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filingDate 2000-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3397cc7c50402317df4ca86de3dffc4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_698dfc77c57a90244856e68973f151ca
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d1d9c7f672f09efe445dce5eff98bcb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f18364696d8ee0e407fb7725fabe290d
publicationDate 2001-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2001192382-A
titleOfInvention Substituted 1,4-dihydropyridine compounds as bradykinin antagonists
abstract (57) [Summary] (Modified)n[Problem] B 2 Antagonist activity and human liver microso B with metabolic stability to 2 Receptor non-pepti Provide antagonists.nThe general formula (I):n Or a pharmaceutically acceptable salt thereof. [A is independently halogen; Y is-(CH 2 ) m −, − C (O)-or -S (O)-; R 1 And R 2 Is German Standing C 1-4 Alkyl; R 3 Is C 7-9 Bicycloal Kill, C 5-7 Azacycloalkyl or C 7-9 Aza Bicycloalkyl and the like; R 4 Is thiazolyl, imidazo Ryl or oxazolyl or the like; R 5 Is hydrogen or C 1 -4 Alkyl; m is 0, 1, or 2; n is 0, 1, 2, 3, 4 or 5] A pharmaceutical composition comprising the above compound.
priorityDate 1999-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14013
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Total number of triples: 367.