# Two New Pentadepsipeptides from the Mangrove Fungus Aspergillus sp. SCSIO 41443

**Authors:** Ying Liu, Yi Chen, Jiao Xiao, Xin Sun, Xuefeng Zhou, Yonghong Liu, Bin Yang

PMC · DOI: 10.3390/metabo16030159 · 2026-02-27

## TL;DR

This paper reports the discovery of two new natural compounds from a mangrove fungus, which could have potential applications in drug development.

## Contribution

The study identifies two new pentadepsipeptides, aspertides F and G, from a mangrove fungus.

## Key findings

- Two new compounds, aspertides F and G, were isolated and structurally characterized.
- The compounds showed weak activity against acetylcholinesterase and neuraminidase.
- The research expanded the known chemical diversity of the mangrove fungus Aspergillus sp. SCSIO 41443.

## Abstract

Background: Mangrove fungi are a prolific source of structurally diverse natural products. Among these, natural peptides with varied biological activities hold high commercial value and have been successfully developed into drugs for treating numerous diseases. Methods: Following rice solid-state fermentation of the strain, extracellular metabolites were extracted from the culture filtrate to obtain a crude extract. Cyclic depsipeptides were isolated from the crude extract by silica gel vacuum liquid chromatography for preliminary fractionation and enrichment, followed by high-performance liquid chromatography (HPLC) purification. The structures of the compounds were determined based on extensive spectroscopic analysis (1D and 2D NMR, ESI-MS-MS analysis) and Marfey’s method for amino acid configuration assignment. Results: Ultimately, two new compounds, aspertides F (1) and G (2), and three known compounds, aspertides C, D, and A (3−5), were identified. The bioassays indicated that these compounds exhibited weak activity against acetylcholinesterase and neuraminidase. Conclusions: The research findings on this strain have not only enriched the metabolic resource library of mangrove fungi but also highlighted their diverse biological activities and significant application potential.

## Full-text entities

- **Diseases:** Alzheimer's disease (MESH:D000544), influenza (MESH:D007251), inflammatory (MESH:D007249), injury to (MESH:D014947), cytotoxic (MESH:D064420)
- **Chemicals:** ester (MESH:D004952), Na (MESH:D012964), CH3CN (MESH:C032159), DMSO (MESH:D004121), DCM (MESH:D008752), peptides (MESH:D010455), CH3OH (MESH:D000432), salt (MESH:D012492), Amino Acid (MESH:D000596), ethyl acetate (MESH:C007650), Fr (MESH:D005605), PBS (MESH:D007854), HCl (MESH:D006851), alkaloids (MESH:D000470), NaHCO3 (MESH:D017693), PE (MESH:C004544), olefin (MESH:D000475), silica (MESH:D012822), H2O (MESH:D014867), formic acid (MESH:C030544), silica gel (MESH:D058428), butenolides (MESH:C004511), nitrogen (MESH:D009584), Tyr (MESH:D014443), tetramethylsilane (MESH:C073196), cyclic peptides (MESH:D010456), H-7 (MESH:D019307), lH (MESH:D007986), 5,5'-Dithio bis-(2-nitrobenzoic acid) (MESH:D004228), H (MESH:D006859), Marfey's reagent (MESH:C047134), Aspertide G (-), terpenes (MESH:D013729), tacrine (MESH:D013619), carbon (MESH:D002244), acetylthiocholine iodide (MESH:C543539), acetone (MESH:D000096), 13C (MESH:C000615229), polyketides (MESH:D061065), brevianamide S (MESH:C577119), depsipeptide (MESH:D047630), amide (MESH:D000577)
- **Species:** Aspergillus tamarii (species) [taxon 41984], Aspergillus sp. (species) [taxon 5065], Aspergillus versicolor (species) [taxon 46472], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Eurotium sp. (species) [taxon 1859957], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Pro3-Ala

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027552/full.md

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Source: https://tomesphere.com/paper/PMC13027552