http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BG-106850-A

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filingDate 2002-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f5b813714f64bf2c9da7f49234a8784
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8bd670ebb7df473c5e5a1c097c16328
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbeb71865d8785b8a850882229ef99c9
publicationDate 2003-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BG-106850-A
titleOfInvention PYRIDO [2,3-d] PYRIMIDINE-2,7-DIAMINE KINASE INHIBITORS
abstract The compounds are potent inhibitors of cdk-kinases and growth factor-mediated kinases. They have the general formula wherein R 2, R 7, R 13, R 14 and R 15 are independently hydrogen or (unsubstituted) lower alkyl, (unsubstituted) lower alkenyl, (unsubstituted) lower alkynyl or (unsubstituted) ; R5 is halogen, cyano, nitro, -R9, -NR9R10 or -OR9; R6 is halogen, cyano, nitro, -R9, -NR9R10, -OR9, -CO2R9, -COR9, -CONR9R10, -NR9COR10, (un) substituted lower alkenyl or (un) substituted lower alkynyl; R8 is -CO2R13, -COR13, -CONR13R14, -CSNR13R14, -C (NR13) NR14R15, -SO3R13, -SO2R13, -SO2NR13R14, -PO3R13R14, -POR13R14, -PO (NR13R14) 2; R9 and R10 are independently hydrogen or (un) substituted lower alkyl; R11 is a heteroaryl or heterocyclic group; R12 is a cycloalkyl, heterocyclic, aryl or heteroaryl group and n has the value of 0, 1, 2 or 3. The compounds and their pharmaceutical compositions are used in the treatment of cell proliferative disorders, for example cancer and restenosis.
priorityDate 2000-01-25-04:00^^<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: 515.