Consequences of Isostructural Main‐Chain Modifications for the Design of Antimicrobial Foldamers: Helical Mimics of Host‐Defense Peptides Based on a Heterogeneous Amide/Urea Backbone

Paul Claudon, Aude Violette, Karen Lamour, Marion Décossas, Sylvie Fournel, Julien Godet, Yves Mély, Brigitte Jamart‐Grégoire, Marie‐Christine Averlant‐Petit, Jean‐Paul Briand,

Angewandte Chemie International Edition · 2009 · 147 citations · 18 references

Concepts

Abstract

Fraternal twins: Oligoureas and γ-peptides are isosteric, quasi-isostructural helical foldamers endowed with distinct biomolecular recognition properties. Combination of the two backbones to generate urea/amide hybrids (see picture) was found to give more potent yet less cytotoxic antimicrobial helical foldamers.

References

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