Molecular Networking-Driven Discovery of Antifungal Azaphilone Dimers from the Marine-Derived Fungus <i>Humicola</i> sp. HK1-8

A novel azaphilone dimer, humilone A (<b>1</b>), along with its related monomer, humilone B (<b>2</b>), was isolated from cultures of the marine-derived fungus <i>Humicola</i> sp. HK1-8 using a molecular networking-guided discovery approach. Further investigation of the molecular family of azaphilone dimers led to the putative identification of four analogues, humilones C-F (<b>3</b>-<b>6</b>), based on systematic analysis of their characteristic MS/MS fragmentation patterns. Detailed fragmentation studies of the dimers revealed that the predominant cleavage fragments originated from C-C bond scission at the dimeric methylene bridge. Compound <b>1</b> displayed antifungal activity against <i>Rhizoctonia solani</i>.

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Publication Details

Journal
Journal of Natural Products
Published
2025-06-16
DOI
https://doi.org/10.1021/acs.jnatprod.5c00531
Citations
3
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
4.18

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article

Molecular Networking-Driven Discovery of Antifungal Azaphilone Dimers from the Marine-Derived Fungus Humicola sp. HK1-8

Li Shen, Xia-Hao Zhu, Zhonghui Li, Chang‐Yun Wang et al.
3 citations
Journal of Natural Products
Microbial Natural Products and Biosynthesis
4.18
article

Molecular Networking-Driven Discovery of Antifungal Azaphilone Dimers from the Marine-Derived Fungus Humicola sp. HK1-8

Li Shen, Xia-Hao Zhu, Zhonghui Li, Chang‐Yun Wang, Likui Zhang, Long Chen, Min Chen, Sheng Wang, Tong Wu
article en
3 citations

Abstract

A novel azaphilone dimer, humilone A (<b>1</b>), along with its related monomer, humilone B (<b>2</b>), was isolated from cultures of the marine-derived fungus <i>Humicola</i> sp. HK1-8 using a molecular networking-guided discovery approach. Further investigation of the molecular family of azaphilone dimers led to the putative identification of four analogues, humilones C-F (<b>3</b>-<b>6</b>), based on systematic analysis of their characteristic MS/MS fragmentation patterns. Detailed fragmentation studies of the dimers revealed that the predominant cleavage fragments originated from C-C bond scission at the dimeric methylene bridge. Compound <b>1</b> displayed antifungal activity against <i>Rhizoctonia solani</i>.

Journal of Natural ProductsVol. 88(6)
Ministry of Education of the People's Republic of China (CN), Wuhan Engineering Science & Technology Institute (CN), Ministry of Agriculture and Rural Affairs (CN), Ocean University of China (CN), Yangzhou University (CN), College of Marin (US)
National Key Research and Development Program of China, National Natural Science Foundation of China - State Grid Corporation Joint Fund for Smart Grid
Life below water
Openalex Percentile: Top 6%
Microbial Natural Products and Biosynthesis
4.18
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