http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0882706-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2602-08
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filingDate 1998-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c77dcc6e51cf342efa67d93acddc6b06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2d0821065662c95ac43927f929b6775
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b6f0e22a5ee14b8b2bd9c2e46ba4144
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_922825754472269a3bca2995ecbe933c
publicationDate 1998-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0882706-A1
titleOfInvention Cell adhesion inhibitors
abstract This invention provides novel indenone derivatives,ntheir pharmaceutical formulations and their use for theninhibition of leukocyte adherence to cells. The indenonenderivative is of the formulan nwhere R 1 and R 2 are each independently hydrogen, hydroxy,nnitro, amino, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or halo;n R 3 is hydrogen, hydroxy, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 nalkynyl, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy, halo, halo (C 1 -C 6 nalkyl), unsubstituted or substituted phenyl; and R 4 is hydrogen or C 1 -C 4 alkyl, or a pharmaceuticallynacceptable salt or solvate thereof; provided that, n   when R 1 , R 2 and R 4 are each hydrogen, R 3 is othernthan C 1 -C 4 alkyl, halo(C 1 -C 4 alkyl), cyclopropylnor phenyl.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6469003-B1
priorityDate 1997-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53670884
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID233640240

Total number of triples: 927.