432554-92-2Relevant academic research and scientific papers
Isoxazolines as Therapeutic Agents
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Paragraph 0702-0703, (2013/03/26)
The present invention provides compound of Formula (I) biologically active metabolites, pro-drugs, isomers, stereoisomers, solvates, hydrates and pharmaceutically acceptable salts thereof wherein the variables are defined herein. The compounds of the invention are useful for treating immunological conditions.
Optimization of 5-vinylaryl-3-pyridinecarbonitriles as PKCθ inhibitors
Boschelli, Diane H.,Subrath, Joan,Niu, Chuansheng,Wu, Biqi,Wang, Yan,Lee, Julie,Brennan, Agnes,Ho, Melisa,Deng, Bijia,Yang, Xiaoke,Xu, Xin,Leung, Louis,Wang, Jianyao,Atherton, James,Chaudhary, Divya
scheme or table, p. 1965 - 1968 (2010/06/20)
Analog 8, a 3-pyridinecarbonitrile with an (E)-2-{6-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}vinyl group at C-5, had an IC50 value of 1.1 nM for the inhibition of PKCθ and potently blocked the production of IL-2 in both stimulated murine T cells (IC50 = 34 nM) and human whole blood (IC50 = 500 nM).
Optimization of 7-alkene-3-quinolinecarbonitriles as Src kinase inhibitors
Boschelli, Diane H.,Wang, Daniel,Wang, Yan,Wu, Biqi,Honores, Erick E.,Barrios Sosa, Ana Carolina,Chaudhary, Inder,Golas, Jennifer,Lucas, Judy,Boschelli, Frank
scheme or table, p. 2924 - 2927 (2010/07/04)
The 7-alkene-3-quinolinecarbonitrile 20, a potent inhibitor of Src enzymatic and cellular activity with IC50 values of 2.1 and 58 nM, respectively, had comparable efficacy to bosutinib in a colon tumor xenograft study.
5-ALKYL/ALKENYL-3-CYANOPYRIDINES AS KINASE INHIBITORS
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Page/Page column 170, (2009/07/17)
Described herein are compounds of formula I: wherein G is and pharmaceutically acceptable salts thereof, wherein J, X, R1, R2, R11, R12' and p are as defined herein. Also provided herein are methods of making the compounds of formula I, and methods of using these compounds for inhibiting or treating a pathological condition or disorder linked to or mediated by a protein kinase in a mammal.
