http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2327946-A1

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filingDate 2000-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20da4a7d407e3babee8f29b8d4c87fd6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4261146e4848054b10bd08cd68ece365
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d2346686e73821ac0cd685d1999fc73
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a48ada9f50de12b70c94e09a01af280c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d066c3ac36b5afedfbddde052a882f51
publicationDate 2001-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2327946-A1
titleOfInvention Substituted 1,4-dihydropyridine compounds as bradykinin antagonists
abstract This invention provides a compound of the formula (I): (see formula I) or the pharmaceutically acceptable salts thereof wherein A is independently halo; Y is -(CH2)m-, -C(O)- or -S(O)-; R1 and R2 are independently C1-4 alkyl; R3 is C7-9 bicycloalkyl, C5-7 azacycloalkyl or C7-9 azabicycloalkyl, the C7-9 bicycloalkyl, C5-7 azacycloalkyl or C7-9 azabicycloalkyl being optionally substituted with one, two or three substituents are independently selected from oxo, hydroxyl, C1-4 alkyl, C1-4 alkyloxy, C1-4 alkyl-carbonyl, formyl, C1-4 alkylenedioxy, and phenyl-C1-4 alkyl; R4 is thiazolyl, imidazolyl or oxazolyl, the thiazolyl, imidazolyl or oxazolyl being optionally substituted with one or two substituents independently selected from C1-4 alkyl and halo; R5 is hydrogen or C1-4 alkyl; m is 0, 1 or 2; and n is 0, 1, 2, 3, 4 or 5. These compounds are useful for the treatment of medical conditions mediated by bradykinin such as inflammation, allergic rhinitis, pain, etc. This invention also provides 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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Total number of triples: 468.