首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Anticancer activity of N-bis(trifluoromethyl)alkyl-N'-(polychlorophenyl) and N'-(1,2,4-triazolyl) ureas.
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Anticancer activity of N-bis(trifluoromethyl)alkyl-N'-(polychlorophenyl) and N'-(1,2,4-triazolyl) ureas.

机译:N-双(三氟甲基)烷基-N'-(聚氯苯基)和N'-(1,2,4-三唑基)脲的抗癌活性。

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摘要

A number of N-bis(trifluoromethyl)alkyl-N'-substituted ureas have been synthesized and evaluated for their in vitro anticancer activity against the human cancer cell lines at the National Cancer Institute (NCI, USA). Marked activity was shown for compounds 4a and 5a. The most sensitive cell lines relative to the tested compounds were: 4a UO-31 (renal cancer, logGI(50) -5.62), HS 578T (breast cancer, logGI(50) -5.50), 5a HCC-2998 (colon cancer, logGI(50) -5.94), NCI-H322M (lung cancer, logGI(50) -5.75) and PC-3 (prostate cancer, logGI(50) -5.66).
机译:已经合成了许多N-双(三氟甲基)烷基-N'-取代的脲,并在美国国家癌症研究所(NCI)评估了它们对人癌细胞系的体外抗癌活性。对于化合物4a和5a显示出明显的活性。相对于测试化合物而言,最敏感的细胞系为:4a UO-31(肾癌,logGI(50)-5.62),HS 578T(乳腺癌,logGI(50)-5.50),5a HCC-2998(结肠癌, logGI(50)-5.94),NCI-H322M(肺癌,logGI(50)-5.75)和PC-3(前列腺癌,logGI(50)-5.66)。

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