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

被引:33
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
中国国家自然科学基金; 美国国家科学基金会;
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
相关论文
共 23 条
[1]   An update on DPP-4 inhibitors in the management of type 2 diabetes [J].
Cahn, Avivit ;
Cernea, Simona ;
Raz, Itamar .
EXPERT OPINION ON EMERGING DRUGS, 2016, 21 (04) :409-419
[2]   Synthesis and protein tyrosine phosphatase 1B inhibition activities of two new synthetic bromophenols and their methoxy derivatives [J].
Cui Yongchao ;
Shi Dayong ;
Hu Zhiqiang .
CHINESE JOURNAL OF OCEANOLOGY AND LIMNOLOGY, 2011, 29 (06) :1237-1242
[3]   BOTH SUBCUTANEOUSLY AND INTRAVENOUSLY ADMINISTERED GLUCAGON-LIKE PEPTIDE-I ARE RAPIDLY DEGRADED FROM THE NH2-TERMINUS IN TYPE-II DIABETIC-PATIENTS AND IN HEALTHY-SUBJECTS [J].
DEACON, CF ;
NAUCK, MA ;
TOFTNIELSEN, M ;
PRIDAL, L ;
WILLMS, B ;
HOLST, JJ .
DIABETES, 1995, 44 (09) :1126-1131
[4]  
Ebert R, 1987, DIABETES-METAB RES, V3, P185
[5]  
Fan X, 2003, CHINESE CHEM LETT, V14, P939
[6]   Bromophenols from the red alga Rhodomela confervoides [J].
Fan, X ;
Xu, NJ ;
Shi, JG .
JOURNAL OF NATURAL PRODUCTS, 2003, 66 (03) :455-458
[7]   Synthesis of three bromophenols from red algae as PTP1B inhibitors [J].
Guo Shuju ;
Li Jing ;
Li Ting ;
Shi Dayong ;
Han Lijun .
CHINESE JOURNAL OF OCEANOLOGY AND LIMNOLOGY, 2011, 29 (01) :68-74
[8]  
H D B C B S, 2012, BIOCH PHARM, V83, P823
[9]   The physiology of glucagon-like peptide 1 [J].
Holst, Jens Juul .
PHYSIOLOGICAL REVIEWS, 2007, 87 (04) :1409-1439
[10]  
Hu HP, 2017, CN106632241A, Patent No. 106632241