20 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Exploration of phenylpropanoic acids as agonists of the free fatty acid receptor 4 (FFA4): Identification of an orally efficacious FFA4 agonist.

Glaxosmithkline
Polar aromatic periphery increases agonist potency of spirocyclic free fatty acid receptor (GPR40) agonists inspired by LY2881835.

Saint Petersburg State University
Free fatty acid receptor 1 (GPR40) agonists containing spirocyclic periphery inspired by LY2881835.

Saint Petersburg State University
Novel free fatty acid receptor 1 (GPR40) agonists based on 1,3,4-thiadiazole-2-carboxamide scaffold.

Saint Petersburg State University
Phenoxymethyl 1,3-oxazoles and 1,2,4-oxadiazoles as potent and selective agonists of free fatty acid receptor 1 (GPR40).

Enamine
Identification of diarylsulfonamides as agonists of the free fatty acid receptor 4 (FFA4/GPR120).

Glaxosmithkline
Discovery and optimization of an azetidine chemical series as a free fatty acid receptor 2 (FFA2) antagonist: from hit to clinic.

Galapagos
Discovery of TAK-875: A Potent, Selective, and Orally Bioavailable GPR40 Agonist.

TBA
The first synthetic agonists of FFA2: Discovery and SAR of phenylacetamides as allosteric modulators.

Amgen
Insights into the recent progress in the medicinal chemistry of pyranopyrimidine analogs.

Mansoura University
Structure-Activity Relationship Study and Biological Evaluation of 2-(Disubstituted phenyl)-indole-5-propanoic Acid Derivatives as GPR40 Full Agonists.

Sungkyunkwan University
Identification of free fatty acid receptor 2 agonists using virtual screening.

TBA
N-Thiazolylamide-based free fatty-acid 2 receptor agonists: Discovery, lead optimization and demonstration of off-target effect in a diabetes model.

Ogeda
Discovery of a Potent Thiazolidine Free Fatty Acid Receptor 2 Agonist with Favorable Pharmacokinetic Properties.

University of Southern Denmark
Microbiota-Host Transgenomic Metabolism, Bioactive Molecules from the Inside.

University of Bologna
Heteroaryl-substituted triazoles as APJ receptor agonists

Amgen
PD-1/PD-L1 inhibitors

Gilead Sciences
Salts and processes of preparing a PI3K inhibitor

Incyte
Substituted aminopyrimidine compounds and methods of use

Calitor Sciences
Inhibitors of the Renal Outer Medullary Potassium channel

Merck Sharp & Dohme