http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H09202764-A

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filingDate 1996-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03c819561464edd1cd9419701195a52f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b70ec8dc593d346ede1f1cb149b5903
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publicationDate 1997-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09202764-A
titleOfInvention Nitro compound
abstract (57) [Abstract] [Purpose] [Constitution] General formula (1) (In the formula, R 1 represents an aromatic hydrocarbon group such as a naphthyl group which may have a substituent; A represents a sulfone group or a sulfonamide which may have a substituent on the nitrogen atom. Group, an amide group; R 2 represents a hydrocarbon group having 1 to 10 carbon atoms; G represents an amino group which may have a substituent, or a cyclic amine such as piperazine or homopiperazine. R 3 represents a hydrocarbon group having 1 to 18 carbon atoms which may have a substituent and in which a hetero atom may be present at any position.) Or A pharmaceutically acceptable salt thereof. [Effect] The compound of the present invention has a proliferation inhibitory action on vascular smooth muscle cells and an inhibitory action on cyclic contraction, It is useful as a therapeutic agent for angina pectoris, which has an effect of preventing restenosis after TCA.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003515526-A
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priorityDate 1996-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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