C-Methylated Flavonoids from Cleistocalyx operculatus and Their Inhibitory Effects on Novel Influenza A (H1N1) Neuraminidase

被引:100
作者
Dao, Trong-Tuan [1 ]
Tung, Bui-Thanh [1 ]
Nguyen, Phi-Hung [1 ]
Thuong, Phuong-Thien [1 ]
Yoo, Sung-Sik [2 ]
Kim, Eun-Hee [2 ]
Kim, Sang-Kyum [3 ]
Oh, Won-Keun [1 ]
机构
[1] Chosun Univ, Coll Pharm, Project Team BK21, Kwangju 501759, South Korea
[2] Choong Ang Vaccine Lab, Taejon 305348, South Korea
[3] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
来源
JOURNAL OF NATURAL PRODUCTS | 2010年 / 73卷 / 10期
关键词
ROXB; MERR; VIRUS NEURAMINIDASE; ESSENTIAL OIL; BUDS; PERRY; ACID; EXTRACT;
D O I
10.1021/np1002753
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
As part of an ongoing study focused on the discovery of anti-influenza agents from plants, four new (1-4) and 10 known (5-14) C-methylated flavonoids were isolated from a methanol extract of Cleistocalyx operculatus buds using an influenza H1N1 neuraminidase inhibition assay. Compounds 4, 7, 8, and 14, with a chalcone skeleton, showed significant inhibitory effects on the viral neuraminidases from two influenza viral strains, H1N1 and H9N2. Compound 4 showed the strongest inhibitory activity against the neuraminidases from novel influenza H1N1 (WT) and oseltamivir-resistant novel H1N1 (H274Y mutant) expressed in 293T cells with IC50 values of 8.15 +/- 1.05 and 3.31 +/- 1.34,mu M, respectively. Compounds 4, 7, 8, and 14 behaved as noncompetitive inhibitors in the kinetic studies. These results indicate that C-methylated flavonoids from C. operculatus have the potential to be developed as neuraminidase inhibitors for novel influenza H1N1.
引用
收藏
页码:1636 / 1642
页数:7
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