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首页> 外文期刊>Bulletin of the Korean Chemical Society >Design, Synthesis, and Biological Evaluation of Selenium-incorporated Aminopyridazines as Anticancer Agents
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Design, Synthesis, and Biological Evaluation of Selenium-incorporated Aminopyridazines as Anticancer Agents

机译:硒结合的氨基哒嗪类抗癌药的设计,合成及生物学评价

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摘要

A new series of 3-alkylseleno-6-alkylaminopyridazines, 3-alkylseleno-6-alkyliminopyridazines, and 3-alkylseleno-6-dialkylaminopyridazines was synthesized from 3,6-dichloropyridazine for development of new anticancer agents. The process involves the selenylation, Se-alkylation, and aralkylamination (or imination). The alkylamines such as ethylamine and the dialkylamines such as dipropylamine were introduced into the 3-position of the pyridazine ring. These new compounds showed antiproliferative activities against breast cancer (MCF-7) and hepatocellular carcinoma (Hep3B) cells in CCK-8 assays and could be promising candidates for chemotherapy of carcinomas.
机译:由3,6-二氯哒嗪合成了一系列新的3-烷基硒基6-烷基氨基哒嗪,3-烷基硒基6-烷基亚氨基哒嗪和3-烷基硒基6-二烷基氨基哒嗪,用于开发新的抗癌药。该过程涉及硒化,硒烷基化和芳烷基氨基化(或氨基化)。将烷基胺如乙胺和二烷基胺如二丙胺引入哒嗪环的3-位。这些新化合物在CCK-8分析中显示出对乳腺癌(MCF-7)和肝细胞癌(Hep3B)细胞的抗增殖活性,并有望成为癌症化学疗法的候选药物。

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