Pharmacological Characterization of JNJ-40068782, a New Potent, Selective, and Systemically Active Positive Allosteric Modulator of the mGlu2 Receptor and Its Radioligand [3H]JNJ-40068782

@article{Lavreysen2013PharmacologicalCO,
  title={Pharmacological Characterization of JNJ-40068782, a New Potent, Selective, and Systemically Active Positive Allosteric Modulator of the mGlu2 Receptor and Its Radioligand [3H]JNJ-40068782},
  author={Hilde Lavreysen and Xavier Langlois and Abdel Ahnaou and Wilhelmus H.I.M. Drinkenburg and Paula te Riele and Ilse Biesmans and Ilse van der Linden and Luc Peeters and Anton A Megens and Cindy Wintmolders and Jos{\'e} Mar{\'i}a Cid and Andr{\'e}s A. Trabanco and Jos{\'e} Ignacio Andr{\'e}s and Frank Matthias Dautzenberg and Robert Johannes L{\"u}tjens and Gregor James Macdonald and John R. Atack},
  journal={The Journal of Pharmacology and Experimental Therapeutics},
  year={2013},
  volume={346},
  pages={514 - 527}
}
Modulation of the metabotropic glutamate type 2 (mGlu2) receptor is considered a promising target for the treatment of central nervous system diseases such as schizophrenia. Here, we describe the pharmacological properties of the novel mGlu2 receptor positive allosteric modulator (PAM) 3-cyano-1-cyclopropylmethyl-4-(4-phenyl-piperidin-1-yl)-pyridine-2(1H)-one (JNJ-40068782) and its radioligand [3H]JNJ-40068782. In guanosine 5′-O-(3-[35S]thio)triphosphate binding, JNJ-40068782 produced a… 

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