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Design, synthesis and biological evaluation of sulphonamide derivatives of benzofuran-imidazopyridines as anticancer agents
Chemical Data Collections Pub Date : 2020-11-28 , DOI: 10.1016/j.cdc.2020.100608
Indraganti Sreenivasa Murthy , Reddymasu Sireesha , Kolli Deepti , P. Srinivasa Rao , R. Ramesh Raju

A novel library of sulphonamide derivatives of benzofuran-imidazopyridines (9a-j) were designed, synthesized and screened for their anticancer activity against four human cancer cell lines such as breast cancer (MCF-7), lung cancer (A549), colon cancer (Colo-205) and ovarian cancer (A2780) by employing MTT assay. The results are expressed with IC50 µM, which indicated that all of the compounds showed good to moderate activity on tested cell lines. Among them, compound 9c showed potent anticancer activities against MCF-7, A549, Colo-205 and A2780 cell lines with IC50 values of 0.011 ± 0.0075 µM, 0.073 ± 0.0012 µM, 0.10 ± 0.19 µM and 0.034 ± 0.0041 µM respectively.



中文翻译:

苯并呋喃-咪唑并吡啶类抗癌药磺酰胺衍生物的设计,合成及生物学评价

设计,合成并筛选了苯并呋喃-咪唑并吡啶(9a-j)的磺酰胺衍生物新文库,它们针对四种人类癌细胞系(例如乳腺癌(MCF-7),肺癌(A549),结肠癌(采用MTT分析法检测Colo-205)和卵巢癌(A2780)。结果用IC 50 µM表示,表明所有化合物对受试细胞系均显示出良好至中等的活性。其中,化合物9c对MCF-7,A549,Colo-205和A2780细胞系显示有效的抗癌活性,IC 50值分别为0.011±0.0075 µM,0.073±0.0012 µM,0.10±0.19 µM和0.034±0.0041 µM。

更新日期:2020-12-16
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