首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and biological evaluation of cinnamido linked pyrrolo(2,1-c)(1,4)benzodiazepines as antimitotic agents.
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Synthesis and biological evaluation of cinnamido linked pyrrolo(2,1-c)(1,4)benzodiazepines as antimitotic agents.

机译:肉桂酸连接的吡咯并(2,1-c)(1,4)苯并二氮杂作为抗有丝分裂剂的合成及生物学评价。

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摘要

A series of new cinnamido-pyrrolo[2,1-c][1,4]benzodiazepine conjugates (4a-d and 5a-d) and their dimers (6a-d) have been designed, synthesized and evaluated for their biological activity. The anticancer screening of compound 4a by the NCI exhibited significant GI50 values ranging from 68 to 732 nM against 53 of 59 human cancer cell lines tested. Compounds 5a-d and 6a-d have also shown remarkable cytotoxic activity with GI50 values <0.1 microM concentrations in a large number of cell lines. Interestingly, compounds 5b and 6b have been identified as a new class of inhibitors of tubulin polymerization and their action has been rationalized by the cell cycle arrest in G0 and G2/M phase.
机译:已设计,合成并评估了一系列新的肉桂吡咯并[2,1-c] [1,4]苯二氮杂共轭物(4a-d和5a-d)及其二聚体(6a-d)。 NCI对化合物4a的抗癌筛选显示出相对于测试的59种人类癌细胞系中的53种,GI68值范围从68到732 nM。化合物5a-d和6a-d在大量细胞系中也显示出显着的细胞毒性活性,GI50值<0.1 microM。有趣的是,化合物5b和6b已被确定为一类新的微管蛋白聚合抑制剂,其作用已通过G0和G2 / M期的细胞周期停滞而合理化。

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