83864-99-7Relevant academic research and scientific papers
Synthesis and evaluation of new sesamol-based phenolic acid derivatives with hypolipidemic, antioxidant, and hepatoprotective effects
Xie, Yundong,Liu, Jiping,Shi, Yongheng,Bin Wang,Wang, Xiaoping,Wang, Wei,Sun, Meng,Xu, Xinya,He, Shipeng
, p. 1688 - 1702 (2021/07/26)
The objective of this study is to synthesize a series of sesamol-based phenolic acid derivatives, which were designed by combination principle. The hypolipidemic activity of all these compounds was preliminarily screened by acute hyperlipidemic mice model induced by Triton WR 1339, in which compound T6 exhibited more significant reducing plasma TG and TC than fenofibrate. Compound T6 was also found to obviously decrease TG and TC both in the plasma and hepatic tissue of high-fat-diet-induced hyperlipidemic mice. Moreover, T6 showed hepatoprotective effects, which remarkable amelioration in characteristic liver enzymes was examined and the histopathological observation displayed that compound T6 inhibited lipids accumulation in the hepatic. The levels of PPAR-α receptor related to lipids metabolism in hepatic tissue were upregulated after T6 treatment. Other potent effects of T6 such as antioxidant and anti-inflammatory activity were also observed. On the bases of these findings, compound T6 may serve as an effective hypolipidemic and hepatoprotective agent. [Figure not available: see fulltext.]
1,3-benzodioxole natural salvianolic acid ester compound and blood fat reduction application thereof
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Paragraph 0061; 0065-0066, (2019/10/17)
The invention discloses a 1,3-benzodioxole natural salvianolic acid ester compound and blood fat reduction application thereof. A sesamol structure is adopted as a functional fragment, a natural salvianolic acid type structure is introduced into the sesam
A one pot process for the preparation of caffeic acid ester derivatives
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Page 5, (2008/06/13)
The present invention relates to a one pot process for the preparation of caffeic acid ester derivatives of the formula I: ???whereinAr is aryl, which is unsubstituted or substituted with halogen, hydroxy, C1-6 alkyl or C1-6 alkoxy,A is C1-6 alkylene, C2-6 alkenylene or C2-6 alkynylene,m is a number from 0 to 6; andB is C1-6 alkyl or aryl, which is unsubstituted or substituted with halogen, hydroxy, C1-6 alkyl or C1-6 alkoxy; ???which process comprises reacting, in a suitable solvent for esterification of a carboxylic acid derivative, a compound of the formula II: ???whereinAr and A are as defined above. ???with a halogenating reagent and alcohol of the formula III:H-(CH2)m-B ???whereinm and B are as defined above.
Chemical and toxicological studies on bracken fern, Pteridium aquilinum var. latiusculum. VI. Isolation of 5-O-caffeoylshikimic acid as an antithiamine factor
Fukuoka
, p. 3219 - 3224 (2007/10/02)
5-O-Caffeoylshikimic acid (dactylifric acid) was isolated from bracken fern as a major constituent of its acutely toxic fraction, which causes depression of leucocytes and thrombocytes in calves. 5-O-Caffeoylshikimic acid exhibited an antithiamine effect in vitro, but had no hematuric effect in guinea pigs.
