1H and 13C NMR assignments for two anthraquinones and two xanthones from the mangrove fungus (ZSUH-36)

Magn Reson Chem. 2007 May;45(5):434-8. doi: 10.1002/mrc.1974.

Abstract

We report the unambiguous assignments of the (1)H and (13)C NMR spectra of one new natural product, namely, 6,8-di-O-methyl versiconol (1) together with one known anthraquinone aversin (2) and two xanthones 5-methoxysterigmatocystin (3) and sterigmatocystin (4). These compounds were all isolated from the mangrove endophytic fungus ZSUH-36 from the South China Sea. 1D and 2D NMR experiments including COSY, HMQC and HMBC were used to elucidate the structures. Variations in the (1)H NMR spectrum of 6,8-di-O-methyl versiconol (1) were also observed in the temperature range 25-75 degrees C. In addition, the plausible biogenetic path from 1 to 2 is discussed.

MeSH terms

  • Anthraquinones / chemistry*
  • Carbon Isotopes
  • China
  • Fungi / chemistry*
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Oceans and Seas
  • Protons
  • Xanthones / chemistry*

Substances

  • 6,8-di-O-methyl versiconol
  • Anthraquinones
  • Carbon Isotopes
  • Protons
  • Xanthones
  • aversin