http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2201923-C2

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filingDate 1997-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf6115b33f61f64f3bc899776a6cc1c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c60c40e13c6309488ec2aaafb0441a6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f1daa44498576911559e9f749445cee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c23df3b9cc4a8e465aa722bc3241adaf
publicationDate 2003-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2201923-C2
titleOfInvention Arylalkanoylpyridazines
abstract FIELD: organic chemistry of heterocyclic compounds, biochemistry, pharmacy. SUBSTANCE: invention relates to arylalkanoylpyridazines of the formula (I) where B means A, OA, NH 2 , CF 3 , aromatic heterocycle taken among pyridine, pyrazine and pyrimidine; Q is absent or means alkylene with 1-6 carbon atoms; R 1 and R 2 mean independently each of other OR 5 where R 5 means A or cycloalkyl with 3-7 carbon atoms; A means alkyl with 1-10 carbon atoms, and to their physiologically acceptable salts. Compounds of the formula (I) and their physiologically acceptable salts are inhibitors of phosphodiesterase IV and can be used for preparing the medicinal agent with indicated action being for treatment of asthmatic diseases preferably. Except for, invention relates also to method of synthesis of compounds of the formula (I), method of preparing pharmaceutical compositions useful for inhibition of activity of phosphodiesterase IV and to pharmaceutical composition. EFFECT: improved method of synthesis and preparing, valuable medicinal and biochemical properties of compounds. 8 cl, 25 ex
priorityDate 1996-08-13-04:00^^<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: 484.