Synthesis, evaluation, molecular dynamics simulation and targets identification of novel pyrazole-containing imide derivatives

被引:13
作者
Cai, Wenxi [1 ,2 ]
Wu, Jingwei [1 ]
Sun, Yingzhan [1 ]
Liu, Ailin [3 ]
Wang, Runling [1 ]
Ma, Ying [1 ]
Wang, Shuqing [1 ]
Dong, Weili [1 ]
机构
[1] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therape, Tianjin 300070, Peoples R China
[2] Characterist Med Ctr PAP, Dept Pharm, Tianjin, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Natl Ctr Pharmaceut Screening, Inst Mat Med, Beijing, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Antitumor agents; biological activity; molecule docking; pharmmapper; molecular dynamics simulation; ACID-BINDING PROTEIN; WEB SERVER; DESIGN; LOCALIZATION; INHIBITORS; RECEPTORS; APOPTOSIS; DOCKING;
D O I
10.1080/07391102.2020.1745284
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new series of novel pyrazole-containing imide derivatives were synthesized and evaluated for their anticancer activities against A-549, Bel7402, and HCT-8 cell lines. Among these compounds A2, A4, A11 and A14 possessed high inhibition activity against A-549 cell lines with IC50 values at 4.91, 3.22, 27.43 and 18.14 mu M, respectively, better than that of 5-fluorouracil (IC50=59.27 mu M). A2, A4, and A11 also exhibited significant inhibitory activity towards HCT-8 and Bel7402 cell lines. Interestingly, the Heat Shock Protein 90 alpha (Hsp90 alpha, PDB ID: 1UYK) was found to be the potential drug target of these synthesized compounds with the aid of PharmMapper server () and docking module of Schrodinger (Maestro 10.2). Additionally, molecular dynamics simulation was performed out to explore the most likely binding mode of compound A2 with Hsp90 alpha. Communicated by Ramaswamy H. Sarma
引用
收藏
页码:2176 / 2188
页数:13
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