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Identification of an Orally Efficacious GPR40/FFAR1 Receptor Agonist.


ABSTRACT: GPR40/FFAR1 is a G protein-coupled receptor predominantly expressed in pancreatic ?-cells and activated by long-chain free fatty acids, mediating enhancement of glucose-stimulated insulin secretion. A novel series of substituted 3-(4-aryloxyaryl)propanoic acid derivatives were prepared and evaluated for their activities as GPR40 agonists, leading to the identification of compound 5, which is highly potent in in vitro assays and exhibits robust glucose lowering effects during an oral glucose tolerance test in nSTZ Wistar rat model of diabetes (ED50 = 0.8 mg/kg; ED90 = 3.1 mg/kg) with excellent pharmacokinetic profile, and devoid of cytochromes P450 isoform inhibitory activity.

SUBMITTER: Agarwal S 

PROVIDER: S-EPMC5150676 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature

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Identification of an Orally Efficacious GPR40/FFAR1 Receptor Agonist.

Agarwal Sameer S   Sasane Santosh S   Deshmukh Prashant P   Rami Bhadresh B   Bandyopadhyay Debdutta D   Giri Poonam P   Giri Suresh S   Jain Mukul M   Desai Ranjit C RC  

ACS medicinal chemistry letters 20160921 12


GPR40/FFAR1 is a G protein-coupled receptor predominantly expressed in pancreatic β-cells and activated by long-chain free fatty acids, mediating enhancement of glucose-stimulated insulin secretion. A novel series of substituted 3-(4-aryloxyaryl)propanoic acid derivatives were prepared and evaluated for their activities as GPR40 agonists, leading to the identification of compound <b>5</b>, which is highly potent in <i>in vitro</i> assays and exhibits robust glucose lowering effects during an ora  ...[more]

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