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Novel ketooxazole based inhibitors of fatty acid amide hydrolase (FAAH)
Authors:Timmons Amy  Seierstad Mark  Apodaca Rich  Epperson Matt  Pippel Dan  Brown Sean  Chang Leon  Scott Brian  Webb Michael  Chaplan Sandra R  Breitenbucher J Guy
Affiliation:Johnson & Johnson Pharmaceutical Research and Development, L.L.C., 3210 Merryfield Row, San Diego, CA 92121, USA.
Abstract:Efforts to improve the properties of the well studied ketooxazole FAAH inhibitor OL-135 resulted in the discovery of a novel propylpiperidine series of FAAH inhibitors that has a modular design and superior properties to OL-135. The efficacy of one of these compounds was demonstrated in a rat spinal nerve ligation model of neuropathic pain in rats.
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