山奈酚
立体化学
亚麻黄酮
化学
苯乙酮
二维核磁共振波谱
糖苷键
细胞病变效应
酶
生物
生物化学
类黄酮
抗氧化剂
体外
催化作用
作者
Ngoc Hoi Nguyen,Thi Kim Quy Ha,Sangho Choi,Sangmi Eum,Chul‐Ho Lee,Vũ Tiến Chính,Won Keun Oh
出处
期刊:Phytochemistry
[Elsevier BV]
日期:2016-10-01
卷期号:130: 291-300
被引量:26
标识
DOI:10.1016/j.phytochem.2016.06.011
摘要
Five acetophenones bearing spiroketal-hexofuranoside rings, one di-C-glycosidic acetophenone and two benzopyrans, along with 16 known compounds were isolated from the leaves of Melicope pteleifolia. Structures of all the isolates were elucidated using extensive spectroscopic methods, including 1D, 2D-NMR and HRESIMS. All the isolates were also evaluated for their neuraminidase inhibitory activities against H1N1, H9N2, wild-type H1N1 and oseltamivir-resistant H1N1 (H274Y mutation) virus strains. Of the isolates, tamarixetin 3-robinobioside was found to exhibit the strongest enzymatic inhibition (IC50 24.93 ± 3.46, 23.19 ± 5.41, 26.67 ± 5.16 and 40.16 ± 4.50 μM, respectively). Selected candidates, kaempferol 3-robinobioside, kaempferol 3-O-β-d-glucopyranosyl (1 → 2)-α-d-xylopyranoside and tamarixetin 3-robinobioside, also showed moderate reductions in H1N1-induced cytopathic effects on MDCK cells.
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