<i>p</i>‐Terphenyl and Orsellinic Acid Derivatives from the European Polyporales <i>Terana coerulea</i> and <i>Sparassis brevipes</i>

Investigation of the secondary metabolites of the solid-state rice cultures from the European basidiomycetes Terana coerulea and Sparassis brevipes afforded three previously undescribed secondary metabolites identified as two p-terphenyl derivatives (1 and 2) and one orsellinic acid congener (3) in addition to another known, isoeverninic acid (4). Chemical structures of the isolated compounds were elucidated through comprehensive 1D and 2D NMR spectroscopic analyses, coupled with HR-MS and other spectral methods. The isolated compounds were assessed for their cytotoxic and antimicrobial activities. Compound 1 revealed weak antimicrobial properties, whereas the inseparable mixture of 3 and 4 featured moderate cytotoxic and antimicrobial effects.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2024-09-19
DOI
https://doi.org/10.1002/cbdv.202401597
Citations
2
Primary Topic
Fungal Biology and Applications
Type
article
Field-Weighted Citation Impact
0.90

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article

p‐Terphenyl and Orsellinic Acid Derivatives from the European Polyporales Terana coerulea and Sparassis brevipes

Marc Stadler, Harald Kellner, Sherif S. Ebada, Winnie Chemutai Sum
2 citations
Chemistry & Biodiversity
Fungal Biology and Applications
0.90
article

p‐Terphenyl and Orsellinic Acid Derivatives from the European Polyporales Terana coerulea and Sparassis brevipes

Marc Stadler, Harald Kellner, Sherif S. Ebada, Winnie Chemutai Sum
article en
2 citations

Abstract

Investigation of the secondary metabolites of the solid-state rice cultures from the European basidiomycetes Terana coerulea and Sparassis brevipes afforded three previously undescribed secondary metabolites identified as two p-terphenyl derivatives (1 and 2) and one orsellinic acid congener (3) in addition to another known, isoeverninic acid (4). Chemical structures of the isolated compounds were elucidated through comprehensive 1D and 2D NMR spectroscopic analyses, coupled with HR-MS and other spectral methods. The isolated compounds were assessed for their cytotoxic and antimicrobial activities. Compound 1 revealed weak antimicrobial properties, whereas the inseparable mixture of 3 and 4 featured moderate cytotoxic and antimicrobial effects.

Chemistry & BiodiversityVol. 22(1)
Ain Shams University (EG), Helmholtz Centre for Infection Research (DE), International University Institute (IHI) Zittau (DE), Technische Universität Dresden (DE), Technische Universität Braunschweig (DE)
Alexander von Humboldt-Stiftung, Deutscher Akademischer Austauschdienst
Openalex Percentile: Top 24%
Fungal Biology and Applications
0.90
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