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filingDate 2000-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60eb4d087bcd7cdb25cc1da696893ef4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d0aba538e93d531004596e15126157e
publicationDate 2004-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2240995-C2
titleOfInvention Aminobenzophenones as inhibitors of interleukin il-1beta and tumor necrosis factor tnf-alpha
abstract FIELD: organic chemistry. n SUBSTANCE: invention relates to compounds of the formula (1): n n n n wherein R 1 , R 2 and R 3 represent independently one or more similar or different substitutes taken among the group consisting of hydrogen, halogen atom, hydroxy-group, mercapto-group, trifluoromethyl, amino-group, (C 1 -C 3 )-alkyl, (C 2 -C 3 )-olefin group, (C 1 -C 3 )-alkoxy-group, (C 1 -C 3 )-alkylthio-group, (C 1 -C 6) -alkylamino-group, (C 1 -C 3 )-alkoxycarbonyl, cyano-group, carbamoyl or phenyl; R 1 and R 2 are represented by nitro-group and R 3 - by carboxy-group additionally; R 4 represents hydrogen atom, (C 1 -C 3 )-alkyl or allyl; Q represents a bond or -C(R 6 )(R 7 )(-O-C=O)- wherein R 6 and R 7 mean independently hydrogen atom, trifluoromethyl or (C 1 -C 4 )-alkyl; Y represents either (C 5 -C 15 )-alkyl, (C 2 -C 15 )-olefin group, (C 3 -C 10 )-monocyclic hydrocarbon or phenyl being each of that can be substituted optionally with one or more similar or different substituted represented by the formula R 5 ; or Y represents (C 5 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 3 -C 6 )-cycloalkyl, (C 5 -C 8 )-cycloalkene group or phenyl bein each can be substituted optionally with one or more similar or different substituted taken among the group including halogen atom, hydroxy-group, amino-group, (C 1 -C 2 )-alkoxy-group, (C 1 -C 4 )-alkylamino-group, (C 1 -C 3 )-alkoxycarbonyl, cyano-group, azido-group, -COOH, -CONH 2 , -CONHR' or -CONRR', wherein R and R' mean (C 1 -C 2 )-alkyl; or Y represents (C 1 -C 4 )-alkyl substituted with at least one or more substituted of the formula R 5 or -CONRR' wherein R and R' mean (C 1 -C 2 )-alkyl; or Y represents group of the formula -CH 2 -(Z-O) n -Z wherein Z represents (C 1 -C 3 )-alkyl and wherein n represents a whole number > 1 being without continuous linear sequence of atoms in the group Y > 15; R 5 represents halogen atom, hydroxy-group, mercapto-group, trifluoromethyl, amino-group, (C 1 -C 3 )-alkoxy-group, (C 1 -C 3 )-alkylthio-group, (C 1 -C 6 )-alkylamino-group, (C 1 -C 3 )-alkoxycarbonyl, cyano-group, azido-group, nitro-group, -COOH, -CONH 2 , -CONHR', -COONR'R' wherein R' means (C 1 -C 3 )-alkyl; X means oxygen or sulfur atom; or pharmaceutically acceptable salts of this compound, or hydrates of this compound, or solvates of this compound that can be used for treatment of humans in veterinary science. n EFFECT: valuable medicinal and veterinary properties of compounds. n 8 cl, 2 tbl, 31 ex
priorityDate 1999-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9811564
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559526
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419525604
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422322624
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID443295
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422322620
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450556737
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9827706
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67230
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422323024
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID74828
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420246818
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ28386
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454973655
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413996884
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ63264
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453130162
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID80271
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23514209
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID403974
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393737
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID50912043
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID450200
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9XS77
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422323361
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP26889
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2757370
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413997016
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21910879

Total number of triples: 309.