Química Nova (Jul 2016)

A STRATEGY FOR THE RAPID IDENTIFICATION OF FUNGAL METABOLITES AND THE DISCOVERY OF THE ANTIVIRAL ACTIVITY OF PYRENOCINE A AND HARZIANOPYRIDONE

  • Laura P. Ióca,
  • Stelamar Romminger,
  • Mario F. C. Santos,
  • Karin F. Bandeira,
  • Fabiana T. Rodrigues,
  • Miriam H. Kossuga,
  • Karen J. Nicacio,
  • Everton L. F. Ferreira,
  • Raquel P. Morais-Urano,
  • Messias S. Passos,
  • Luciana K. Kohn,
  • Clarice W. Arns,
  • Lara D. Sette,
  • Roberto G. S. Berlinck

DOI
https://doi.org/10.5935/0100-4042.20160092
Journal volume & issue
Vol. 39, no. 6
pp. 720 – 731

Abstract

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The isolation and identification of bioactive metabolites from complex extracts obtained from microbial growth media is a time consuming, costly, and labor-intensive task. A strategy to rapidly identify secondary metabolites isolated from extracts obtained from the culture media of marine-derived and endophytic fungal strains is described. Identification was achieved by HPLC-UV-MS and 1H NMR analyses in combination with data obtained from the Dictionary of Natural Products. Among the compounds identified, (-)-naphthoquinoneimine, citreorosein, emodin, pyrenocine A and harzianopyridone displayed moderate to potent antiviral activity. (-)-Naphthoquinoneimine was isolated as the enantiomer of its previously reported dextrorotatory congener, while 6,7-dihydroxy-2,2-dimethyl-4-chromanone is herein reported for the first time as a natural product.

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