http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1322641-A1

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filingDate 2001-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a5fb128096fa12a132f1718862fd68fb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ca284647c7234fcde45b6c812dd9be6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04a6d0ca1a38eb53ca3d73b8c6892b6f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7bfc7743e3d264a7343417b8fbc89530
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3e7ab6d4afe11906584bf23d8f82c40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_073bedb7ed392d71eb36b989be347d6f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f20eb53f4b0b5d6449ed88086a73b608
publicationDate 2003-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1322641-A1
titleOfInvention Pharmaceutically active hydrophilic sulfonamide derivatives as inhibitors of protein junkinases
abstract The present invention is related to substantially hydrophilic sulfonamide derivatives, or sulfonamide derivatives having a substantially hydrophilic moiety, of formula (I) notably for use as pharmaceutically active compounds, as well as to pharmaceutical formula-tions containing such sulfonamide derivatives. Said sulfonamide derivatives are effi-cient modulators of the JNK pathway, they are in particular efficient and selective in-hibitors of JNK 3. The present invention is furthermore related to novel sulfonamide derivatives as well as to methods of their preparation. The compounds of formula (I) according to the present invention being suitable pharma-ceutical agents are those wherein Ar1 is a substituted or unsubstituted aryl or heteroaryl; Ar2 is an aryl or heteroaryl group carrying at least one hydrophilic substituent;X is O or S, preferably O; R1 is hydrogen or a C¿1?-C6-alkyl group, or R?1¿ forms a substituted or unsubstituted 5-6-membered saturated or unsaturated ring with Ar1; n is an integer from 0 to 5, preferably between 1-3 and most preferred 1; Y within formula (I) is an unsubstituted or a substituted 4-12-membered saturated cyclic or bicyclic alkyl containing at least one nitrogen atom, whereby one nitrogen atom within said ring is forming a bond with the sulfonyl group of formula (I) thus providing a sulfonamide.
priorityDate 2000-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9XT91
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10797
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Total number of triples: 729.