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filingDate 1998-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_202eee7414f4389462faa543cd035898
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publicationDate 2003-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2197490-C2
titleOfInvention Derivatives of 4-oxo-3,5-dihydro-4h-pyridazino[4,5-b]-indol-1-acetamide, their synthesis and application in therapy
abstract FIELD: organic chemistry, medicine, pharmacy. SUBSTANCE: invention relates to novel derivatives of 4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1- acetamide of the formula (I): where X means H, methyl-, methoxy-, phenylmethoxy-group; Y means H, one or two halogen atoms, OH, ; R 1 means H, C 1 -C 4 -alkyl; R 2 and R 3 each and independently each of other means H, C 1 -C 4 -alkyl, phenylmethyl group; or R 2 and R 3 with nitrogen atom that carries their form azethidinyl-, pyrrolidinyl-, 3-ethoxypyrrolidinyl-, piperidinal-, morpholinyl-, 4-methylpiperazinyl- or 1,3- thiazolidinyl-group. Compounds of the formula (I) are agonists of ω 1 - and ω 2 -benzodi-azepine receptors located in macromolecular gamma-aminobutyric acid (GABA) complex and therefore they can be used for treatment of diseases associated with disorder of GABA-ergic transmission. EFFECT: improved method of synthesis, valuable medicinal properties of compounds. 4 cl, 1 tbl
priorityDate 1997-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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