http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002530390-A

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filingDate 1999-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2002-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002530390-A
titleOfInvention IL-5 inhibitory 6-azauracil derivative
abstract (57) [Summary]nIn the present invention, p is 0 to 3; q is 0 to 4; -AB- is-(CH Two ) r -,-(CH Two ) t -O-,-(CH Two ) t -S (= O) u -Or-(CH Two ) t -NR Three R is 2 to 4; t is 1 to 3; u is 0 to 2; 1 Is O, S, NR Three Or a direct bond; 1 And R Four Is C 1-6 Alkyl, halo, polyhalo C 1-6 Alkyl, hydroxy, mercapto, C 1-6 Alkyloxy, C 1-6 Alkylthio, C 1-6 Alkylcarbonyloxy, aryl, cyano, nitro, Het Three , R 6 , NR 7 R 8 Or substitution C 1-4 Alkyl; R Two Is aryl, Het 1 , C 3-7 Cycloalkyl, cyano, optionally substituted C 1-6 Alkyl, -C (= Q) -X Two -R Fifteen And R Three Is hydrogen or C 1-4 Alkyl; R Fifteen Is hydrogen, optionally substituted C 1-6 Alkyl, C 3-7 Cycloalkyl, aryl; X Two Is a direct bond, Fifteen But also halo or Het 1 Can also be; X Two Is NR Five R if Fifteen Can also be hydroxy; X Two Is C (= O) -NH-NH or NH-NH-C (= O), Fifteen Is R 11 Q can be replaced by O, S or NR Three And X Two Is O, S, NR Five , C (= O) -NH-NH, NH-NH-C (= O) or a direct bond; Five Is hydrogen, C 1-6 Alkyl, C 1-6 Alkyloxy or aryl C 1-6 Alkyl; R 6 Is a sulfonyl or sulfinyl derivative; R 7 And R 8 Is independently hydrogen, optionally substituted C 1-4 Alkyl, aryl, carbonyl-containing moiety, C 3-7 Cycloalkyl, -YC 1-4 Alkanediyl-C (= O) -OR 14 , Het Three And R 6 And R 11 Is hydroxy, mercapto, cyano, nitro, halo, trihalomethyl, C 1-4 Alkyloxy, formyl, trihalo C 1-4 Alkylsulfonyloxy, R 6 , NR 7 R 8 , C (= O) NR 7 R 8 , C 1-4 Alkanediyl-C (= O) -OR 14 , -C (= O) -OR 14 , -YC 1-4 Alkanediyl-C (= O) -OR 14 , Aryl, aryloxy, arylcarbonyl, C 3-7 Cycloalkyl, C 3-7 Cycloalkyloxy, phthalimido-2-yl, Het Three , Het Four And C (= O) Het Three An aryl is an optionally substituted phenyl; Het 1 , Het Two , Het Three And Het Four Is a heterocyclic ring which may be optionally substituted, their N-oxides, pharmaceutically acceptable addition salts and stereochemical isomers; Composition comprising the composition. The invention further relates to their use as medicaments.nEmbedded image
priorityDate 1998-11-23-04:00^^<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/protein/ACCA0A803JUX3
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419906515
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID396991
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456636940
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP01587
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ60481
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ2MH06
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP20096
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCB4DNV3
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17841212
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411317346

Total number of triples: 302.