167394-67-4

Upstream product

• 161443-22-7 methyl 4,6-O-(4-methoxybenzylidene)-α-D-glucopyranoside 
• 161443-23-8 methyl 2,3-di-O-benzyl-4,6-O-(4-methoxybenzylidene)-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 90633-95-7 methyl 2,3-bis-O-benzyl-4-O-[(4-methoxyphenyl)methyl]-α-D-glucopyranoside 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 18929-63-0 methyl 4,6-O-para-methoxybenzylidene-α-D-glucopyranoside 
• 108-24-7 acetic anhydride 
• 130523-98-7 (2S,3S,4S,5R,6S)-4,5-Bis-benzyloxy-6-methoxy-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-carbaldehyde 

Downstream Products

• 161364-91-6 (1S,2R,3S,4S,5R,6R)-4,5-Bis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexane-1,2,3-triol 
• 209050-73-7 (1R,2S,3R,4R,5S,6S)-3,4-Bis-benzyloxy-2,6-bis-benzyloxymethoxy-5-(4-methoxy-benzyloxy)-cyclohexanol 
• 167394-68-5 1-O-acetyl-3,4-bis-O-benzyl-5-O-[(4-methoxyphenyl)methyl]-D-myo-inositol 
• 161364-90-5 (2R,3R,4S,5R,6S)-2-acetoxy-3-hydroxy-4,5-bis-O-benzyl-6-O-[(4-methoxyphenyl)methyl]-cyclohexanone 

Relevant academic research and scientific papers

Synthesis of L-α-phosphatidyl-D-myo-inositoi 5-phosphate and L-α- phosphatidyl-D-myo-inositol 3,5-bisphosphate

Two new 5-phosphorylated phosphatidylinositols have been synthesized from methyl α-D-glucopyranoside as the chiral precursor. These new PtdInsP(n)s have been recently detected in mammalian cells.

Synthesis of P-5 tethered inositol-1,2,6-trisphosphate, an affinity reagent for α-trinositol receptors

The synthesis of D-myo-P-5-(O-aminopropyl)-Ins(1,2,5,6)P4, a phosphodiester analog of Ins(1,2,6)P3 tethered at the C-5 position, has been achieved and a photoaffinity label has been prepared.