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

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 (IC<sub>50</sub> = 20.85 μM).

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Publication Details

Journal
Natural Products and Bioprospecting
Published
2026-02-03
DOI
https://doi.org/10.1007/s13659-025-00580-1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Jie-Chun Zeng, Wei‐Guang Wang, Xuping Zhang, Lu Gao et al.
Natural Products and Bioprospecting
Microbial Natural Products and Biosynthesis
article

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

Jie-Chun Zeng, Wei‐Guang Wang, Xuping Zhang, Lu Gao, Qian-Qian Yin
article en

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 (IC<sub>50</sub> = 20.85 μM).

Natural Products and BioprospectingVol. 16(1)
Minzu University of China (CN), Yunnan University (CN), State Ethnic Affairs Commission (CN)
National Natural Science Foundation of China, Natural Science Foundation of Yunnan Province, Yunnan Provincial Department of Education, Yunnan Provincial Department of Education Science Research Fund Project
Openalex Percentile: Top 69%
Microbial Natural Products and Biosynthesis
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