http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20000035818-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a717ea5b2ac78ac329ab3a9659d834d2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4725
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-34
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-404
filingDate 1997-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47639cdab7100238495b34e411282df2
publicationDate 2000-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20000035818-A
titleOfInvention 4-aminoethoxy indolone derivatives
abstract Compounds of formula (I) or pharmaceutically acceptable salts thereof are dopamine synthesis and release useful for treating schizophrenia, Parkinson's Disease, Tourette's Syndrome, alcoholism, cocaine addiction and similar drug addiction It is an inhibitor of.n n n Formula In n n n n n n n In Formula I above,n n n Y is hydrogen, halogen or lower alkoxy,n n n R 1 is hydrogen, lower alkyl or aryl (lower) alkyl,n n n R 2 is hydrogen, lower alkyl or — (CH 2 ) n X p Ar where X is oxygen or carbonyl, Ar is cycloalkyl, aryl or arylaryl, oxindolinyl, benzimidazolyl, indolyl, 2-oxobenzimidazolyl or 2-thiooxobenzimidazolyl, n is one of integers from 1 to 6, p is an integer of 0 or 1), orn n n R 1 and R 2 together with the nitrogen atom to which they are attached form 3,4-dihydro-1H-isoquinolinyl or 1,3-dihydro-isoindolyl.
priorityDate 1996-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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