1211875-20-5Relevant academic research and scientific papers
Identification of a potent, state-dependent inhibitor of Nav1.7 with oral efficacy in the formalin model of persistent pain
Bregman, Howard,Berry, Loren,Buchanan, John L.,Chen, April,Du, Bingfan,Feric, Elma,Hierl, Markus,Huang, Liyue,Immke, David,Janosky, Brett,Johnson, Danielle,Li, Xingwen,Ligutti, Joseph,Liu, Dong,Malmberg, Annika,Matson, David,McDermott, Jeff,Miu, Peter,Nguyen, Hanh Nho,Patel, Vinod F.,Waldon, Daniel,Wilenkin, Ben,Zheng, Xiao Mei,Zou, Anruo,McDonough, Stefan I.,Dimauro, Erin F.
, p. 4427 - 4445 (2011/09/14)
Clinical human genetic studies have recently identified the tetrodotoxin (TTX) sensitive neuronal voltage gated sodium channel Nav1.7 (SCN9A) as a critical mediator of pain sensitization. Herein, we report structure-activity relationships for a novel series of 2,4-diaminotriazines that inhibit hNav1.7. Optimization efforts culminated in compound 52, which demonstrated pharmacokinetic properties appropriate for in vivo testing in rats. The binding site of compound 52 on Nav1.7 was determined to be distinct from that of local anesthetics. Compound 52 inhibited tetrodotoxin-sensitive sodium channels recorded from rat sensory neurons and exhibited modest selectivity against the hERG potassium channel and against cloned and native tetrodotoxin-resistant sodium channels. Upon oral administration to rats, compound 52 produced dose- and exposure-dependent efficacy in the formalin model of pain.
ARYL CARBOXAMIDE DERIVATIVES AS SODIUM CHANNEL INHIBITORS FOR TREATMENT OF PAIN
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, (2011/09/19)
The present invention provides compounds that are inhibitors of voltage-gated sodium channels (Nav), in particular Nav 1.7, and are therefore useful for the treatment of diseases treatable by inhibition of these channels, in particular, chronic pain disorders. Also provided are pharmaceutical compositions containing such compounds and processes for preparing such compounds.
