1629041-92-4Relevant articles and documents
Discovery of non-zwitterionic aryl sulfonamides as Nav1.7 inhibitors with efficacy in preclinical behavioral models and translational measures of nociceptive neuron activation
Wu, Yong-Jin,Guernon, Jason,McClure, Andrea,Luo, Guanglin,Rajamani, Ramkumar,Ng, Alicia,Easton, Amy,Newton, Amy,Bourin, Clotilde,Parker, Dawn,Mosure, Kathleen,Barnaby, Omar,Soars, Matthew G.,Knox, Ronald J.,Matchett, Michele,Pieschl, Rick,Herrington, James,Chen, Ping,Sivarao,Bristow, Linda J.,Meanwell, Nicholas A.,Bronson, Joanne,Olson, Richard,Thompson, Lorin A.,Dzierba, Carolyn
, p. 5490 - 5505 (2017)
Since zwitterionic benzenesulfonamide Nav1.7 inhibitors suffer from poor membrane permeability, we sought to eliminate this characteristic by replacing the basic moiety with non-basic bicyclic acetals and monocyclic ethers. These efforts led to
DIAMINO-ALKYLAMINO-LINKED ARYLSULFONAMIDE COMPOUNDS WITH SELECTIVE ACTIVITY IN VOLTAGE-GATED SODIUM CHANNELS
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, (2018/06/06)
Disclosed are compounds of Formula A, or a salt thereof: Formula (A), wherein: Het, Q and R1A to R4A are defined herein, which compounds have properties for blocking Nav 1.7 ion channels found in peripheral and sympathetic
BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS
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Paragraph 0684-0685, (2018/06/29)
This invention is directed to benzenesulfonamide compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment of diseases or conditions associated with voltage-gated sodium channels, such as epilepsy and/or epileptic seizure disorders.