微管蛋白
部分
尿素
化学
对接(动物)
立体化学
解聚
氨基酸
有丝分裂
微管
主轴装置
组合化学
生物化学
细胞
细胞分裂
生物
有机化学
细胞生物学
医学
护理部
作者
Rakhi Chaudhary,Shuaib,Syed Riaz Hashim,Prem Shankar Mishra
出处
期刊:Der Pharma Chemica
日期:2015-01-01
卷期号:7 (10): 493-503
摘要
Substituted cinnamoyl ureas have been identified as novel compounds with their various biological acti vities. The novel cinnamoyl ureas were synthesized successfully by various substitutions, at the various position, which further were evaluated for their tubulin inhibitor activity .Thus in this research work, we aimed to use all th ese active moieties with urea and phenyl urea substitutions at carbonyl moiety. Molecular docking study was used for confirming their interaction with tubulin protein t aking MSE137, ACO 201 and MSE148 as tubulin molecu le for their antitumor activity. Through molecular docking study, the result showed that all the synthesized compounds act by inhibiting cell mitosis by binding to the protei n tubulin in the mitotic spindle and preventing pol ymerization or depolymerization into the microtubules . Among the synthesized compounds 3a,3b, 3d showed higher no of interaction with amino acids of tubulin molecule , thus they were considered as good antitumor agents.
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