Dimer and Tetramer of Gallic Acid: Facile Synthesis, Antioxidant and Antiproliferative Activities

被引:0
|
作者
Pan, Junzhu [1 ]
Yin, Dongqin [2 ]
Ma, Lifang [3 ]
Zhao, Yi [1 ]
Zhao, Jing [1 ]
Guo, Li [1 ]
机构
[1] Sichuan Univ, West China Sch Pharm, Key Lab Drug Targeting & Drug Delivery Syst, Educ Minist,Dept Med Chem, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Lab Stem Cell Biol, Chengdu 610041, Peoples R China
[3] Sichuan Univ, Sch Chem Engn, Chengdu 610041, Peoples R China
关键词
Gallic acid; Polyphenol; Antioxidant activity; Antiproliferative activity; Vanlency effects; Convergent synthesis; INDUCED OXIDATIVE STRESS; PELTIPHYLLUM-PELTATUM; RESVERATROL ANALOGS; ANTICANCER ACTIVITY; SIGNALING PATHWAYS; CANCER CELLS; APOPTOSIS; GALLATE; DERIVATIVES; DENDRIMERS;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In view of the various and promising biological activities of gallic acid, we designed and prepared a series of poly-phenolic compounds carrying multi-gallic acids residues. These dimer and tetramer of gallic acids were facilely synthesized by convergent approach. Subsequently, antioxidant activity evaluation was carried out using DPPH assay, and the resulting polyphenol exerted enhanced activity to gallic acid monomer. Antiproliferative activity evaluation was performed using MTT assay with three human cancer cell lines (Hela, A549 and MCF-7) and two human normal cell lines (HEK293 and HUVEC). The cytotoxicity of the dimer and tetramer of gallic acid were higher than that of the monomer against both cancer and normal cell lines, however the cytotoxicity of the dimer and tetramer against cancer cells was much fiercer than normal cells, which resulted in better selectivity. Consequently, vanlency effects embodied in both antioxidant and antiproliferative activities of the obtained multi-gallic acid derivatives.
引用
收藏
页码:27 / 32
页数:6
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