N-substituted indazole sulfonamide compounds with selective activity in voltage-gated sodium channels
Disclosed are compounds of Formula AA and Formula AB: wherein "Heteroaryl-1", RA1, RA2, RB1, and RC are defined herein, which novel compounds have properties for blocking Nav 1.7 ion channels found in peripheral and sympathetic neurons. Also described are pharmaceutical formulations compri...
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creator | KELLY, III MICHAEL J PERO JOSEPH E LEHMAN HANNAH D. G. F ROSSI MICHAEL A LAYTON MARK E |
description | Disclosed are compounds of Formula AA and Formula AB: wherein "Heteroaryl-1", RA1, RA2, RB1, and RC are defined herein, which novel compounds have properties for blocking Nav 1.7 ion channels found in peripheral and sympathetic neurons. Also described are pharmaceutical formulations comprising the compounds of Formulae AA and AB or their salts, and methods of treating neuropathic pain disorders using the same. |
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F ; ROSSI MICHAEL A ; LAYTON MARK E</creatorcontrib><description>Disclosed are compounds of Formula AA and Formula AB: wherein "Heteroaryl-1", RA1, RA2, RB1, and RC are defined herein, which novel compounds have properties for blocking Nav 1.7 ion channels found in peripheral and sympathetic neurons. Also described are pharmaceutical formulations comprising the compounds of Formulae AA and AB or their salts, and methods of treating neuropathic pain disorders using the same.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>2016</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20160712&DB=EPODOC&CC=US&NR=9388179B2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20160712&DB=EPODOC&CC=US&NR=9388179B2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KELLY, III MICHAEL J</creatorcontrib><creatorcontrib>PERO JOSEPH E</creatorcontrib><creatorcontrib>LEHMAN HANNAH D. 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F</creatorcontrib><creatorcontrib>ROSSI MICHAEL A</creatorcontrib><creatorcontrib>LAYTON MARK E</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KELLY, III MICHAEL J</au><au>PERO JOSEPH E</au><au>LEHMAN HANNAH D. G. F</au><au>ROSSI MICHAEL A</au><au>LAYTON MARK E</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>N-substituted indazole sulfonamide compounds with selective activity in voltage-gated sodium channels</title><date>2016-07-12</date><risdate>2016</risdate><abstract>Disclosed are compounds of Formula AA and Formula AB: wherein "Heteroaryl-1", RA1, RA2, RB1, and RC are defined herein, which novel compounds have properties for blocking Nav 1.7 ion channels found in peripheral and sympathetic neurons. 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title | N-substituted indazole sulfonamide compounds with selective activity in voltage-gated sodium channels |
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