Neuraminidase inhibitory activity by compounds isolated from aerial parts of Rhinacanthus nasutus

被引:14
|
作者
Kwak, Hee Jae [1 ]
Park, SeonJu [1 ]
Kim, Nanyoung [1 ]
Yoo, Guijae [1 ]
Park, Jun Hyung [1 ]
Oh, Youngse [1 ]
Nguyen Xuan Nhiem [2 ]
Kim, Seung Hyun [1 ]
机构
[1] Yonsei Univ, Yonsei Inst Pharmaceut Sci, Coll Pharm, Incheon, South Korea
[2] Vietnam Acad Sci & Technol, Inst Marine Biochem, Hanoi, Vietnam
基金
新加坡国家研究基金会;
关键词
Rhinacanthus nasutus; lignan; neuraminidase; INFLUENZA-VIRUS; IN-VITRO; CONSTITUENTS; LIGNANS; GLYCOSIDES; ROOTS; BARK;
D O I
10.1080/14786419.2017.1365067
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Rhinacanthus nasutus (L.) Kurz (Acanthaceae) is known as traditional medicine for the treatment of various diseases, such as cancer, fungal infections, herpes virus infections and several types of skin diseases in South-East Asian countries. In this study, eight compounds 1-8 were isolated from the aerial parts of R. nasutus. The structures of compounds were determined by the spectroscopic methods, including 1D and 2D NMR. The isolated compounds were evaluated for neuraminidase inhibitory activity. Several lignans, 2,3-bis[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-1,4-butanediol (5) and 8,8-bisdihydrosiringenin glucoside (6), significantly inhibited neuraminidase activity, which was comparable to the positive controls, mangiferin and oseltamivir. In addition, a structure-based virtual screening against neuraminidase using bioactive components was demonstrated. [GRAPHICS] .
引用
收藏
页码:2111 / 2115
页数:5
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