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filingDate 1978-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9425c06b3cd837bd368baa37125dda8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5396d9847ac39e91ab6a58c40935253
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9aac8a7e33596f82753e3a85a4cbbcde
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15833e9037e75c946510d2c69246aab4
publicationDate 1980-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-784779-A3
titleOfInvention Method of preparing 7-beta-halogenarylmalonamido-7-alpha-methoxy-heterocyclylthiomethyl-1-dethia-1-oxa-3-cephem-4-carboxylic acid derivatives or their salts with organic or inorganic bases
abstract Antibacterial haloarylmalonamido-1-dethia-1-oxacephalosporins of the following formula: <IMAGE> wherein Ar is <IMAGE> <IMAGE> +TR <IMAGE> (in which Hal and Hal' each is halogen and RO is hydroxy or protected hydroxy); COA and COB each is carboxy or protected carboxy including a pharmaceutically acceptable salt group; and Het is 1-lower alkyl-5-tetrazolyl, 1,3,4-thiadiazol-2-yl or 5-lower alkyl-1,3,4-thiadiazol-2-yl, a pharmaceutical or veterinary composition comprising the said haloarylmalonamido-1-dethia-1-oxacephalosporin and pharmaceutical carrier, and a method for treating or preventing human or veterinary infectious diseases comprising administering an effective amount of the said antibacterial compound.
priorityDate 1977-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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