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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5deddb47ccaab1d4da2aacc344dd8717
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-32
filingDate 1981-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84c52c76da2649a0e1b84da579505ca3
publicationDate 1982-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4337259-A
titleOfInvention Pyridine derivatives
abstract The invention relates to a pharmaceutical composition comprising an anti-ulcer effective amount of a compound of formula I <IMAGE> wherein R represents hydrogen, lower alkyl, phenyl, halophenyl, loweralkylphenyl, loweralkoxyphenyl, or aralkyl of 7 to 12 carbon atoms, R1 represents hydrogen or lower alkoxy, R2 represents hydrogen, chlorine or trifluoromethyl and n is 1 or 2, or a pharmaceutically acceptable acid addition salt thereof, and a pharmaceutically acceptable carrier. A method of treating ulcers or hypersecretion in a mammal which comprises administering a compound of formula I is also disclosed. Some compounds of formula I are novel and within the scope of the invention.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4631287-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4839353-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4394509-A
priorityDate 1980-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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