Planta Med 2013; 79(15): 1447-1452
DOI: 10.1055/s-0033-1350768
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Phenanthrenes from Juncus effusus

Authors

  • Xue-Hui Su

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
  • Zhi-Peng Yuan

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
  • Cong-Ying Li

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
  • Yu-Jiao Zhong

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
  • Hong-Jian Du

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
  • Ya-Ya Wen

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
  • Yan-Fang Li

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
  • Bing Liang

    Department of Pharmaceutics & Bioengineering, School of Chemical Engineering, Sichuan University, Chengdu, China
Further Information

Publication History

received 06 January 2013
revised 06 July 2013

accepted 22 July 2013

Publication Date:
26 August 2013 (online)

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Abstract

A chemical investigation of the EtOAc-soluble fraction from the ethanol extract of the medullae of Juncus effusus led to the isolation of three new 9,10-dihydrophenanthrenes, juncuenins EG (13); two new phenanthrenes, dehydrojuncuenins DE (45); one new feruloylated glycoside (6); and one known 9,10-dihydrophenanthrene (7). The structures of these compounds were determined by analyzing their spectroscopic data. Metabolites 14 and 7 were further evaluated for their in vitro cytotoxic activities against seven human cancer lines (A549, MCF-7, BEL-7402, HeLa, COLO205, BGC-823, and SK-OV-3). Among them, compound 1 exhibited weak cytotoxicity against MCF-7 and HeLa cell lines. Compound 7 showed moderate cytotoxicity against MCF-7 and HeLa cell lines, with IC50 values of 9.17 and 19.6 µM, respectively.

Supporting Information