Synthesis of new conjugated coumarin-benzimidazole hybrids and their anticancer activity

被引:128
|
作者
Paul, Kamaldeep [1 ]
Bindal, Shweta [1 ]
Luxami, Vijay [1 ]
机构
[1] Thapar Univ, Sch Chem & Biochem, Patiala 147004, Punjab, India
关键词
Coumarin; Benzimidazole; Hybrids; Anticancer agents; Molecular docking; VIRUS NS5B POLYMERASE; NATIONAL-CANCER-INSTITUTE; DRUG DISCOVERY; IN-VITRO; ANTITUMOR-ACTIVITY; DERIVATIVES; INHIBITORS; DESIGN; POTENT; ACID;
D O I
10.1016/j.bmcl.2012.12.071
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel coumarin-benzimidazole hybrids, 3-(1H-benzo[d]imidazol-2-yl)-7-(substituted amino)-2H-chromen-2-one derivatives of biological interest were synthesized. Six out of the newly synthesized compounds were screened for in vitro antitumor activity against preliminary 60 tumor cell lines panel assay. A significant inhibition for cancer cells was observed with compound 8 (more than 50% inhibition) compared with other compounds and active known drug 5-fluorouracil (in some cell lines) as positive control. Compound 8 displayed appreciable anticancer activities against leukemia, colon cancer and breast cancer cell lines. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3667 / 3672
页数:6
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