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
相关论文
共 50 条
  • [21] Diterpenoid alkaloids from Delphinium albiflorum
    Ulubelen, A
    Desai, HK
    Joshi, BS
    Venkateswarlu, V
    Pelletier, SW
    Mericli, AH
    Mericli, F
    Ozcelik, H
    JOURNAL OF NATURAL PRODUCTS, 1995, 58 (10): : 1555 - 1561
  • [22] Diterpenoid Alkaloids from Delphinium liangshanense
    Liu, Yue
    Zhao, Yi-Dan
    Zhong, He-Yang
    Chen, Si-Yang
    Huang, Shuai
    Chen, Lin
    Zhou, Xian-Li
    CHEMISTRY & BIODIVERSITY, 2024, 21 (06)
  • [23] Diterpenoid alkaloids from Delphinium trichophorum
    Pu, Yang-Li
    Tian, Ling-Feng
    Chen, Lin
    Deng, Meng-Yi
    Xie, Jiang
    Huang, Shuai
    Zhou, Xian-Li
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2023, 25 (12) : 1175 - 1183
  • [24] Diterpenoid alkaloids from Delphinium uncinatum
    Ulubelen, A
    Arfan, M
    Sönmez, U
    Meriçli, AH
    Meriçli, F
    PHYTOCHEMISTRY, 1998, 47 (06) : 1141 - 1144
  • [25] Diterpenoid alkaloids from Delphinium trichophorum
    Huang, Shuai
    Wang, Jian-Zhu
    Pu, Yang-Li
    Liu, Yu-Yan
    Chen, Ying
    Chen, Lin
    Zhou, Xian-Li
    PHYTOCHEMISTRY, 2024, 225
  • [26] Diterpenoid Alkaloids from Delphinium Tongolense
    Lan HE
    Xuan PAN
    Bo Gang LI
    Yao Zu CHEN(The Chemistry Department of Zhejian Univ.
    The Department of Pharmacy of Lanzhou Medical College
    The Chengdu Institute of Biology
    Chinese Chemical Letters, 1997, (09) : 791 - 792
  • [27] Diterpenoid Alkaloids from Delphinium yunnanense
    Chen, Feng-Zheng
    Chen, Qiao-Hong
    Wang, Feng-Peng
    HELVETICA CHIMICA ACTA, 2011, 94 (02) : 254 - 260
  • [28] Diterpenoid Alkaloids from Delphinium aemulans
    Ablajan, Nurfida
    Zhao, Bo
    Xue, Wenjuan
    Ruzi, Zukela
    Zhao, Jiangyu
    Aisa, Haji Akber
    NATURAL PRODUCT COMMUNICATIONS, 2018, 13 (11) : 1429 - 1431
  • [29] Diterpenoid alkaloids from Delphinium gracile
    Reina, M.
    Mancha, R.
    Gonzalez-Coloma, A.
    Bailen, M.
    Rodriguez, M. L.
    Martinez-Diaz, R. A.
    NATURAL PRODUCT RESEARCH, 2007, 21 (12) : 1048 - 1055
  • [30] Diterpenoid alkaloids from Delphinium tongolense
    He, L
    Pan, X
    Li, BG
    Chen, YZ
    CHINESE CHEMICAL LETTERS, 1997, 8 (09) : 791 - 792