A derivative of trihydroxynaphthalenone and a pyrone metabolite from the endophytic fungus Talaromyces purpurpgenus

J Asian Nat Prod Res. 2024 May;26(5):555-561. doi: 10.1080/10286020.2024.2333359. Epub 2024 Apr 2.

Abstract

A newly discovered trihydroxynaphthalenone derivative, epoxynaphthalenone (1) involving the condensation of ortho-hydroxyl groups into an epoxy structure, and a novel pyrone metabolite characterized as pyroneaceacid (2), were extracted from Talaromyces purpurpgenus, an endophytic fungus residing in Rhododendron molle. The structures of these compounds were elucidated through a comprehensive analysis of their NMR and HRESIMS data. The determination of absolute configurations was accomplished using electronic circular dichroism (ECD) calculations and CD spectra. Notably, these recently identified metabolites exhibited a moderate inhibitory activity against xanthine oxidase (XOD).

Keywords: Talaromyces purpurpgenus; endophyte; structural elucidation; xanthine oxidase.

MeSH terms

  • Circular Dichroism
  • Molecular Structure
  • Naphthalenes / chemistry
  • Naphthalenes / isolation & purification
  • Naphthalenes / pharmacology
  • Nuclear Magnetic Resonance, Biomolecular
  • Pyrones* / chemistry
  • Pyrones* / isolation & purification
  • Pyrones* / pharmacology
  • Talaromyces* / chemistry
  • Xanthine Oxidase* / antagonists & inhibitors

Substances

  • Pyrones
  • Xanthine Oxidase
  • Naphthalenes