细胞毒性
IC50型
体外
阳性对照
立体化学
化学
癌细胞系
细胞培养
拉伤
传统医学
生物
癌细胞
生物化学
癌症
医学
遗传学
解剖
作者
Huong T. M. Nguyen,Phung Kim Phi Nguyen,Ngo Thi Thuy Duong,Jirapast Sichaem,T. M. Lien
标识
DOI:10.1080/14786419.2022.2126467
摘要
Two previously unreported dimethylpyranoflavanones, pyronomelodorones A and B (1 and 2), along with five known compounds, 7-O-methyldihydrowogonin (3), 5,6,7-trimethoxyflavanone (4), 5,6-dihydroxy-7-methoxy-dihydroflavone (5), 5,7,8-trimethoxydihydroflavone (6), and pinostrobin (7), were isolated from the roots of Melodorum fruticosum. The structures of all isolates were fully characterized using spectroscopic data and comparison with the previous literature. All isolates were evaluated for their in vitro α-glucosidase inhibition and their cytotoxicity against KB, HepG2, and MCF7 cell lines. Among the isolates, compound 1 exhibited the most inhibitory activity against α-glucosidase and was superior to the positive control with an IC50 value of 1.32 μM. Compounds 1 and 2 showed weak cytotoxicity against the three human cancer cell lines, with IC50 values in the range of 53.3–79.0 μM.
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