Evidence map›Paper›PMID 42741900›Full record

ArticleChemistry & biodiversity2026

New γ-Unsaturated Lactone and Aliphatic Acid From the Deep-Sea-Derived Fungus Penicillium crustosum HDN17-68.

Naritsara Yusawat, Wenxue Wang, Xiaonan Deng, Hengyi Xu, Chuanteng Ma, Dehai Li, Wanwimol Klaypradit, Juta Mookdasanit, Guojian Zhang

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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5 · Who and what money

Authors and funding

9 authors.

Naritsara YusawatKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.ORCID https://orcid.org/0009-0000-6132-8622
Wenxue WangKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.ORCID https://orcid.org/0000-0002-3469-1765
Xiaonan DengKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.
Hengyi XuKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.ORCID https://orcid.org/0009-0003-2176-195X
Chuanteng MaKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.
Dehai LiKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.ORCID https://orcid.org/0000-0002-7191-2002
Wanwimol KlaypraditDepartment of Fishery Products, Faculty of Fisheries, Kasetsart University, Bangkok, Thailand.
Juta MookdasanitDepartment of Fishery Products, Faculty of Fisheries, Kasetsart University, Bangkok, Thailand.
Guojian ZhangKey Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.ORCID https://orcid.org/0000-0002-4976-8083

Funding

Kasetsart University-Ocean University of China (KU-OUC) Dual Degree ProgramMajor Basic Research Programs of Natural Science Foundation of Shandong Province ZR2023ZD29National Natural Science Foundation of China 32370061National Natural Science Foundation of China 325B2002Taishan Scholar Youth Expert Program in Shandong Province tsqn 202103153
6 · The paper itself

Abstract

Marine fungal natural products are valuable sources of structurally diverse and biologically active compounds with potential applications in drug discovery and biotechnology. The fungus Penicillium crustosum is an important source of bioactive natural products that display significant antibacterial properties. This study describes the isolation and characterization of two new structures including one γ-unsaturated lactone named crustosulin A and one aliphatic acid named crustosenoic acid A along with ten known compounds from a marine-derived fungus Penicillium crustosum HDN17-68, which is isolated from the Western Pacific deep-sea mud sample. Compounds were isolated and purified through column chromatography and HPLC, and structures were elucidated using spectroscopic tools including NMR, MS, and ECD. Compound 1 represents the first example of a dimeric γ-unsaturated butyrolactone incorporating a β-to-α connectivity and it exhibited weak activity against Salmonella enterica and methicillin-resistant Staphylococcus aureus (MRSA), with MIC values of 32 and 64 µg/mL, respectively. These findings expand the chemical diversity of secondary metabolites from deep-sea-derived Penicillium fungi.

Indexed as

Anti-Bacterial AgentsFatty AcidsLactonesPenicilliumMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMolecular StructureAnti-Bacterial AgentsFatty AcidsLactonesantimicrobialfungal metabolitemarine‐derived fungusOSMAC strategystructure elucidationunsaturated lactone

Identifiers

PMID42741900
PMCPMC13575841

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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.