New 3-Acyl Tetramic Acid Derivatives from the Deep-Sea-Derived Fungus Lecanicillium fusisporum

Mar Drugs. 2022 Apr 6;20(4):255. doi: 10.3390/md20040255.

Abstract

Seven rare C3-C6 reduced 3-acyl tetramic acid derivatives, lecanicilliumins A-G (1-7), along with the known analogue cladosporiumin D (8), were obtained from the extract of the deep-sea-derived fungus Lecanicillium fusisporum GXIMD00542 within the family Clavipitacae. Their structures were elucidated by extensive spectroscopic data analysis, quantum chemistry calculations and chemical reaction. Compounds 1, 2, 5-7 exhibited moderate anti-inflammatory activity against NF-κB production using lipopolysaccharide (LPS) induced RAW264.7 cells with EC50 values range of 18.49-30.19 μM.

Keywords: Lecanicillium fusisporum; anti-inflammatory activity; clavipitacae; deep-sea fungus; tetramic acid derivatives.

MeSH terms

  • Animals
  • Hypocreales*
  • Mice
  • Molecular Structure
  • Pyrrolidinones* / chemistry
  • Pyrrolidinones* / pharmacology
  • RAW 264.7 Cells

Substances

  • Pyrrolidinones
  • tetramic acid

Supplementary concepts

  • Lecanicillium fusisporum