Secondary Metabolites with α-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus Talaromyces sp. CY-3

Mar Drugs. 2021 Aug 28;19(9):492. doi: 10.3390/md19090492.

Abstract

Eight new compounds, including two sambutoxin derivatives (1-2), two highly oxygenated cyclopentenones (7-8), four highly oxygenated cyclohexenones (9-12), together with four known sambutoxin derivatives (3-6), were isolated from semimangrove endophytic fungus Talaromyces sp. CY-3, under the guidance of molecular networking. The structures of new isolates were elucidated by analysis of detailed spectroscopic data, ECD spectra, chemical hydrolysis, 13C NMR calculation, and DP4+ analysis. In bioassays, compounds 1-5 displayed better α-glucosidase inhibitory activity than the positive control 1-deoxynojirimycin (IC50 = 80.8 ± 0.3 μM), and the IC50 value was in the range of 12.6 ± 0.9 to 57.3 ± 1.3 μM.

Keywords: Talaromyces sp.; molecular networking; polyketides; sambutoxin; α-glucosidase.

MeSH terms

  • Endophytes / metabolism*
  • Glycoside Hydrolase Inhibitors / chemistry
  • Glycoside Hydrolase Inhibitors / metabolism*
  • Malvaceae / microbiology*
  • Molecular Structure
  • Mycotoxins / chemistry
  • Mycotoxins / metabolism*
  • Polyketides / chemistry
  • Polyketides / metabolism*
  • Secondary Metabolism
  • Talaromyces / metabolism*
  • alpha-Glucosidases / chemistry

Substances

  • Glycoside Hydrolase Inhibitors
  • Mycotoxins
  • Polyketides
  • sambutoxin
  • alpha-Glucosidases