http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4549014-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4b8a28caa5561d6dbc92d613367b7ad2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D265-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D265-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-34
filingDate 1984-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1985-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f96f2d92afaea47214c39bc4f3190359
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_595347c19467315f7b91922ecad2863a
publicationDate 1985-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4549014-A
titleOfInvention Adamantyl containing 1,4-oxazinone derivatives
abstract Antimicrobial or anti-inflammatory 1,4-oxazinone derivatives of the structure: ##STR1## wherein one of R and R 1 is hydrogen and the other is --CH 2 CO 2 R 6 (R 6 =alkyl) or R and R 1 together represent the group ═CHCO 2 R 6 , R 2 and R 3 are hydrogen, alkyl, substituted alkyl, phenyl or substituted phenyl or R 2 and R 3 together represent a single adamantyl group, and R 4 and R 5 are hydrogen, alkyl, substituted alkyl, phenyl, substituted phenyl, or benzyl, are disclosed herein.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8892495-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9535563-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5532363-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10361802-B1
priorityDate 1984-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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