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filingDate 2015-09-04^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-10-24^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e52b932e68f95184bd60359088e5e72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5cb07150da1319189a0358e8905f729
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a7971fb355fa5c1fdbf7f7abcd4393d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1cfdb49f4e9903487f08649ad5141713
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbf115029ca6ed9183edc8423897176a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a26f489cf45ffbe3cb2c75364b4fea87
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publicationDate 2017-10-24^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9796704-B2
titleOfInvention Substituted quinazolines as receptor-type kinase inhibitors
abstract The present invention provides compounds of structural formula I, n nfor modulating receptor kinase activity, particularly ephrin and EGFR, and methods of treating diseases mediated by receptor kinase activity utilizing the compounds and pharmaceutical compositions thereof. Diseases mediated by receptor kinase activity include, but are not limited to, diseases characterized in part by abnormal levels of cell proliferation (i.e. tumor growth), programmed cell death (apoptosis), cell migration and invasion and angiogenesis associated with tumor growth. Compounds of the invention include “spectrum selective” kinase modulators, compounds that inhibit, regulate and/or modulate signal transduction across subfamilies of receptor-type tyrosine kinases, including ephrin and EGFR.
priorityDate 2002-07-15^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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