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filingDate 1991-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f632955cf288ba272ac37c8407f66c6b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30dd9b7895e4e090019202c67c85fef0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1399f36444f0ff63e5568fce0c181209
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_570cd69e4d277e2b46a5c39769bca03c
publicationDate 1991-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IE-911757-A1
titleOfInvention Anti-tumour compounds
abstract The invention relates to quinazoline derivatives, or pharmaceutically-acceptable salts thereof, which possess anti-tumour activity; to processes for their manufacture; and to pharmaceutical compositions containing them. The invention provides a quinazoline of the formula:- wherein R<1> includes hydrogen, amino and alkyl or alkoxy each of up to 4 carbon atoms; R<2> includes hydrogen, alkyl, hydroxyalkyl and halogenoalkyl each of up to 4 carbon atoms; R<3> is hydrogen or alkyl or up to 3 carbon atoms; Ar is phenylene or heterocyclene; L is a group of the formula -CO.NH-, -NH.CO-, -CO.NR<4>-, -NR<4>.CO-, -CH=CH- or -CO.O-, wherein R<4> is alkyl of up to 4 carbon atoms; and Y is a branched alkyl group bearing substituents Y<2> and Y<3> the definition of each independently including hydroxy, cyano, aryl and heteroaryl, and the definition of Y<3> also optionally including sulpho, N-phenylsulphonylcarbamoyl and 5-tetrazolyl; or a pharmaceutically-acceptable salt thereof.
priorityDate 1990-05-30-04:00^^<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: 1197.