Issue 33, 2015

Disulfide-bridged peptide macrobicycles from nature

Abstract

Disulfide-bridged peptide bicycles (DBPBs) are molecules that contain a transannular disulfide bridge within a macrocyclic framework. While DBPBs are precedented in nature, the development of synthetic analogues and their use as therapeutic agents has yet to realize their full potential. A series of naturally-occurring DBPBs and their respective structural and biological features is presented, followed by a description of synthetic methods used to prepare and understand these unique bicyclic systems. The synergy of high-throughput biology and synthetic chemistry should facilitate the development of novel DBPBs in the near future.

Graphical abstract: Disulfide-bridged peptide macrobicycles from nature

Article information

Article type
Review Article
Submitted
04 Jun 2015
Accepted
23 Jun 2015
First published
23 Jun 2015

Org. Biomol. Chem., 2015,13, 8768-8779

Author version available

Disulfide-bridged peptide macrobicycles from nature

B. K. W. Chung and A. K. Yudin, Org. Biomol. Chem., 2015, 13, 8768 DOI: 10.1039/C5OB01115A

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