Antioxidant and antiviral activities of silybin fatty acid conjugates

被引:54
作者
Gazak, Radek [1 ]
Purchartova, Katerina [1 ]
Marhol, Petr [1 ]
Zivna, Lucie [1 ]
Sedmera, Petr [1 ]
Valentova, Katerina [2 ]
Kato, Nobuo [3 ]
Matsumura, Hiroyo [3 ]
Kaihatsu, Kunihiro [3 ]
Kren, Vladimir [1 ]
机构
[1] Acad Sci Czech Republ, Inst Microbiol, CZ-14220 Prague, Czech Republic
[2] Palacky Univ, Dept Med Chem & Biochem, Fac Med & Dent, CZ-77515 Olomouc, Czech Republic
[3] Osaka Univ, Inst Sci & Ind Res, Dept Organ Fine Chem, Osaka 5670047, Japan
关键词
Silybin; Silibinin; Influenza virus; Lipophilic derivatives; Lipid peroxidation; Antiviral; LIPID-PEROXIDATION; PHOSPHATIDYLCHOLINE COMPLEX; PHOSPHOLIPID COMPLEX; VITAMIN-E; SILYMARIN; DERIVATIVES; INHIBITION; MECHANISM; SILIPIDE; MARIANUM;
D O I
10.1016/j.ejmech.2009.11.056
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two selective acylation methods for silybin esterification with long-chain fatty acids were developed, yielding a series of silybin 7-O- and 23-O-acyl-derivatives of varying acyl chain lengths. These compounds were tested for their antioxidant (inhibition of lipid peroxidation and DPPH-scavenging) and anti-influenza virus activities. The acyl chain length is an important prerequisite for both biological activities, as they improved with increasing length of the acyl moiety. (C) 2009 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1059 / 1067
页数:9
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