# Eight new α-pyrone and γ-butenolide derivatives from the plant endophytic fungus Diaporthe sp. CCY4

**Authors:** Jie-Chun Zeng, Xu-Ping Zhang, Lu Gao, Qian-Qian Yin, Wei-Guang Wang

PMC · DOI: 10.1007/s13659-025-00580-1 · Natural Products and Bioprospecting · 2026-02-03

## TL;DR

Researchers discovered eight new chemical compounds from a plant fungus and found some inhibit a key enzyme involved in protein regulation.

## Contribution

The paper reports the isolation and characterization of eight new α-pyrone and γ-butenolide derivatives from an endophytic fungus.

## Key findings

- Eight new compounds were isolated and structurally identified using advanced spectroscopic methods.
- Four compounds showed significant anti-ubiquitination activity against USP4, with one being particularly potent.
- The study highlights the potential of fungal metabolites as sources of bioactive compounds.

## Abstract

Five new α-pyrones, diaporpyrones G-K (1–5) and three new γ-butenolide derivatives, porbutenolides A-C (6–8), along with seven known compounds (9–15), were isolated from the culture extract of the endophytic fungus Diaporthe sp. CCY4. Their structures were elucidated by comprehensive spectroscopic analysis, including 1D/2D NMR and HRESIMS data. The absolute configurations of 7 and 8 were assigned using electronic circular dichroism (ECD) calculations. All compounds were evaluated for inhibitory activity against ubiquitin-specific peptidase 4 (USP4). Compounds 2, 5, 9, and 13 exhibited significant anti-ubiquitination effects at 40 μM, with 13 showing the most potent inhibition (IC50 = 20.85 μM).

The online version contains supplementary material available at 10.1007/s13659-025-00580-1.

## Linked entities

- **Proteins:** USP4 (ubiquitin specific peptidase 4)

## Full-text entities

- **Genes:** USP4 (ubiquitin specific peptidase 4) [NCBI Gene 7375] {aka UNP, Unph}
- **Diseases:** neurodegenerative diseases (MESH:D019636), cytotoxicity (MESH:D064420), cancer (MESH:D009369), metastasis (MESH:D009362)
- **Chemicals:** C-6 (MESH:C117224), methanol (MESH:D000432), vialinin A (MESH:C508745), polyketide (MESH:D061065), lovastatin (MESH:D008148), 13C (MESH:C000615229), Na (MESH:D012964), naphthoquinone (MESH:D009285), CH3CN (MESH:C032159), epoxide (MESH:D004852), H2-12 (-), chromene (MESH:D001578), alternariol (MESH:C005197), 3H (MESH:D014316), silica gel (MESH:D058428), acetone (MESH:D000096), DMSO (MESH:D004121), CaCl2 (MESH:D002122), pyrone (MESH:D011753), H-7 (MESH:D019307), penicillin (MESH:D010406), CH2Cl2 (MESH:D008752), C (MESH:D002244), C2 (MESH:C023714), H2O (MESH:D014867), B2 (MESH:C023970), TMS (MESH:C073196), oil (MESH:D009821), H (MESH:D006859), ethyl acetate (MESH:C007650), hexane (MESH:D006586), agar (MESH:D000362), PR-619 (MESH:C570894), alternariol 9-methylether (MESH:C018206)
- **Species:** Camellia japonica (common camellia, species) [taxon 4443], Thelephora vialis (species) [taxon 139392], Diaporthe sp. (species) [taxon 1756133]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12864556/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12864556/full.md

---
Source: https://tomesphere.com/paper/PMC12864556