885671-70-5

Upstream product

• 295320-98-8 3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose 
• 196868-07-2 1,2-O-isopropylidene-5-O-(tert-butyl)dimethylsilyl-α-D-ribofuranoside 
• 518332-44-0 5-O-tert-butyldimethylsilyl-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose 
• 518332-60-0 3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-α-D-glucopyranosyl]-1,2-O-isopropylidene-5-phenyl-α-D-ribofuranose 
• 518332-46-2 5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose 
• 518332-41-7 2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-1-phenylsulfinyl-β-D-glucopyranoside 
• 108-24-7 acetic anhydride 

Downstream Products

• 912567-61-4 2-benzyl-4-hydroxytetrahydrofuran-3-yl 3,4-di-O-acetyl-2,6-di-O-benzyl-α-D-glucopyranoside 
• 912567-63-6 C₅₅H₅₇O₁₇P₃ 
• 912567-62-5 2-benzyl-4-tetrahydrofuran-3-yl 2,6-di-O-benzyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of adenophostin A analogues conjugating an aromatic group at the 5′-position as potent IP3 receptor ligands

Previous structure-activity relationship studies of adenophostin A, a potent IP3 receptor agonist, led us to design the novel adenophostin A analogues 5a-c, conjugating an aromatic group at the 5′-position to develop useful IP3 recep