The aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyte glutathione reductase†
Abstract
Various aza-analogues of
* Corresponding authors
a Université Joseph Fourier, Département de Chimie Moléculaire, CNRS UMR-5250, ICMG FR-2607, BP-53, Grenoble Cedex 9, France
b
Biochemie-Zentrum der Universität Heidelberg, Im Neuenheimer Feld 504, Heidelberg, Germany
E-mail:
elisabeth.davioud@gmx.de
Fax: +49-6221-54-5586
c Interdisciplinary Research Center, Justus Liebig University, Heinrich-Buff-Ring 26-32, Giessen, Germany
d Centre National de la Recherche Scientifique, Paris, France
Various aza-analogues of
C. Morin, T. Besset, J. Moutet, M. Fayolle, M. Brückner, D. Limosin, K. Becker and E. Davioud-Charvet, Org. Biomol. Chem., 2008, 6, 2731 DOI: 10.1039/B802649C
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.
Fetching data from CrossRef.
This may take some time to load.
Loading related content