| Literature DB >> 25082126 |
Eun Ju Park1, Young Gil Ahn2, Seung Hyun Jung2, Hyo Jeong Bang1, Mira Kim1, Dong Jin Hong1, Jisook Kim2, Kwee Hyun Suh2, Young Jin Kim3, Doran Kim3, Eun-Yeong Kim4, Kiho Lee4, Kyung Hoon Min5.
Abstract
Takeda G-protein-coupled receptor 5 (TGR5) is a promising molecular target for metabolic diseases. A series of 4-(2,5-dichlorophenoxy)pyrimidine and cyclopropylmalonamide derivatives were synthesized as potent agonists of TGR5 based on a bioisosteric replacement strategy. Several compounds exhibited improved potency, compared to a reference compound with a pyridine scaffold. The pharmacokinetic profile of the representative compound 18 was considered moderate.Entities:
Keywords: Agonist; Bioisostere; Malonamide; Pyrimidine; TGR5
Mesh:
Substances:
Year: 2014 PMID: 25082126 DOI: 10.1016/j.bmcl.2014.07.026
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823