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filingDate 2002-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e61afeda822b62c47e2cd189a52d22b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdc60a4bffa1b41aaa487ae51c1002d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d460b248630dfa54f2135b0c068b0c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_386d9786d36b2800b4daa7bb835e4723
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publicationDate 2013-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-304035-B6
titleOfInvention N-phenylarylsulfonamide compound, a pharmaceutical composition containing the compound as an active ingredient, a synthetic intermediate for the compound and a method for its preparation
abstract N-phenylarylsulfonylamide compounds of formula I (R.sup.1. Denotes COOH, etc .; R.sup.2. Denotes hydrogen, methyl, etc .; R.sup.3. 4 is a combination of a methyl group and a methyl group, etc .; R 5 denotes an isopropyl group, etc .; Ar represents a thiazolyl group, a pyridyl group, a 5-methyl-2-furyl group, each optionally substituted by methyl; n represents 0 or 1). The compound of formula I binds to and antagonizes the prostagladin E.sub.2.n receptor, in particular the EP.sub.1.n receptor subtype. It is less influenced by protein binding, so it has satisfactory in vivo activity. It is therefore considered to be useful as an analgesic, antipyretic, agent for the treatment of pollakiuria and / or lower urinary tract disease or an antitumor agent.
priorityDate 2001-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 508.