Nuclear Magnetic Resonance Screening Approach for Discovery of 5‐Hydroxymethylfurfural Derivatives from Marine Fungus <i>Fusarium oxysporum</i> SP7

By tracing the characteristic proton and carbon nuclear magnetic resonance signals of the furan ring and aldehyde group, four novel 5-hydroxymethylfurfural derivatives, fusaroxysporins A-D (1-4), together with 10 known compounds were obtained from the marine fungus Fusarium oxysporum SP7. Their structures were elucidated by comprehensive spectroscopic analysis. The possible biogenic synthesis pathways of these compounds were speculated. Compound 1 showed moderate cytotoxic activity against the human type II alveolar epithelial cell A-549 and the human hepatocarcinoma cell line HepG2 with IC<sub>50</sub> values of 48.0 and 92.0 µM, respectively, while the other compounds had no activity (IC<sub>50</sub> > 200 µM).

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Journal
Chemistry & Biodiversity
Published
2025-02-20
DOI
https://doi.org/10.1002/cbdv.202500248
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Nuclear Magnetic Resonance Screening Approach for Discovery of 5‐Hydroxymethylfurfural Derivatives from Marine Fungus Fusarium oxysporum SP7

Kailei Chen, Yejing Xuan, Hou‐Jin Li, Yuhua Zhang et al.
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
article

Nuclear Magnetic Resonance Screening Approach for Discovery of 5‐Hydroxymethylfurfural Derivatives from Marine Fungus Fusarium oxysporum SP7

Kailei Chen, Yejing Xuan, Hou‐Jin Li, Yuhua Zhang, Wen-Jian Lan, Yajie Zhou
article en

Abstract

By tracing the characteristic proton and carbon nuclear magnetic resonance signals of the furan ring and aldehyde group, four novel 5-hydroxymethylfurfural derivatives, fusaroxysporins A-D (1-4), together with 10 known compounds were obtained from the marine fungus Fusarium oxysporum SP7. Their structures were elucidated by comprehensive spectroscopic analysis. The possible biogenic synthesis pathways of these compounds were speculated. Compound 1 showed moderate cytotoxic activity against the human type II alveolar epithelial cell A-549 and the human hepatocarcinoma cell line HepG2 with IC<sub>50</sub> values of 48.0 and 92.0 µM, respectively, while the other compounds had no activity (IC<sub>50</sub> > 200 µM).

Chemistry & BiodiversityVol. 22(7)
Sun Yat-sen University (CN)
Life below water
Openalex Percentile: Top 96%
Microbial Natural Products and Biosynthesis
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