http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0629200-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_61f88efcda59d7062a4252ecf6886f58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
filingDate 1993-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da17a27999d74dbe0b0de67cbaeca04c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5064ecf7c9d544d3141741f350a6a8e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d3a39c5b237e8da8297d3180a8f64fa
publicationDate 1994-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0629200-A1
titleOfInvention Epibatidine and derivatives, compositions and methods of treating pain
abstract The present invention relates to compounds and compositions and methods for the treatment of pain, and derivatives thereof which have potent analgesic activity. The compounds have the formula (I) in which R1 is selected from H, lower alkyl, C3-C9 cycloalkyl, acyl, and C3-C9 cycloalkylalkyl, haloalkyl, alkenyl, alkynyl, hydroxyalkyl, or C3-C8 cycloalkenyl or C3-C8 cycloalkynyl ; and wherein R is selected from cycloalkyl, aryl, heteroaryl (selected from the group consisting of pyrridyl, thienyl, furanyl, imidazolyl, pyrazinyl and pyrimidyl) or phenoxy; the groups of said R can be substituted with hydroxyl, C1-C6 lower alkyl, C2-C6 alkenyl, C1-C6 lower alkoxyl, halo, C1-C6 haloalkyl, amino, C1-C6 alkylamino and C2-C10 dialkylamino, and sulfonamido or a pharmaceutically acceptable salt thereof.
priorityDate 1992-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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