Synthesis and in vitro cytotoxic activity of chromenopyridones.

International Journal of Medicinal Chemistry Pub Date : 2013-01-01 Epub Date: 2012-01-08 DOI:10.1155/2013/984329

Balwinder Singh, Vishal Sharma, Gagandeep Singh, Rakesh Kumar, Saroj Arora, Mohan Paul Singh Ishar

引用次数: 0

Abstract

Novel substituted chromenopyridones (3a-j and 6a-d) were synthesized and evaluated in vitro for the cytotoxic activity against various human cancer cell lines such as prostate (PC-3), breast (MCF-7), CNS (IMR-32), cervix (Hela), and liver (Hep-G2). preliminary cytotoxic screening showed that all the compounds possess a good to moderate inhibitory activity against various cancer cell lines. Particularly, compound 6b bearing allyl moiety displayed a significant cytotoxic potential in comparison to standard drugs.

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铬吡啶酮的合成和体外细胞毒性活性。

研究人员合成了新型取代的铬吡啶酮类化合物（3a-j 和 6a-d），并在体外评估了这些化合物对前列腺癌（PC-3）、乳腺癌（MCF-7）、中枢神经系统癌症（IMR-32）、宫颈癌（Hela）和肝癌（Hep-G2）等多种人类癌细胞株的细胞毒性活性。特别是与标准药物相比，含有烯丙基的化合物 6b 显示出显著的细胞毒性潜力。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

International Journal of Medicinal Chemistry CHEMISTRY, MEDICINAL-

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期刊介绍： International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis. International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis.