77377-07-2

Usage

InChI:InChI=1/C13H11NO/c15-13-8-5-11(6-9-13)4-7-12-3-1-2-10-14-12/h1-10,15H/b7-4+

Upstream product

• 109-06-8 α-picoline 
• 123-08-0 4-hydroxy-benzaldehyde 
• 19036-99-8 2-(4-Methoxy-styryl)-pyridin 
• 1145-93-3 diethyl 4-methoxybenzylphosphonate 
• 121-98-2 methyl 4-methoxybenzoate 
• 824-94-2 p-methoxybenzyl chloride 
• 105-13-5 4-Methoxybenzyl alcohol 
• 99-96-7 4-hydroxy-benzoic acid 

Downstream Products

• 57439-26-6 1-ethyl-2-(4-hydroxy-styryl)-pyridinium; iodide 
• 38039-57-5 (E)-1-methyl-2-[4-(hydroxybenzyl)-vinyl]-pyridinium iodide 
• 3767-85-9 4-(2-[2]pyridyl-ethyl)-phenol 

Relevant academic research and scientific papers

Synthesis, theoretical, and experimental study of radical scavenging activity of 3-pyridinol containing trans-resveratrol analogs

In the search of more powerful and versatile antioxidant agents for biomedical applications, a structural modification of the resveratrol scaffold was carried out. Six trans-resveratrol (TR) analogs with a trans-stilbazole framework were obtained. Quantum

Synthesis and anti-inflammatory activity of resveratrol analogs

Seventeen novel resveratrol derivatives were synthesized. Their anti-inflammatory activities were tested on xylene-induced mouse ear edema. The pharmacological results showed that some compounds have potent anti-inflammatory activities.