124575-21-9

Upstream product

• 124575-20-8 C₄₀H₆₄O₁₀ 
• 100-39-0 benzyl bromide 
• 6763-49-1 (+/-)-1,2:5,6-dicyclohexylidene-myo-inositol 
• 41545-19-1 (+)-1,2:5,6-di-O-cyclohexylidene-myo-inositol 
• 124601-98-5 (-)-6-O-benzyl-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 108-24-7 acetic anhydride 
• 124589-02-2 C₂₀H₃₀O₇ 
• 101636-71-9 1,6-Di-O-acetyl-2,3:4,5-di-O-cyclohexylidene-D/L-myo-inositol 

Downstream Products

• 2068-89-5 D-myo-inositol 1,4,5-triphosphate 
• 108268-52-6 (D)-4-O-benzyl-2,3-O-cyclohexylidene-myo-inositol 1,4,5-(hexabenzyl)trisphosphate 
• 943026-95-7 C₂₁H₂₈O₇ 
• 108233-91-6 (D)-4-O-benzyl-2,3-O-cyclohexylidene-myo-inositol 

Relevant academic research and scientific papers

Modulation of the inositol 1,4,5-trisphosphate receptor by inositol phosphates

The mode of recognition at the binding site of the Ins(1,4,5)P3 receptor was assessed by examining the structure-activity relationships of different Ca2+-mobilizing inositol phosphates.

An efficient chemoenzymic access to optically active myo-inositol polyphosphates

The 1,4,5-tris-, 1,3,4-tris-, and 1,3,4,5-tetrakis-phosphates of 1D-myo-inositol have been prepared in their enantiomerically pure forms from the two enantiomers of 1,2:5,6-di-O-cyclohexylidene-myo-inositol. A facile enzymic preparation is also described

AN EFFICIENT SYNTHESIS OF OPTICALLY ACTIVE D-MYO-INOSITOL 1,4,5-TRIPHOSPHATE

An effective synthesis of D-myo-inositol 1,4,5-triphosphate was developed using a chiral inositide precursor which can be prepared via a facile enzymatic or chemical method.