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Solid‐phase synthesis and screening of a library of C‐terminal arginine peptide aldehydes against Murray Valley encephalitis virus protease

Identifieur interne : 001E22 ( Main/Exploration ); précédent : 001E21; suivant : 001E23

Solid‐phase synthesis and screening of a library of C‐terminal arginine peptide aldehydes against Murray Valley encephalitis virus protease

Auteurs : Nicholas J. Ede [Australie] ; Jeffrey Hill [Singapour] ; Joma K. Joy [Singapour] ; Anne-Marie Ede [Australie] ; Merran L. Koppens [Australie]

Source :

RBID : ISTEX:BD9E692FC34F28635BD5C07CCFE3E4E86CDBCCE0

English descriptors

Abstract

Murray Valley encephalitis virus is a member of the flavivirus group, a large family of single‐stranded RNA viruses, which cause serious disease in all regions of the world. Unfortunately, no suitable antivirals are available, and there are commercial vaccines for only three flaviviruses. The solid‐phase synthesis of a library of 400 C‐terminal arginine peptide aldehydes and their screening against Murray Valley encephalitis virus protease are demonstrated. The library was utilised to elucidate several tripeptide sequences that can be used as inhibitors in further SAR studies. Copyright © 2012 European Peptide Society and John Wiley & Sons, Ltd.
The solid‐phase synthesis of a library of 400 C‐terminal arginine peptide aldehydes and their screening against Murray Valley encephalitis virus protease are demonstrated. The library was utilised to elucidate several tripeptide sequences that can be used as inhibitors in further SAR studies.

Url:
DOI: 10.1002/psc.2450


Affiliations:


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Le document en format XML

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