Exploiting thiol-functionalized benzosiloxaboroles for achieving diverse substitution patterns - synthesis, characterization and biological evaluation of promising antibacterial agents

Nowicki, Krzysztof; Krajewska, Joanna; Stepniewski, Tomasz Maciej, 1988-; Wielechowska, Monika; Wińska, Patrycja; Kaczmarczyk, Anna; Korpowska, Julia; Selent, Jana; Marek-Urban, Paulina H.; Durka, Krzysztof; Woźniak, Krzysztof; Laudy, Agnieszka E.; Luliński, Sergiusz

Exploiting thiol-functionalized benzosiloxaboroles for achieving diverse substitution patterns - synthesis, characterization and biological evaluation of promising antibacterial agents

Mostra el registre complet Registre parcial de l'ítem

dc.contributor.author Nowicki, Krzysztof
dc.contributor.author Krajewska, Joanna
dc.contributor.author Stepniewski, Tomasz Maciej, 1988-
dc.contributor.author Wielechowska, Monika
dc.contributor.author Wińska, Patrycja
dc.contributor.author Kaczmarczyk, Anna
dc.contributor.author Korpowska, Julia
dc.contributor.author Selent, Jana
dc.contributor.author Marek-Urban, Paulina H.
dc.contributor.author Durka, Krzysztof
dc.contributor.author Woźniak, Krzysztof
dc.contributor.author Laudy, Agnieszka E.
dc.contributor.author Luliński, Sergiusz
dc.date.accessioned 2025-07-16T07:34:22Z
dc.date.available 2025-07-16T07:34:22Z
dc.date.issued 2024
dc.description.abstract 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.
dc.description.sponsorship 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.
dc.format.mimetype application/pdf
dc.identifier.citation Nowicki K, Krajewska J, Stępniewski TM, Wielechowska M, Wińska P, Kaczmarczyk A, et al. Exploiting thiol-functionalized benzosiloxaboroles for achieving diverse substitution patterns - synthesis, characterization and biological evaluation of promising antibacterial agents. RSC Med Chem. 2024 Mar 20;15(5):1751-72. DOI: 10.1039/d4md00061g
dc.identifier.doi http://dx.doi.org/10.1039/d4md00061g
dc.identifier.issn 2632-8682
dc.identifier.uri http://hdl.handle.net/10230/70930
dc.language.iso eng
dc.publisher Royal Society of Chemistry
dc.relation.ispartof RSC Med Chem. 2024 Mar 20;15(5):1751-72
dc.relation.projectID info:eu-repo/grantAgreement/EC/H2020/730897
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.rights.uri http://creativecommons.org/licenses/by/3.0/
dc.subject.other Química clínica
dc.title Exploiting thiol-functionalized benzosiloxaboroles for achieving diverse substitution patterns - synthesis, characterization and biological evaluation of promising antibacterial agents
dc.type info:eu-repo/semantics/article
dc.type.version info:eu-repo/semantics/publishedVersion

Col·leccions

Articles (Hospital del Mar Research Institute)
Documents OpenAIRE (Open Access Infrastructure for Research in Europe)