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filingDate 2009-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6acd4b0a023d1e38dbfdba185be3968f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ffc2c7b3ab48ddd54aa0e6741c076e6
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0dce3e0d85517549995d553dda8351b0
publicationDate 2010-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2010029719-A1
titleOfInvention Arylsulfonamide derivatives as c-jun-n-terminal kinases (jnk's) inhibitors
abstract The present invention relates to sulfonamide derivatives of formula I notably for use as pharmaceutically active compounds, as well as to pharmaceutical formulations containing such sulfonamide derivatives. Said sulfonamide derivatives are useful in the treatment of neuronal disorders, autoimmune diseases, cancer and cardiovascular diseases. Furthermore, said sulfonamide derivatives are efficient modulators of the JNK pathway, they are in particular efficient and selective inhibitors of JNK2 and -3. The present invention is furthermore related to novel sulfonamide derivatives as well as to methods of their preparation. n n n n n n n n n n n n Ar 1 is a substituted or unsubstituted aryl or heteroaryl group; n X is O or S, preferably O; n Ar 2 a substituted or unsubstituted arylene or heteroarylene group; n R 1 and R 2 are independently selected from the group consisting of hydrogen and a C 1 -C 6 -alkyl group;
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2018110729-A1
priorityDate 2001-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 854.