| Literature DB >> 27825762 |
Cheng Chen1, He Li2, Ya-Qiu Long3.
Abstract
GPR40 belongs to the GPCR family and the activation of GPR40 has been shown to induce glucose-stimulated insulin secretion (GSIS) from pancreatic beta cells as well as incretin secretion from intestinal endocrine cells. Therefore, GPR40 has emerged as a viable and promising therapeutic target for type 2 diabetes mellitus (T2DM) without the risk of hypoglycemia. However, the termination of TAK-875 in phase III clinical trials for the hepatotoxicity issue threw doubt over the long-term safety of targeting GPR40. Herein, we summarized the newly disclosed biological characteristics and the druglikeness-based structural evolution of GPR40 agonists to advance the development of GPR40-based anti-diabetic drugs.Entities:
Keywords: Biased agonism; FFA1; GPR40; Glucose-stimulated insulin secretion; Type 2 diabetes
Mesh:
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Year: 2016 PMID: 27825762 DOI: 10.1016/j.bmcl.2016.10.074
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823