Design, synthesis and biological evaluation of 2-(phenoxymethyl)-5-phenyl-1,3,4-oxadiazole derivatives as anti-breast cancer agents

被引:50
作者
Lakshmithendral, K. [1 ]
Saravanan, K. [1 ]
Elancheran, R. [1 ]
Archana, K. [1 ]
Manikandan, N. [2 ]
Arjun, H. A. [1 ]
Ramanathan, M. [2 ]
Lokanath, N. K. [3 ]
Kabilan, S. [1 ]
机构
[1] Annamalai Univ, Drug Discovery Lab, Dept Chem, Annamalainagar 608002, Tamil Nadu, India
[2] PSG Coll Pharm, Dept Pharmacol, Coimbatore 641004, Tamil Nadu, India
[3] Univ Mysore, Dept Studies Phys, Manasagangotri 570006, Mysuru, India
关键词
Estrogen receptor; Breast cancer; 1,3,4-Oxadiazoles; Molecular docking; RECOGNITION; CELLS; DNA;
D O I
10.1016/j.ejmech.2019.02.033
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Structural based molecular docking approach revealed the findings of 2-(phenoxymethyl) -5-phenyl-1,3,4-oxadiazole derivatives. The compounds (7a-o) were synthesized and characterized well by using conventional methods. The compounds, 7b and 7m were reconfirmed through single crystal XRD analysis. The synthesized compounds (7a-o) were evaluated their antiproliferative activities against MCF-7 and MDA-MB-453. Furthermore, Lipinski's rule of five and pharmacokinetic properties were predicted for the test compounds. These results demonstrate that the compounds 7b and 7d exhibit more potent cytotoxicity and 7d exhibits dose-dependent activity and reduced cell viability. Further, the mechanism of action for the induced apoptosis was observed through morphological changes and western blotting analysis. These findings may furnish the lead for further development. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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