1438867-75-4

Upstream product

• 100-39-0 benzyl bromide 
• 24677-78-9 2,3-dihydroxybenzaldehyde 
• 86734-59-0 3-benzyloxy-2-hydroxybenzaldehyde 

Downstream Products

• 1438868-63-3 11-(benzyloxy)-9-(ethylsulfonyl)-3-(1-hydroxy-3,3-dimethylbutyl)-4-methoxydibenzo[b,g][1,5]dioxocin-5(7H)-one 
• 1438868-61-1 11-(benzyloxy)-3-(1-hydroxy-3,3-dimethylbutyl)-4-methoxy-9-(methylsulfonyl)dibenzo[b,g][1,5]dioxocin-5(7H)-one 
• 1438868-59-7 11-(benzyloxy)-9-(ethylthio)-3-(1-hydroxy-3,3-dimethylbutyl)-4-methoxydibenzo-[b,g][1,5]-dioxocin-5(7H)-one 
• 1438868-57-5 11-(benzyloxy)-3-(1-hydroxy-3,3-dimethylbutyl)-4-methoxy-9-(methylthio)dibenzo[b,g][1,5]dioxocin-5(7H)-one 
• 1438868-52-0 11-(benzyloxy)-9-(ethylthio)-4-methoxy-5-oxo-5,7-dihydrodibenzo[b,g][1,5]dioxocine-3-carbaldehyde 
• 1438868-50-8 11-(benzyloxy)-4-methoxy-9-(methylthio)-5-oxo-5,7-dihydrodibenzo[b,g][1,5]dioxocine-3-carbaldehyde 
• 1438868-44-0 C₂₅H₂₄O₇S 
• 1438868-41-7 C₂₄H₂₂O₇S 
• 1438868-31-5 methyl 6-(2-(benzyloxy)-4-(ethylthio)-6-(hydroxymethyl)phenoxy)-3-formyl-2-methoxybenzoate 
• 1438868-29-1 methyl 6-(2-(benzyloxy)-6-(hydroxymethyl)-4-(methylthio)phenoxy)-3-formyl-2-methoxybenzoate 
• 1438868-23-5 methyl 6-(2-(benzyloxy)-4-(ethylthio)-6-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)phenoxy)-3-formyl-2-methoxybenzoate 
• 1438868-20-2 methyl 6-(2-(benzyloxy)-4-(methylthio)-6-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)phenoxy)-3-formyl-2-methoxybenzoate 
• 1438868-11-1 2-(benzyloxy)-4-(ethylthio)-6-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)phenol 
• 1438868-08-6 2-(benzyloxy)-4-(methylthio)-6-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)phenol 

Relevant academic research and scientific papers

Synthesis and evaluation of the analogues of penicillide against cholesterol ester transfer protein

A series of penicillide analogues, with modifications at C-3 and C-9 positions, are synthesized as potential cholesteryl ester transfer protein (CETP) inhibitors. The preliminary in vitro inhibition assay provided some valuable structure-activity relationship information about penicillide. Copyright