63427-87-2

Upstream product

• 530-59-6 sinapinic acid 
• 530-59-6 trans-3,5-dimethoxy-4-hydroxycinnamic acid 

Downstream Products

• 69854-18-8 2,6-Bis(3,4,5-trimethoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane-4,8-dione 
• 26350-60-7 trans-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid 

Relevant academic research and scientific papers

Hydroxycinnamic acids as DNA-cleaving agents in the presence of Cu II ions: Mechanism, structure-activity relationship, and biological implications

The effectiveness of hydroxycinnamic acids (HCAs), that is, caffeic acid (CaA), chlorogenic acid (ChA), sinapic acid (SA), ferulic acid (FA), 3hydroxycinnamic acid (3-HCA), and 4hydroxycinnamic acid (4-HCA), as pBR322 plasmid DNA-cleaving agents in the pr

Determination of free diferulic, disinapic and dicoumaric acids in plants and foods

Hydroxycinnamates are common phenolic compounds of plants and plant foods, often found in substantial quantities. Due to their high in vitro antioxidant activity they can easily be oxidized under oxidative conditions. In this study, we found that in vitro

Biotransformation of sinapic acid catalyzed by Momordica charantia Peroxidase

Biotransformation of sinapic acid (1) with H2O 2/Momordica charantia peroxidase, which exists in the widely used food M. charantia, at pH 5.0, 43 °C, in the presence of acetone resulted in six compounds, including four new compounds. Compound 2 was the first isolation of a new unique sinapic acid tetrameric derivate, which is formed by peroxidase catalysis in vitro. Besides 2, three other new sinapic acid dimers, 3-5 have also been isolated. Their structures were established on the basis of spectroscopic data. Compound 5 showed a stronger antioxidative activity than the parent sinapic acid (1). Compounds 4 and 5 significantly inhibited the growth of HL-60 cell at the concentration of 10-5 mol/L.

Stereochemistry of phellinsin A: A concise synthesis of α-arylidene-γ-lactones

Phellinsin A (1a) was prepared in a concise way, thereby elucidating the relative stereochemistry of the aryl and carboxylic acid groups in 1a. The synthesis employed selective monohydrolysis of the dilactones derived from oxidative dimerization of cinnamic acid derivatives. This approach provided a practical synthetic route to α-arylidene-γ-lactones. Copyright Taylor & Francis, Inc.