http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PT-88260-B

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_571b8abacacea64d3f7089d0983b8b3b
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5025
filingDate 1988-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98c0143fad4a22735c3690702ffcd5a4
publicationDate 1995-03-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PT-88260-B
titleOfInvention METHOD FOR THE PREPARATION OF IMIDAZOPIRIDAZINE DERIVATIVES WITH CYTOTOXIC ACTIVITY
abstract Compounds of general formula (I) <CHEM> wherein R<1> represents an optionally substituted carbocyclic or heterocyclic aryl group, or an optionally substituted alkyl, alkenyl, cycloalkyl or cycloalkenyl group; R<2> represents an optionally substituted alkyl, alkenyl, alkynyl, cycloakyl or cycloalkenyl group or an optionally substituted carbocyclic or heterocyclic aryl or aralkyl group; R<3> represents a hydrogen atom or an alkyl group; and either X represents an oxygen or sulphur atom, a group -CH2- or a group NR<4> where R<4> represents a hydrogen atom or a C1-4 alkyl group; and Y represents a group -CH2- or -CH2CH2- or X-Y together represent the group -CH=CH-; and salts and physiologically functional derivatives thereof are useful in the treatment of tumours. Processes for preparing the compounds, intermediates useful in their preparation, pharmaceutical compositions containing them and their use in the treatment of tumours are also described.
priorityDate 1987-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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