Lasiodiplactone A, a novel lactone from the mangrove endophytic fungus Lasiodiplodia theobromae ZJ-HQ1

Org Biomol Chem. 2017 Aug 2;15(30):6338-6341. doi: 10.1039/c7ob01657c.

Abstract

Lasiodiplactone A (1), an unprecedented lactone, was obtained from the mangrove endophytic fungus Lasiodiplodia theobromae ZJ-HQ1. The structure of 1 was established by analysis of NMR spectroscopic data and electronic circular dichroism (ECD) spectra. Lasiodiplactone A (1) was the first example of lactone that possesses a unique tetracyclic system (12/6/6/5) of RAL12 (12-membered β-resorcylic acid lactone) with a pyran ring and a furan ring. A possible biogenetic pathway for 1 was proposed. Compound 1 showed anti-inflammatory activity by inhibiting nitric oxide (NO) production in lipopolysaccharide activated in RAW264.7 cells with IC50 value of 23.5 μM and exhibited potential α-glucosidase inhibitory activity with IC50 values of 29.4 μM.

MeSH terms

  • Animals
  • Ascomycota / chemistry*
  • Ascomycota / metabolism
  • Endophytes / chemistry*
  • Endophytes / metabolism
  • Glycoside Hydrolase Inhibitors / chemistry*
  • Glycoside Hydrolase Inhibitors / isolation & purification
  • Glycoside Hydrolase Inhibitors / metabolism
  • Glycoside Hydrolase Inhibitors / pharmacology*
  • Inhibitory Concentration 50
  • Lactones / chemistry*
  • Lactones / isolation & purification
  • Lactones / metabolism
  • Lactones / pharmacology*
  • Mice
  • RAW 264.7 Cells
  • alpha-Glucosidases / metabolism

Substances

  • Glycoside Hydrolase Inhibitors
  • Lactones
  • lasiodiplactone A
  • alpha-Glucosidases