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Diversity-oriented synthesis derived indole based spiro and fused small molecules kills artemisinin-resistant

机译:以分集为主的合成衍生的基于吲哚螺旋和融合的小分子杀死了抗石英素的抗体

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摘要

Screening of DOS-synthesised compounds for anti-plasmodial activity. a Synchronized parasite culture in ring stage were seeded to adjust parasitaemia to 1%. This synchronized culture was then treated either with DMSO or compounds (5 µM) for 48 h. Giemsa-stained slides were prepared at 0 and 48 h post-treatment to monitor the parasitaemia. Graphs were prepared for the average value of three independent experiments performed in duplicate with ± SD. b Parasites at different stages of the IDC at 0 and 48 h post-treatment were calculated. Table shows the percentage of remaining parasites in different stages of IDC from three independent experiments with ± SD
机译:筛选DOS合成化合物的抗疟原虫活性。环阶段的同步寄生虫培养均接种将寄生虫调节至1%。然后用DMSO或化合物(5μM)处理该同步培养物48小时。在治疗后0和48小时制备Giemsa染色的幻灯片以监测寄生虫。为与±SD重复进行的三个独立实验的平均值制备图。计算IDC的不同阶段的B寄生物在0和48小时后进行治疗。表显示了IDC不同阶段的剩余寄生虫的百分比,来自三个独立实验,±SD

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