http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-0301562-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-10
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filingDate 2001-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f326fbfe60270de02657f14439c066a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6cf245668557724ae878214231a99379
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa6839f8ebd1abb241ce52733f47ee83
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_395b0258f48efd94551252991b277651
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4cb8072bd9193dd1271d9046b25c5dfc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ca12c07b1cbcc02aab8df1ed4755787
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publicationDate 2003-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0301562-A2
titleOfInvention New oxazolidinone derivatives and methods for their preparation, pharmaceutical compositions containing them
abstract The present invention relates to oxazolidinone derivatives of formula (1) and their pharmaceutically acceptable salts having a broad spectrum inhibitory effect on bacteria. Another object of the present invention is a process for the preparation of oxazolidinone derivatives of formula (1) or pharmaceutically acceptable salts thereof. The present invention further provides pharmaceutical compositions having a therapeutic agent of the general formula (1) oxazolidinone derivative or a pharmaceutically acceptable salt thereof. In the general formula (1), R1 is hydrogen, fluorine, chlorine or CF3; R2 is a group of formula (a) or (b) wherein R3 is an amino group or a substituted piperazinyl group, or a 5- or 6-membered heterocyclic group containing one or more nitrogen or oxygen atoms or both. SHE
priorityDate 2000-06-05-04:00^^<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: 437.