Unsaturated N-acetyl- D-glucosaminuronic acid glycosides as inhibitors of influenza virus sialidase.

Abstract:

:The threat of pandemic influenza is a significant concern of governments worldwide. There is a very limited and relatively expensive armament to tackle such a pandemic should it occur. This fact provides much impetus to the scientific community for the discovery of new and less expensive anti-influenza drugs. Our longstanding interest in the inhibition of influenza virus sialidase, coupled with the development of simple carbohydrates that mimic an unsaturated derivative of the enzyme's naturally-occurring ligand, N-acetylneuraminic acid, has led us to investigate the development of influenza virus sialidase inhibitors based on these mimetics. We have successfully prepared a range of these compounds, in good yield, from the relatively inexpensive carbohydrate N-acetylglucosamine utilising a short synthetic procedure. We have employed a sialidase inhibition assay for biological evaluation of the target compounds and to our delight these mimetics have displayed significant inhibition of influenza virus sialidase.

journal_name

Glycoconj J

journal_title

Glycoconjugate journal

authors

Mann MC,Islam T,Dyason JC,Florio P,Trower CJ,Thomson RJ,von Itzstein M

doi

10.1007/s10719-006-5445-9

subject

Has Abstract

pub_date

2006-02-01 00:00:00

pages

127-33

issue

1-2

eissn

0282-0080

issn

1573-4986

journal_volume

23

pub_type

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