http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BG-62403-B1

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filingDate 1995-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ed4c2c19e0c3d7c4d86d6332b24d02b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00f70c5f34cfe85f7ec401c0d30e5af7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c88a00cfa8ceaa4fb0c98e8facc314a
publicationDate 1999-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BG-62403-B1
titleOfInvention ISOHINOLINE DERIVATIVES IN THE QUALITY OF THERAPY
abstract The tetrahydroisoquinoline compounds and theirpharmaceutically acceptable salts are applied in analgesia and thetreatment of psychoses, the Parkinson Disease, the Lesch-Nyansyndrome, in impairment of the concentration and congnitiveabilities, or in the release of drug addiction, and in delayeddyskinesia. They have the formulawhere R1 is one or more substituents selected from H, halogen,hydroxy alkyl (optionally substituted with hydroxy), alkoxy,alkylthio, alkylsulphenyl, alkylsulphonyl, nitro, cyano,polyhaloalkyl, polyhaloalkoxy, phenyl (optionally substituted byone or more halogen, alkyl, alkoxy), or R1 is optionally alkylatedcarbamoyl; R2 means saturated or unsaturated aliphatic group,optionally substituted by hydroxy or alkoxy; E is alkylene chainoptionally substituted by one or more alkyl groups; G means (a)optionally substituted saturated or unsaturated alicylic groupcontaining from 3 to 8 carbon atoms, or (b) optionally substitutedsaturated or unsaturated aliphatic chain containing 1 to 12 carbonatoms, or (c) optionally substituted 5- or 6-member heterocyclicring containing one or more N or O atoms, or SOn groups where n is0, 1 or 2. The invention also relates to their O-acylatedderivatives which ensure lipophilic esters.18 claims
priorityDate 1993-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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