Talarodride I, an Unusual Penta‐Nor‐Nonadride and Other Derivatives Characterized From the Deep‐Sea Seamount‐sourced Endozoic <i>Talaromyces scorteus</i> AS‐242

Talarodride I (1), the first representative of penta-nor-nonadride derivative having a caged bicyclo[4.3.1]deca-2,6-diene core skeleton with an aldehyde group at C-15, together with a new congener talarodride J (2) and five known secondary metabolites (3-7), were isolated and identified from the Magellan seamount-sourced sea-anemone endozoic fungus Talaromyces scorteus AS-242. Their structures were assigned by nuclear magnetic resonance and mass spectroscopic data analysis and time-dependent density functional theory electronic circular dichroism calculations. In the antibacterial assays compounds 1-5 displayed activities against a broad spectrum of human- and aquatic pathogens, with compounds 1 and 2 showing potent inhibitory effects against Escherichia coli and Aeromonas hydrophilia (minimum inhibitory concentration values 1-4 µg/mL).

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-04-07
DOI
https://doi.org/10.1002/cbdv.202500726
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Talarodride I, an Unusual Penta‐Nor‐Nonadride and Other Derivatives Characterized From the Deep‐Sea Seamount‐sourced Endozoic Talaromyces scorteus AS‐242

Ling‐Hong Meng, Ying Wang, Bin‐Gui Wang, Xiaoming Li et al.
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
article

Talarodride I, an Unusual Penta‐Nor‐Nonadride and Other Derivatives Characterized From the Deep‐Sea Seamount‐sourced Endozoic Talaromyces scorteus AS‐242

Ling‐Hong Meng, Ying Wang, Bin‐Gui Wang, Xiaoming Li, Guan‐Hai Dong
article en

Abstract

Talarodride I (1), the first representative of penta-nor-nonadride derivative having a caged bicyclo[4.3.1]deca-2,6-diene core skeleton with an aldehyde group at C-15, together with a new congener talarodride J (2) and five known secondary metabolites (3-7), were isolated and identified from the Magellan seamount-sourced sea-anemone endozoic fungus Talaromyces scorteus AS-242. Their structures were assigned by nuclear magnetic resonance and mass spectroscopic data analysis and time-dependent density functional theory electronic circular dichroism calculations. In the antibacterial assays compounds 1-5 displayed activities against a broad spectrum of human- and aquatic pathogens, with compounds 1 and 2 showing potent inhibitory effects against Escherichia coli and Aeromonas hydrophilia (minimum inhibitory concentration values 1-4 µg/mL).

Chemistry & BiodiversityVol. 22(9)
Chinese Academy of Sciences (CN), Institute of Oceanology (CN), Qingdao National Laboratory for Marine Science and Technology (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Life below water
Openalex Percentile: Top 92%
Microbial Natural Products and Biosynthesis
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