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Usage

Uses

Used in Pharmaceutical Industry:
(2R-trans)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-5,7-dihydroxy-2H-1-benzopyran-3-yl palmitate is used as a potential bioactive compound for its possible antioxidant properties. The presence of multiple hydroxyl groups on the benzopyran ring may contribute to its ability to combat oxidative stress and protect cells from damage, making it a candidate for development in pharmaceutical applications.
Used in Cosmetic Industry:
In the cosmetic industry, (2R-trans)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-5,7-dihydroxy-2H-1-benzopyran-3-yl palmitate may be utilized for its potential antioxidant and bioactive properties. Its complex structure could offer benefits in skincare products, such as anti-aging formulations, where antioxidants are crucial for protecting the skin from environmental stressors and promoting overall skin health.

InChI:InChI=1/C31H44O7/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-30(36)37-29-21-24-26(34)19-23(32)20-28(24)38-31(29)22-16-17-25(33)27(35)18-22/h16-20,29,31-35H,2-15,21H2,1H3/t29-,31+/m0/s1

Upstream product

• 87292-49-7 5,7,3',4'-tetra-O-benzylepicatechin 
• 490-46-0 (2R,3R)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-1[2H]-benzopyran-3,5,7-triol 
• 909798-95-4 (2R,3R)-3',4',5,7-tetra-O-benzylflavan-3-yl hexadecanoate 
• 112-67-4 n-hexadecanoyl chloride 
• 154-23-4 catechin 

Relevant academic research and scientific papers

Antimicrobial activity of 3-O-Acyl-(-)-epicatechin and 3-O-Acyl-(+)- catechin derivatives

As an exploratory investigation of antimicrobial promoting compounds, 3-O-acyl-(-)-epicatechins and 3-O-acyl-(+)-catechins possessing various aromatic groups and aliphatic chains of varying length from C4 to C16 for increasing lipophilicity were synthesiz

Inhibitory effects of 3-O-acyl-(+)-catechins on Epstein-Barr virus activation

In the course of an exploratory investigation of antitumor-promoting catechins, 3-O-acyl-(+)-catechins of varying carbon lengths from C4 to C18 were assessed for inhibitory effects on the activation of the Epstein-Barr virus early an

Epicatechin conjugated with fatty acid is a potent inhibitor of DNA polymerase and angiogenesis

Anti-cancer and anti-angiogenesis effects of green tea catechins have been demonstrated. It has been found that chemical modification of tea catechins improves their biological activities. We examined the chemical modification of epicatechin enhanced anti

Cerium(III) chloride-promoted chemoselective esterification of phenolic alcohols

A mild and operationally simple method for the chemoselective esterification of phenolic alcohols is described. The reaction overcomes the tyranny of protection, and capitalizes on the activation of acyl halides with cerium(III) chloride to selectively esterify alcohol hydroxyls in the presence of phenolic ones. The generality of the reaction was demonstrated with a series of phenolic alcohols of dietary relevance (vanillol, hydroxytyrosol, epicatechin), providing an expeditious entry into a series of compounds of relevance for biomedical research, some of which previously available only by enzymatic methods.

ANTIMICROBIAL COMPOSITIONS AND METHODS OF USE

A catechin is modified in at least one position (most preferably in the 3-position of the C-ring) to increase its lipophilicity. Contemplated catechins are demonstrated to have significantly improved antibacterial properties, likely due to catastrophic membrane damage.

Anticancer activity of 3-O-acyl and alkyl-(-)-epicatechin derivatives

We report the synthesis and anticancer effects of 3-O-acyl and alkyl-(-)-epicatechin derivatives.