A novel benzazepinone sodium channel blocker with oral efficacy in a rat model of neuropathic pain
摘要:
A series of benzazepinones were synthesized and evaluated for block of Na(v)1.7 sodium channels. Compound 30 from this series displayed potent channel block, good selectivity versus other targets, and dose-dependent oral efficacy in a rat model of neuropathic pain. (C) 2013 Elsevier Ltd. All rights reserved.
A novel benzazepinone sodium channel blocker with oral efficacy in a rat model of neuropathic pain
摘要:
A series of benzazepinones were synthesized and evaluated for block of Na(v)1.7 sodium channels. Compound 30 from this series displayed potent channel block, good selectivity versus other targets, and dose-dependent oral efficacy in a rat model of neuropathic pain. (C) 2013 Elsevier Ltd. All rights reserved.