http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-9904238-A3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c8cbc6261d883f27c8339ffb4b4cfeaa
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-75
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 1998-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f32c92e7cdf6ea609c28715e14f55b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1fd5e4459b399c2a6490821954439e9e
publicationDate 2001-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-9904238-A3
titleOfInvention Cyanoguanidines as Cell Proliferation Inhibitors
abstract The solution relates to hitherto unknown compoundsncharacterized by formula I, or tautomers thereofnforms, the connection of the pyridine ring being in the 3-positionnor 4, and wherein R is one or moren, substituents which may be the same or different and arenselected from the group consisting of hydrogen, halogen, trifluoromethyl,n*, C 1-4 alkyl, alkoxy or alkyloxycarbonyl, nitro, amino orn; cyano substituents, and X represents a direct bond,nsubstituted C 1-6 cycloalkylene, divalent heterocyclicna ring (with one or more nitrogen, oxygen or sulfur atoms),narylene, oxygen, one or two sulfur atoms or amino groups,nwhich may be substituted by hydrogen or C 1-4 alkyl; andnQ 1 and Q 2 represent C divalent hydrocarbon radical,nwhich may be aliphatic, branched cyclic, saturated ornunsaturated; and pharmaceutically acceptable non-toxic salts thereof andnN-oxides. These compounds have meaning in human i; '.nveterinary medical practice for diseasesncharacterized by unwanted cell proliferation
priorityDate 1998-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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