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BY-NC-ND 3.0 license Open Access Published by De Gruyter June 2, 2014

Kuehneromycins A and B, Two New Biological Active Compounds from a Tasmanian Kuehneromyces sp. (Strophariaceae, Basidiomycetes)

  • Gerhard Erkel , Kirsten Lorenzen , Timm Anke , Robert Velten , Alberto Gimenez and Wolfgang Steglich

Abstract

In a search for new inhibitors of RNA-directed DNA-polymerases kuehneromycin A (1) was isolated from fermentations of a Tasmanian Kuehneromyces species. Its structure was elucidated by spectroscopic methods. Kuehneromycin A (1) is a non-competitive inhibitor of avian myeloblastosis virus (Ki 200 μᴍ) and moloney murine leukemia virus (Ki 40 μᴍ) reverse transcriptases. The second compound, kuehneromycin B (2) is a strong inhibitor of platelet aggregation stimulated with different inducers. In addition, both compounds exhibit cytotoxic and antimicrobial activities.

Received: 1994-10-5
Published Online: 2014-6-2
Published in Print: 1995-2-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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