84092-47-7

Upstream product

• 84092-46-6 2-hydroxy-4,4',6-tri(methoxymethoxy)-3-(3,3-dimethylallyl)chalcone 
• 870-63-3 prenyl bromide 
• 27364-71-2 2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone 
• 480-66-0 2,4,6-trihydroxyacetophenone 
• 65490-09-7 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone 
• 84092-45-5 2',4'-bis(methoxymethoxy)-5'-(3,3-dimethylallyl)-6'-hydroxyacetophenone 

Downstream Products

• 68682-02-0 5,7-Dihydroxy-2-(4-hydroxy-phenyl)-8-(3-methyl-but-2-enyl)-chroman-4-one 
• 72357-31-4 4',5,7-trihydroxy-8-prenylflavone 

Relevant academic research and scientific papers

Synthesis, biological evaluation of prenylflavonoids as vasorelaxant and neuroprotective agents

A series of prenylflavonoids with multiple hydroxyl groups were synthesized and evaluated for their vasorelaxant activities against rat aorta rings pre-contracted by phenylephrine (PE), as well as their neuroprotective effects against OGD induced PC12 cel

Synthesis of four natural prenylflavonoids and their estrogen-like activities

Four prenylflavonoids, bavachin 1, isobavachin 2, 7,4′-dihydroxy-8- prenylflavone 3, and 8-prenylapigenin 4 were synthesized and recognized for possessing estrogen-like activity in MCF-7/BOS cells, as evaluated by an estrogen-screening assay. All compound

A New Synthesis of 4',5,7-Trihydroxy-8-(3,3-dimethylallyl)flavanone

The title prenylated flavanone (V) isolated from the roots of Marshallia grandiflora has been synthesised by a new route starting from 2-hydroxy-4,6-di-(methoxymethoxy) acetophenone (I).Prenylation of I gives 3-C-prenyl ke