Secondary metabolites from the Colletotrichum gloeosporioides A12, an endophytic fungus derived from Aquilaria sinensis

Nat Prod Res. 2018 Oct;32(19):2360-2365. doi: 10.1080/14786419.2017.1410810. Epub 2017 Dec 4.

Abstract

Two new cyclohexene derivatives colletotricones A and B (1 and 2) and a new thiazole derivative colletotricole A (5), along with six known natural metabolites were isolated from the extract of Colletotrichum gloeosporioides A12, an endophytic fungus derived from Aquilaria sinensis. Among them, the colletotricones A and B possess a cyclohexenone skeleton, whereas the colletotricole A is a thiazole derivative. Their structures were fully assigned with the aid of extensive spectroscopic analysis and data from the literature. Moreover, cytotoxic activity in vitro of compounds 1 and 3-9 were evaluated against MCF-7, NCI-H460, HepG-2 and SF-268 tumour cell lines. The new compound 1 exhibited growth inhibitory activity against all the four tumour cell lines with IC50 values ranging from 15.7 to 46.8 μM.

Keywords: Aquilaria sinensis; Colletotrichum gloeosporioides; cyclohexene derivative; cytotoxicity; thiazole.

MeSH terms

  • Antineoplastic Agents / isolation & purification
  • Cell Line
  • Cell Line, Tumor
  • Colletotrichum / chemistry*
  • Cyclohexenes / chemistry
  • Cyclohexenes / isolation & purification
  • Endophytes
  • Humans
  • Molecular Structure
  • Spectrum Analysis
  • Thiazoles / chemistry
  • Thiazoles / isolation & purification
  • Thymelaeaceae / microbiology

Substances

  • Antineoplastic Agents
  • Cyclohexenes
  • Thiazoles