Rational design, synthesis and anti-proliferative evaluation of novel 1,4-benzoxazine-[1,2,3]triazole hybrids

被引:52
|
作者
Bollu, Rajitha [1 ]
Palem, Jyothsna Devi [1 ]
Bantu, Rajashaker [1 ]
Guguloth, Vijayacharan [1 ]
Nagarapu, Lingaiah [1 ]
Polepalli, Sowjanya [2 ]
Jain, Nishant [2 ]
机构
[1] Indian Inst Chem Technol, CSIR, Organ Chem Div CPC 2, Hyderabad 500007, Andhra Pradesh, India
[2] Indian Inst Chem Technol, CSIR, Ctr Chem Biol, Hyderabad 500007, Andhra Pradesh, India
关键词
1,2,3-Triazoles; 1,4-Benzoxazine; Anti-proliferative; Apoptosis; Cell lines; POTENTIAL ANTICANCER AGENTS; CLICK CHEMISTRY; DERIVATIVES; CANCER; 1,2,3-TRIAZOLES; INHIBITORS; SCAFFOLD; ANALOGS;
D O I
10.1016/j.ejmech.2014.10.051
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel 1,2,3-triazole-1,4-benzoxazine hybrids 5a-n were efficiently synthesized employing click chemistry approach and evaluated for anti-proliferative activity against four cancer cell lines such as HeLa (cervical), MIAPACA (pancreatic), MDA-MB-231 (breast) and IMR32 (neuroblastoma). Compounds 5n and 5g exhibited promising anti-proliferative activity with GI(50) values ranging from 1.2 to 2.5 mu M and 0.1-1.1 mu M respectively against all cell lines, like HeLa, MDA-MB-231, MIAPACA and IMR32, while compound 51 showed significant activity against MDA-MB-231 and IMR32 with GI(50) values ranging from 1.1 and 1.4 mu M. This is the first report on the synthesis and in vitro anti-proliferative evaluation of 1,2,3-triazole-1,4-benzoxazine hybrids. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:138 / 146
页数:9
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