56290-55-2

Usage

Type

Synthetic derivative of resveratrol

Resveratrol source

Natural polyphenol found in plants like grapes and peanuts

Potential activities

Antioxidant, anticancer

Therapeutic effects

Inhibits cancer cell proliferation, reduces inflammation, protects against oxidative stress

Research areas

Skincare and cosmetic products, due to antioxidant properties

Current status

Further research needed to understand potential benefits and safety profile

Upstream product

• 674-82-8 4-methyleneoxetan-2-one 
• 106-42-3 para-xylene 
• 2142-73-6 1-(2,5-dimethylphenyl)-1-ethanone 
• 141-78-6 ethyl acetate 

Downstream Products

• 147251-61-4 2-(2,5-dimethylbenzoyl)-3-methylquinoxaline 1,4-dioxide 

Relevant academic research and scientific papers

Substituted phenyl-1,3-diketones as protectants against skin damage

The subject invention relates to pharmaceutical compositions comprising a safe and effective amount of a compound having the structure: STR1 wherein each R is alkyl or hydrogen, at least two being alkyl; R' is hydrogen, alkyl or aryl; R" is alkyl or halo; and each X is independently oxygen or sulfur; and a pharmaceutically-acceptable carrier. The subject invention also relates to methods for preventing damage to skin by topically applying a safe and effective amount of such compounds to the skin.

U.V. Irradiation of 3-Substituted 2-Arylquinoxalines; Photocyclization to Indoloquinoxalines or Related Heterocyclic Systems

Upon irradiation in methanol in the presence of p-toluenesulphonic acid, a series of 2-aroyl-3-methylquinoxalines 8 (aroyl group = o-methyl-, p-methyl-, m-methoxy-, p-methoxy-, p-bromo-, and 2,5-dimethyl-benzoyl) underwent cyclisation to the corresponding