TY - JOUR
T1 - Drug discovery approaches targeting the incretin pathway
AU - Deng, Xinxian
AU - Tavallaie, Mojdeh S.
AU - Sun, Ran
AU - Wang, Juntao
AU - Cai, Qingqing
AU - Shen, Jian
AU - Lei, Shuwen
AU - Fu, Lei
AU - Jiang, Faqin
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/6
Y1 - 2020/6
N2 - 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 action mechanisms of 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.
AB - 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 action mechanisms of 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.
KW - DPP-4 inhibitors
KW - Drug discovery
KW - GLP-1 receptor agonists
KW - Incretin pathway
KW - Ligand-receptor interactions
UR - http://www.scopus.com/inward/record.url?scp=85083364813&partnerID=8YFLogxK
U2 - 10.1016/j.bioorg.2020.103810
DO - 10.1016/j.bioorg.2020.103810
M3 - Review article
C2 - 32325333
AN - SCOPUS:85083364813
SN - 0045-2068
VL - 99
JO - Bioorganic Chemistry
JF - Bioorganic Chemistry
M1 - 103810
ER -