912353-07-2

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 82314-88-3 7-hydroxy-8-formyl-2-methylchromone 
• 912353-05-0 7-(4-methoxybenzyloxy)-2-methyl-8-formylchromone 
• 912353-08-3 7-(4-methoxybenzyloxy)-2-methyl-8-((phenethylamino)methyl)-4H-chromen-4-one 
• 912353-06-1 8-((4-methoxybenzylamino)methyl)-7-(4-methoxybenzyloxy)-2-methyl-4H-chromen-4-one 
• 103-63-9 1-phenyl-2-bromoethane 

Relevant academic research and scientific papers

Synthesis and?anticancer activity of?lavendustin A derivatives containing arylethenylchromone substituents

2-Styrylchromones, which are relatively scarce in nature, have been reported to possess potent cytotoxicities on KB cell line. Lavendustin A, a metabolite of Streptomyces griseolavendus, has been shown to inhibit a growth of A431 cell line. Accordingly, a