HCV-NS3/4A Protease Inhibitory Iridoid Glucosides and Dimeric Foliamenthoic Acid Derivatives from Anarrhinum orientale

被引:14
作者
El Dine, Riham Salah [1 ,2 ]
Monem, Azza R. Abdel [1 ]
El-Halawany, Ali M. [1 ,2 ]
Hattori, Masao [2 ]
Abdel-Sattar, Essam [1 ,3 ]
机构
[1] Cairo Univ, Dept Pharmacognosy, Fac Pharm, Cairo 11562, Egypt
[2] Toyama Univ, Inst Nat Med, Toyama 9300194, Japan
[3] King Abdulaziz Univ, Dept Nat Prod, Fac Pharm, Jeddah 21589, Saudi Arabia
来源
JOURNAL OF NATURAL PRODUCTS | 2011年 / 74卷 / 05期
关键词
VIRUS; GLYCOSIDES; RIBAVIRIN; PEGINTERFERON; CHEMISTRY;
D O I
10.1021/np100554h
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Four new compounds were isolated from the methanol extract of the aerial parts of Anarrhinum orientale: 6'-O-cinnamoylmussaenosidic acid (1), 6'-O-cinnamoyl-8-O-(6 '''-O-cinnamoylglucopyranosyl)mussaenosidic acid (2), (2E,6E)-8-{[(2E,6E)-8-hydroxy-2,6-dimethylocta-2,6-dienoyl]oxy}-2, 6-dimethylocta-2,6-dienoic acid (3), and (2E,6E)-8-{[(2E,6E)-8-acetoxy-2,6-dimethylocta-2,6-dienoyl]oxy}-2,6-dimethylocta-2,6-dienoic acid (4). The known 8-O-cinnamoylmussaenosidic acid (5) was also identified. All five compounds were tested for inhibition of the hepatitis C virus (HCV) protease. Compounds 1 and 5 exhibited moderate activity, while 2 and 3 showed weak effects. No inhibitory activity on the human serine protease was observed for any of these compounds, which may infer the selectivity toward the viral protease. A computational docking study of the isolated compounds against HCV protease was used to formulate a hypothetical mechanism for the inhibitory activity of the active compounds on the enzymes tested.
引用
收藏
页码:943 / 948
页数:6
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