97227-86-6

Upstream product

• 100-39-0 benzyl bromide 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 50637-28-0 (3-(benzyloxy)-5-methoxyphenyl)methanol 
• 50637-26-8 methyl 3-(benzyloxy)-5-methoxybenzoate 

Downstream Products

• 247086-79-9 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzoic acid 
• 247086-81-3 (4-benzyloxy-2-hydroxymethyl-6-methoxy-phenyl)-(2,6-bis-benzyloxy-4-methyl-phenyl)-methanone 
• 178749-82-1 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzoic acid methyl ester 
• 178749-81-0 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzaldehyde 
• 519-57-3 sulochrin 
• 178749-80-9 2,6-bis-benzyloxy-4-methyl-benzoic acid 5-benzyloxy-2-bromo-3-methoxy-benzyl ester 

Relevant academic research and scientific papers

Effects of ortho-substituent groups of sulochrin on inhibitory activity to eosinophil degranulation

Sulochrin, a metabolite of fungi, has been shown to have an inhibitory activity to eosinophil degranulation. A series of sulochrin derivatives substituted at ortho-positions to the 10-carbonyl group was examined the activity. The importance of alkylester