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2021 Dec 1 [cited 2024 Nov 23];12(1):412

Overall, structural modifications, including the stapling motif ( i,i + 7), specific positioning of the staple, N- and C-terminal residues, conservation of leucine side chains, and preservation of charged/polar residues D146, E151, and N153 directed the improved potency and specificity of 1907 as a FAK scaffold inhibitor

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