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filingDate 1991-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f100139b11fd6bbd323f281dab1656b0
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publicationDate 1992-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2057777-A1
titleOfInvention Cephalosporin derivatives
abstract Abstract Cephalosporin derivatives of the general formula in which R3 is a group of the formula (a) R60 and R65 are hydrogen or lower alkyl, R15-R19 are each independently hydrogen, halogen or hydroxy, n is zero or 1, R4 and R5 are each hydrogen, halogen, lower alkyl, lower alkoxy or amino, R7 is hydrogen or lower alkyl and R8 is lower alkyl, halo-lower alkyl, C3-C7 cycloalkyl or mono-, di- or trihalophenyl, and Z is N or C-R9, where R9 is hydrogen, halogen, lower alkyl or lower alkoxy; and, when R4 is fluoro, R5 and R7 are hydrogen, R8 is cyclopropyl and Z is C-H, R3 can also be one of the groups (b) (c) in which R61 and R66 are hydrogen or methyl, R15-R19 are as above and R90 is hydrogen, hydroxy, carboxy, amino or [[4-(lower alkyl)-2,3-dioxo-1-piperazinyl]carbonyl]amino; pharmaceutically acceptable acid or base addition salts thereof, hydrates of compounds of formula I and hydrates of such salts. The products have antibacterial activity.
priorityDate 1990-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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