CHRISTOPHER JAMES WEST
Pilots at Chancellors Rdg Ct, Cary, NC
License number
North Carolina A1703860
Issued Date
Apr 2016
Expiration Date
Oct 2016
Category
Airmen
Type
Authorized Aircraft Instructor
Address
Address
107 Chancellors Ridge Ct, Cary, NC 27513
Personal information
See more information about CHRISTOPHER JAMES WEST at radaris.comName
Address
Phone
46 Chinaberry Crse, Chapel Hill, NC 27516
481 Tuttles Grove Rd, Beaufort, NC 28516
5133 Autumncrest Dr, Greensboro, NC 27407
511 W E St, Erwin, NC 28339
345 Lee Ave, Lexington, NC 27295
Professional information
Sodium Channel Inhibitors
US Patent:
8124610, Feb 28, 2012
Filed:
Jul 14, 2008
Appl. No.:
12/173012
Inventors:
Alan Bradley Fulp - Williow Spring NC, US
Matthew Scott Johnson - Durham NC, US
Christopher John Markworth - Durham NC, US
Brian Edward Marron - Durham NC, US
Darrick Conway Seconi - Cary NC, US
Christopher William West - Cary NC, US
Xiaodong Wang - Chapel Hill NC, US
Shulan Zhou - Chapel Hill NC, US
Matthew Scott Johnson - Durham NC, US
Christopher John Markworth - Durham NC, US
Brian Edward Marron - Durham NC, US
Darrick Conway Seconi - Cary NC, US
Christopher William West - Cary NC, US
Xiaodong Wang - Chapel Hill NC, US
Shulan Zhou - Chapel Hill NC, US
Assignee:
Icagen Inc. - Durham NC
International Classification:
C07D 409/12, A61K 31/44
US Classification:
514275, 514342, 514370, 544322, 5462707, 548197
Abstract:
Compounds, compositions and methods are provided which are useful in the treatment of diseases through the inhibition of sodium ion flux through voltage-gated sodium channels. More particularly, the invention provides substituted sulfonamides, compositions comprising these compounds, as well as methods of using these compounds or compositions in the treatment of central or peripheral nervous system disorders, particularly pain and chronic pain by blocking sodium channels associated with the onset or recurrence of the indicated conditions. The compounds, compositions and methods of the present invention are of particular use for treating neuropathic or inflammatory pain by the inhibition of ion flux through a voltage-gated sodium channel.