http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61129168-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0d6256baf554e46784d8daa478a2ddc6
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04
filingDate 1984-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba146266244c12722e0ccb36919cb49b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64620767fb87b646acf6c5bf2b1c6aa7
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41456e69750deffeb1b451760e1e19af
publicationDate 1986-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61129168-A
titleOfInvention 2-(4-substituted piperazin-4-oxyd-1-yl)-4-phenyl-quinoline derivative
abstract NEW MATERIAL:The compound of formula I [R 1 is lower alkyl, OH (lower) alkayl or aralkyl wherein the alkyl is substitutd with OH (said aryl part may b substituted with halogen, lower alkyl or lower alkoxy); R 2 and R 3 are H, halogen, lower alkyl, CF 3 or lower alkoxy) and its salt. n EXAMPLE: 2-(4-Ethylpierazin-4-oxid-1-yl)-4-phenylquinoline.1/4-hydrate. n USE: An antiulcer agent having excellent activity to suppress the secretion of acid in the stomach. n PREPARATION: The compound of formula I can be prepared by the ordinary oxidization reaction of the compound of formula II (some of which are novel) with an oxidizing agent such as m-chloroperbenzoic acid in a solvent such as chloroform at 0W100°C. n COPYRIGHT: (C)1986,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104557696-A
priorityDate 1984-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 21.