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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D505-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D505-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
filingDate 1984-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1986-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5396d9847ac39e91ab6a58c40935253
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_008934664c89a60190681a0940b9345b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b01fb5939f54da52f377c088538d663
publicationDate 1986-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4569993-A
titleOfInvention Malonyloxacephemcarboxylic acid derivatives
abstract An antibacterial 7beta-substituted malonamido-7alpha-methoxy-3-tetrazolylthiomethyl-1-dethia-1-oxa-3-ceph em-4-carboxylic acid and its derivative represented by the following formula: <IMAGE> (wherein R1 is alkyl, hydroxyaryl, or thienyl; R2 and R4 each is hydrogen, light metal or a carboxy-protecting group; and R3 is optionally protected hydroxyalkyl, carbamoylalkyl, dialkylaminoalkyl, or sulfamoylalkyl) are disclosed.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2466743-C1
priorityDate 1983-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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