Two new cytotoxic diterpenoid alkaloids from Delphinium grandiflorum

被引:0
|
作者
Nan, Ze-dong [1 ,2 ,3 ]
Shang, Ying [1 ,2 ]
Deng, Chao-fan [1 ,2 ]
Zhu, Yi-dong [1 ,2 ]
Jiang, Guo-dong [1 ,2 ]
Wang, Zhen-zhen [1 ,2 ]
Li, Chong-long [1 ,2 ]
Ma, Xiao-li [1 ,2 ]
Jiang, Zhi-Bo [1 ,2 ,3 ]
机构
[1] North Minzu Univ, Sch Chem & Chem Engn, Dept Pharmaceut Engn, Yinchuan 750001, Peoples R China
[2] North Minzu Univ, Key Lab Chem Engn & Technol, State Ethn Affairs Commiss, Yinchuan 750001, Peoples R China
[3] Ningxia Low Grade Resource High Value Utilizat & E, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
Ranunculaceae; Delphinium grandiflorum; C- 18 -diterpenoid alkaloid; C- 19 -diterpenoid alkaloid; Cytotoxic activities;
D O I
10.1016/j.phytol.2024.03.003
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Delphinium grandiflorum, one of the well-known Delphinium species, contains diverse bioactive diterpenoid alkaloids (DAs), which promoted a systematic phytochemical study on this plant. As a result, two new DAs, namely 16-demethyl tuguaconitine (1) and 6-O-acetyl-16-demethyldelsoline (2), together with one known analogue pseudophnine A (3) were obtained from the whole herbs of D. grandiflorum. Their structures were elucidated by use of extensive spectroscopic analysis (HR-ESIMS, IR, 1D and 2D NMR). Additionally, the inhibitory effects of these obtained individual compounds were also evaluated in vitro for lung cancer cell line (A549), liver cancer cell line (SMMC-7721), and breast cancer cell line (MCF-7). The results of cytotoxic activities showed that only compound 2 exhibit weak inhibitory effect on SMMC-7721 and MCF-7, and their IC50 values were 37.4 and 33.1 mu M, respectively. However, compound 1 and 3 had no obvious cytotoxic activities (IC50>80 mu M).
引用
收藏
页码:11 / 15
页数:5
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