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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).
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页码:11 / 15
页数:5
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