Dao Trong-Tuan, Tung Bui-Thanh, Nguyen Phi-Hung, Thuong Phuong-Thien, Yoo Sung-Sik, Kim Eun-Hee, Kim Sang-Kyum, Oh Won-Keun
BK21 Project Team, College of Pharmacy, Chosun University, 375 Seosuk-dong, Dong-gu, Gwangju 501-759, Republic of Korea.
J Nat Prod. 2010 Oct 22;73(10):1636-42. doi: 10.1021/np1002753. Epub 2010 Oct 1.
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 μM, 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.
作为一项正在进行的从植物中发现抗流感药物研究的一部分,使用甲型H1N1流感病毒神经氨酸酶抑制试验,从水翁花的甲醇提取物中分离出4种新的(1-4)和10种已知的(5-14)C-甲基化黄酮类化合物。具有查耳酮骨架的化合物4、7、8和14对两种流感病毒株H1N1和H9N2的病毒神经氨酸酶表现出显著抑制作用。化合物4对在293T细胞中表达的新型甲型H1N1流感病毒(野生型)和耐奥司他韦新型甲型H1N1流感病毒(H274Y突变体)的神经氨酸酶表现出最强的抑制活性,IC50值分别为8.15±1.05和3.31±1.34μM。在动力学研究中,化合物4、7、8和14表现为非竞争性抑制剂。这些结果表明,水翁花中的C-甲基化黄酮类化合物有潜力被开发为新型甲型H1N1流感病毒的神经氨酸酶抑制剂。