http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0142361-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D267-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D267-14
filingDate 1984-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4546a9c2e344e4dc58abfbbb6b35a639
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e81c5d7e7e69b093f452040114c1dce7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5ad34058153439310bfd6eb38fe088f
publicationDate 1985-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0142361-A2
titleOfInvention N-substituted-5-phenyl-4,1-benzoxazepin-2(3H)-ones having therapeutic utility
abstract Compounds of the formulan wherein R, is cyclopropylmethyl, 2-phenylethyl, aminoalkyl, cycloaminoalkyl, optionally ring-substituted phenoxyalkyl, optionally ring-substituted phenylthioalkyl, optionally ring-substituted phenylsulphinylalkyl, optionally ring-substituted phenylsulphonylalkyl, cycloalkoxyalkyl, optionally ring-substituted phenylalkyl, hydroxyalkyl, alkoxyalkyl or phthali- midoalkyl; R 2 is H, alkyl or phenyl; and Y, is H, CI, Br, F, MO 2 or CF 3 , can have utility as inhibitors of phospholipase A 2 and thus as inhibitors of arachidonic acid cascade biosynthesis.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
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Total number of triples: 397.