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Molecular Pharmacology|January 4, 2008
Activation of TRPA1 by farnesyl thiosalicylic acidMichael Maher, Hong Ao, Tue Banke, et al.
British Journal of Pharmacology|February 28, 2006
Inhibition of fatty acid amide hydrolase produces analgesia by multiple mechanismsLeon Chang, Lin Luo, James A Palmer, et al.
Bioorganic & Medicinal Chemistry Letters|February 22, 2008
Novel ketooxazole based inhibitors of fatty acid amide hydrolase (FAAH)Amy Timmons, Mark Seierstad, Rich Apodaca, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 11, 2007
Pharmacology and antitussive efficacy of 4-(3-trifluoromethyl-pyridin-2-yl)-piperazine-1-carboxylic acid (5-trifluoromethyl-pyridin-2-yl)-amide (JNJ17203212), a transient receptor potential vanilloid 1 antagonist in guinea pigsAnindya Bhattacharya, Brian P Scott, Nadia Nasser, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 25, 2003
Neuronal hyperpolarization-activated pacemaker channels drive neuropathic painSandra R Chaplan, Hong-Qing Guo, Doo Hyun Lee, et al.
Bioorganic & Medicinal Chemistry Letters|August 10, 2011
Discovery of a novel series of selective HCN1 blockersKelly J McClure, Michael Maher, Nancy Wu, et al.
Journal of Biomolecular Screening|April 1, 2005
Identifying modulators of hERG channel activity using the PatchXpress planar patch clampAdrienne E Dubin, Nadia Nasser, Jutta Rohrbacher, et al.
Bioorganic & Medicinal Chemistry Letters|September 6, 2016
The discovery and preclinical characterization of 6-chloro-N-(2-(4,4-difluoropiperidin-1-yl)-2-(2-(trifluoromethyl)pyrimidin-5-yl)ethyl)quinoline-5-carboxamide based P2X7 antagonistsJason C Rech, Anindya Bhattacharya, Bryan J Branstetter, et al.
European Journal of Pharmacology|May 22, 2020
Selective inhibition of peripheral cathepsin S reverses tactile allodynia following peripheral nerve injury in mouseWilliam A Eckert, John J M Wiener, Hui Cai, et al.
Anesthesia and Analgesia|December 20, 2008
Biochemical and biological properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a mechanism-based inhibitor of fatty acid amide hydrolaseMark J Karbarz, Lin Luo, Leon Chang, et al.
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