828268-89-9

Upstream product

• 933-40-4 cycloxexanone dimethyl ketal 
• 69982-70-3 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-5a-carba-β-DL-glucopyranosyl bromide 
• 74766-78-2 3,4-di-O-acetyl-1,5-anhydro-6-bromo-2,6-dideoxy-5a-carba-DL-arabino-hex-1-enitol 
• 432547-07-4 3-O-benzoyl-1,5-anhydro-2,6-dideoxy-4-O-mesyl-5a-carba-L-arabino-hex-1-enitol 
• 115225-42-8 3,4-di-O-acetyl-1,5-anhydro-6-bromo-2,6-dideoxy-5a-carba-L-arabino-hex-1-enitol 
• 432547-06-3 3,4-di-O-acetyl-1,5-anhydro-2,6-dideoxy-5a-carba-L-arabino-hex-1-enitol 
• 432547-08-5 1,5-anhydro-2,6-dideoxy-5a-carba-L-lyxo-hex-1-enitol 
• 828268-88-8 1,5-anhydro-3,4-O-(cyclohexane-1,1-diyl)-2,6-dideoxy-5a-carba-L-lyxo-hex-1-enitol 

Relevant academic research and scientific papers

Synthesis and glycosidase inhibitory activity of some N-substituted 5a-carba-β-fuco- and β-galactopyranosylamines, and selected derivatives

In the course of chemical modification of α-fucosidase inhibitors of 5a-carba-fucopyranosylamine type, an N-dodecyl derivative of the enantiomer 6-deoxy-5a-carba-β-d-galactopyranosylamine demonstrated very strong inhibition of β-galactosidase and β-glucos

Synthesis and glycosidase inhibitory activity of some N-substituted 6-deoxy-5a-carba-β-dl- and L-galactopyranosylamines

Chemical modification of 5a-carba-β-DL-fucopyranosylamine (3) generated six N-substituted derivatives 9a-f, among which N-octyl 9b, decyl 9c, and phenylbutyl ones 9f were found to be very strong β-galactosidase as well as β-glucosidase inhibitors. The inh