,增加了选择性指标。这些初步结果表明姜黄素衍生物作为潜在的抗疟性化合物。

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