Evidence map›Paper›PMID 41629543›Full record

ArticleNatural products and bioprospecting2026

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

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

Abstract read
In one paragraph

Article in Natural products and bioprospecting, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jie-Chun ZengKey Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming, 650031, Yunnan, People's Republic of China.
Xu-Ping ZhangKey Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming, 650031, Yunnan, People's Republic of China.
Lu GaoKey Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming, 650031, Yunnan, People's Republic of China.
Qian-Qian YinKey Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming, 650031, Yunnan, People's Republic of China. yinqianpharm@163.com.
Wei-Guang WangKey Laboratory of Chemistry in Ethnic Medicinal Resources of Ministry of Education, Yunnan Minzu University, Kunming, 650031, Yunnan, People's Republic of China. wwg@live.cn.ORCID http://orcid.org/0000-0003-3395-767X

Funding

National Natural Science Foundation of China 22377105National Natural Science Foundation of China 82160670Natural Science Foundation of Yunnan Province 202401AV070003Yunnan Provincial Department of Education Science Research Fund Project 2025J0492Yunnan Provincial Science and Technology Talent and Platform Program 202505AF350066
6 · The paper itself

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

Indexed as

Deubiquitinating enzymesDiaporthe sp.PolyketidesUSP4α-pyroneγ-butenolide

Identifiers

PMID41629543
PMCPMC12864556

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.