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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-18
filingDate 1993-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d06f71e74cabf5da771aef34e0b2cfb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db6b523c93aa983ca995c09e7627119b
publicationDate 1995-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0674639-A1
titleOfInvention Azanoradamantanes
abstract This invention relates to methods of treating conditions responsive to 5-HT4 agonists and/or antagonists and 5-HT3 antagonists by administering compounds of the formula: <IMAGE> or a pharmaceutically acceptable salt thereof wherein Z is selected from the group consisting of <IMAGE> R1 is alkoxy of one to six carbon atoms; R2, R3, R4 and R5 are the same or different and are selected from the group consisting of hydrogen, halogen, CF3, hydroxy, alkoxy of one to six carbon atoms, acyl of two to seven carbon atoms, amino, amino substituted by one or two alkyl groups of one to six carbon atoms, C2-C7 acylamino, aminocarbonyl, aminosulfone optionally substituted by one or two alkyl groups of one to six carbon atoms, C1-C6 alkylsulfone and nitro; n is 0, 1 or 2; m is 0 or 1; X is O or NR7; and R7 is hydrogen or alkyl of 1 to 6 carbon atoms.
priorityDate 1992-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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