Synthesis of polybrominated benzimidazole and benzotriazole derivatives containing a tetrazole ring and their cytotoxic activity

被引:12
作者
Lukowska-Chojnacka, Edyta [1 ]
Winska, Patrycja [1 ]
Wielechowska, Monika [1 ]
Bretner, Maria [1 ]
机构
[1] Warsaw Univ Technol, Inst Biotechnol, Fac Chem, Noakowskiego St 3, PL-00664 Warsaw, Poland
来源
MONATSHEFTE FUR CHEMIE | 2016年 / 147卷 / 10期
关键词
Antitumor agents; Azole; Benzimidazole; Heterocycles; Tetrazole; Total synthesis; PROTEIN-KINASE CK2; INHIBITORS; ANTICANCER;
D O I
10.1007/s00706-016-1785-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of new benzimidazole and benzotriazole derivatives containing a tetrazole moiety was synthesized by N-alkylation of 5-aryltetrazole with 4,5,6,7-tetrabromo-1-(3-chloropropyl)-1H-benzimidazole and 4,5,6,7-tetrabromo-2-(3-chloropropyl)-2H-benzotriazole. The reaction was regioselective and mostly 2,5-disubstituted tetrazole derivatives were obtained. The effect of all synthesized compounds on human recombinant casein kinase 2alpha subunit (rhCK2 alpha) and cytotoxicity against human T-cell lymphoblast (CCRF-CEM) and breast adenocarcinoma (MCF-7) cell lines were evaluated. The results have shown that many of the synthesized compounds exhibit significant cytotoxicity at micromolar concentration. [GRAPHICS]
引用
收藏
页码:1789 / 1796
页数:8
相关论文
共 30 条