http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0163238-A2

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filingDate 1985-05-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d8f0425065d0029a020d57d59b20fa3
publicationDate 1985-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0163238-A2
titleOfInvention Substituted and bridged pyridines useful as pharmaceutical agents
abstract There are disclosed novel substituted and bridged pyridines having the formulan wherein:n R is hydrogen; C 1 -C 8 straight chain or branched alkyl; benzyl; R 1 and R 4 are, e.g., hydrogen or hydrocarbon having up to 8 carbon atoms; R 2 and R 3 are, e.g., hydrocarbon having up to 8 carbon atoms; C3-C e cycloalkyl; C 2 -C 8 alkyl interrupted by 1 to 2 oxygen atoms or substituted with NR 5 R 6 wherein R 5 and R 6 can independently by hydrogen, C 1 -C 8 alkyl, aralkyl wherein the alkyl groups has up to 8 carbon atoms and the aryl has 6 carbon atoms, or R 5 and R 6 together with the N atom can be joined to form a 5-or 6-membered ring wherein the 6-membered ring can contain an 0 or N hetereoatom and the N heteroatom can be substituted with C 1 -C 6 alkyl; X, W, Z and U can independently by, e.g., hydrogen; phenyl; halo or NO 2 ; provided that two of X, W, Z and U are hydrogen; or, X and W, W and Z, or Z and U, together with the phenyl ring form naphthyl or benzooxadiazole rings; Y is O; S; SO; n is 0 or 1; and, the pharmaceutically acceptable acid addition salts thereof. Those compounds are useful as calcium entry blockers.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011506440-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0005209-A1
priorityDate 1984-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 467.