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Current Opinion in Pharmacology|October 30, 2007
Sodium channels and nociception: recent concepts and therapeutic opportunitiesDouglas S Krafte, Anthony W BannonEuropean Biophysics Journal : EBJ|November 27, 2002
Decrease of inward rectification as a mechanism for arachidonic acid-induced potentiation of hKir2.3Yi Liu, Dong Liu, Douglas S KrafteEuropean Journal of Pharmacology|February 1, 2002
Tenidap, a novel anti-inflammatory agent, is an opener of the inwardly rectifying K+ channel hKir2.3Yi Liu, Dong Liu, David Printzenhoff, et al.Anesthesia and Analgesia|July 18, 2009
The effect of kappa-opioid receptor agonists on tetrodotoxin-resistant sodium channels in primary sensory neuronsXin Su, Neil A Castle, Brett Antonio, et al.Channels (Austin, Tex.)|August 12, 2008
Block of Nav1.8 by small moleculesDouglas S Krafte, Mark Chapman, Brian Marron, et al.Neuropharmacology|June 23, 2010
A-887826 is a structurally novel, potent and voltage-dependent Na(v)1.8 sodium channel blocker that attenuates neuropathic tactile allodynia in ratsXu-Feng Zhang, Char-Chang Shieh, Mark L Chapman, et al.Epilepsia|March 26, 2018
A comprehensive approach to identifying repurposed drugs to treat SCN8A epilepsyTalia A Atkin, Chani M Maher, Aaron C Gerlach, et al.Proceedings of the National Academy of Sciences of the United States of America|July 3, 2013
Voltage sensor interaction site for selective small molecule inhibitors of voltage-gated sodium channelsKen McCormack, Sonia Santos, Mark L Chapman, et al.Bioorganic & Medicinal Chemistry|October 23, 2010
Discovery and biological evaluation of potent, selective, orally bioavailable, pyrazine-based blockers of the Na(v)1.8 sodium channel with efficacy in a model of neuropathic painMarc J C Scanio, Lei Shi, Irene Drizin, et al.Bioorganic & Medicinal Chemistry|May 27, 2008
Discovery of potent furan piperazine sodium channel blockers for treatment of neuropathic painIrene Drizin, Robert J Gregg, Marc J C Scanio, et al.Pageof 2