http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-2011009489-A

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filingDate 2010-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc99776e5ea322d90a0c03605950801a
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publicationDate 2011-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-2011009489-A
titleOfInvention PIRROLO DERIVATIVES [2,3-B] PIRIDINE FOR THE INHIBITION OF RAF KINASES.
abstract The {2,4-difluoro-3- [5- (2-methoxy-pyrimidin-5-yl) -1 H-pyrrolo [2,3-b] pyridine-3- propane-1-sulfonic acid compounds are described carbonyl] -phenyl} -amide, [3- (5- cyano-1 H -pyrrolo [2,3-b] pyridine-3-c arbonyl) -2,4-difficult-phenyl] - propane-1-sulfonic acid - amide, [3- (5- cyano-1 H -pyrrolo [2,3-b] pyridine-3-carbonyl) -2-fluoro-phenyl] -amide propane-1-sulfonic acid, N- [3- (5 -cyano-1H-pyrrolo [2,3-bJpyridine-3-carbonyl) -2,4-ciifluoro-phenyl] -2,5-difluoro-benzenesulfonamide, N- [3- (5-cyano-1H-pyrrolo [2 , 3-bjpyridine-3-carbonyl) -2,4-difluoro-phenyl] -3-fluoro-benzenesulfonamide, [3- (5- cyano-1H-pyrrolo [2,3-b] pyrrolidine-1-sulfonic acid) pyridine-3-carbonyl) -2,4-difluoro-phenyl] -amide, [3- (5-cyano-1H-pyrrolo [2,3-b] pyridine-3-carbonyl] N, N-dimethylamino-sulfonic acid ) -2,4-difluoro-fe nil] -amide, and salts thereof, formulations thereof, conjugates thereof, derivatives thereof, forms thereof and uses thereof. In certain aspects and embodiments, the described compounds or salts thereof, formulations thereof, conjugates thereof, derivatives thereof and forms thereof are active on at least one Raf protein kinase. Methods of using them to treat diseases and conditions, including diseases and conditions associated with the activity of Raf kinase proteins, including melanoma, glioma, colorectal cancer, thyroid cancer, lung cancer, ovarian cancer, cancer are also described. of prostate and biliary tract cancer.
priorityDate 2009-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 1058.