A new sesquiterpenoid quinone with cytotoxicity from Abelmoschus sagittifolius

被引:5
作者
Chen, De-Li [1 ,2 ]
Zhang, Xiao-Po [3 ]
Ma, Guo-Xu [4 ,5 ]
Wu, Hai-Feng [4 ,5 ]
Yang, Jun-Shan [4 ,5 ]
Xu, Xu-Dong [4 ,5 ]
机构
[1] Chinese Acad Med Sci, Hainan Prov Key Lab Resources Conservat & Dev Sou, Inst Med Plant Dev, Hainan Branch, Wanning 571533, Peoples R China
[2] Peking Union Med Coll, Wanning 571533, Peoples R China
[3] Hainan Med Univ, Sch Pharmaceut Sci, 3 Xueyuan Rd, Haikou 571101, Peoples R China
[4] Chinese Acad Med Sci, Inst Med Plant Dev, 151 Malianwa North Rd, Beijing 100193, Peoples R China
[5] Peking Union Med Coll, 151 Malianwa North Rd, Beijing 100193, Peoples R China
关键词
Abelmoschus sagittifolius; sesquiterpenoid; cytotoxicity;
D O I
10.1080/14786419.2015.1033624
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new sesquiterpenoid quinone, Acyl hibiscone B (1), together with five known compounds, (R)-lasiodiplodin (2), (R)-de-O-methyllasiodiplodin, (3) dibutyl phthalate (4), (R)-9-phenylnonan-2-ol (5) and hibiscone B (6), was obtained from the stem tuber of Abelmoschus sagittifolius. The structure of compound 1 was elucidated by analysing its H-1 and C-13 NMR, H-1-H-1 COSY, HSQC, HMBC, NOESY and HR-ESI-MS values. Compound 1 showed significant cytotoxicity against Hela and HepG-2 human cancer cell lines.
引用
收藏
页码:565 / 569
页数:5
相关论文
共 10 条
  • [1] Enantiodivergent synthesis of both enantiomers of the macrocyclic lactone lasiodiplodin
    Bracher, F
    Schulte, B
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1996, (21): : 2619 - 2622
  • [2] Chen HY, 1965, FLORA OF HAINAN, V2
  • [3] Chinese Herbalism Editorial Board State Administration of Traditional Chinese Medicine of the People's Republic of China, 1999, CHINESE MAT MED
  • [4] Ferreira MA, 1980, J CHEM SOC PERK T, V1, P249, DOI [10.1039/p19800000249, DOI 10.1039/P19800000249]
  • [5] A new triterpenoid saponin from Ardisia gigantifolia
    Mu, Li-Hua
    Huang, Xiao-Wu
    Guo, Dai-Hong
    Dong, Xian-Zhe
    Liu, Ping
    [J]. JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2013, 15 (10) : 1123 - 1129
  • [6] PHOTOLACTONIZATION - A NOVEL SYNTHETIC ENTRY TO MACROLIDES
    QUINKERT, G
    BILLHARDT, UM
    JAKOB, H
    FISCHER, G
    GLENNEBERG, J
    NAGLER, P
    AUTZE, V
    HEIM, N
    WACKER, M
    SCHWALBE, T
    KURTH, Y
    BATS, JW
    DURNER, G
    ZIMMERMANN, G
    KESSLER, H
    [J]. HELVETICA CHIMICA ACTA, 1987, 70 (03) : 771 - 861
  • [7] Wang YF, 2009, J ANHUI AGR SCI, V37, P11001
  • [8] A new periplogenin cardenolide from the seeds of Antiaris toxicaria
    Wu, Xiu-Li
    Wu, Yu-Ling
    Li, Hou-Gang
    Liu, He-Tao
    Fu, Xue-Yan
    Cui, Rui-Qin
    Wang, Jian-Huan
    Liu, Cheng
    Chen, Jing
    [J]. JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2014, 16 (04) : 418 - 421
  • [9] [杨瑞云 YANG Ruiyun], 2007, [分析测试学报, Journal of Instrumental Analysis], V26, P12
  • [10] Ethnobotanical study on medicinal plants around Limu Mountains of Hainan Island, China
    Zheng, Xi-long
    Wei, Jian-he
    Sun, Wei
    Li, Rong-tao
    Liu, Shou-bai
    Dai, Hao-fu
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2013, 148 (03) : 964 - 974