Identification of novel PPARα/γ dual agonists by virtual screening, ADMET prediction and molecular dynamics simulations

被引:10
作者
Liu, Xin [1 ]
Jing, Zhi [1 ]
Jia, Wen-Qing [1 ]
Wang, Shu-Qing [1 ]
Ma, Ying [1 ]
Xu, Wei-Ren [4 ]
Liu, Jian-Wen [2 ,3 ]
Cheng, Xian-Chao [1 ]
机构
[1] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therape, Tianjin 300070, Peoples R China
[2] East China Univ Sci & Technol, Sch Pharm, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab New Drug Design, Shanghai 200237, Peoples R China
[4] Tianjin Inst Pharmaceut Res, Tianjin Key Lab Mol Design & Drug Discovery, Tianjin 300193, 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
PPAR alpha; PPAR gamma; virtual screening; ADMET; molecular dynamics; PROLIFERATOR-ACTIVATED RECEPTORS; ACCURATE DOCKING; LIGAND-BINDING; GAMMA; ALPHA; METABOLISM; ABSORPTION; RESISTANCE; GLIDE;
D O I
10.1080/07391102.2017.1373706
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
PPAR alpha and PPAR gamma have been the most widely studied Peroxisome proliferator-activated receptor (PPAR) subtypes due to their important roles in regulating glucose, lipids, and cholesterol metabolism. By combining the lowering serum triglyceride levels benefit of PPAR alpha agonists (such as fibrates) with the glycemic advantages of the PPAR gamma agonists (such as TZD), the dual PPAR agonists approach can both improve the metabolic effects and minimize the side effects caused by either agent alone, and hence, has become a promising strategy for designing effective drugs against type-2 diabetes. In this study, by means of virtual screening, ADMET prediction and molecular dynamics (MD) simulations techniques, one compound-ASN15761007 with high binding score, low toxicity were gained. It was observed by MD simulations that ASN15761007 not only possessed the same function as AZ242 did in activating PPAR alpha and BRL did in activating PPAR gamma, but also had more favorable conformation for binding to the two receptors. Our results provided an approach to rapidly produce novel PPAR alpha/gamma dual agonists which might be a potential lead compound to develop against insulin resistance and hyperlipidemia.
引用
收藏
页码:2988 / 3002
页数:15
相关论文
共 50 条