http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0984940-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-78
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filingDate 1998-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b976b576b2cf5d3a3d565357a674412d
publicationDate 2000-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0984940-A1
titleOfInvention Cyanoamidines as cell proliferation inhibitors
abstract The present invention relates to hitherto unknown compounds of formula (I), or their tautomeric forms, the attachment to the pyridine being in the 2-, 3- or 4-position, in which formula R1 stands for one or more substituents which can be the same or different and are selected from the group consisting of: hydrogen, halogen, amino, trifluoromethyl, nitro, cyano, carboxy, or alkyl, alkoxy, or alkoxycarbonyl, the C-content of which can be from 1 to 4; Q stands for C4-C9 divalent hydrocarbon radical which can be straight, branched, saturated or unsaturated; X stands for methylene, oxygen, sulphur or nitrogen, and R stands for hydrogen or for one or more substituents which can be the same or different and are selected from the group consisting of: hydroxy, amino, halogen, trifluoromethyl, cyano, nitro, carboxy, carbamoyl, methylenedioxy, or alkyl, alkoxy, alkylthio, alkylamino, or alkoxycarbonyl, the C-content of which can be from 1 to 4; and pharmaceutically acceptable, non-toxic salts and N-oxides thereof. The present compounds are of value in the human and veterinary practice.
priorityDate 1997-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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