24672-86-4

Usage

Uses

(±)-Isobavachin is recognized for possessing estrogen-like activity in MCF-7/BOS cells.

Upstream product

• 948307-22-0 7,4'-dimethoxymethoxy-8-(3,3-dimethylallyl)-flavanone 
• 1134396-40-9 8-allyl-7-(methoxymethoxy)-2-(4-(methoxymethoxy)phenyl)chroman-4-one 
• 65490-08-6 2-hydroxy-4-(methoxymethoxy)acetophenone 
• 870-63-3 prenyl bromide 
• 115-18-4 2-methyl-3-buten-2-ol 
• 69097-97-8 7,4'-dihydroxy-dihydroflavone 
• 124775-22-0 1-<2-Hydroxy-4-(methoxymethoxy)phenyl>-3-<4-(methoxymethoxy)phenyl>prop-2-en-1-on 
• 54730-26-6 4-methoxymethoxy-3-(3,3-dimethylallyl)-2-hydroxyacetophenone 
• 19825-40-2 2,4-Dihydroxy-3-C-prenylacetophenone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 

Downstream Products

• 78332-22-6 4'-hydroxy-2,2-dimethylpyrano<5,6:8,7>flavone 
• 78316-30-0 4'-hydroxy-2,2-dimethylpyrano<5,6:8,7>flavanone 

Relevant academic research and scientific papers

8-Prenylflavanones through Microwave Promoted Tandem Claisen Rearrangement/6-endo-trig Cyclization and Cross Metathesis

Prenylated flavanones were obtained from ortho-allyloxy chalcones through a one-pot sequence of Claisen rearrangement and 6-endo-trig cyclization, followed by olefin cross metathesis of the intermediate allyl flavanones with 2-methyl-2-butene. The synthet

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

New Syntheses of 4',7-Dihydroxy-6,8-di-C-prenylflavanone, Bavachin, Isobavachin and Related Compounds

The titel compounds have been synthesised by nuclear prenylation of 4',7-dihydroxyflavanone(liquiritigenin, III), Cyclodehydrogenation of bavachin and isobavachin with DDQ yields the chromenoflavanones (VIII) and (X) respectively which on dehydrogenation