http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1385844-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a910d33c239980f3a705e312c5bad6a
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
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filingDate 2002-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6892d1059def48b23790094c61f15ce3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95230f5743ee99c8844c353202365b52
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bee76c24cb25cd80697be1c70fe0c085
publicationDate 2004-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1385844-A1
titleOfInvention Oxazolidinones containing a sulfonimid group as antibiotics
abstract Compounds of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, wherein, for example, HET is an N-linked 5-membered, fully or partially unsaturated heterocyclic ring, or an N-linked 6-membered di-hydro-heteroaryl ring; and Q is, for example, Q1 or Q2: wherein R<2 >and R<3 >are independently hydrogen or fluoro; T is selected, for example, from a group of the formula (TA1) or (TA2): wherein, for example, X1m is O= and X2m is R2s-(E)ms-N-; wherein E is an electron withdrawing group, for example, -SO2- or -CO-; and, for example, R2s is hydrogen or (1-6C)alkyl; are useful as pharmaceutical agents; and processes for their manufacture and pharmaceutical compositions containing them are described.
priorityDate 2001-04-07-04:00^^<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: 736.