http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-0400370-A2

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filingDate 2002-06-24^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed3b1c08e47f0bfafffd710cd8317f66
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a2b63a5c6848942bdbbd49aa8956ef0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d9fb3e7cce7aafc494ecf9d7acd97d2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c484698f0fd7d05c28c1fbd16d5a0e92
publicationDate 2004-08-30^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0400370-A2
titleOfInvention Antibacterial oxazolidinone derivatives, process for their preparation, pharmaceutical preparations containing them, their use and intermediates
abstract The present invention relates to fluoroquinolone derivatives of the new oxazolidinone compounds of formula I, their pharmaceutically acceptable salts or solvates, or their geometric or optical isomers, or mixtures or polymorphic forms of any of the isomers. R1 is an organic group; R 2 is hydrogen, C 1-4 alkyl or phenyl; R3 is hydrogen, halogen, C1-C4 alkyl, C1-C4 alkoxy or amino; R4 is hydrogen or halogen; R5 is an organic group; Meaning is an organic group; W is a 4-, 5-, 6-, 7-, or 8-membered heterocyclic ring containing one or more nitrogen atoms. The invention further relates to a process for the preparation of the compounds of the invention, to pharmaceutical compositions containing them as active ingredient, to their use and to their intermediates. SHE
priorityDate 2001-06-27^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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