• J. Med. Chem. · Oct 2011

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

    • Elisabeth Christiansen, Christian Urban, Manuel Grundmann, Maria E Due-Hansen, Ellen Hagesaether, Johannes Schmidt, Leonardo Pardo, Susanne Ullrich, Evi Kostenis, Matthias Kassack, and Trond Ulven.
    • Department of Physics and Chemistry, University of Southern Denmark, Campusvej 55, DK-5230 Odense M, Denmark.
    • J. Med. Chem. 2011 Oct 13; 54 (19): 6691-703.

    AbstractThe free fatty acid receptor 1 (FFA1, also known as GPR40) enhances glucose-stimulated insulin secretion from pancreatic β-cells and is recognized as an interesting new target for treatment of type 2 diabetes. Several series of selective FFA1 agonists are already known. Most of these are derived from free fatty acids (FFAs) or glitazones and are relatively lipophilic. Aiming for the development of potent, selective, and less lipophilic FFA1 agonists, the terminal phenyl of a known compound series was replaced by nitrogen containing heterocycles. This resulted in the identification of 37, a selective FFA1 agonist with potent activity on recombinant human FFA1 receptors and on the rat insulinoma cell line INS-1E, optimal lipophilicity, and excellent in vitro permeability and metabolic stability.

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