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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ac40ffdd0f9b7563bab9d5dccaa8a6b3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D205-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-04
filingDate 1980-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71e3604da70d7407e9b6107ed5326328
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16d3ee01375b0eeceaeccd3e23ab3990
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7e02535922cabe572bc5e9d3da182a1
publicationDate 1987-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-193505-B
titleOfInvention Process for producing citostatic quinazoline derivatives
abstract Quinazoline derivatives of formula:n wherein r represents: 1) a straight or branched chain unsaturated hydrocarbon group, or 2) a straight or branched chain saturated or unsaturated hydrocarbon group which is substituted by at least one: heteroatom, the or each heteroatom being halogeno when R is a C 1 hydrocarbon group; or saturated carbocyclic group; or group containing at least one heteroatom, the or each heteroatom being 0, N or S when R contains a cyclic group; and n is 0 or an integer of 1-4; X or, when n is an integer of at least 2, each X independently, represents a halogeno, C 1 -C 4 alkyl, aryl or aralkyl group or a group including at least one heteroatom; and Y represents a group of formula:-n wherein m . 1 (poly-L-glutamates); and the pharmaceutically acceptable salts and esters thereof, which are suitable as anti-cancer agents.
priorityDate 1979-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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