http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0918770-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ba045776bcd32d32e3100da8dfce4e28
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-496
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12
filingDate 1997-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b156a60e330f311c25caafc08f67451
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b2e62a72c41a9453be3eb9a8d2728ce
publicationDate 1999-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0918770-A1
titleOfInvention Pyridyl-piperazinyl-phenyl-oxazolidinone derivatives and their use as antibacterials
abstract The invention concerns a compound of formula (I) wherein, for example: R<1> is of the formula -NHC(=O)R<a> wherein R<a> is for example (1-4C)alkyl; R<2> and R<3> hydrogen or fluoro; R<4> and R<5> are independently are independently hydrogen or methyl; R<6> is pyridyl, optionally substituted by substituents selected from (1-4C)alkyl (optionally substituted), halo, trifluoromethyl, (1-4C)alkylS(O)n- (wherein n is 0, 1 or 2), (1-4C)alkylS(O)2amino, (1-4C)alkanoylamino, carboxy, hydroxy, amino, (1-4C)alkylamino, di-(1-4C)alkylamino, (1-4C)alkoxycarbonyl, carbamoyl, <u>N</u>-(1-4C)alkylcarbamoyl, di-(<u>N</u>-(1-4C)alkyl)carbamoyl [wherein the (1-4C)alkyl group or groups in the last two-mentioned carbamoyl substituents is optionally substituted by hydroxy, (1-4C)alkoxy or (1-4C)alkoxycarbonyl], (2-4C)alkenyl (optionally substituted by carboxy or (1-4C)alkoxycarbonyl), (1-4C)alkoxy, cyano or nitro; pharmaceutically-acceptable salts, suitable N-oxides and in vivo hydrolysable esters thereof; processes for their preparation; pharmaceutical compositions containing them and their use as antibacterial agents.
priorityDate 1996-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399517
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14049689
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21226386
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233835664
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ67E05
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408037842
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID164602
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129183405
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233835557
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17609701
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129394664
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127489368
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516000
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127781398
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423576818
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419535018
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID94459
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233835134
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127456315
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426180661
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID437234
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6038
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136044219
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID56996182
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13445090
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419503254
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67629937
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423568350

Total number of triples: 644.