http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0725870-A

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filingDate 1994-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3da4a27e11590273f1b5533ee37088ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bc9303184dd4d82f9db696698000e87
publicationDate 1995-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0725870-A
titleOfInvention 2,3,6-Substituted quinazolinones with angiotensin II receptor blocking properties
abstract (57) [Summary] (Modified) [Purpose] 6- (Polycyclic heterocyclic) -2- (lower alkyl) -3- showing activity as angiotensin II antagonist Provided (substituted) quinazolinone compounds. A quinazolinone compound having the formula I and a pharmaceutically acceptable salt thereof, a process for producing them, and an effective amount of the compound or a pharmaceutically acceptable salt thereof, hypertension or depressive heart attack. A pharmaceutical composition useful for the treatment of. [Wherein R is 1H-tetrazol-5-yl, carboxyl or -NHSO 2 CF 3 ; X is C 3 -C 5 It is alkyl; R 6 is -C (= CH 2) -COOR 7 (However, R 7 is H, CH 3 ) or a condensed complex such as hexahydropyrrolo [1,2-b] isoxazol-2-yl, tetrahydro-2H-isoxazolo [3,2-b] isoquinolin-2-yl, etc. It is a ring group]
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5883773-A
priorityDate 1993-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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