108233-91-6

Upstream product

• 123994-35-4 C₃₁H₅₄O₇Si₂ 
• 124575-21-9 (-)-1-O-acetyl-6-O-benzyl-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 100-39-0 benzyl bromide 
• 33021-17-9 (-)-2,3:4,5-di-O-cyclohexylidene-myo-inositol 
• 87-89-8 D-myo-inositol 
• 124589-02-2 C₂₀H₃₀O₇ 
• 101636-71-9 1,6-Di-O-acetyl-2,3:4,5-di-O-cyclohexylidene-D/L-myo-inositol 
• 123994-34-3 C₃₁H₅₂O₆Si₂ 
• 123994-33-2 C₂₆H₄₀O₅Si 
• 123994-32-1 C₂₅H₃₈O₄SeSi 
• 123994-31-0 methyl (3S,4R,5R)-3-O-benzoyl-4,5-O-cyclohexylidene-3,4,5-trihydroxycyclohec-1-ene-1-carboxylate 
• 124575-20-8 C₄₀H₆₄O₁₀ 
• 6763-49-1 (+/-)-1,2:5,6-dicyclohexylidene-myo-inositol 
• 108340-80-3 6-O-benzyl-1-O-camphanoyl-2,3:4,5-di-O-cyclohexylidene-myo-inositol 

Downstream Products

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

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.

SYNTHESIS, POTENTIOMETRIC AND 31P-NMR INVESTIGATIONS OF THE IONIZATION STATE AND COMPLEXATION PROPERTIES OF INOSITOL-PHOSPHATES: BIOLOGICAL CONSEQUENCES

The synthesis and the potentiometric studies of inositol-phosphates allow, particularly for Ins(1,4,5)P3, the correlation between the ionization state of the phosphate functions and the binding properties of the 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.

Enantiospecific Synthesis of D-myo-Inositol 1,4,5-Trisphosphate from (-)-Quinic Acid

A versatile, enentiospecific approach to functionalized cyclitols from (-)-quinic acid is illustrated by a synthesis of D-myo-inositol 1,4,5-trisphosphate, the calcium-mobilizing intracellular second messenger of the phosphatidylinositol cycle.

THE TOTAL SYNTHESIS OF myo-INOSITOL POLYPHOSPHATES

Total synthesis of the individual enentiomers of myo-inositol 4-phosphate (15), myo-inositol 1,4-biphosphate (2) and myo-inositol 1,4,5-triphosphate (1), together with syntheses of racemic myo-inositol 1,3,4-triphosphate (4) and myo-inositol 2,4,5-triphos