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filingDate 2005-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_255c628315363298402aecd6d32674bb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9823987fea677303b92b2cf1cca176fb
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f13049e817df25466b1b9d63b10bcc1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_baa505b66b4a994ae40d9ce5e25b6c6b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90c0d95ece6ec9cc383ed86e9326a60f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_839318846c3bce7160b335afd7b560b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f1c022344db10b2a91b6d883a9287b6
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publicationDate 2007-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1773817-A1
titleOfInvention Substituted aryl-amine derivatives and methods of use
abstract The present invention provides classes of compounds, including-their pharmaceutically acceptable derivatives, useful for treating angiogenesis and related diseases such as cancer. Formula I and II wherein R is a 9- or 10-membered heterocyclyl ring selected from 7-isoquinolinyl,..2-methyl-3-oxo-2,3-dihydroindazol-6-yl, [1,6]-naphthydrin-3-yl, [1,7]-naphthydrin-2-yl, 1-oxo-2,3-dihydrobenzofuran-4-yl, 3-oxo-2,3-dihydrobenzofuran-5-yl, dihydro-benzodioxinyl, 6-quinazolinyl, 2-amino-6-quinazolinyl, 4-methylamino-6-quinazolinyl, 2,4-diamino-6 quinazolinyl, 3-oxo-3,4-dihydro-1,4-benzoxazin-6-yl, 2,2-difluoro-l;3-benzodioxol-5-yl and 2,2,3,3 tetrafluoro-2,3-dihydro-l,4-benzodioxin-6-yl, each of which is optionally substituted with one or more substituents selected from halo, haloakyl, C1-6 alkyl, C2-8 alkenyl, C2-8 alkynyl, N-dimethylamino-C1-6-alkyl, N-dimethylamino-C1-6-alkoxy, amino, alkyl-carbonylamino, morpholino-sulfonyl, amino-sulfonyl, oxazolyl, pyrrolyl,4 morpholinyl, carboxyl, cyano, and acetyl; wherein R1 in formula I is selected from unsubstituted or substituted phenyl, 5-6 membered heteroaryl, 9-10 membered bicyclic heterocyclyl and 11-14 membered tricyclic heterocyclyl, and R1 in formula II is selected from specific bicyclic heterocycles.
priorityDate 2004-07-22-04:00^^<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: 6070.