Issue 30, 2010
From the journal:

Chemical Communications

Stereochemistry of 4-hydroxyproline affects the conformation of conopeptides†

Jia Xu,a   Yanli Wang,a   Bingbing Zhang,a   Baohuai Wangb  and  Weihong Du*a  

* Corresponding authors

a Department of Chemistry, Renmin University of China, Beijing, China

b Institute of Physical Chemistry, Peking University, Beijing, China

Abstract

The cis/trans isomerization of 4-hydroxyproline is shown to remarkably affect the conformation of conopeptides with or without disulfide bonds.

Graphical abstract: Stereochemistry of 4-hydroxyproline affects the conformation of conopeptides

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0CC00075B
Article type
Communication
Submitted
02 Mar 2010
Accepted
31 Mar 2010
First published
29 Apr 2010

Chem. Commun., 2010,46, 5467-5469

Permissions

Request permissions

Stereochemistry of 4-hydroxyproline affects the conformation of conopeptides

J. Xu, Y. Wang, B. Zhang, B. Wang and W. Du, Chem. Commun., 2010, 46, 5467 DOI: 10.1039/C0CC00075B

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