Cytotoxic Naphthoquinone and Azaanthraquinone Derivatives from an Endophytic Fusarium solani

J Nat Prod. 2017 Apr 28;80(4):1173-1177. doi: 10.1021/acs.jnatprod.6b00610. Epub 2017 Mar 3.

Abstract

Bioactivity-guided fractionation of the ethyl acetate extract obtained from the culture of the endophytic fungus Fusarium solani resulted in the isolation of one new naphthoquinone, 9-desmethylherbarine (1), and two azaanthraquinone derivatives, 7-desmethylscorpinone (2) and 7-desmethyl-6-methylbostrycoidin (3), along with four known compounds. Their structures were elucidated by spectral analysis, as well as a direct comparison of spectral data with those of known compounds. Azaanthraquinones 2 and 3 showed cytotoxic activity against four human tumor cell lines, MDA MB 231, MIA PaCa2, HeLa, and NCI H1975. A molecular docking study suggested DNA interactions as the mode of action of these naphthoquinones and azaanthraquinones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates
  • Anthraquinones / chemistry
  • Anthraquinones / isolation & purification*
  • Anthraquinones / pharmacology*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology*
  • Aza Compounds / chemistry
  • Aza Compounds / isolation & purification*
  • Aza Compounds / pharmacology*
  • Drug Screening Assays, Antitumor
  • Fusarium / chemistry*
  • HeLa Cells
  • Humans
  • Molecular Docking Simulation
  • Molecular Structure
  • Naphthoquinones / chemistry
  • Naphthoquinones / isolation & purification*
  • Naphthoquinones / pharmacology*
  • Nuclear Magnetic Resonance, Biomolecular

Substances

  • Acetates
  • Anthraquinones
  • Antineoplastic Agents
  • Aza Compounds
  • Naphthoquinones
  • ethyl acetate