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首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis, characterization and anticancer activity of novel ferrocene containing quinolinones: 1-Allyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-allyl-2-ferrocenylquinolin-4(1H)-ones
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Synthesis, characterization and anticancer activity of novel ferrocene containing quinolinones: 1-Allyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-allyl-2-ferrocenylquinolin-4(1H)-ones

机译:新型二茂铁的合成,表征和抗癌活性含喹啉酮:1-烯丙基-2-铁核基-2,3-二氢喹啉-4(1H) - 酮和1-烯丙基-2-铁烯基喹啉-4(1H) - 酮

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摘要

A two new series of ferrocene containing quinolinones -1-allyl-2-ferrocenyl-2,3-dihydroquinolin-4(1H)-ones and 1-allyl-2-ferrocenylquinolin-4(1H)-ones - were prepared and characterized by standard spectroscopic techniques and cyclic voltammetry. The in vitro antitumor activity of all synthesized compounds was investigated against Human Cervix Carcinoma (HeLa), Chronic Myelogenous Leukemia (K562) and normal endothelial (HUVEC) cell lines using the MIT method. Quinolone derivative 5c exhibited the highest cytotoxic activity in the cell growth inhibition of HeLa cell line while 5f was the most toxic against K562 cells. (C) 2018 Elsevier B.V. All rights reserved.
机译:制备并表征了两种新的二氯醌-1-烯丙基-2-铁烯基-2,3-二氢喹啉-4(1H)和1-烯丙基-2-铁烯基喹啉-4(1H) - 酮 - 酮 - 酮 - 酮和1-烯丙基-2-二铁蛋白-4(1H) - 标准光谱技术和循环伏安法。 使用MIT方法对所有合成化合物的体外抗肿瘤活性研究所有合成的化合物,慢性髓性白血病(K562)和正常内皮(HUVEC)细胞系。 喹啉衍生物5C在Hela细胞系的细胞生长抑制中表现出最高的细胞毒性活性,而5F对K562细胞最有毒。 (c)2018年elestvier b.v.保留所有权利。

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