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filingDate 2000-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_902b9e452257f540db9feac6f863439a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed9148e78db8af61518ed514f383aac5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ac19599da1bf6762acdfe5fe310f2dc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3e97131b3a32c9c83942c27e984db39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1182a8adf9a6cb931586dc81f011049
publicationDate 2005-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2257382-C2
titleOfInvention Derivatives of benzodiazepine, medicinal agent comprising thereof and method for their preparing
abstract FIELD: organic chemistry, chemical technology, medicine, pharmacy. n SUBSTANCE: invention describes derivatives of benzodiazepine of the general formula (I) n and their pharmaceutically acceptable acid-additive salts wherein X means a ordinary bond or ethynediyl group; when X means ordinary bond then R 1 means halogen atom, (lower)-alkyl, (lower)-alkylcarbonyl, (lower)-cycloalkyl, benzoyl, phenyl substituted optionally with halogen atom, hydroxyl, (lower)-alkyl, (lower)-alkoxy-group, halogen-(lower)-alkoxy-group or cyano-group; styryl, phenylethyl, naphthyl, diphenyl, benzofuranyl, or 5- or 6-membered heterocyclic ring representing thiophenyl, furanyl, pyridinyl, dihydropyridinyl, tetrahydropyridinyl which are optionally substituted; when X means ethynediyl group then R 1 means hydrogen atom, (lower)-alkyl substituted optionally with oxo-group; (lower)-cycloalkyl substituted with hydroxyl; (lower)-cycloalkenyl substituted optionally with oxo-group; (lower)-alkenyl, optionally substituted phenyl; 5- or 6-membered heterocyclic ring representing thiophenyl, thiazolyl, pyridinyl, dihydropyridinyl, tetrahydropyridinyl or dihydropyranyl and substituted optionally; R 3 means phenyl, pyridyl, thiophenyl or thiazolyl which are substituted optionally. These compounds can be used for treatment or prophylaxis of acute and/or chronic neurological diseases, such as psychosis, schizophrenia, Alzheimer's disease, disorder of cognitive ability and memory disorder. Also, invention describes a medicinal agent based on these compounds and a method for preparing compounds of the formula (I). n EFFECT: improved method for preparing, valuable medicinal properties of compounds. n 10 cl, 1 tbl, 173 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2610262-C2
priorityDate 1999-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 1046.