1186608-83-2Relevant academic research and scientific papers
FIVE-AND-SIX-MEMBERED HETEROCYCLIC COMPOUND AND USE THEREOF AS PROTEIN RECEPTOR KINASE INHIBITOR
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Paragraph 0060; 0067-0068, (2021/12/18)
A class of five-membered fused with six-membered heterocyclic compounds represented by formula I and a pharmaceutical composition, preparation, and an application thereof are disclosed. These compounds have TRK kinase inhibitory activity and can treat diseases related to TRK dysfunction.
Methyl-1H-indazole ROR gamma conditioning agent and application thereof
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Paragraph 0111; 0112; 0113; 0114; 0115, (2019/01/24)
The invention relates to a compound or a stereisomer, a tautomer or pharmaceutically acceptable salt or a solvate or a prodrug thereof, a preparation method thereof, a pharmaceutical composition containing the conditioning agents and application of the ph
1H-PYRAZOLO [3, 4-B] PYRIDINE COMPOUNDS FOR INHIBITING RAF KINASE
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Page/Page column 49, (2011/04/14)
Compounds of Formula I are useful for inhibition of Raf kinases. Methods of using compounds of Formula I and stereoisomers, tautomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed. [FORMULA I]
Pyrazolopyridine inhibitors of B-RafV600E. Part 1: The development of selective, orally bioavailable, and efficacious inhibitors
Wenglowsky, Steve,Ren, Li,Ahrendt, Kateri A.,Laird, Ellen R.,Aliagas, Ignacio,Alicke, Bruno,Buckmelter, Alex J.,Choo, Edna F.,Dinkel, Victoria,Feng, Bainian,Gloor, Susan L.,Gould, Stephen E.,Gross, Stefan,Gunzner-Toste, Janet,Hansen, Joshua D.,Hatzivassiliou, Georgia,Liu, Bonnie,Malesky, Kim,Mathieu, Simon,Newhouse, Brad,Raddatz, Nicholas J.,Ran, Yingqing,Rana, Sumeet,Randolph, Nikole,Risom, Tyler,Rudolph, Joachim,Savage, Scott,Selby, Leann T.,Shrag, Michael,Song, Kyung,Sturgis, Hillary L.,Voegtli, Walter C.,Wen, Zhaoyang,Willis, Brandon S.,Woessner, Richard D.,Wu, Wen-I,Young, Wendy B.,Grina, Jonas
scheme or table, p. 342 - 347 (2011/07/09)
The V600E mutation of B-Raf kinase results in constitutive activation of the MAPK signaling pathway and is present in approximately 7% of all cancers. Using structure-based design, a novel series of pyrazolopyridine inhibitors of B-RafV600E was
PYRAZOLE [3, 4-B] PYRIDINE RAF INHIBITORS
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Page/Page column 87-88, (2009/10/22)
Compounds of Formula I are useful for inhibition of Raf kinases. Methods of using compounds of Formula I and stereoisomers, tautomers, prodrugs and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed.
