http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0420464-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7f6e33603375c486b0ab3505830af9e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-20
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-20
filingDate 1990-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1994-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_178fbf6fb061de8659b4de4453357b14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a714b40d3f7ed82cf031e0dae624ff0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c57bf23f4b6c0e344ee9fd43b31a4787
publicationDate 1994-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0420464-B1
titleOfInvention 3-Isoxazolone derivatives, their preparation and their therapeutic uses
abstract Compounds of formula (I): <CHEM> [in which R<1> is hydrogen, halogen, alkyl, alkenyl, alkynyl, optionally substituted benzyl or optionally substituted phenyl; R<2> is hydrogen, alkyl, optionally substituted phenyl, or a heterocycle having from 5 to 7 ring atoms; or R<1> and R<2>, together with the carbons to which they are attached, form an optionally substituted hydrocarbon ring fused to the isoxazole ring; -NR<3>R<4> represents an alicyclic amino group; and A is optionally substituted phenyl, optionally substituted benzyl, alkyl, alkoxy, optionally substituted benzyloxy, or optionally substituted phenoxy]; and acid addition salts thereof have valuable activity for the treatment of cerebrovascular disorders and for use as centrally acting muscle relaxants.
priorityDate 1989-09-26-04:00^^<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: 533.