1. Academic Validation
  2. Discovery of non-zwitterionic aryl sulfonamides as Nav1.7 inhibitors with efficacy in preclinical behavioral models and translational measures of nociceptive neuron activation

Discovery of non-zwitterionic aryl sulfonamides as Nav1.7 inhibitors with efficacy in preclinical behavioral models and translational measures of nociceptive neuron activation

  • Bioorg Med Chem. 2017 Oct 15;25(20):5490-5505. doi: 10.1016/j.bmc.2017.08.012.
Yong-Jin Wu 1 Jason Guernon 2 Andrea McClure 2 Guanglin Luo 2 Ramkumar Rajamani 2 Alicia Ng 3 Amy Easton 2 Amy Newton 2 Clotilde Bourin 2 Dawn Parker 2 Kathleen Mosure 2 Omar Barnaby 2 Matthew G Soars 2 Ronald J Knox 2 Michele Matchett 2 Rick Pieschl 2 James Herrington 2 Ping Chen 2 D V Sivarao 2 Linda J Bristow 2 Nicholas A Meanwell 2 Joanne Bronson 2 Richard Olson 2 Lorin A Thompson 2 Carolyn Dzierba 2
Affiliations

Affiliations

  • 1 Bristol-Myers Squibb Research and Development, 5 Research Parkway, Wallingford, CT 06492-7660, USA. Electronic address: yong-jin.wu@bms.com.
  • 2 Bristol-Myers Squibb Research and Development, 5 Research Parkway, Wallingford, CT 06492-7660, USA.
  • 3 One Squibb Drive, New Brunswick, NJ 08903, USA.
Abstract

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 the discovery of the non-zwitterionic aryl sulfonamide 49 as a selective Nav1.7 inhibitor with improved membrane permeability. Despite its moderate cellular activity, 49 exhibited robust efficacy in mouse models of neuropathic and inflammatory pain and modulated translational electromyogram measures associated with activation of nociceptive neurons.

Keywords

Benzenesulfonamide; Membrane permeability; Na(v)1.7 inhibitor; Neuropathic and inflammatory pain; Nociceptive flexion reflex (NFR); Translational electromyogram.

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