611225-63-9Relevant articles and documents
Discovery of RAF265: A Potent mut-B-RAF inhibitor for the treatment of metastatic melanoma
Williams, Teresa E.,Subramanian, Sharadha,Verhagen, Joelle,McBride, Christopher M.,Costales, Abran,Sung, Leonard,Antonios-Mccrea, William,McKenna, Maureen,Louie, Alicia K.,Ramurthy, Savithri,Levine, Barry,Shafer, Cynthia M.,MacHajewski, Timothy,Renhowe, Paul A.,Appleton, Brent A.,Amiri, Payman,Chou, James,Stuart, Darrin,Aardalen, Kimberly,Poon, Daniel
, p. 961 - 965 (2015/09/22)
Abrogation of errant signaling along the MAPK pathway through the inhibition of B-RAF kinase is a validated approach for the treatment of pathway-dependent cancers. We report the development of imidazo-benzimidazoles as potent B-RAF inhibitors. Robust in
Design and synthesis of orally bioavailable benzimidazole reverse amides as pan RAF kinase inhibitors
Subramanian, Sharadha,Costales, Abran,Williams, Teresa E.,Levine, Barry,McBride, Christopher M.,Poon, Daniel,Amiri, Payman,Renhowe, Paul A.,Shafer, Cynthia M.,Stuart, Darrin,Verhagen, Joelle,Ramurthy, Savithri
, p. 989 - 992 (2014/12/10)
Benzimidazole reverse amides were designed and synthesized as Pan RAF kinase inhibitors. Investigation of the structure-activity relationship of the compounds revealed that they were potent in vitro and exhibited desirable in vivo properties.
SOLID FORMS OF A RAF KINASE INHIBITOR
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, (2009/01/20)
The present invention is directed to solid forms of the Raf kinase inhibitor 1-methyl-5-(2-(5-(trifluoromethyl)-1H-imidazol-2-yl)pyridin-4-yloxy)-N-(4-(trifluoromethyl)phenyl)-1H-benzo[d]imidazol-2-amine, as well as compositions thereof and uses of the sa
Design and synthesis of orally bioavailable benzimidazoles as raf kinase inhibitors
Ramurthy, Savithri,Subramanian, Sharadha,Aikawa, Mina,Amiri, Payman,Costales, Abran,Dove, Jeff,Fong, Susan,Jansen, Johanna M.,Levine, Barry,Ma, Sylvia,McBride, Christopher M.,Michaelian, Jonah,Pick, Teresa,Poon, Daniel J.,Girish, Sandhya,Shafer, Cynthia M.,Stuart, Darrin,Sung, Leonard,Renhowe, Paul A.
supporting information; experimental part, p. 7049 - 7052 (2009/11/30)
A series of arylaminobenzimidazoles was designed and synthesized as Raf kinase inhibitors. Exploration of the structure-activity relationship resulted in compounds that are potent in vitro and show desirable in vivo properties.
FORMULATIONS FOR BENZIMIDAZOLYL PYRIDYL ETHERS
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Page/Page column 26, (2008/06/13)
Formulations are provided, comprising: a compound of Formula (I), a pharmaceutically acceptable salt thereof, or a mixture of any two or more thereof; and an ingredient selected from a hydrophilic solvent, a lipophilic solvent, an emulsifier, or a mixture
SALTS OF BENZIMIDAZOLYL PYRIDYL ETHERS AND FORMULATIONS THEREOF
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Page/Page column 26-27, (2008/06/13)
Salts of benzimidazolyl pyridyl ethers are provided, particularly salts of { 1 -methyl-5- [2-(5-trifluoromethyl- 1 H-imidazol-2-yl)-pyridin-4-yloxy] - 1 H-benzoimidazol-2-yl } -(4- trifluoromethyl-phenyl)amine. Compositions and formulations including such
Substituted benzimidazoles and methods of preparation
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Page/Page column 18, (2008/06/13)
Methods for preparing new substituted benzimidazole compounds having formula (I) useful for treating kinase mediated disorders are provided wherein R1, R2, R3, R4, a, b, and c are defined herein
Substituted benzazoles and methods of their use as inhibitors of Raf kinase
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Page 88-89, (2008/06/13)
New substituted benz-azole compounds, compositions and methods of inhibition of Raf kinase activity in a human or animal subject are provided. The new compounds compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.