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filingDate 1989-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_968763e0133d4a50fabcdc1ecf6a145e
publicationDate 1990-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02134321-A
titleOfInvention 6-halo-4-quinolone compound for producing agent for treating osteoartheritis and application such pharmaceutical composition
abstract PURPOSE: To obtain an agent capable of treating osteoarthritis without causing prominent adverse effect by compounding a 6-halo-4-quinolone compound. n CONSTITUTION: This agent is obtained by compounding a compound of formula I or II (R is ethyl, cyclopropyl, NHCH 3 or a phenyl group substituted with F at para position; R 1 is H or a 1-2C alkyl; R 2 is a halogen; A is CH or N; X is O or S; R 3 is methyl when X is O and H when X is S) or an addition base with a pharmaceutically permissible acid or base, e.g. 1-cyclopropyl-7- piperazinyl-6-fluoro-1,4-dihydro-3-carboxy-4-quinolone. The agent enables the therapy both for a single arthrosis and whole peripheral arthroses of an arthritis patient. The agent is administered once a week by injection, and arthrosis infiltration is carried out in initial five days of the week of the injection. Total dose in a week is in a range of 50-500mg, and the treatment is repeated 7-10 times. n COPYRIGHT: (C)1990,JPO
priorityDate 1988-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 29.