http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-404937-B

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filingDate 1997-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b623ad9264aa79f8f5873cdff0b7ed40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77c4f8ece7377ecb33d61221e930c4ca
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5759e7e977274db2107f6915e07432e
publicationDate 2000-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-404937-B
titleOfInvention 2-Chloro-5-trifluoromethyl-benzoylguanidines having an action of inhibiting cellular Na<+>/H<+> exchange mechanism, process for their preparation, and their pharmaceutical compositions
abstract Ortho-substituted benzoylguanidines of the formula I in which R2 and R3 have the meanings given in the claims, are suitable, as antiarrhythmic pharmaceuticals having a cardioprotective component, for the prophylaxis and treatment of infarction and for the treatment of angina pectoris. They also inhibit, in a preventive manner, the pathophysiological processes associated with the development of ischemically induced damage, in particular in association with the triggering of ischemically induced cardiac arrhythmias. An ortho-substituted benzoylguanidine of the formula I in which: either one of R2 and R3 is hydrogen, and the other one is selected from C1, Br, I, (C1-C8)-alkyl, (C3-C8)-cycloaklyl or -OR5; R5 is (C1-C8)-alkyl or -CdH2d-(C3-C8)-cycloalkyl; d is zero, 1 or 2; and the pharmaceutically tolerated salts thereof.
priorityDate 1996-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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