http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54135763-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_39ae96c0ecc22ff90ff986371a3cea0f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4427
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
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filingDate 1978-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4033ad1a1b92f838732412ebfdea6df
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publicationDate 1979-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S54135763-A
titleOfInvention Azetidinone derivative having substituted amino group, its salt, and their preparation
abstract NEW MATERIAL:An azetidinone derivative having substituted amino group or its salt of formula I(R 1 is lower alkyl substituted by COOH, OH, etc., lower alkanoyl substituted by OH, phenyl which may be substituted by OH, etc., R 2 is H, lower alkyl substituted by OH; R 3 is H, CH 2 COOH). n EXAMPLE: 2- [3- [2- [4- (3-caboxy-3-caboxymethylaminopropoxy)phenyl] -2-hydroxyimino-acetamido] -2-oxo-1-azetidinyl] -2- (4-hydroxyphenyl) acetic acid. n USE: Antibacterial agent having specific antibacterial spectrum, and its intermediate. n PROCESS: A compound I wherein R 1 is Ra 1 , and R 2 is Ra 2 is prepared by reacting a compound II or its salt with a compound III (Ra 1 is COOH, etc.; Ra 2 is H, etc.), and reducing the resultant compound. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1978-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 23.