2026-04-13T03:03:52Zhttps://recercat.cat/oai/request

oai:recercat.cat:10230/709302025-07-17T17:46:34Zcom_2072_6col_2072_452952

00925njm 22002777a 4500 dc Nowicki, Krzysztof author Krajewska, Joanna author Stepniewski, Tomasz Maciej, 1988- author Wielechowska, Monika author Wińska, Patrycja author Kaczmarczyk, Anna author Korpowska, Julia author Selent, Jana author Marek-Urban, Paulina H. author Durka, Krzysztof author Woźniak, Krzysztof author Laudy, Agnieszka E. author Luliński, Sergiusz author 2025-07-16T07:34:22Z 2025-07-16T07:34:22Z 2024 Benzosiloxaboroles are an emerging class of medicinal agents possessing promising antimicrobial activity. Herein, the expedient synthesis of two novel thiol-functionalized benzosiloxaboroles 1e and 2e is reported. The presence of the SH group allowed for diverse structural modifications involving the thiol-Michael addition, oxidation, as well as nucleophilic substitution giving rise to a series of 27 new benzosiloxaboroles containing various polar functional groups, e.g., carbonyl, ester, amide, imide, nitrile, sulfonyl and sulfonamide, and pendant heterocyclic rings. The activity of the obtained compounds against selected bacterial and yeast strains, including multidrug-resistant clinical strains, was investigated. Compounds 6, 12, 20 and 22-24 show high activity against Staphylococcus aureus, including both methicillin-sensitive (MSSA) and methicillin-resistant (MRSA) strains, with MIC values in the range of 1.56-12.5 μg mL-1, while their cytotoxicity is relatively low. The in vitro assay performed with 2-(phenylsulfonyl)ethylthio derivative 20 revealed that, in contrast to the majority of known antibacterial oxaboroles, the plausible mechanism of antibacterial action, involving inhibition of the leucyl-tRNA synthetase enzyme, is not responsible for the antibacterial activity. Structural bioinformatic analysis involving molecular dynamics simulations provided a possible explanation for this finding. This research was financially supported by National Science Centre (Poland) in the framework of the project UMO-2018/31/B/ST5/00210. Work implemented as a part of Operational Project Knowledge Education Development 2014–2020 co-financed by the European Social Fund (the TRIBIOCHEM interdisciplinary PhD Program for P. H. M.-U.). The computational part of the work has been performed under the Project HPC-EUROPA3 (INFRAIA-2016-1-730897), with the support of the EC Research Innovation Action under the H2020 Program; in particular, the authors gratefully acknowledge the support of Hospital del Mar Medical Research Institute (IMIM), Pompeu Fabra University and the computer resources and technical support provided by Barcelona Supercomputing Center (BSC). The work was supported by the Warsaw University of Technology. http://hdl.handle.net/10230/70930 Química clínica Exploiting thiol-functionalized benzosiloxaboroles for achieving diverse substitution patterns - synthesis, characterization and biological evaluation of promising antibacterial agents