Cyclo(dehydroala-L-Leu), an alpha-glucosidase inhibitor from Penicillium sp. F70614

J Antibiot (Tokyo). 2000 Sep;53(9):954-8. doi: 10.7164/antibiotics.53.954.

Abstract

A diketopiperazine (1) has been isolated from the culture broth of Penicillium sp. F70614 and its structure has been determined to be cyclo(dehydroala-L-Leu) by various spectroscopic analyses. This compound selectively inhibited yeast alpha-glucosidase and porcine intestinal alpha-glucosidase with IC50 values of 35 and 50 microg/ml, respectively. However, it did not show significant inhibitory effects against almond beta3-glucosidase, Aspergillus alpha-galactosidase, Escherichia coli beta-galactosidase and jack bean alpha-mannosidase.

MeSH terms

  • Binding, Competitive
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / isolation & purification
  • Enzyme Inhibitors / pharmacology*
  • Fermentation
  • Glycoside Hydrolase Inhibitors*
  • Inhibitory Concentration 50
  • Penicillium / chemistry*
  • Penicillium / metabolism
  • Peptides, Cyclic / chemistry
  • Peptides, Cyclic / isolation & purification
  • Peptides, Cyclic / pharmacology*
  • Piperazines / chemistry
  • Piperazines / isolation & purification
  • Piperazines / pharmacology*
  • alpha-Glucosidases / metabolism

Substances

  • Cyclo(dehydroala-Leu)
  • Enzyme Inhibitors
  • Glycoside Hydrolase Inhibitors
  • Peptides, Cyclic
  • Piperazines
  • alpha-Glucosidases