整合生物学期刊网

应用天然产物 ›› 2013, Vol. 3 ›› Issue (4): 137-140.DOI: 10.1007/s13659-013-0036-5

• Regular Article • 上一篇    下一篇

Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi

Timo H. J. NIEDERMEYER, Thomas JIRA, Michael LALK, Ulrike LINDEQUIST   

  1. Institute of Pharmacy, Ernst-Moritz-Arndt-University, Friedrich-Ludwig-Jahn-Straße 17, 17487 Greifswald, Germany
  • 收稿日期:2013-04-30 修回日期:2013-06-02 出版日期:2013-08-24 发布日期:2018-02-11
  • 通讯作者: Timo H.J.NIEDERMEYER,E-mail:timo.niedermeyer@uni-greifswald.de
  • 基金资助:
    We thank K. Weisz for recording the NMR spectra. Financial support by the federal state of MecklenburgVorpommern and the EU ("Landesforschungsschwerpunkt" EMAU 02 015 20) is gratefully acknowledged.

Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi

Timo H. J. NIEDERMEYER, Thomas JIRA, Michael LALK, Ulrike LINDEQUIST   

  1. Institute of Pharmacy, Ernst-Moritz-Arndt-University, Friedrich-Ludwig-Jahn-Straße 17, 17487 Greifswald, Germany
  • Received:2013-04-30 Revised:2013-06-02 Online:2013-08-24 Published:2018-02-11
  • Supported by:
    We thank K. Weisz for recording the NMR spectra. Financial support by the federal state of MecklenburgVorpommern and the EU ("Landesforschungsschwerpunkt" EMAU 02 015 20) is gratefully acknowledged.

摘要: Two farnesylhydroquinones were isolated from the fruiting bodies of Ganoderma pfeifferi, farnesylhydroquinone (1) and the new compound ganomycin K (2), (5S)-3-[(E)-7,8-dihydroxy-4,8-dimethylnon-3-enyl]-5-(2,5-dihydroxyphenyl)-furan-2(5H)-one. The structures of 1 and 2 were determined on the basis of mass spectrometric and NMR spectroscopic evidence. The antibacterial activity of the isolated compounds was neglectable.

关键词: Ganoderma pfeifferi, farnesylhydroquinone, ganomycin

Abstract: Two farnesylhydroquinones were isolated from the fruiting bodies of Ganoderma pfeifferi, farnesylhydroquinone (1) and the new compound ganomycin K (2), (5S)-3-[(E)-7,8-dihydroxy-4,8-dimethylnon-3-enyl]-5-(2,5-dihydroxyphenyl)-furan-2(5H)-one. The structures of 1 and 2 were determined on the basis of mass spectrometric and NMR spectroscopic evidence. The antibacterial activity of the isolated compounds was neglectable.

Key words: Ganoderma pfeifferi, farnesylhydroquinone, ganomycin