131146-97-9

Upstream product

• 131146-94-6 (+/-)-1,6-di-O-allyl-3-O-benzyl-myo-inositol 
• 131146-96-8 (±)-2,3-O-isopropylidene-1,5,6-tri-O-allyl-4-O-benzyl-myo-inositol 
• 6404-82-6 (+/-)-1,2-O-isopropylidene-myo-inositol 
• 87-89-8 D-myo-inositol 
• 111392-28-0 (±)-1-O-allyl-2,3:5,6-di-O-isopropylidene-myo-inositol 
• 129094-34-4 Benzoic acid (3aR,4S,4aR,7aS,8S,8aR)-8-hydroxy-2,2,6,6-tetramethyl-hexahydro-benzo[1,2-d;4,5-d']bis[1,3]dioxol-4-yl ester 
• 131146-87-7 (±)-1-O-allyl-4-O-benzyl-2,3:5,6-di-O-isopropylidene-myo-inositol 
• 131146-88-8 (±)-1-O-allyl-4-O-benzyl-2,3-O-isopropylidene-myo-inositol 
• 58706-24-4 (+/-)-6-O-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 51548-88-0 (+/-)-1,2:4,5-di-O-isopropylidene-myo-inositol 
• 131146-95-7 (+/-)-1,6-di-O-allyl-3-O-benzyl-4,5-O-isopropylidene-myo-inositol 
• 115072-69-0 (+/-)-1,6-di-O-allyl-2,3:4,5-di-O-isopropylidene-myo-inositol 
• 115072-70-3 (+/-)-1,6-di-O-allyl-myo-inositol 
• 131146-96-8 (+/-)-1,2,6-tri-O-allyl-3-O-benzyl-4,5-O-isopropylidene-myo-inositol 

Downstream Products

• 131146-98-0 (+/-)-5,6-di-O-acetyl-2,3,4-tri-O-allyl-1-O-benzyl-myo-inositol 
• 131147-17-6 C₅₄H₆₀O₁₂ 
• 131147-17-6 C₅₄H₆₀O₁₂ 
• 131146-82-2 C₅₄H₆₀O₁₂ 
• 131146-82-2 C₅₄H₆₀O₁₂ 
• 131146-93-5 (+/-)-1,5,6-tri-O-benzyl-myo-inositol 
• 131233-74-4 2-O,3-O,4-O,5-O-tetrabenzyl-L-myo-inositol 
• 6195-66-0 (+/-)-1,2,5,6-tetra-O-benzyl-myo-inositol 
• 131147-14-3 (+/-)-1,3,4,5-tetra-O-benzyl-myo-inositol 
• 135182-40-0 (1R,2R,3S,4R,5R,6R)-3,4,5-Tris-allyloxy-2,6-bis-benzyloxy-cyclohexanol 
• 135182-41-1 {3-[Benzyloxy-((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxy-3,4,5-trihydroxy-cyclohexyloxy)-phosphoryloxy]-propyl}-carbamic acid benzyl ester 
• 131146-99-1 (+/-)-2,3,4-tri-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 

Relevant academic research and scientific papers

Synthesis and in vitro anticancer activity evaluation of novel bioreversible phosphate inositol derivatives

The chemistry and biology of phosphorylated inositols have become intense areas of research during the last two decades due to their involvement in various cellular signaling processes. However, the metabolic instability by phosphatases or kinases and poo

Affinity probes for ins(1,3,4,5)P4 receptors

A P-1-tethered derivative of Ins(1,3,4,5)P4 was synthesized and used to prepare a bioselective affinity matrix and a photoaffinity label for purification and covalent modification of IP4 receptor proteins.

The synthesis and resolution of (+/-)-1,5,6-tri-O-benzyl-myo-inositol

Racemic 1,5,6-O-benzyl-myo-inositol was prepared by five routes and converted into 1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol, the camphanates of which were readily separated by chromatography.The absolute configurations of the chiral derivative