http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5112832-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5deddb47ccaab1d4da2aacc344dd8717
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D221-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-14
filingDate 1990-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84c52c76da2649a0e1b84da579505ca3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e7347735936f3ded44cf160f8132248
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_880ad195686b9fede375c1c9acb2baf3
publicationDate 1992-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5112832-A
titleOfInvention Certain cyclopenta[b]pyridines and 5,6,7,8-tetrahydroquinolines having anti-inflammatory activity
abstract The invention concerns compounds of formula I ##STR1## or a salt thereof, wherein R 1 and R 2 each independently represent hydrogen, lower alkyl, lower alkoxy, carboxyloweralkyl, carboxy, hydroxyloweralkyl, halogen, haloloweralkyl, lower alkoxycarbonyl, optionally substituted aryl or optionally substituted aralkyl, n represents an integer from 3 to 6; R 3 represents hydrogen or single or multiple substitution on one or more of the aliphatic carbons by one or more substituents selected from lower alkyl, optionally substituted aryl and optionally substituted aralkyl; A represents a group of formula (i) or (ii) below: n n --CR.sup.4 R.sup.5 --(CR.sup.6 R.sup.7).sub.m -- (i) n n n --CX--(CR.sup.6 R.sup.7).sub.m -- (ii) n n in which R 4 , R 6 and R 7 each independently represent hydrogen or lower alkyl (providing that when R 5 is NH 2 , R 0 is hydrogen); m is 0 or 1; R 5 represents hydrogen, NH 2 , OH or loweralkoxy, and X is ═O, ═NH or ═NOH, the attachment of A to B being from either end, and B represents an optionally substituted aryl or heteroaryl radical which compounds possess anti-inflammatory activity. Also disclosed is a process for preparing a useful intermediate to compounds of formula I.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5604238-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5593943-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2004281959-B9
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2004281959-B2
priorityDate 1988-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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