Diverse Secondary Metabolites From the <i>Ligia exotica‐</i> Derived Fungus <i>Diaporthe melitensis</i> HZ‐1

One new phenolic derivative diameliresorcin (1), one new natural product N-(2'-oxopiperidin-3'-yl) picolinamide (2), one new α-pyrone derivative diameliphyone (3), and six known secondary metabolites (4-9) were isolated from the Ligia exotica-derived fungus Diaporthe melitensis HZ-1. The structures of three new compounds were identified by IR, NMR, and HR-ESI-MS, whereas their absolute configurations were validated either through single-crystal x-ray diffraction analysis or via time-dependent density functional theory (TDDFT)-electronic circular dichroism (ECD) calculations. It is noted that the absolute configuration of compound 2 was determined for the first time. Meanwhile, all the isolated compounds were evaluated for their antibacterial activities. Among them, diameliresorcin (1) exhibited weak anti-Vibrio vulnificus activity with minimum inhibitory concentration (MIC) value of 46 µg/mL.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-04-29
DOI
https://doi.org/10.1002/cbdv.202500919
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.39

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article

Diverse Secondary Metabolites From the Ligia exotica‐ Derived Fungus Diaporthe melitensis HZ‐1

Xu‐Wen Li, Ming Zhu, Zhen Gao, Yang Jin et al.
1 citations
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
1.39
article

Diverse Secondary Metabolites From the Ligia exotica‐ Derived Fungus Diaporthe melitensis HZ‐1

Xu‐Wen Li, Ming Zhu, Zhen Gao, Yang Jin, Yan Bao, Yi Hao
article en
1 citations

Abstract

One new phenolic derivative diameliresorcin (1), one new natural product N-(2'-oxopiperidin-3'-yl) picolinamide (2), one new α-pyrone derivative diameliphyone (3), and six known secondary metabolites (4-9) were isolated from the Ligia exotica-derived fungus Diaporthe melitensis HZ-1. The structures of three new compounds were identified by IR, NMR, and HR-ESI-MS, whereas their absolute configurations were validated either through single-crystal x-ray diffraction analysis or via time-dependent density functional theory (TDDFT)-electronic circular dichroism (ECD) calculations. It is noted that the absolute configuration of compound 2 was determined for the first time. Meanwhile, all the isolated compounds were evaluated for their antibacterial activities. Among them, diameliresorcin (1) exhibited weak anti-Vibrio vulnificus activity with minimum inhibitory concentration (MIC) value of 46 µg/mL.

Chemistry & BiodiversityVol. 22(9)
Chinese Academy of Sciences (CN), Shanghai Institute of Materia Medica (CN), University of Chinese Academy of Sciences (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 21%
Microbial Natural Products and Biosynthesis
1.39
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Diverse Secondary Metabolites From the <i>Ligia exotica‐</i> Derived Fungus <i>Diaporthe melitensis</i> HZ‐1 — Xu‐Wen Li, Ming Zhu, et al. · Chemistry & Biodiversity (2025) | TGRS Research Map | TGRS