49570-46-9

Upstream product

• 117-39-5 quercetol 
• 2051-90-3 Dichlorodiphenylmethane 
• 1258551-29-9 acetic acid 5-acetoxy-7-hydroxy-2-(2-methyl-2-phenylbenzo-[1,3]dioxol-5-yl)-4-oxo-4H-chromen-3-yl ester 
• 1258551-28-8 acetic acid 3,5-diacetoxy-2-(2,2-diphenyl-benzo[1,3]dioxol-5-yl)-4-oxo-4H-chromen-7-yl ester 
• 357194-03-7 2-(2,2-diphenylbenzo[1,3]dioxol-5-yl)-3,5,7-trihydroxychromen-4-one 
• 1258551-30-2 acetic acid 5-acetoxy-7-benzyloxy-2-(2,2-diphenyl-benzo[1,3]dioxol-5-yl)-4-oxo-4H-chromen-3-yl ester 

Downstream Products

• 1310686-94-2 C₂₀H₁₈O₁₀ 

Relevant academic research and scientific papers

Quercetin-POC conjugates: Differential stability and bioactivity profiles between breast cancer (MCF-7) and colorectal carcinoma (HCT116) cell lines

In the course of our ongoing efforts to develop novel quercetin conjugates with enhanced stability profiles, we introduced an isopropyloxycarbonylmethoxy (POC) group to 7-OH and/or 3-OH of quercetin and prepared three novel quercetin conjugates. The querc

Enhanced stability and intracellular accumulation of quercetin by protection of the chemically or metabolically susceptible hydroxyl groups with a pivaloxymethyl (POM) promoiety

In order to increase stability of quercetin, its metabolically and chemically susceptible hydroxyl groups 7-OH and 3-OH respectively were transiently blocked with a pivaloxymethyl (POM) promoiety to provide two novel quercetin conjugates [7-O-POM-Q (2), 3