Two New Cytotoxic Decalin Derivatives from Marine-Derived Fungus Talaromyces sp

Chem Biodivers. 2022 Mar;19(3):e202100990. doi: 10.1002/cbdv.202100990. Epub 2022 Jan 27.

Abstract

Two new decalin derivatives named fusarielins O (1) and P (2), together with seven known compounds (3-9) were isolated from the crude extract of the marine-derived fungus Talaromyces sp. The planar structures of the new compounds were elucidated by comprehensive spectroscopic analyses of NMR and HR-ESI-MS. The absolute configuration of 1 was assigned by Snatzke's method and comparison of experimental and calculated electronic circular dichroism (ECD) spectra. Compounds 1-9 were evaluated for their cytotoxic activities against three tumor cell lines and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activities.

Keywords: antioxidant activity; cytotoxicity; secondary metabolites; structural elucidation.

MeSH terms

  • Antineoplastic Agents* / chemistry
  • Circular Dichroism
  • Molecular Structure
  • Naphthalenes
  • Talaromyces* / chemistry

Substances

  • Antineoplastic Agents
  • Naphthalenes
  • decalin