Author: Butters Terry Alonzi Dominic Kukushkin Nikolay Ren Yuan Blériot Yves
Publisher: Springer Publishing Company
ISSN: 0282-0080
Source: Glycoconjugate Journal, Vol.26, Iss.9, 2009-12, pp. : 1109-1116
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Abstract
Multiple isoforms of mammalian α-mannosidases are active in the pathways of N-linked glycoprotein synthesis and catabolism. They differ in specificity, function and location within the cell and can be selectively inhibited by imino sugar monosaccharide mimics. Previously, a series of structurally related novel 7-membered iminocyclitols were synthesised and found to be inhibitors of α-mannosidase using
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