Antifungal profile against Candida auris clinical isolates of tyroscherin and its new analog produced by the deep-sea-derived fungal strain Scedosporium apiospermum FKJ-0499

J Antibiot (Tokyo). 2024 Mar;77(3):156-162. doi: 10.1038/s41429-023-00696-x. Epub 2024 Jan 11.

Abstract

A new antifungal compound, named N-demethyltyroscherin (1), was discovered from the static fungal cultured material of Scedosporium apiospermum FKJ-0499 isolated from a deep-sea sediment sample together with a known compound, tyroscherin (2). The structure of 1 was elucidated as a new analog of 2 by MS and NMR analyses. The absolute configuration of 1 was determined by chemical derivatization. Both compounds showed potent in vitro antifungal activity against clinically isolated Candida auris strains, with MIC values ranging from 0.0625 to 4 µg ml-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents* / pharmacology
  • Antifungal Agents* / therapeutic use
  • Candida auris
  • Epinephrine / analogs & derivatives*
  • Fatty Alcohols*
  • Fungi
  • Microbial Sensitivity Tests
  • Scedosporium*

Substances

  • Antifungal Agents
  • tyroscherin
  • Epinephrine
  • Fatty Alcohols