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filingDate 1991-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd410a2295d4e7edb1662722a5556914
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e53068e71b96a8ba410118195d8bf185
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09c923d3708d915246ee0445d12a7233
publicationDate 1993-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FI-88793-B
titleOfInvention FRAMEWORK FOR THE PHARMACOLOGICAL ACTIVATION OF ACTIVE PHENYLNAFTAL
abstract The invention relates to a process for the preparation of pharmacologically active benzonaphthalene derivatives of the formula <IMAGE> wherein: R1 is i) <IMAGE> or ii) -CH2OH -R6 is a radical <IMAGE> or a radical -OR7, wherein R7 is a hydrogen atom, alkyl radical, monohydroxyalkyl radical or polyhydroxyalkyl radical, r' and r" are each a hydrogen atom, lower alkyl radical, a mono or polyhydroxyalkyl radical, an optionally substituted aryl radical or a residue of an amino acid or an aminated sugar, or together form a heterocycle, R2 is a hydrogen atom, an alkyl radical, an alkoxy radical or a cycloaliphatic radical, R3 is a hydrogen atom, a hydroxyl radical, an alkyl radical, an alkoxy radical, an optionally substituted cycloaliphatic radical, a thiocycloaliphatic radical or a radical of the formula -O-Si(CH3)2-R8, wherein R8 is an alkyl radical, R4 and R5, identical or different, are a hydrogen atom, a lower alkyl radical, a hydroxy radical or a lower acyloxy radical, and the preparation of salts of benzonaphthalene derivatives of the aforementioned formula I. These compounds are useful in the topical and systemic treatment of dermatological, rheumatic, respiratory and ophthalmic illnesses.
priorityDate 1985-04-11-04:00^^<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/gene/GID18263
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153875675
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423400858
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426078961
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10907
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP78599
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419535942
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9855836
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415893423
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10788316
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559552
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14928
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2752044
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409851389
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419506465
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419536434
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7123
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68794058
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419520247
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415715112
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393647
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409856317
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID343798
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409851735
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16314
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429378005
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1080
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413484378
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429378004
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP49725
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420961648
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2202
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18952768
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID429378006
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13633552
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419552768
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10526466

Total number of triples: 326.