Planta Med 2015; 81(05): 382-387
DOI: 10.1055/s-0035-1545721
Natural Product Chemistry
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Antichlamydial Sterol from the Red Sea Sponge Callyspongia aff. implexa

Authors

  • Usama Ramadan Abdelmohsen

    1   Department of Botany II, Julius-von-Sachs Institute for Biological Sciences, University of Würzburg, Würzburg, Germany
    5   Permanent address: Department of Pharmacognosy, Faculty of Pharmacy, Minia University, Minia, Egypt
  • Cheng Cheng

    1   Department of Botany II, Julius-von-Sachs Institute for Biological Sciences, University of Würzburg, Würzburg, Germany
  • Anastasija Reimer

    2   Department of Microbiology, Biocenter, University of Würzburg, Würzburg, Germany
  • Vera Kozjak-Pavlovic

    2   Department of Microbiology, Biocenter, University of Würzburg, Würzburg, Germany
  • Amany K. Ibrahim

    3   Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt
  • Thomas Rudel

    2   Department of Microbiology, Biocenter, University of Würzburg, Würzburg, Germany
  • Ute Hentschel

    1   Department of Botany II, Julius-von-Sachs Institute for Biological Sciences, University of Würzburg, Würzburg, Germany
  • RuAngelie Edrada-Ebel

    4   Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK
  • Safwat A. Ahmed

    3   Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt
Further Information

Publication History

received 12 September 2014
revised 10 January 2015

accepted 24 January 2015

Publication Date:
17 March 2015 (online)

Abstract

Marine sponges are rich sources of natural products exhibiting diverse biological activities. Bioactivity-guided fractionation of the Red Sea sponge Callyspongia aff. implexa led to the isolation of two new compounds, 26,27-bisnorcholest-5,16-dien-23-yn-3β,7α-diol, gelliusterol E (1) and C27-polyacetylene, callimplexen A (2), in addition to the known compound β-sitosterol (3). The structures of the isolated compounds were determined by 1D- and 2D-NMR techniques as well as high-resolution tandem mass spectrometry and by comparison to the literature. The three compounds (13) were tested against Chlamydia trachomatis, an obligate intracellular gram-negative bacterium, which is the leading cause of ocular and genital infections worldwide. Only gelliusterol E (1) inhibited the formation and growth of chlamydial inclusions in a dose-dependent manner with an IC50 value of 2.3 µM.