Issue 5, 2012

β-Hairpin stabilization through an interstrand triazole bridge

Abstract

β-Hairpin peptides were conformationally stabilized through a 1,4 disubstituted 1,2,3-triazole interstrand linkage. A NMR conformational analysis revealed that the β-hairpin content depends on the number and position of substituent methylene units of the 1,2,3-triazole ring. These results will allow the design of metabolically stable peptidomimetic analogs of bioactive β-hairpin peptides.

Graphical abstract: β-Hairpin stabilization through an interstrand triazole bridge

Supplementary files

Article information

Article type
Communication
Submitted
27 Sep 2011
Accepted
17 Nov 2011
First published
01 Dec 2011

Chem. Commun., 2012,48, 762-764

β-Hairpin stabilization through an interstrand triazole bridge

V. Celentano, D. Diana, L. De Rosa, A. Romanelli, R. Fattorusso and L. D. D'Andrea, Chem. Commun., 2012, 48, 762 DOI: 10.1039/C1CC16017F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements