http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01301683-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_39ae96c0ecc22ff90ff986371a3cea0f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-546
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-20
filingDate 1988-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f760d05d57e66c9a644a0e276503d74f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f4f162d2c7385bb7f995d0d0e0d98ab
publicationDate 1989-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01301683-A
titleOfInvention Novel cephem compound
abstract NEW MATERIAL:Dibenzylamine salt of 7-[2-(2-aminothiazol-4-yl)-2-methoxyimino- acetamido]-3-cephem-4-carboxylic acid (syn-isomer) shown by the formula. n USE: An antibacterial agent against Gram-positive and Gram-negative bacteria, maintaining effective blood concentration for many hours. n PREPARATION: 7-[2-(2-Aminothiazol-4-yl)-2-methoxyiminoacetamido] -3-cephem-4- carboxylic acid (syn-isomer) is treated with dibenzylamine. n COPYRIGHT: (C)1989,JPO&Japio
priorityDate 1987-09-25-04:00^^<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: 30.