http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0148004-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20
filingDate 1984-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d16e3aa6578894d8171f91d87e256135
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c2303b58a11fed4d87ef900f9fc6cb50
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publicationDate 1985-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0148004-A2
titleOfInvention Cephalosporin antibiotics
abstract Cephalosporin compounds of general formulan (whereinn Q represents a cyclopropylmethyl goup, Y represents an optionally blocked carboxyl group or an optionally N-mono- or N,N-di-alkyl substituted carbamoyl group, Z represents hydrogen, optionally N-substituted carbamoyloxy, heterocyclicthio or optionally substituted pyridinium or bicyclicpyridinium, R represents an optionally protected amino group, R 2 represents a hydrogen atom or a carboxyl blocking group, B represents -S- or >S-0, and the dotted line indicates Δ 2 or Δ 3 unsaturation) and salts thereof. n The Δ 3 sulphide compounds exhibit a particularly advantageous profile of antibiotic activity against both Gram-positive and Gram-negative and organisms, including β-lactamase-producing strains. n Methods of preparing the compounds of the invention are described, as is the use of the compounds as active antibiotics and as precursors therefor.
priorityDate 1983-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 409.