含亚胺化合物的抗癌和抗菌活性

S. Qazia, Asia Naz, Aneela Javedc
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引用次数: 0

摘要

以胶质瘤细胞株(U87)为实验对象,采用MTT法检测了一系列亚胺衍生物(3 -m)的体外抗癌活性,其中包括硫氨基脲、氨基氨基脲、噻唑和恶唑的功能部分。其中,化合物3m的IC50值为8.86±0.15µM,最强。用正常人胚胎肾细胞系HEK-293评价化合物的细胞毒性。采用圆盘扩散法对合成的衍生物进行抑菌活性评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticancer and antimicrobial activities of Imine containing compounds
A series of imine derivatives (3a-m) including thio-semicarbazone, semicarbazone, thiazole and oxazole functional moieties were examined for anti-cancer activity in-vitro by MTT assay using glioblastoma cell line (U87). Among all compound 3m was most potent compound with IC50 value of 8.86 ± 0.15 µM. Cytotoxicity of compounds were evaluated using normal human embryonic kidney cell line i.e HEK-293. Moreover, antibacterial activity of synthesized derivatives was also evaluated by disc diffusion method.
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