716361-85-2

Upstream product

• 99-10-5 3,5-Dihydroxybenzoic acid 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 24131-32-6 3,5-bis(benzyloxy)benzyl bromide 
• 100-39-0 benzyl bromide 
• 616-76-2 2-hydroxy-5-formylbenzoic acid 
• 50513-72-9 (3,5-di-benzyloxy)benzoic acid benzyl ester 

Downstream Products

• 716361-86-3 (E)-1-[3'-(4''-t-butylbenzoyl)benzamido-4'-benzyloxy]phenyl-2-(3''',5'''-dibenzyloxy)phenylethene 
• 716361-87-4 (E)-1-[3'-(4''-carboxybenzamido)-4'-benzyloxy]phenyl-2-(3''',5'''-dibenzyloxy)phenylethene 

Relevant academic research and scientific papers

Synthesis of a piceatannol analog: Replacement of hydroxy group with amide functionality

Polyhydroxylated stilbene analogs of piceatannol are shown to possess protein-tyrosine kinase (PTK) inbibitory activity. We have developed a novel approach to introduce an amide moiety into the structure of piceatannol. The amido substituted stilbene deri