418766-76-4

Upstream product

• 418766-78-6 [(2S)-2,3-epoxypropyl] 2-O-benzyl-3,4-O-[(2S,3S)-(2,3-dimethoxybutane-2,3-diyl)]-α-D-xylopyranoside 
• 866935-49-1 (2(S)-hydroxy-3-azidopropyl) 2-O-benzyl-3,4-O-[(2S,3S)-(2,3-dimethoxybutane-2,3-diyl)]-α-D-xylopyranoside 
• 100-39-0 benzyl bromide 
• 418766-77-5 [(2S)-2,3-epoxypropyl] 3,4-O-[(2S,3S)-(2,3-dimethoxybutane-2,3-diyl)]-α-D-xylopyranoside 
• 172795-17-4 allyl 2-O-benzyl-α-D-xylopyranoside 
• 201043-07-4 allyl 3,4-O-[(2S,3S)-(2,3-dimethoxybutane-2,3-diyl)]-α-D-xylopyranoside 

Downstream Products

• 866935-50-4 (2(S)-hydroxy-3-aminopropyl) 2-O-benzyl-α-D-xylopyranoside 

Relevant academic research and scientific papers

New sugar-based permeant analogs of D-Myo-inositol 1,4,5-trisphosphate mimicking the effect of vasopressin: Synthesis and biologic evaluation

On the basis of the xylose-inositol analogy, a series of permeant analogs of D-myo-inositol 1,4,5-trisphosphate (InsP3) have been synthesized by various esterifications of the phosphate groups. Their ability to cross the cell membrane has been

D-myo-Inositol-1,4,5-trisphosphate and adenophostin mimics: Importance of the spatial orientation of a phosphate group on the biological activity

Three different routes for the synthesis of heterocyclic analogues of the second messenger D-myo-inositol-1,4,5-trisphosphate (InsP3) and the natural adenophostins, starting from allyl D-xyloside are described. The two diastereoisomers at C-2 o