Leveraging the Pre-DFG Residue Thr-406 To Obtain High Kinase Selectivity in an Aminopyrazole-Type PAK1 Inhibitor Series.
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F. Diederich | G. Manning | I. Aliagas | K. Hoeflich | Weiru Wang | J. Rudolph | C. Heise | Q. Chao | Yanzhou Liu | J. Crawford | H. La | P. Dong | Wendy Lee | Lesley J. Murray | S. Mathieu | L. Rougé