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filingDate 1996-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cef4285469ed12d329d56f0e9bc551b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc8a784923740947581c452d6fff4d37
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f02022e7347cac19e678ea734d0991eb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d90087a80fbbaccfb5b468711a333ba0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_349dee61792650e7bdd02d4bce96f284
publicationDate 1997-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09278780-A
titleOfInvention Quinolone derivative
abstract (57) Abstract: The present invention provides a novel quinolone derivative useful as a cell adhesion inhibitor. SOLUTION: The formula (I) (In the formula, R 1 represents a substituted or unsubstituted aryl, a substituted or unsubstituted aromatic heterocyclic group, cyano or acetamido, R 2 and R 3 are the same or different, and hydrogen, Represents lower alkyl, halogenated lower alkyl, halogen, hydroxyl, lower alkoxyl, lower alkylthio, nitro, amino, lower alkylamino, dilower alkylamino, lower alkanoylamino, or lower alkoxycarbonyl, and R 4 and R 5 are the same or Differently representing hydrogen or lower alkyl, n and m are 0, 1, Represents an integer of 2. ) A quinolone derivative represented by or a pharmacologically acceptable salt thereof.
priorityDate 1996-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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