204450-10-2

Upstream product

• 4282-40-0 1-Iodoheptane 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 204450-05-5 benzyl 3-O-n-heptyl-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 204450-07-7 benzyl 2-O-benzyl-3-O-n-heptyl-4,6-(p-methoxybenzylidene)-α-D-glucopyranoside 
• 204450-08-8 benzyl 2-O-benzyl-3-O-n-heptyl-4-(p-methoxybenzyl)-α-D-glucopyranoside 
• 204450-06-6 benzyl 3-O-n-heptyl-4,6-(p-methoxybenzylidene)-α-D-glucopyranoside 
• 133692-61-2 3-O-n-heptyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 204450-14-6 (2R,3R,4S,5R,6S)-5,6-Bis-benzyloxy-4-heptyloxy-2-isobutyl-tetrahydro-pyran-3-ol 
• 204450-15-7 (2S,3R,4S,5R,6R)-2,3-Bis-benzyloxy-4-heptyloxy-6-isobutyl-5-methoxy-tetrahydro-pyran 
• 204450-11-3 benzyl 2-O-benzyl-3-O-n-heptyl-4-(p-methoxybenzyl)-6-deoxy-6-isopropyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Design, synthesis, and evaluation of the multidrug resistance-reversing activity of D-glucose mimetics of hapalosin

When five substituents of hapalosin were placed on D-glucose, molecular modeling revealed that the substituents on mimetics 2 and 3 occupy similar spatial positions as the corresponding substituents on hapalosin. Mimetic 3 and all the glucopyranoside inte