Planta Med 2014; 80(11): 936-941
DOI: 10.1055/s-0034-1368612
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Two New 2,3-Seco-Hopane Triterpene Derivatives from Megacodon stylophorus and Their Antiproliferative and Antimicrobial Activities

Authors

  • Chao Liu

    1   Department of Pharmaceutical Engineering, School of Chemistry and Chemical Engineering, Southeast University, Nanjing, P. R. China
    3   Jiangsu Province Hi-Tech Key Laboratory for Bio-medical Research, Southeast University, Nanjing, P. R. China
  • Zhi-Xin Liao

    1   Department of Pharmaceutical Engineering, School of Chemistry and Chemical Engineering, Southeast University, Nanjing, P. R. China
    3   Jiangsu Province Hi-Tech Key Laboratory for Bio-medical Research, Southeast University, Nanjing, P. R. China
  • Shi-Jun Liu

    1   Department of Pharmaceutical Engineering, School of Chemistry and Chemical Engineering, Southeast University, Nanjing, P. R. China
  • Lan-Ju Ji

    2   Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, P. R. China
  • Hong-Fa Sun

    2   Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, P. R. China
Further Information

Publication History

received 28 November 2013
revised 18 May 2014

accepted 20 May 2014

Publication Date:
04 July 2014 (online)

Abstract

Chemical investigation of the ethanol extract of the whole plant of Megacodon stylophorus led to the isolation and identification of two new seco-hopane triterpenoids, 2,3-seco-22(29)-hopene-2-carboxyl-3-aldehyde (1) and 2,3-seco-4(23),22(29)-hopene-2-carboxyl-3-aldehyde (2), along with 10 known compounds, 312. All the isolates were reported from this plant for the first time. The structures of compounds 1 and 2 were determined by detailed analysis of their spectral data including 1D and 2D NMR. In addition, compound 1 was further analyzed by X-ray crystallography. Compounds 13 were evaluated for their in vitro anti-proliferative activities on HeLa, MCF-7, and Hep-G2 tumor cell lines. Compound 2 was active against the three cell lines with IC50 values of 3.6, 7.5, and 13.6 µM, respectively, while compound 1 exhibited cytotoxicity on MCF-7 (IC50 14.0 µM) and HeLa (IC50 18.2 µM) cell lines. Antimicrobial activities of compounds 12 (minimum inhibitory concentration values in the range of 3.12–12.50 mg/mL) were also observed.