HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities

被引:23
作者
Li, Fang-Ru [1 ]
Liu, Lu [1 ,2 ]
Liu, Ya-Ping [1 ]
Wang, Jin-Tang [1 ]
Yang, Mei-Lian [1 ]
Khan, Afsar [3 ]
Qin, Xu-Jie [5 ]
Wang, Yu-Dan [4 ]
Cheng, Gui-Guang [1 ]
机构
[1] Kunming Univ Sci & Technol, Fac Agr & Food, Kunming 650500, Yunnan, Peoples R China
[2] Yunnan Univ Chinese Med, Yunnan Prov Key Lab Mol Biol Sinomed, Kunming 650500, Yunnan, Peoples R China
[3] COMSATS Univ Islamabad, Dept Chem, Abbottabad Campus, Abbottabad 22060, Pakistan
[4] Yunnan Minzu Univ, Natl & Local Joint Engn Res Ctr Green Preparat Te, Kunming 650500, Yunnan, Peoples R China
[5] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Melodinus cochinchinensis (Lour.) Merr. (Apocynaceae); melokhanines; Bisindole alkaloids; Anti-inflammatory; Cytotoxicity; MONOTERPENOID INDOLE ALKALOIDS; CHEMISTRY; FRUITS;
D O I
10.1016/j.phytochem.2021.112673
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Melodinus species have been proved to be good resources of bisindole alkaloids. Six bisindole alkaloids were isolated from the leaves and stems of Melodinus cochinchinensis (Lour.) Merr. guided by HRESIMS data analysis. Among them, melokhanines K-M, epi-scandomelonine, and epi-scandomeline possessed aspidosperma-scandine skeleton linked by a C-C bond while meloyine II had a scandine-scandine skeleton. The structures were established by extensive spectroscopic analysis of their HRESIMS and NMR data. Melokhanines K-M were undescribed compounds, while epi-scandomelonine, epi-scandomeline and meloyine II were known compounds, which were reported from Melodinus species for the first time. The anti-inflammatory and cytotoxic activities of the isolates were also evaluated in vitro. Melokhanine K and meloyine II showed potent inhibitory activity on the production of nitric oxide, interleukin-6, and tumor necrosis factor-alpha in LPS-induced RAW 264.7 macrophages, whereas episcandomelonine and epi-scandomeline exhibited certain cytotoxic activity against MOLT-4 cells with IC50 values 5.2 and 1.5 mu M, respectively.
引用
收藏
页数:7
相关论文
共 40 条
  • [1] STRUCTURAL STUDIES ON VINDOLININE
    ATTAURRAHMAN
    MALIK, S
    ALBERT, K
    [J]. ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 1986, 41 (03): : 386 - 392
  • [2] SpecDis: Quantifying the Comparison of Calculated and Experimental Electronic Circular Dichroism Spectra
    Bruhn, Torsten
    Schaumloeffel, Anu
    Hemberger, Yasmin
    Bringmann, Gerhard
    [J]. CHIRALITY, 2013, 25 (04) : 243 - 249
  • [3] Alkaloids from Melodinus yunnanensis
    Cai, Xiang-Hai
    Li, Yan
    Liu, Ya-Ping
    Li, Xiao-Ning
    Bao, Mei-Fen
    Luo, Xiao-Dong
    [J]. PHYTOCHEMISTRY, 2012, 83 : 116 - 124
  • [4] Cai Xiang-Hai, 2011, Chinese Journal of Natural Medicines, V9, P259, DOI 10.1016/S1875-5364(11)60061-7
  • [5] Melokhanines A-J, Bioactive Monoterpenoid Indole Alkaloids with Diverse Skeletons from Melodinus khasianus
    Cheng, Gui-Guang
    Li, Dan
    Hou, Bo
    Li, Xiao-Nian
    Liu, Lu
    Chen, Ying-Ying
    Lunga, Paul-Keilah
    Khan, Afsar
    Liu, Ya-Ping
    Zuo, Zhi-Li
    Luo, Xiao-Dong
    [J]. JOURNAL OF NATURAL PRODUCTS, 2016, 79 (09): : 2158 - 2166
  • [6] Indole alkaloids from cultivated Vinca major
    Cheng, Gui-Guang
    Zhao, Yun-Li
    Zhang, Yu
    Lunga, Paul-Keilah
    Hu, Dong-Bao
    Li, Yan
    Gu, Ji
    Song, Chang-Wei
    Sun, Wei-Bang
    Liu, Ya-Ping
    Luo, Xiao-Dong
    [J]. TETRAHEDRON, 2014, 70 (45) : 8723 - 8729
  • [7] C-13 NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY OF NATURALLY OCCURRING SUBSTANCES .48. DIMERIC QUINOLINIC MELODINUS ALKALOIDS
    DAUDON, M
    MEHRI, MH
    PLAT, MM
    HAGAMAN, EW
    WENKERT, E
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1976, 41 (20) : 3275 - 3278
  • [8] Cytotoxic Indole Alkaloids from Melodinus tenuicaudatus
    Feng, Tao
    Li, Yan
    Wang, Yuan-Yuan
    Cai, Xiang-Hai
    Liu, Ya-Ping
    Luo, Xiao-Dong
    [J]. JOURNAL OF NATURAL PRODUCTS, 2010, 73 (06): : 1075 - 1079
  • [9] Frisch M.J., 2009, GAUSSIAN 09 D01
  • [10] Angustifonines A and B, Cytotoxic Bisindole Alkaloids from Bousigonia angustifolia
    Fu, Yan-hui
    Di, Ying-tong
    He, Hong-ping
    Li, Shun-lin
    Zhang, Yu
    Hao, Xiao-jiang
    [J]. JOURNAL OF NATURAL PRODUCTS, 2014, 77 (01): : 57 - 62