党参
植物化学
糖苷
立体化学
细胞毒性
化学
二维核磁共振波谱
传统医学
生物
生物化学
中医药
医学
体外
病理
替代医学
作者
Nguyễn Hữu Toàn Phần,Nguyễn Thị Thuần,Nguyễn Thị Hiển,Phạm Văn Huyến,Nguyen Huu Huong Duyen,Trần Thị Hồng Hạnh,Nguyen Xuan Cuong,Trần Hồng Quang,Châu Văn Minh
标识
DOI:10.1016/j.phytol.2020.10.002
摘要
Phytochemical study of the Codonopsis javanica roots led to isolation of 12 secondary metabolites, including three new sesquiterpenoid glycosides, named codojavanosides A-C (1-3) and nine known compounds, (3R,6E,10S)-2,6,10-trimethyl-3-hydroxydodeca-6,11-diene-2,10-diol (4), (E)-2-hexenyl O-β-d-glucopyranoside (5), oct-1-en-3-ol O-α-l-arabinopyranosyl-(1′′→6′)-O-β-d-glucopyranoside (6), (Z)-3-hexenyl O-α-l-arabinopyranosyl-(1→6)-β-d-glucopyranoside (7), tangshenosides I (8) and II (9), tangshenosides V (10) and VI (11), and corchoionoside C (12). Their structures were identified by comprehensive analyses of the 1D and 2D NMR and mass spectra. Evaluation of their cytotoxic effects toward three human cancer cell lines, including lung (A549), liver (HepG2), and breast (MCF7) revealed that compounds 1, 2, 4 and 11 exhibit weak cytotoxicity toward the A549 cell line, with the induction of cell death ranging from 40.8–66.4 % at the concentration of 100 μM.
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