http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2010116740-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
filingDate 2010-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-WO2010116740-A1
titleOfInvention Pyridinethio derivatives and pharmaceutical compositions containing them having anti-Helicobacter pylori activity
abstract The present invention provides a novel pyridine derivative and a pharmaceutical composition using the same, particularly a pharmaceutical composition having selective antibacterial activity against Helicobacter pylori. In the present invention, the following general formula (I), wherein R 1 and R 2 represent a hydrogen atom or a C 1-8 alkyl group, R 3 and R 4 represent a hydrogen atom, and a C 1-8 Represents an alkyl group, X represents —O—, —S— or the like, Y represents a C 1-12 alkyl group which may be substituted with a substituent, or — (R 5 —O) n —R. 6 (wherein R 5 represents a C 1-5 alkylene group, R 6 represents a C 1-8 alkyl group which may be substituted with a substituent, and n represents an integer of 1 to 10). And Z represents a hydrogen atom or the like.) Or a pharmacologically acceptable salt thereof, and a pharmaceutical composition containing the same.
priorityDate 2009-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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