Cytotoxicity of New Ferulic-Acid Derivatives on Human Colon Carcinoma (HCT116) Cells

被引:2
作者
Bakholdina, L. A. [1 ,2 ]
Markova, A. A. [3 ]
Khlebnikov, A., I [4 ]
Sevodin, V. P. [1 ]
机构
[1] II Polzunov Altai State Tech Univ, Biisk Technol Inst Filial, 27 Trofimov St, Biisk 659305, Altai Krai, Russia
[2] Russian Acad Sci, Inst Problems Chem & Energet Technol, Siberian Branch, Biisk 659322, Altai Krai, Russia
[3] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, Moscow 119991, Russia
[4] Natl Res Tomsk Polytech Univ, Tomsk 634050, Russia
关键词
feruloyl oligosaccharides; synthesis; ferulic-acid esters; cytotoxicity; HCT116 human colon carcinoma; ESTER; RICE;
D O I
10.1007/s11094-019-02030-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of esters of ferulic acid and alcohols were synthesized and characterized structurally. All tested synthetic compounds were more cytotoxic against HCT116 cell line (human colon carcinoma) than ferulic acid. Benzyl and phenylethyl esters of ferulic acid were the most active compounds (IC50 = 0.0077 and 0.0065 g/L, respectively). Feruloylated wheat-bran oligosaccharides were less active than free ferulic acid against HCT116 tumor cells.
引用
收藏
页码:516 / 520
页数:5
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