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Discovery of AM-1638: A Potent and Orally Bioavailable GPR40/FFA1 Full Agonist.

Authors :
Brown SP
Dransfield PJ
Vimolratana M
Jiao X
Zhu L
Pattaropong V
Sun Y
Liu J
Luo J
Zhang J
Wong S
Zhuang R
Guo Q
Li F
Medina JC
Swaminath G
Lin DC
Houze JB
Source :
ACS medicinal chemistry letters [ACS Med Chem Lett] 2012 Aug 15; Vol. 3 (9), pp. 726-30. Date of Electronic Publication: 2012 Aug 15 (Print Publication: 2012).
Publication Year :
2012

Abstract

GPR40 (FFA1) is a G-protein-coupled receptor, primarily expressed in pancreatic islets, the activation of which elicits increased insulin secretion only in the presence of elevated glucose levels. A potent, orally bioavailable small molecule GPR40 agonist is hypothesized to be an effective antidiabetic posing little or no risk of hypoglycemia. We recently reported the discovery of AMG 837 (1), a potent partial agonist of GPR40. Herein, we present the optimization from the GPR40 partial agonist 1 to the structurally and pharmacologically distinct GPR40 full agonist AM-1638 (21). Moreover, we demonstrate the improved in vivo efficacy that GPR40 full agonist 21 exhibits in BDF/DIO mice as compared to partial agonist 1.

Details

Language :
English
ISSN :
1948-5875
Volume :
3
Issue :
9
Database :
MEDLINE
Journal :
ACS medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
24900539
Full Text :
https://doi.org/10.1021/ml300133f