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

机译:含四唑环的多溴苯并咪唑和苯并三唑衍生物的合成及其细胞毒性

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摘要

AbstractA 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 (rhCK2α) 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.
机译:摘要通过5-芳基四唑与4,5,6,7-四溴-1-(3-氯丙基)-1H-苯并咪唑和4,5,6的N-烷基化反应合成了一系列含有四唑部分的新苯并咪唑和苯并三唑衍生物,7-四溴-2-(3-氯丙基)-2H-苯并三唑。该反应是区域选择性的,并且大部分获得了2,5-二取代的四唑衍生物。评估了所有合成化合物对人重组酪蛋白激酶2α亚基(rhCK2α)的影响以及对人T细胞淋巴母细胞(CCRF-CEM)和乳腺癌细胞(MCF-7)的细胞毒性。结果表明,许多合成的化合物在微摩尔浓度下均表现出明显的细胞毒性。

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