http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2184971-A1

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filingDate 1996-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c003d994ad83a762dbcd17ab87ccbd42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c0e87272971de281cd6f72dc7fc2d55
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publicationDate 1997-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2184971-A1
titleOfInvention Cephalosporin derivatives
abstract The present invention relates to cephalosporin derivatives of the general formula I wherein R1 is a group selected from 2-, 3- and 4-hydroxyphenyl, 2- and 3-methoxyphenyl, 4-carboxyphenyl, 4-carbamoylphenyl, 3-trifluoro-methylphenyl, 2- and 3-fluorophenyl, 3-nitrophenyl, 3-fluoro-4-hyroxyphenyl, 2-fluoro-4-hydroxyphenyl, 3-fluoro-2-hydroxy-phenyl, 3-, 4-dihydroxyhenyl, benzyl, -CHR-phenyl, 3-hydroxy-benzyl, 4-aminobenzyl, 2-, 3- and 4-fluorobenzyl, 2-, 3- and 4-methoxybenzyl, 4-nitrobenzyl, 4-carboxybenzyl, 4-trifluoromethyl-benzyl, 1-naphthyl and 2-naphthyl, all hydroxy, amino, carboxy and carbamoyl substituents optionally being substituted, or is pyridinyl mono-substituted with halogen, pyrimidyl, pyrazinyl di-substituted with lower alkyl, pyridazinyl mono-substituted with halogen, piperidinyl in which the amino group may be substituted by an acyl group, thiadiazolyl, oxo-tetrahydrofuranyl, thiophenyl mono-substituted with lower alkoxycarbonyl or carbamoyl, tetrazolyl-lower alkyl, tetrahydrofuranyl-lower alkyl, thiophenyl-lower alkyl or benzimidazolyl-lower alkyl; and R is carboxy or esterified carboxy; readily hydrolyzable esters thereof, pharmaceutically acceptable salts of said compounds and hydrates of the compounds of formula I and of their esters and salts, as well as the their use and the process for manufacturing such compounds.
priorityDate 1995-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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