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首页> 外文期刊>Molecules >Preliminary LC-MS Based Screening for Inhibitors of Plasmodium falciparum Thioredoxin Reductase (PfTrxR) among a Set of Antimalarials from the Malaria Box
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Preliminary LC-MS Based Screening for Inhibitors of Plasmodium falciparum Thioredoxin Reductase (PfTrxR) among a Set of Antimalarials from the Malaria Box

机译:基于初步LC-MS的疟疾药房中一组抗疟药中恶性疟原虫硫氧还蛋白还原酶(PfTrxR)抑制剂的筛选

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摘要

Plasmodium falciparum thioredoxin reductase (PfTrxR) has been identified as a potential drug target to combat growing antimalarial drug resistance. Medicines for Malaria Venture (MMV) has pre-screened and identified a set of 400 antimalarial compounds called the Malaria Box. From those, we have evaluated their mechanisms of action through inhibition of PfTrxR and found new active chemical scaffolds. Five compounds with significant PfTrxR inhibitory activity, with IC50 values ranging from 0.9-7.5 mu M against the target enzyme, were found out of the Malaria Box.
机译:恶性疟原虫硫氧还蛋白还原酶(PfTrxR)已被确定为对抗日益增长的抗疟药耐药性的潜在药物靶标。疟疾风险药物公司(MMV)已预先筛选并鉴定出400种抗疟化合物,称为“疟疾盒”。从中,我们评估了它们通过抑制PfTrxR的作用机理,并发现了新的活性化学支架。在疟疾箱中发现了五种具有显着PfTrxR抑制活性的化合物,针对目标酶的IC50值为0.9-7.5μM。

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