921942-45-2

Upstream product

• 125553-69-7 1-(2-hydroxy-4,6-dimethoxyphenyl)-3-(4-nitrophenyl)propane-1,3-dione 
• 1609456-12-3 2-acetyl-3,5-dimethoxyphenyl-4-bromobenzoate 
• 182618-23-1 4-nitro-2'-hydroxy-4',6'-dimethoxychalcone 
• 555-16-8 4-nitrobenzaldehdye 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 
• 836608-01-6 2-(4-nitrophenyl)-5,7-dimethoxy-4H-chromen-4-one 

Downstream Products

• 16290-50-9 3-(4-hydroxyphenyl)-5,7-dimethoxy-4H-chromen-4-one 
• 132018-33-8 2-(4-aminophenyl)-5,7-dihydroxy-4H-chromen-4-one 
• 22812-39-1 2-(4-acetoxy-phenyl)-5,7-dimethoxy-chromen-4-one 
• 437-64-9 genkwanin 

Relevant academic research and scientific papers

Collateral sensitivity of resistant MRP1-overexpressing cells to flavonoids and derivatives through GSH efflux

The multidrug resistance protein 1 (MRP1) is involved in multidrug resistance of cancer cells by mediating drug efflux out of cells, often in co-transport with glutathione (GSH). GSH efflux mediated by MRP1 can be stimulated by verapamil. In cells overexp

Copper-mediated trimethylsilyl azide in amination of bromoflavonoids to synthesize unique aminoflavonoids

Aminoflavonoids are unique antioxidants comparing to other abundant flavonoids in nature. Their syntheses and biological activities were scarcely reported. An effectively copper-mediated amination of the corresponding bromoflavonoids to synthesize a serie

Synthesis and structure elucidation of five series of aminoflavones using 1D and 2D NMR spectroscopy

Twenty-six new aminoflavones have been synthesised by two different methods and the structure elucidation was accomplished using extensive 1D ( 1H, 13C) and 2D NMR spectroscopic studies (COSY, HSQC and HMBC experiments). Copyright