Bioactive isopimarane and 3,4-seco isopimarane diterpenoids from Isodon amethystoides

被引:2
作者
Zhao, Chenliang [1 ,2 ]
Zhou, Lang [1 ]
Xie, Wenjian [2 ]
Zhao, Lihan [2 ]
Zhang, Chiyuan [2 ]
He, Kang [1 ]
Ye, Jianghai [1 ]
Zhang, Jingjie [1 ]
Pan, Lutai [1 ]
Zou, Juan [1 ]
Zhang, Hongjie [2 ]
机构
[1] Guizhou Univ Tradit Chinese Med, Coll Pharm, 4 Dongging Rd, Guiyang 550025, Guizhou, Peoples R China
[2] Hong Kong Baptist Univ, Sch Chinese Med, Kowloon Tong, Kowloon, 7 Baptist Univ Rd, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Isodon amethystoides; Lamiaceae; Isopimarane diterpenoids; Cytotoxicity; Antibacterial;
D O I
10.1186/s13065-022-00880-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isodon amethystoides (Lamiaceae) is a popular plant in folk medicine in the southern provinces of China. Our phytochemical investigation of the twigs and leaves of this plant led to the discovery of five new diterpenoids with isopimarane and 3,4-seco isopimarane scaffolds [isoamethinols A-E (1-5)], along with the known compound 3,4-seco isopimara-4(18),7,15-triene-3-oic acid methylester (6). The chemical structures of these compounds, including the absolute configurations of the new diterpenoids, were determined by comprehensive spectroscopic analyses and single crystal X-ray diffraction measurements. These compounds were evaluated for their biological activities against a panel of human cancer cell lines, gram-positive bacterial strains and HIV. Notably, the 3,4-seco-isopimarane isoamethinol D (4) showed toxicity to the cervical Hela cancer (Hela) cells with an IC50 value of 27.21 mu M and the lung (A549) cancer cells with an IC50 value of 21.47 mu M. Compound 4 also exhibited mild antimicrobial activity against the oral bacterial strain Streptococcus mutans. These findings suggested that the diterpenoids with a 3,4-seco-isopimarane diterpenoids isolated from I. amethystoides could provide a novel structure scaffold for the discovery of anticancer and antimicrobial compounds.
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页数:11
相关论文
共 18 条
  • [11] Rumschlag-Booms Emily, 2011, J Antivir Antiretrovir, V3, P8
  • [12] SHELXT - Integrated space-group and crystal-structure determination
    Sheldrick, George M.
    [J]. ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2015, 71 : 3 - 8
  • [13] Sheldrick GM, 2015, ACTA CRYSTALLOGR C, V71, P3, DOI [10.1107/S2053273314026370, 10.1107/S2053229614024218, 10.1107/S0108767307043930]
  • [14] Sun H.D., 2001, Diterpenoids from Isodon species
  • [15] Diterpenoids from Isodon species and their biological activities
    Sun, Han-Dong
    Huang, Sheng-Xiong
    Han, Quan-Bin
    [J]. NATURAL PRODUCT REPORTS, 2006, 23 (05) : 673 - 698
  • [16] Wang XR., 1994, CHIN HERB MED, V25, P285
  • [17] Anti-HIV diphyllin glycosides from Justicia gendarussa
    Zhang, Hong-Jie
    Rumschlag-Booms, Emily
    Guan, Yi-Fu
    Liu, Kang-Lun
    Wang, Dong-Ying
    Li, Wan-Fei
    Nguyen, Van Hung
    Cuong, Nguyen Manh
    Soejarto, Djaja Doel
    Fong, Harry H. S.
    Rong, Lijun
    [J]. PHYTOCHEMISTRY, 2017, 136 : 94 - 100
  • [18] Isolation, evaluation of bioactivity and structure determination of amethinol A, a prototypic amethane diterpene from Isodon amethystoides bearing a six/five/seven-membered carbon-ring system
    Zhao, Chen-Liang
    Sarwar, Md. Shahid
    Ye, Jiang-Hai
    Ku, Chuen Fai
    Li, Wan-Fei
    Luo, Guo-Yong
    Zhang, Jing-Jie
    Xu, Jun
    Huang, Zhao-Feng
    Tsang, Siu Wai
    Pan, Lu-Tai
    Zhang, Hong-Jie
    [J]. ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 2018, 74 : 635 - +