首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Synthesis of novel fluoro 1,2,3-triazole tagged amino bis(benzothiazole) derivatives, their antimicrobial and anticancer activity
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Synthesis of novel fluoro 1,2,3-triazole tagged amino bis(benzothiazole) derivatives, their antimicrobial and anticancer activity

机译:新型含氟1,2,3-三唑标记的氨基双(苯并噻唑)衍生物的合成,抗菌和抗癌活性

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摘要

A new series of fluoro 1,2,3-triazole tagged amino bis (benzothiazole) derivatives 8, 9 were prepared starting from 2-amino benzothiazole in four steps via amination, cyclization, alkylation followed by reaction with various azides under sharpless conditions through click chemistry approach. All newly synthesized compounds were screened for their antimicrobial and cytotoxic activity against four human cancer cell lines (U937, THP-1, Colo205, and A549), and promising compounds have been identified.
机译:从2-氨基苯并噻唑开始,经胺化,环化,烷基化,分四个步骤从2-氨基苯并噻唑开始,制备了一系列新的含氟1,2,3-三唑标记的氨基双(苯并噻唑)衍生物8、9,然后在无尖锐条件下通过点击反应与各种叠氮化物反应化学方法。筛选了所有新合成的化合物对四种人类癌细胞系(U937,THP-1,Colo205和A549)的抗微生物和细胞毒性活性,并鉴定了有前途的化合物。

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