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Aromatic Oligoamide Foldamers with a “Wet Edge” as Inhibitors of the α-Helix-Mediated p53–hDM2 Protein–Protein Interaction

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Abstract

This paper describes the design, synthesis and structural analysis of a 3-O-alkylated aromatic oligoamide that incorporates an additional hydrophilic 6-O-alkyl substituent in the central monomer. This oligomer exhibits low μM inhibitory potency against the p53–hDM2 interaction compared with its unfunctionalised counterpart and significantly improved solubility.

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