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grantDate 1992-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d4fd5b868e645b1acd21183e974ae30
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publicationDate 1992-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1300626-C
titleOfInvention Dihydropyridine compounds, processes for their preparation and their use
abstract ABSTRACT Blood-sugar-lowering dihydropyridines of the formula in which R1 represents phenyl, naphthyl, thienyl, pyridyl, chromenyl or thiochromenyl, it being possible for the radicals mentioned each to carry up to 2 iden-tical or different substituents from the series comprising halogen alkyl, alkoxy and alkylthio with in each case up to 6 carbon atoms, fluoro-alkyl and fluoroalkoxy with in each case up to 3 carbon atoms and 3 fluorine atoms, nitro and cyano, R2 represents straight-chain, branched or cyclic alkyl which has up to 8 carbon atoms, can be interrupted in the alkyl chain by an oxygen or a sulphur atom and can be substituted by halogen, phenyl, cyano, hydroxyl, amino, alkylamino or dialkylamino with in each case up to 3 carbon atoms per alkyl group or by N-benzylmethylamino, R3 represents straight-chain, branched or cyclic alkyl which has up to 6 carbon atoms, can be interrupted in the alkyl chain by an oxygen atom and can be substituted by halogen, hydroxyl, amino, phenyl, morpholino, carboxy or alkoxycar-bonyl with up to 4 carbon atoms and R4 and R5 each represent hydroxyl, or R4 and R5 together represent -O-, or a physiologically acceptable salt thereof. Le A 24 766
priorityDate 1986-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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