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Design, Synthesis, and Structure–Activity Relationships of 3,4,5‐Trisubstituted 4,5‐Dihydro‐1,2,4‐oxadiazoles as TGR5 Agonists
Author(s) -
Zhu Junjie,
Ye Yangliang,
Ning Mengmeng,
Mándi Attila,
Feng Ying,
Zou Qingan,
Kurtán Tibor,
Leng Ying,
Shen Jianhua
Publication year - 2013
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.201300144
Subject(s) - pharmacophore , g protein coupled bile acid receptor , chemistry , rational design , stereochemistry , ligand (biochemistry) , bile acid , biochemistry , receptor , materials science , nanotechnology
Given its role in the mediation of energy and glucose homeostasis, the G‐protein‐coupled bile acid receptor 1 (TGR5) is considered a potential target for the treatment of type 2 diabetes mellitus and other metabolic disorders. By thorough analysis of diverse structures of published TGR5 agonists, a hypothetical ligand‐based pharmacophore model was built, and a new class of potent TGR5 agonists, based on the novel 3,4,5‐trisubstituted 4,5‐dihydro‐1,2,4‐oxadiazole core, was discovered by rational design. Three distinct synthetic methods for constructing 4,5‐dihydro‐1,2,4‐oxadiazoles and extensive structure–activity relationship studies are reported herein. Compound ( R )‐ 54 n , the structure of which was determined by single‐crystal X‐ray diffraction and quantum chemical solid‐state TDDFT‐ECD calculations, showed the best potency, with an EC 50 value of 1.4 n M toward hTGR5. Its favorable properties in vitro warrant further investigation.