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 : 001E23Solid‐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 :
- Journal of Peptide Science [ 1075-2617 ] ; 2012-11.
English descriptors
- Teeft :
- Aldehyde, Arginine, Arginine peptide aldehydes, Chem, Cleavage, Copyright, Cysteine proteases, Encephalitis, European peptide society, Fmoc, Inhibition constants, Inhibitor, John wiley sons, Library synthesis, Linker, Mass spectrometry mimotopes sample, Microtitre plate format, Mimotopes, Mmol, Molecular weight, Mvev, Mvev protease, Oxazolidine, Pept, Peptide, Peptide aldehyde library, Peptide aldehydes, Peptide inhibitor, Peptide synthesis, Protease, Protease assay, Reaction mixture, Solid phase, Solid phase synthesis, Spectrometry.
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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<front><div type="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.</div>
<div type="abstract">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.</div>
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