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American Chemical Society, ACS Medicinal Chemistry Letters, 6(6), p. 711-715, 2015

DOI: 10.1021/acsmedchemlett.5b00151

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Leveraging the Pre-DFG Residue Thr-406 To Obtain High Kinase Selectivity in an Aminopyrazole-Type PAK1 Inhibitor Series

This paper is available in a repository.
This paper is available in a repository.

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