Vermistatin derivatives with α-glucosidase inhibitory activity from the mangrove endophytic fungus Penicillium sp. HN29-3B1

Planta Med. 2014 Jul;80(11):912-7. doi: 10.1055/s-0034-1382859. Epub 2014 Aug 12.

Abstract

Three new vermistatin derivatives, 6-demethylpenisimplicissin (1), 5'-hydroxypenisimplicissin (2), and 2''-epihydroxydihydrovermistatin (3), along with five known vermistatin analogues, methoxyvermistatin (4), vermistatin (5), 6-demethylvermistatin (6), hydroxyvermistatin (7), and penisimplicissin (8), were isolated from the culture of the mangrove endophytic fungus Penicillium sp. HN29-3B1 from Cerbera manghas. Their structures were elucidated mainly by nuclear magnetic resonance spectroscopy. The absolute configurations of compounds 1 and 2 were deduced on the basis of circular dichroism data. The absolute structures of compounds 3 and 5 were confirmed by a single-crystal X-ray diffraction experiment using Cu Kα radiation. In the bioactivity assay, compounds 1 and 3 exhibited α-glucosidase inhibitory activity with IC50 values of 9.5 ± 1.2 and 8.0 ± 1.5 µM, respectively. The plausible biosynthetic pathways for all compounds are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apocynaceae / microbiology*
  • Endophytes
  • Glycoside Hydrolase Inhibitors / chemistry
  • Glycoside Hydrolase Inhibitors / isolation & purification
  • Glycoside Hydrolase Inhibitors / pharmacology*
  • Molecular Structure
  • Penicillium / chemistry*
  • Pyrones / chemistry
  • Pyrones / isolation & purification
  • Pyrones / pharmacology*
  • X-Ray Diffraction
  • alpha-Glucosidases / drug effects

Substances

  • 2'-epihydroxydihydrovermistatin
  • 5'-hydroxypenisimplicissin
  • 6-demethylpenisimplicissin
  • Glycoside Hydrolase Inhibitors
  • Pyrones
  • vermistatin
  • alpha-Glucosidases