http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9906048-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36
filingDate 1998-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d1875c4689cd217b3f52f4b6f825e05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f2ee7e338cf54158222b85f71ff71da
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb1bf5bdec1d00bf094b27f0f5bc7e41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a36d467b234203ef1d2c7bd2e471bc68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ebf31dd356e282b4a0d63270141b342
publicationDate 1999-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9906048-A1
titleOfInvention Bis quaternary mrsa cephem derivatives
abstract Provided by the present invention are cephem derivatives represented by general formulae (IA) or (IB) or (IC) wherein Ar is an optionally substituted lipophilic phenyl, naphthyl or pyridyl group; L1 and L2 are (C1-C6)alkyl optionally substituted with hydroxy or keto and/or optionally interrupted with a vinyl group, S, O, aryl, heteroaryl, (a) or (b); in which R1 is H or (C1-C6)alkyl; A is CO2H, PO3H, SO3H, tetrazole, squaric acid or a hydroxyl group; and Q is a quaternized nitrogen group. The derivatives are gram-positive antibacterial agents especially useful in the treatment of diseases caused by methicillin-resistant Staphylococcus aureus.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109535174-A
priorityDate 1997-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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