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Discovery of potent dipeptidyl peptidase IV inhibitors derived from β-aminoamides bearing substituted [1,2,3]-triazolopiperidines for the treatment of type 2 diabetes

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成果类型:
期刊论文
作者:
Shan, Zhenwei;Peng, Min;Fan, Houxing;Lu, Qingtao;Lu, Peng;...
通讯作者:
Chen, Yilang
作者机构:
[Lu, Qingtao; Shan, Zhenwei] Shandong Univ Tradit Chinese Med, Dept Med Chem, Jinan 250355, Shandong, Peoples R China.
[Fan, Houxing; Zhao, Chuansheng; Lu, Peng; Chen, Yilang] Shanghai Sun Sail Pharmaceut Sci & Technol Co Ltd, Dept Med Chem, Shanghai 201203, Peoples R China.
[Peng, Min] Hunan Univ Chinese Med, Dept Med Chem, Changsha 410208, Hunan, Peoples R China.
通讯机构:
[Chen, Yilang] S
Shanghai Sun Sail Pharmaceut Sci & Technol Co Ltd, Dept Med Chem, Shanghai 201203, Peoples R China.
语种:
英文
关键词:
Dipeptidyl peptidase IV inhibitors;Type 2 diabetes;Triazolopiperidine
期刊:
Bioorganic & Medicinal Chemistry Letters
ISSN:
0960-894X
年:
2011
卷:
21
期:
6
页码:
1731-1735
基金类别:
The authors are thankful for the financial support from Shanghai Municipal Natural Science Foundation (Project 09431901800).
机构署名:
本校为其他机构
院系归属:
药学院
摘要:
A series of novel [1,2,3]-triazolopiperidine derivatives 5a-5y were synthesized and evaluated as inhibitors of dipeptidyl peptidase IV (DPP-4) for the treatment of type 2 diabetes, most of the compounds exhibited excellent in vitro potency (IC50 <50 nM) against DPP-4. Among these, compound 5d with potent in vitro activity against DPP-4 and good pharmacokinetic profiles exhibited pronounced in vivo efficacy in an oral glucose tolerance test (OGTT) in ICR mice. On the base of these properties, compound 5d was selected as a potential new candidate for the tr...

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