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Structure-based design of covalent Siah inhibitors.
Stebbins JL, Santelli E, Feng Y, De SK, Purves A, Motamedchaboki K, Wu B, Ronai ZA, Liddington RC, Pellecchia M. Stebbins JL, et al. Chem Biol. 2013 Aug 22;20(8):973-82. doi: 10.1016/j.chembiol.2013.06.008. Epub 2013 Jul 25. Chem Biol. 2013. PMID: 23891150 Free PMC article.
Design, synthesis, and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-Jun N-terminal kinase.
De SK, Stebbins JL, Chen LH, Riel-Mehan M, Machleidt T, Dahl R, Yuan H, Emdadi A, Barile E, Chen V, Murphy R, Pellecchia M. De SK, et al. Among authors: stebbins jl. J Med Chem. 2009 Apr 9;52(7):1943-52. doi: 10.1021/jm801503n. J Med Chem. 2009. PMID: 19271755 Free PMC article.
Structure-based discovery of a new class of Bcl-xL antagonists.
Rega MF, Leone M, Jung D, Cotton NJ, Stebbins JL, Pellecchia M. Rega MF, et al. Among authors: stebbins jl. Bioorg Chem. 2007 Aug;35(4):344-53. doi: 10.1016/j.bioorg.2007.03.001. Epub 2007 May 21. Bioorg Chem. 2007. PMID: 17512966 Free PMC article.
37 results