Cytotoxic Diketopiperazine Alkaloids and Polyketides Isolated From the Deep‐Sea Fungus <i>Subuliphorum</i> sp. SCSIO 41053

Fermentation of the deep-sea fungus Subuliphorum sp. SCSIO 41053 on rice medium yielded two novel metabolites, aspergiamide G (1) and palitantin D (6), along with 12 previously reported compounds (2-5 and 7-14). Comprehensive spectroscopic analyses, including nuclear magnetic resonance, mass spectrometry, and electronic circular dichroism, were used to establish the chemical structures and stereochemistry, which were corroborated by literature comparison. Biological evaluation revealed that compounds 4, 6, and 9 exhibited moderate cytotoxicity against the mouse melanoma cell line (B16F10), with half-maximal inhibitory concentration values of 10.07 ± 1.68, 10.93 ± 5.60, and 30.00 ± 7.33 µM, respectively. Molecular docking studies suggested that compounds 4 and 6 interact strongly with the active site of tyrosinase, a key enzyme in melanogenesis, highlighting their potential as enzyme inhibitors.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-12-20
DOI
https://doi.org/10.1002/cbdv.202503516
Primary Topic
melanin and skin pigmentation
Type
article
Field-Weighted Citation Impact
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article

Cytotoxic Diketopiperazine Alkaloids and Polyketides Isolated From the Deep‐Sea Fungus Subuliphorum sp. SCSIO 41053

Yingying Song, Jianglian She, Zhenzhou Tang, Chenghai Gao et al.
Chemistry & Biodiversity
melanin and skin pigmentation
article

Cytotoxic Diketopiperazine Alkaloids and Polyketides Isolated From the Deep‐Sea Fungus Subuliphorum sp. SCSIO 41053

Yingying Song, Jianglian She, Zhenzhou Tang, Chenghai Gao, Junfeng Wang, Kai Liu, Yonghong Liu
article en

Abstract

Fermentation of the deep-sea fungus Subuliphorum sp. SCSIO 41053 on rice medium yielded two novel metabolites, aspergiamide G (1) and palitantin D (6), along with 12 previously reported compounds (2-5 and 7-14). Comprehensive spectroscopic analyses, including nuclear magnetic resonance, mass spectrometry, and electronic circular dichroism, were used to establish the chemical structures and stereochemistry, which were corroborated by literature comparison. Biological evaluation revealed that compounds 4, 6, and 9 exhibited moderate cytotoxicity against the mouse melanoma cell line (B16F10), with half-maximal inhibitory concentration values of 10.07 ± 1.68, 10.93 ± 5.60, and 30.00 ± 7.33 µM, respectively. Molecular docking studies suggested that compounds 4 and 6 interact strongly with the active site of tyrosinase, a key enzyme in melanogenesis, highlighting their potential as enzyme inhibitors.

Chemistry & BiodiversityVol. 23(2)
Guangxi University (CN), South China Sea Institute Of Oceanology (CN), Guangxi University of Chinese Medicine (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 57%
melanin and skin pigmentation
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Cytotoxic Diketopiperazine Alkaloids and Polyketides Isolated From the Deep‐Sea Fungus <i>Subuliphorum</i> sp. SCSIO 41053 — Yingying Song, Jianglian She, et al. · Chemistry & Biodiversity (2025) | TGRS Research Map | TGRS