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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D241-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-12
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filingDate 1994-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbe3816ac0c40f44affe45a1240b18cd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df6d785f751641d19a5cb08194bb4944
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publicationDate 1995-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07233153-A
titleOfInvention 7-Substituted 1- (2-hydroxyphenyl) -2 (1H) -quinoxalinone derivative
abstract (57) [Summary] [Structure] 1-substituted 7-position represented by the following chemical formula 1 (2-Hydroxyphenyl) -2 (1H) -quinoxalinone derivative or its alkali metal salt. [Chemical 1] (In the formula, R is hydrogen, lower alkyl, phenyl, etc., W is oxygen atom or sulfur atom, X is halogen, trifluoromethyl, cyano, etc., Y is halogen, etc., Z is hydrogen, lower alkyl, substituted lower alkyl or raw. It means a group capable of being converted into a hydrogen atom in the body.) [Effect] Since the compound of the above chemical formula 1 and its alkali metal salt have a vasodilatory action and a blood pressure lowering action based on the smooth muscle relaxing action, cardiovascular diseases It is useful as a medicine such as a therapeutic drug.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4869225-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008505874-A
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