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首页> 外文期刊>Research Journal of Pharmaceutical, Biological and Chemical Sciences >Synthesis, Molecular Docking and Cytotoxicity Evaluation of Novel 1,2-Disubstituted Benzimidazole Derivatives Against Liver and Breast Cancer Cell Lines.
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Synthesis, Molecular Docking and Cytotoxicity Evaluation of Novel 1,2-Disubstituted Benzimidazole Derivatives Against Liver and Breast Cancer Cell Lines.

机译:新型1,2-二取代苯并咪唑衍生物对肝脏和乳腺癌细胞系的合成,分子对接和细胞毒性评估。

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摘要

ABSTRACT A series of novel 1, 2-disubstituted benzo[d]imidazole derivatives was synthesized, which bearing at position-1 different bioactive side chains or heterocyclic moieties. While, they are linked to 2,4,6-trisubstituted pyridine ring at position-2. In vitro Cytotoxic evaluation of all the new synthesized benzimidazole compounds (315a,b) against hepatocellular carcinoma (HepG-2) and breast carcinoma (MCF-7) cell lines showed that most of them gave significant cytotoxicity. Moreover, compou.
机译:摘要合成了一系列新颖的1、2-二取代的苯并[d]咪唑衍生物,它们在1位具有不同的生物活性侧链或杂环部分。同时,它们在2位连接到2,4,6-三取代的吡啶环上。对所有新合成的苯并咪唑化合物(315a,b)对肝细胞癌(HepG-2)和乳腺癌(MCF-7)细胞系的体外细胞毒性评估表明,它们中的大多数具有明显的细胞毒性。而且,compou。

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