Issue 90, 2014

Synthetic turn mimetics and hairpin nucleators: Quo Vadimus?

Abstract

Structural mimicry of peptides has witnessed perceptible progress in the last three decades. Reverse turn and β-hairpin units are the smallest secondary structural motifs that are some of the most scrutinized functional cores of peptides and proteins. The practice of mimicking, without altering the function of the bioactive core, ranges from conformational locking of the basic skeleton to total replacement of structural architecture using synthetic analogues. Development of heterogeneous backbones – using unnatural residues in place of natural ones – has broadened further opportunities for efficient structural rigidification. This feature article endeavours to trail the path of progress achieved hitherto and envisage the possibilities that lie ahead in the development of synthetic turn mimetics and hairpin nucleators.

Graphical abstract: Synthetic turn mimetics and hairpin nucleators: Quo Vadimus?

Article information

Article type
Feature Article
Submitted
27 Apr 2014
Accepted
11 Jul 2014
First published
15 Jul 2014

Chem. Commun., 2014,50, 13874-13884

Author version available

Synthetic turn mimetics and hairpin nucleators: Quo Vadimus?

R. V. Nair, S. B. Baravkar, T. S. Ingole and G. J. Sanjayan, Chem. Commun., 2014, 50, 13874 DOI: 10.1039/C4CC03114H

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