Penifuranone A: A Novel Alkaloid from the Mangrove Endophytic Fungus Penicillium crustosum SCNU-F0006

Int J Mol Sci. 2024 May 5;25(9):5032. doi: 10.3390/ijms25095032.

Abstract

One previously undescribed alkaloid, named penifuranone A (1), and three known compounds (2-4) were isolated from the mangrove endophytic fungus Penicillium crustosum SCNU-F0006. The structure of the new alkaloid (1) was elucidated based on extensive spectroscopic data analysis and single-crystal X-ray diffraction analysis. Four natural isolates and one new synthetic derivative of penifuranone A, compound 1a, were screened for their antimicrobial, antioxidant, and anti-inflammatory activities. Bioassays revealed that penifuranone A (1) exhibited strong anti-inflammatory activity in vitro by inhibiting nitric oxide (NO) production in lipopolysaccharide-activated RAW264.7 cells with an IC50 value of 42.2 μM. The docking study revealed that compound 1 exhibited an ideal fit within the active site of the murine inducible nitric oxide synthase (iNOS), establishing characteristic hydrogen bonds.

Keywords: alkaloid; anti-inflammatory activity; antimicrobial activity; mangrove fungus.

MeSH terms

  • Alkaloids* / chemistry
  • Alkaloids* / isolation & purification
  • Alkaloids* / pharmacology
  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology
  • Antioxidants / chemistry
  • Antioxidants / pharmacology
  • Lipopolysaccharides
  • Mice
  • Molecular Docking Simulation
  • Molecular Structure
  • Nitric Oxide Synthase Type II / metabolism
  • Nitric Oxide* / metabolism
  • Penicillium* / chemistry
  • Penicillium* / metabolism
  • RAW 264.7 Cells

Substances

  • Alkaloids
  • Nitric Oxide
  • Anti-Inflammatory Agents
  • Nitric Oxide Synthase Type II
  • Lipopolysaccharides
  • Antioxidants