14 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Non-Acidic Free Fatty Acid Receptor 4 Agonists with Antidiabetic Activity.

University of Southern Denmark
Development and Characterization of a Potent Free Fatty Acid Receptor 1 (FFA1) Fluorescent Tracer.

University of Southern Denmark
Discovery of a Potent Free Fatty Acid 1 Receptor Agonist with Low Lipophilicity, Low Polar Surface Area, and Robust in Vivo Efficacy.

University of Southern Denmark
Discovery of TUG-770: A Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatment of Type 2 Diabetes.

University of Southern Denmark
Discovery of a potent and selective free fatty acid receptor 1 agonist with low lipophilicity and high oral bioavailability.

University of Southern Denmark
Synthesis and in vitro evaluation of a selective antagonist and the corresponding radioligand for the prostaglandin D2 receptor CRTH2.

University of Southern Denmark
Discovery of a potent and selective GPR120 agonist.

University of Southern Denmark
Identification of a potent and selective free fatty acid receptor 1 (FFA1/GPR40) agonist with favorable physicochemical and in vitro ADME properties.

University of Southern Denmark
Free fatty acid receptor 1 (FFA1/GPR40) agonists: mesylpropoxy appendage lowers lipophilicity and improves ADME properties.

University of Southern Denmark
Thermodynamic and biological evaluation of a thrombin binding aptamer modified with several unlocked nucleic acid (UNA) monomers and a 2'-C-piperazino-UNA monomer.

University of Southern Denmark
Discovery of potent and selective agonists for the free fatty acid receptor 1 (FFA(1)/GPR40), a potential target for the treatment of type II diabetes.

University of Southern Denmark
Hit-to-Lead Identification and Validation of a Triaromatic Pleuromutilin Antibiotic Candidate.

University of Southern Denmark
Reading and erasing of histone crotonyllysine mimics by the AF9 YEATS domain and SIRT2 deacylase.

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

University of Southern Denmark