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filingDate 1999-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75339224daea7bb1cae3510fdfb590be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f6dde47f88f040869318f63f1e5c1a7f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb4855d517d2fe3bdea709be042a0834
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47a6896ca8b2223d472a6a6c3c6b9ad1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f80b7cd48b77bf7129ff314f813d5d7c
publicationDate 2004-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1460072-A1
titleOfInvention Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors
abstract Compounds of formula (I) and salts or solvates thereof are disclosedn wherein Y is CR 1 and V is N; or Y is CR 1 and V is CR 2 ; R 1 represents CH 3 SO 2 CH 2 CH 2 NHCH 2 -Ar-, wherein Ar is furan or thiazole, each of which may optionally be substituted by one or two halo, C 1-4 alkyl or C 1-4 alkoxy groups; R 2 is hydrogen C 1-4 alkoxy or halo; R 3 is benzyl, halo-, dihalo- or trihalobenzyl, benzoyl, pyridylmethyl, pyridylmethoxy, phenoxy, benzyloxy, halo-, dihalo- or trihalobenzyloxy or benzenesulphonyl; R 4 is halo or C 1-4 alkoxy or is not present; nand wherein either (a) R 3 represents 3-fluorobenzyloxy; and/or (b) R 4 is halo and is substituted in the 3-position of the phenyl ring; nand wherein halo represents fluoro, chloro or bromo. n Processes for the preparation of the compounds, pharmaceutical formulations of the compounds, the use of the compounds in therapy, and methods of treatment of inter alia cancer and malignant tumours by administration of the compounds is also disclosed.
priorityDate 1998-01-12-04:00^^<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: 511.