http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2848606-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c41f271d87fd7b8685fc23adf2fc4988
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0e6416a017df9338e8decc2280d4dff8
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-16
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C279-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P11-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C279-16
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filingDate 2013-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad79cd4428b782d1234bb2252259bf44
publicationDate 2015-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2848606-A2
titleOfInvention Fluoro-substituted (3r, 4r, 5s)-5-guanidino-4-acylamino-3-(pentan-3-yloxy) cyclohexene-1-carboxylic acids, esters thereof and a method for the use thereof
abstract The present invention relates to novel neuraminidase activity inhibitors and use thereof for prophylaxis and treatment of influenza infection, that is, to fluorosubstituted 4-acetamido-5-guanidino-3-(pentan-3-yloxy)cyclohex-1-enecarboxylic acids, their esters of the general formula 1, pharmaceutically acceptable salts and/or hydrates thereof, nwherein R represents hydrogen, optionally substituted C 1 -C 5 alkyl, C 2 -C 5 alkenyl or C 2 -C 5 alkynyl; Rf represents CH 2 F or CHF 2 . Pharmaceutical composition is given, method for its preparation, as well as method for prophylaxis and treatment of viral diseases.
priorityDate 2012-05-12-04:00^^<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: 488.