Synthesis and biological evaluation of pyrimidine bridged combretastatin derivatives as potential anticancer agents and mechanistic studies

Abstract

A number of pyrimidine bridged combretastatin derivatives were designed, synthesized and evaluated for anticancer activities against breast cancer (MCF-7) and lung cancer (A549) cell lines using MTT assays. Most of the synthesized compounds displayed good anticancer activity with IC50 values in low micro-molar range. Compounds 4a and 4p were found most potent in the series with IC50 values of 4.67 ?M & 3.38 ?M and 4.63 ?M & 3.71 ?M against MCF7 and A549 cancer cell lines, respectively. Biological evaluation of these compounds showed that selective cancer cell toxicity (in vitro using human lung and breast cancer cell lines) might be due to the inhibition of antioxidant enzymes instigating elevated ROS levels which triggers intrinsic apoptotic pathways. These compounds were found nontoxic to the normal human primary cells. Compound 4a, was found to be competitive inhibitor of colchicine and in the tubulin binding assay it showed tubulin polymerization inhibition potential comparable to colchicine. The molecular modeling studies also showed that the synthesized compounds fit well in the colchicine-binding pocket. ? 2018 Elsevier Inc.

Description

Keywords

2 methyl 4 (4 tolyl) 6 (3,4,5 trimethoxyphenyl)pyrimidine, 2 methyl 4 phenyl 6 (3,4,5 trimethoxyphenyl)pyrimidine, 2 methyl 4,6 diphenylpyrimidine, 4 (2,4 dichlorophenyl) 6 (3,4,5 trimethoxyphenyl)pyrimidin 2 amine, 4 (3,4 dimethoxyphenyl) 2 methyl 6 (4 tolyl)pyrimidine, 4 (3,4 dimethoxyphenyl) 2 methyl 6 phenylpyrimidine, 4 (3,4 dimethoxyphenyl) 6 (4 methoxyphenyl) 2 methylpyrimidine, 4 (4 chlorophenyl) 2 methyl 6 (3,4,5 trimethoxyphenyl)pyrimidine, 4 (4 chlorophenyl) 6 (3,4 dimethoxyphenyl)pyr

Citation

Kumar, B., Sharma, P., Gupta, V. P., Khullar, M., Singh, S., Dogra, N., & Kumar, V. (2018). Synthesis and biological evaluation of pyrimidine bridged combretastatin derivatives as potential anticancer agents and mechanistic studies. Bioorganic Chemistry, 78, 130-140. doi: 10.1016/j.bioorg.2018.02.027