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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-496
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
filingDate 2009-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5077d8d8bb7906635ed64a7501f372b0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_208733bb0892206ab29c0e0f8a548fe9
publicationDate 2013-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2712619-C
titleOfInvention Dihydropyridine calcium antagonist compounds, preparation methods and medical uses thereof
abstract Dihydropyridine calcium antagonist compounds, preparation methods and medical uses thereof are disclosed. Particularly, preparation methods of compounds of general formula (I) and (II) and pharmaceutically acceptable salts thereof, and their uses in the treatment of cardiovascular diseases are disclosed, wherein R1 represents substituted or unsubstituted heterocyclic, aromatic ring or aralkyl group, the substituents may be C1-C4alkyl, C1-C4alkoxyl, halogen, cyano, trifluoromethyl, trifluoromethoxyl, methylthio, nitro, amino or hydroxyl; R2 represents C1-C8alkyl; R3 and R4 may be same or different, and each independently represents hydrogen, halogen, cyano, trifluoromethyl, trifluoromethoxyl, methylthio, nitro, amino or C1-C4alkyl, C1-C4alkoxyl, C1-C4alkenyl, C1-C4alkynyl; R5 and R6 are same or different, and each represents C1-C4alkyl; X represents O, S or a single bond; m=0-6, n=1-6, and m and n may be same or different.
priorityDate 2008-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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