Total synthesis of a sorrentanone ester library and evaluation of its antimicrobial potential

Sorrentanone belongs to the class of monomeric sorbicillinoids and displays bioactivities against various Gram-positive bacteria including Bacillus subtilis, Enterococcus faecalis, and Streptococcus as well as Staphylococcus species. Within this work, we present the optimization of the synthetic access towards the sorrentanone scaffold, facilitating the formation of a focused library of structural analogs with ester side chains. Exploration of the bioactivities of this compound library displayed the improvement of antibacterial properties and the presence of additional antifungal activities. Initial mode of action analyses showed the influence of the compounds on fungal filament propagation and biofilm production. Overall, this work reveals the pharmaceutical relevance of less studied monomeric sorbicillinoids.

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Journal
Scientific Reports
Published
2025-07-04
DOI
https://doi.org/10.1038/s41598-025-05360-y
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Total synthesis of a sorrentanone ester library and evaluation of its antimicrobial potential

Tobias M. Milzarek, Tobias A. M. Gulder, Jasmina Nikodinović‐Runić, Sandra Vojnović et al.
Scientific Reports
Microbial Natural Products and Biosynthesis
article

Total synthesis of a sorrentanone ester library and evaluation of its antimicrobial potential

Tobias M. Milzarek, Tobias A. M. Gulder, Jasmina Nikodinović‐Runić, Sandra Vojnović, Dušan Milivojević, Sanja Škaro Bogojević, Finn H Gattwinkel
article en

Abstract

Sorrentanone belongs to the class of monomeric sorbicillinoids and displays bioactivities against various Gram-positive bacteria including Bacillus subtilis, Enterococcus faecalis, and Streptococcus as well as Staphylococcus species. Within this work, we present the optimization of the synthetic access towards the sorrentanone scaffold, facilitating the formation of a focused library of structural analogs with ester side chains. Exploration of the bioactivities of this compound library displayed the improvement of antibacterial properties and the presence of additional antifungal activities. Initial mode of action analyses showed the influence of the compounds on fungal filament propagation and biofilm production. Overall, this work reveals the pharmaceutical relevance of less studied monomeric sorbicillinoids.

Scientific ReportsVol. 15(1)
University of Belgrade (RS), Institute of Molecular Genetics (RU), Helmholtz Institute for Pharmaceutical Research Saarland (DE), Technische Universität Berlin (DE), Technische Universität Dresden (DE)
Deutsche Forschungsgemeinschaft, Technische Universität Dresden
Openalex Percentile: Top 81%
Microbial Natural Products and Biosynthesis
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Total synthesis of a sorrentanone ester library and evaluation of its antimicrobial potential — Tobias M. Milzarek, Tobias A. M. Gulder, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS