http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2335288-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-24
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
filingDate 1999-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23ad87a073a8e16178219fe69598f6d7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_037e59f9554c70ff97c56559eee6d3ba
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0bb557b723ea9073d7a58697f652afa7
publicationDate 1999-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2335288-A1
titleOfInvention Propenyl cephalosporin derivatives
abstract Disclosed are cephalosporin derivatives of general formula (I) wherein R is an organic residue with a molecular weight not exceeding 400 bonded to the adjacent sulphur atom via carbon and consisting of carbon, hydrogen, and optional oxygen, sulfur, nitrogen and/or halogen atoms; R1 is hydrogen, lowe r alkyl or phenyl; and A is a secondary, tertiary or quaternary nitrogen atom bound directly to the propenyl group and being substituted by an organic residue with a molecular weight not exceeding 400 and consisting of carbon, hydrogen, and optional oxygen, sulfur, nitrogen and/or halogen atoms, as wel l as readily hydrolyzable esters thereof, pharmaceutically acceptable salts of said compounds and hydrates of the compounds of formula (I) and of their esters and salts. Also disclosed is a process for their manufacture, intermediates useful therein, medicaments containing the end products and us e of the latter for the treatment and prophylaxis of infectious diseases or fo r the manufacture of the medicaments.
priorityDate 1998-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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