http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2162463-C2

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filingDate 1994-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebc77a86e64ab6361d0fd03eb330dd7b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_464d71bd01b7ed447d59401406057db7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1cd428d9e03ebe3c2ec58f8d15367c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63abc0a50342e77da551e850a33fd43d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ce4b74f4c0ae8c6e2bde940b1c049510
publicationDate 2001-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2162463-C2
titleOfInvention Novel 1h-indole-3-acetamides as inhibitors of spla2 and pharmaceutical composition based on thereof
abstract FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to 1H-indole- -3-acetamides of the general formula (I) where X means oxygen atom; R 1 is taken among the group (i), (iii) where: (i) means C 6 -C 20 -alkyl, C 4 -C 12 -cycloalkyl; (iii) means -(CH 2 ) n -(R 80 ) where n = 1-8 and R 80 is the group indicated in (i); R 2 means hydrogen, halogen atom, C 1 -C 3 -alkyl, C 1 -C 2 -alkylthio-, C 1 -C 2 -alkoxy- -group; each of R 3 means independently hydrogen atom or methyl group; R 4 ,R 5 ,R 6 ,R 7 each means independently C 1 -C 10 -alkyl, C 2 -C 10 -alkenyl, C 3 -C 8 -cycloalkyl, C 1 -C 10 -alkoxy-, C 4 -C 8 -cycloalkoxy-, phenoxy-group, halogen atom, hydroxy-group, carboxyl, -C(O)O(C 1 -C 10 )- -alkyl), hydrazide, hydrazino-group, NH 2 ,NO 2 ,-C(O)NR 82 R 83 where R 82 and R 83 means independently hydrogen atom, C 1 -C 10 -alkyl or the group of the formula: a) where R 84 and R 85 mean independently hydrogen atom, C 1 -C 10 -alkyl; p = 1-5; Z means a bond, -O-, -NH-; Q means , phenyl, group of the formula: b) , c) , d) is taken independently among hydrogen atom, R 86 -alkyl and its pharmaceutically acceptable salts, esters or amides. Compounds of the formula (I) show inhibitory activity with respect to fatty acids release mediated by C 1 -C 10 , phospholipase and they can be used for preparing the pharmaceutical composition. Invention describes intermediate compounds used for synthesis of compounds of the formula (I). EFFECT: new compounds indicated above, valuable pharmacological properties. 15 cl, 2 tbl, 101 ex
priorityDate 1993-04-16-04:00^^<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: 824.