Cytotoxic triquinane-type sesquiterpenoids from the endophytic fungus Cerrena sp. A593

Nat Prod Res. 2020 Sep;34(17):2430-2436. doi: 10.1080/14786419.2018.1539977. Epub 2019 Jan 2.

Abstract

The culture broth of Cerrena sp. A593, which was isolated from Pogostemon cablin, showed potent cytotoxicity against several human tumor cell lines. The following chemical study resulted in the isolation of two new triquinane-type sesquiterpenoids, named cerrenins D (1) and E (2), along with two known compounds plerocybellone A (3) and chloriolin B (4). Their structures were fully assigned with the aid of extensive spectroscopic analysis (1H and 13C NMR, HSQC, HMBC, 1H-1H COSY, HRESIMS, and IR) and data from the literature. Moreover, cytotoxic activity in vitro of compounds 1-4 were evaluated against SF-268, MCF-7, NCI-H460, and HepG-2 tumor cell lines. The new compound 1 exhibited weak growth inhibitory activity against all the four tumor cell lines with IC50 values of 41.01, 14.43, 29.67, 44.32 μM.

Keywords: Cerrena sp.; Pogostemon cablin; cytotoxicity; sesquiterpenoids.

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / isolation & purification*
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor
  • Endophytes / chemistry
  • Fungi / pathogenicity*
  • Humans
  • Inhibitory Concentration 50
  • Molecular Structure
  • Pogostemon / microbiology
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / isolation & purification*
  • Sesquiterpenes / pharmacology
  • Spectrum Analysis

Substances

  • Antineoplastic Agents
  • Sesquiterpenes