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filingDate 2000-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee05ad94aa3ce747c6a2e911c045f570
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd0aed395d27fb818f9734bfb4ec9d89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d607b8cfa82e79000193712e741b9e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_994087fbb6b982973bc2988f93510c3f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_802ac0eefc5547e83d02d8fcdf1e61f2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14938dd519b9a442c5ee65921f0bf3a1
publicationDate 2002-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0201832-A2
titleOfInvention Quinazoline derivatives, pharmaceutical compositions and methods for their preparation
abstract The present invention relates to bicyclic heterocyclic compounds of the formula wherein R a is hydrogen or alkyl; Rb is optionally substituted phenyl, benzyl or 1-phenethyl; Rc and Rd are hydrogen, fluorine or chlorine, methoxy or methyl substituted by various groups; X is N or = C (CN) -; A and C are alkylene, substituted alkylene oxy, or substituted alkylene amino; B and D (alkoxycarbonyl) alkenylamino, (alkoxyphosphoryl) alkenylamino or various substituted ring amino groups which are physiologically acceptable salts thereof which inhibit signal transduction mediated by atirosin kinases and are therefore useful in the treatment of various diseases. compounds. SHE
priorityDate 1999-03-15-04:00^^<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: 477.