Cytotoxic and Cell Proliferation Activities of Isocoumarin Derivatives Isolated from <i>Phialocephala scopiformis</i> FC-1873

Phialocephala scopiformis (Ascomycota, Helotiales, Mollisiaceae) are fungi known as both saprophytes and endophytes, forming small apothecia (1 - 3 mm in diameter) on decaying wood. In this study, three novel isocoumarin derivatives (+)-phaeosphaerin A (1), (+)-phaeosphaerin B (2), and (S)-6-demethylkigelin (3) were isolated from Phialocephala scopiformis FC-1873 collected in Japan, along with two known isocoumarins, lignicol (4) and 6,8-dihydroxy-3,5-dimethyl-1H-2-benzopyran-1-one (5). The cytotoxicity of 1 and 4 were evaluated against HL-60, PANK-1, HepG2, HT-29, and T98G cell lines, as well as their effects on cell proliferation in the skin keratinocyte cell line HaCaT. These findings highlight the potential of mollisioid fungi as a source of novel bioactive compounds.

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Publication Details

Journal
Advances in Microbiology
Published
2025-01-01
DOI
https://doi.org/10.4236/aim.2025.155020
Primary Topic
Synthesis and Biological Activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Cytotoxic and Cell Proliferation Activities of Isocoumarin Derivatives Isolated from Phialocephala scopiformis FC-1873

Yuji Doi, Daigo Wakana, Hiyori Itagaki, Tomoo Hosoe et al.
Advances in Microbiology
Synthesis and Biological Activity
article

Cytotoxic and Cell Proliferation Activities of Isocoumarin Derivatives Isolated from Phialocephala scopiformis FC-1873

Yuji Doi, Daigo Wakana, Hiyori Itagaki, Tomoo Hosoe, Nobutomo Ikarashi, Tsuyoshi Hosoya, Fumiaki Sato, Hisashi Takeda, S Kitaoka, Yuji Higashira
article en

Abstract

Phialocephala scopiformis (Ascomycota, Helotiales, Mollisiaceae) are fungi known as both saprophytes and endophytes, forming small apothecia (1 - 3 mm in diameter) on decaying wood. In this study, three novel isocoumarin derivatives (+)-phaeosphaerin A (1), (+)-phaeosphaerin B (2), and (S)-6-demethylkigelin (3) were isolated from Phialocephala scopiformis FC-1873 collected in Japan, along with two known isocoumarins, lignicol (4) and 6,8-dihydroxy-3,5-dimethyl-1H-2-benzopyran-1-one (5). The cytotoxicity of 1 and 4 were evaluated against HL-60, PANK-1, HepG2, HT-29, and T98G cell lines, as well as their effects on cell proliferation in the skin keratinocyte cell line HaCaT. These findings highlight the potential of mollisioid fungi as a source of novel bioactive compounds.

Advances in MicrobiologyVol. 15(05)
Hoshi University
Zero hunger
Openalex Percentile: Top 83%
Synthesis and Biological Activity
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