| Literature DB >> 32325333 |
Xinxian Deng1, Mojdeh S Tavallaie1, Ran Sun1, Juntao Wang1, Qingqing Cai2, Jian Shen3, Shuwen Lei1, Lei Fu4, Faqin Jiang5.
Abstract
Incretin pathway plays an important role in the development of diabetes medications. Interventions in DPP-4 and GLP-1 receptor have shown remarkable efficacy in experimental and clinical studies and imperatively become one of the most promising therapeutic approaches in the T2DM drug discovery pipeline. Herein, we analyzed the actionmechanismsof DPP-4 and GLP-1 receptor targeting the incretin pathway in T2DM treatment. We gave an insight into the structural requirements for the potent DPP-4 inhibitors and revealed a classification of DPP-4 inhibitors by stressing on the binding modes of these ligands to the enzyme. We then reviewed the drug discovery strategies for the development of peptide and non-peptide GLP-1 receptor agonists (GLP-1 RAs). Furthermore, the drug design strategies for DPP-4 inhibitors and GLP-1R agonists were detailed accurately. This review might provide an efficient evidence for the highly potent and selective DPP-4 inhibitors and the GLP-1 RAs, as novel medicines for patients suffering from T2DM.Entities:
Keywords: DPP-4 inhibitors; Drug discovery; GLP-1 receptor agonists; Incretin pathway; Ligand-receptor interactions
Year: 2020 PMID: 32325333 DOI: 10.1016/j.bioorg.2020.103810
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275