Synthesis and In Vitro Cytotoxic Evaluation of 7-Chloro-4-anilino-quinoline Amide Derivatives

被引:0
作者
Bui Trung Hieu [1 ]
Vu Thu Thuy [1 ]
Hoang Xuan Tien [1 ]
Tran Khac Vu [1 ]
机构
[1] Hanoi Univ Sci & Technol, Dept Pharmaceut Chem & Pesticides Technol, Sch Chem Engn, Hanoi, Vietnam
关键词
Anticancer; Amide; Cell line; Cytotoxic; Quinoline; QUINOLINES;
D O I
10.14233/ajchem.2013.14016
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of new amide derivatives of 4-anilino-quinoline have been synthesized and evaluated in vitro cytotoxic activity against the human hepatocellular carcinoma (HepG2), human lung carcinoma (SK-LU-1) and human breast cancer (MCF-7). Compound 5g was found to be most potent cytotoxic activity against HepG2 and MCF-7 cell lines with IC50 values of 2.09 and 4.63 mu g/mL, respectively. Compound 5e exhibited significant cytotoxic activity against three cell lines with IC50 values ranging from 5-10 mu g/mL.
引用
收藏
页码:4453 / 4456
页数:4
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