146294-07-7

Upstream product

• 146288-31-5 (+/-)-(1,3/2,4)-1,4-Di-O-(2-acetoxyethyl)-2,3-di-O-acetyl-5-cyclohexene-1,2,3,4-tetrol 
• 146294-06-6 (+/-)-(1,3/2,4)-1,4-Di-O-(2-hydroxyethyl)-5-cyclohexene-1,2,3,4-tetrol 
• 39078-08-5 rac-(3R,4R,5R,6R)-3,4:5,6-diepoxycyclohex-1-ene 
• 108-24-7 acetic anhydride 

Downstream Products

• 146288-32-6 (+/-)-(1,3/2,4)-2,3-Di-O-acetyl-1,4-di-O-(2-hydroxyethyl)-5-cyclohexene-1,2,3,4-tetrol 

Relevant academic research and scientific papers

A spacer-modified disaccharide as a photoaffinity reagent for the acceptor-binding area of bovine (1->4)-β-D-galactosyltransferase: comparison of its acceptor properties with those of other 2-acetamido-2-deoxy-β-D-glucopyranosides

The spacer-modified disaccharide 1,10-di-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2-azi-1,10-decanediol (10) that mimics the biantennary core heptasaccharide of N-glycoproteins has been synthesised.Compound 10 is an excellent acceptor in galactosyltransferase-catalysed galactosylation by UDP-galactose, is superior (7-8 fold) to analogues that have only one GlcNAc unit, and is an efficient photoaffinity reagent for galactosyltransferase.In the presence of UDP-Gal, no photoaffinity labelling by 10 takes place, which agrees with the mechanism of galactosyltransferase action.