Design, synthesis and biological evaluation of novel pyrimidinedione derivatives as DPP-4 inhibitors

被引:30
|
作者
Li, Ning [1 ,2 ,3 ,4 ]
Wang, Li-Jun [1 ,2 ,4 ]
Jiang, Bo [1 ,2 ,4 ]
Guo, Shu-Ju [1 ,2 ,4 ]
Li, Xiang-Qian [1 ,2 ,4 ]
Chen, Xue-Chun [5 ]
Luo, Jiao [1 ,2 ,3 ,4 ]
Li, Chao [1 ,2 ,3 ,4 ]
Wang, Yi [5 ]
Shi, Da-Yong [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266235, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Ctr Ocean Mega Sci, Qingdao 266071, Peoples R China
[5] Zhejiang Univ, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Pyrimidinedionederivatives; DPP-4; inhibitor; Molecular hybrid; SARs; Type; 2; diabetes; ALGA RHODOMELA-CONFERVOIDES; DIPEPTIDYL PEPTIDASE-4 INHIBITORS; PHOSPHATASE 1B INHIBITOR; C57BL/KSJ-DB/DB MICE; BROMOPHENOLS; DISCOVERY; HPN;
D O I
10.1016/j.bmcl.2018.05.022
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel pyrimidinedione derivatives were designed and evaluated for in vitro dipeptidyl peptidase-4 (DPP-4) inhibitory activity and in vivo anti-hyperglycemic efficacy. Among them, the representative compounds 11, 15 and 16 showed excellent inhibitory activity of DPP-4 with IC50 values of 64.47 nM, 188.7 nM and 65.36 nM, respectively. Further studies revealed that compound 11 was potent in vivo hypoglycemic effect. The structure-activity relationships of these pyrimidinedione derivatives had been discussed, which would be useful for developing novel DPP-4 inhibitors as treating type 2 diabetes.
引用
收藏
页码:2131 / 2135
页数:5
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