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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-72
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-72
filingDate 1986-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1989-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8853921c33244dd27de9e20d44e6b6f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_548e98ee589f77003d794b0ef033e541
publicationDate 1989-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4839367-A
titleOfInvention Antihypertensive amide compounds
abstract Provided are antihypertensive compounds of the formula <IMAGE> wherein R1, R2, R3, R4, R5, and R6 are hydrogen, alkyl, alkenyl, alkynyl, phenyl-alkyl, or cycloalkyl, and may be the same or different, m is an integer from 0 to 2 inclusive, n is an integer from 0 to 4 inclusive, M is alkyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, polycycloalkyl, polycycloalkyl-alkyl, aryl, aralkyl, heteroaryl, heteroaryl-alkyl, hetero-cycloalkyl, hetero-cycloalkyl-alkyl, fused aryl-cycloalkyl, fused aryl-cycloalkyl-alkyl, fused heteroaryl-cycloalkyl, fused heteroaryl-cycloalkyl-alkyl, alkoxyalkyl, alkylthioalkyl, alkylamino-alkyl, or dialkylaminoalkyl, Y is hydroxy, alkoxy, amino, or substituted amino, aminoalkanoyl, aryloxy, aminoalkoxy, or hydroxyalkoxy, and R7 is alkyl, aryl, aralkyl, cycloalkyl, cycloalkyl-alkyl, heterocyclic, -CO-SR, -CS-SR, <IMAGE> CH2COR, -CHM-CO2R, -CH2-CO-SR, -CN, <IMAGE> -CO-NH-CH2CO2R, <IMAGE> or -CO-CO2CO2R, wherein R is hydrogen, alkyl, or aryl, and where Y is hydroxy, their pharmaceutically acceptable, nontoxic alkali metal, alkaline earth metal, and amine salts.
priorityDate 1981-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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