Issue 15, 1985
From the journal:

Journal of the Chemical Society, Chemical Communications

N-oxide as a potential function in the design of enzyme inhibitors. Application to 2,3-epoxysqualene-sterol cyclases

Maurizio Cerutti,   Laura Delprino,   Luigi Cattel,   Pierrette Bouvier-Navé,   Albert Duriatti,   Francis Schuber  and  Pierre Benveniste  

Abstract

The N-oxides of several tertiary amines possessing an aliphatic long chain are more potent inhibitors of 2,3-epoxysqualene-β-amyrin and -lanosterol cyclases than their parent amines.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39850001054
Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1054-1055

Permissions

Request permissions

N-oxide as a potential function in the design of enzyme inhibitors. Application to 2,3-epoxysqualene-sterol cyclases

M. Cerutti, L. Delprino, L. Cattel, P. Bouvier-Navé, A. Duriatti, F. Schuber and P. Benveniste, J. Chem. Soc., Chem. Commun., 1985, 1054 DOI: 10.1039/C39850001054

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.

Spotlight

Advertisements