Synthesis of the naringinase inhibitors l-swainsonine and related 6-C-methyl-l-swainsonine analogues: (6R)-C-methyl-l-swainsonine is a more potent inhibitor of l-rhamnosidase by an order of magnitude than l-swainsonine-Reference-Cited by-同舟云学术

Synthesis of the naringinase inhibitors l-swainsonine and related 6-C-methyl-l-swainsonine analogues: (6R)-C-methyl-l-swainsonine is a more potent inhibitor of l-rhamnosidase by an order of magnitude than l-swainsonine

Published:2008-01 Issue:1 Volume:49 Page:179-184
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Håkansson Anders E.,van Ameijde Jeroen,Horne Graeme,Nash Robert J.,Wormald Mark R.,Kato Atsushi,Besra Gurdyal S.,Gurcha Sudagar,Fleet George W.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference61 articles.

1. A Spectroscopic Investigation of Swainsonine: An α-Mannosidase Inhibitor Isolated from Swainsona canescens

2. Cloning and expression of mouse cytosolic α-mannosidase (Man2c1)

3. Swainsonine prevents the processing of the oligosaccharide chains of influenza virus hemagglutinin.

4. Swainsonine: an inhibitor of glycoprotein processing.

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