http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0339562-B1

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filingDate 1989-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1993-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0339562-B1
titleOfInvention Benzopyran compound and its pharmaceutical use
abstract A benzopyran compound of the general formula (I) <CHEM> wherein A represents -OR<1> or -NH-COR<2> (wherein R<1> represents hydrogen, a lower alkyl, formyl, an alkanoyl, an aroyl or an aralkyl and R<2> represents hydrogen, a lower alkyl, a lower alkoxy, amino, mono- or di-lower alkylamino, an amino-lower alkyl, a hydroxy-lower alkyl, a halo-lower alkyl, a lower alkoxy-lower alkyl, an acyloxy-lower alkyl, a lower alkoxycarbonyl-lower alkyl, an aryl or a heteroaryl); R<3> represents hydrogen, a lower alkyl, a lower alkoxy, amino, a mono- or di-lower alkylamino, an amino-lower alkyl, a hydroxy-lower alkyl, a halo-lower alkyl, a lower alkoxy-lower alkyl, an acyloxy-lower alkyl, a lower alkoxycarbonyl-lower alkyl, an aryl or a heteroaryl, or R<2> and R<3> combined together form an alkylene having 1 to 2 carbon atoms; R<4> and R<5> are the same or different, and respectively represent hydrogen or a lower alkyl, or combined together form an alkylene having 2 to 5 carbon atoms; R<6> represents hydroxyl group, formyloxy, an alkanoyloxy, a haloalkanoyloxy, a lower alkoxycarbonyloxy, an aroyloxy, a heteroaroyloxy, carbamoyloxy, a mono- or di-lower alkylcarbamoyloxy and R<7> represents hydrogen, or R<6> and R<7> combined together form a bond and X and Y are the same or different, and respectively represent hydrogen, halogen, nitro, cyano, a lower alkyl, a lower alkoxy, a halo-lower alkyl, carboxyl, formyl, an alkanoyl, an aroyl, a haloalkanoyl, carbamoyl, a lower alkylsulfinyl, an arylsulfinyl, a lower alkylsulfonyl, an arylsulfonyl, sulfonamido or a mono- or di-lower alkylsulfonamido, or their pharmaceutically acceptable salts and its pharmaceutical use. The compounds of the present invention exhibit remarkable and long lasting antihypertensive actions and peripheral vascular relaxant actions and therefore are useful as therapeutic medicines for hypertensive. Since they also display selective coronary vasodilating actions and the duration of actions are very long, they are of use as therapeutic medicines for cardiovascular disturbances such as angina pectoris and cardiac insufficiency.
priorityDate 1988-04-26-04:00^^<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/CID88456755
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54111104
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15414
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129808683
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16908
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID73905
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234806198
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127717499
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88456759
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128081169
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12184
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129028366
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234942990
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234942991
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127707120
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88456746
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234942988
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127763829
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88456747
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129029416
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234942989
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129935955
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88456744
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129816438

Total number of triples: 944.