Cytotoxic pyrone derivatives from the deep-sea-derived fungus Cladosporium halotolerans FS702

Nat Prod Res. 2024 Feb-Mar;38(4):594-600. doi: 10.1080/14786419.2023.2187794. Epub 2023 Mar 20.

Abstract

Two new compounds (R)-6-((8S)-hydroxypropyl)-2-methyl-5,6-dihydro-4H-pyran-4-one (1) and (R)-6-((8R)-hydroxypropyl)-2-methyl-5,6-dihydro-4H-pyran-4-one (2), together with four known compounds were isolated from the marine-derived fungus Cladosporium halotolerans FS702. The structures of these compounds were determined on the basis of extensive spectroscopic analysis including 1D/2D NMR, IR, UV, HRESIMS, ECD calculations as well as the modified Mosher's method. Cytotoxic assay results showed that compound 2 had significant cytotoxic activity against SF-268, MCF-7, HepG-2, and A549 cells lines with IC50 values of 0.16, 0.47, 0.33 and 0.23 µM, respectively.

Keywords: Cladosporium halotolerans; cytotoxic activity; marine-derived fungus.

MeSH terms

  • Antineoplastic Agents* / chemistry
  • Cell Line, Tumor
  • Cladosporium / chemistry
  • Fungi / chemistry
  • Molecular Structure
  • Pyrones* / pharmacology

Substances

  • Pyrones
  • Antineoplastic Agents

Supplementary concepts

  • Cladosporium halotolerans