Non-Acidic Free Fatty Acid Receptor 4 Agonists with Antidiabetic Activity

Azevedo, Carlos and Watterson, Kenneth and Wargent, Edward T. and Hansen, Steffen and Hudson, Brian and Kępczyńska, Malgorzata A. and Dunlop, Julia and Shumpukade, Bharat and Christiansen, Elisabeth and Milligan, Graeme and Stocker, Claire J. and Ulven, Trond (2016) Non-Acidic Free Fatty Acid Receptor 4 Agonists with Antidiabetic Activity. Journal of Medicinal Chemistry, 59 (19). pp. 8868-8878. ISSN 0022-2623

[img]
Preview
Text
s1-ln2165809-1218727287-1939656818Hwf-86736386IdV2036941942165809PDF_HI0001 (002).pdf

Download (1MB) | Preview
[img]
Preview
Text
SI_Banyu_revised_160713.pdf

Download (206kB) | Preview
Official URL: http://pubs.acs.org/doi/abs/10.1021/acs.jmedchem.6...

Abstract

The free fatty acid receptor 4 (FFA4 or GPR120) has appeared as an interesting potential target for the treatment of metabolic disorders. At present, most FFA4 ligands are carboxylic acids that are assumed to mimic the endogenous long-chain fatty acid agonists. Here, we report preliminary structure-activity relationship studies of a previously disclosed nonacidic sulfonamide FFA4 agonist. Mutagenesis studies indicate that the compounds are orthosteric agonists despite the absence of a carboxylate function. The preferred compounds showed full agonist activity on FFA4 and complete selectivity over FFA1, although a significant fraction of these noncarboxylic acids also showed partial antagonistic activity on FFA1. Studies in normal and diet-induced obese (DIO) mice with the preferred compound 34 showed improved glucose tolerance after oral dosing in an oral glucose tolerance test. Chronic dosing of 34 in DIO mice resulted in significantly increased insulin sensitivity and a moderate but significant reduction in bodyweight, effects that were also present in mice lacking FFA1 but absent in mice lacking FFA4.

Item Type: Article
Uncontrolled Keywords: Free fatty acid receptors; FFA4; GPR120; Insuline sensitivity
Subjects: Q Science > QD Chemistry
Q Science > QP Physiology
Divisions: School of Science > Metabolic Research
Depositing User: Julie Cakebread
Date Deposited: 01 Nov 2016 11:59
Last Modified: 03 Feb 2017 12:51
URI: http://bear.buckingham.ac.uk/id/eprint/152

Actions (login required)

View Item View Item