http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004077632-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_a24834ab8d23a67a47ec3f7637385704
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_051d7b3a22d13f0effeace3224523055
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d5f8a8090382203a0383dfa4ec03512
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b07281ae1332018a949b881fac0ad5d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80765eff46d03e3d464610fa0aa3bfae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8550ae52b86e826f5b3b5e3b94780b44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d1ff9cd6d00c728221c017347b1597e
publicationDate 2004-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004077632-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 formulations containing such sulfonamide derivatives. Said sulfonamide derivatives are efficient modulators of the JNK pathway, they are in particular efficient and selective inhibitors of JNK 3. The present invention is furthermore related to novel sulfonamide derivatives as well as to methods of their preparation. n n n The compounds of formula I according to the present invention being suitable pharmaceutical agents are those wherein n Ar 1 is a substituted or unsubstituted aryl or heteroaryl; n Ar 2 is an aryl or heteroaryl group carrying at least one hydrophilic substituent; n X is O or S, preferably O; n R 1 is hydrogen or a C 1 -C 6 -alkyl group, or R 1 forms a substituted or unsubstituted 5-6-membered saturated or unsaturated ring with Ar 1 ; n n is an integer from 0 to 5, preferably between 1-3 and most preferred 1; n 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.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8946197-B2
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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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Total number of triples: 926.