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首页> 外文期刊>Molecules >Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs
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Synthesis, Cytotoxicity and Mechanistic Evaluation of 4-Oxoquinoline-3-carboxamide Derivatives: Finding New Potential Anticancer Drugs

机译:4-氧喹啉-3-羧酰胺衍生物的合成,细胞毒性和机理评价:寻找新的潜在抗癌药物

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摘要

As part of a continuing search for new potential anticancer candidates, we describe the synthesis, cytotoxicity and mechanistic evaluation of a series of 4-oxoquinoline-3-carboxamide derivatives as novel anticancer agents. The inhibitory activity of compounds 10-18 was determined against three cancer cell lines using the MTT colorimetric assay. The screening revealed that derivatives 16b and 17b exhibited significant cytotoxic activity against the gastric cancer cell line but was not active against a normal cell line, in contrast to doxorubicin, a standard chemotherapeutic drug in clinical use. Interestingly, no hemolytical activity was observed when the toxicity of 16b and 17b was tested against blood cells. The in silico and in vitro mechanistic evaluation indicated he potential of 16b as a lead for the development of novel anticancer agents against gastric cancer cells.
机译:作为不断寻找新的潜在抗癌候选药物的一部分,我们描述了一系列4-氧代喹啉-3-羧酰胺衍生物作为新型抗癌剂的合成,细胞毒性和机理评估。使用MTT比色测定法测定化合物10-18对三种癌细胞系的抑制活性。筛选显示,与临床上使用的标准化疗药物阿霉素相比,衍生物16b和17b对胃癌细胞系表现出显着的细胞毒性活性,但对正常细胞系没有活性。有趣的是,当测试16b和17b对血细胞的毒性时,未观察到任何溶血活性。计算机和体外机理评估表明,他可能具有16b作为开发针对胃癌细胞的新型抗癌药的潜力。

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