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Bromo-cyclobutenaminones as new covalent UDP-N-acetylglucosamine enolpyruvyl transferase (MurA) inhibitors
ID Hamilton, David J. (Author), ID Ábrányi-Balogh, Péter (Author), ID Keeley, Aaron (Author), ID Petri, László (Author), ID Hrast, Martina (Author), ID Imre, Tímea (Author), ID Wijtmans, Maikel (Author), ID Gobec, Stanislav (Author), ID de Esch, Iwan J. P. (Author), ID Keserü M., György (Author)

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Abstract
Drug discovery programs against the antibacterial target UDP-N-acetylglucosamine enolpyruvyl transferase (MurA) have already resulted in covalent inhibitors having small three- and five-membered heterocyclic rings. In the current study, the reactivity of four-membered rings was carefully modulated to obtain a novel family of covalent MurA inhibitors. Screening a small library of cyclobutenone derivatives led to the identification of bromo-cyclobutenaminones as new electrophilic warheads. The electrophilic reactivity and cysteine specificity have been determined in a glutathione (GSH) and an oligopeptide assay, respectively. Investigating the structure-activity relationship for MurA suggests a crucial role for the bromine atom in the ligand. In addition, MS/MS experiments have proven the covalent labelling of MurA at Cys115 and the observed loss of the bromine atom suggests a net nucleophilic substitution as the covalent reaction. This new set of compounds might be considered as a viable chemical starting point for the discovery of new MurA inhibitors.

Language:English
Keywords:covalent inhibitor, MurA, cyclobutenaminone, antibacterial, irreversible
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FFA - Faculty of Pharmacy
Publication status:Published
Publication version:Version of Record
Year:2020
Number of pages:14 str.
Numbering:Vol. 13, iss. 11, art. 362
PID:20.500.12556/RUL-134708 This link opens in a new window
UDC:615.4:54
ISSN on article:1424-8247
DOI:10.3390/ph13110362 This link opens in a new window
COBISS.SI-ID:46907907 This link opens in a new window
Publication date in RUL:27.01.2022
Views:1309
Downloads:183
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Record is a part of a journal

Title:Pharmaceuticals
Shortened title:Pharmaceuticals
Publisher:MDPI
ISSN:1424-8247
COBISS.SI-ID:517582617 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:03.11.2020

Secondary language

Language:Slovenian
Keywords:zaviralci MurA, antibakterijske učinkovine, zdravila, farmacevtska kemija

Projects

Funder:EC - European Commission
Funding programme:H2020
Project number:675899
Name:FRAGments training NETwork
Acronym:FRAGNET

Funder:Other - Other funder or multiple funders
Project number:SNN 125496

Funder:Other - Other funder or multiple funders
Funding programme:OTKA
Project number:PD124598

Funder:Other - Other funder or multiple funders
Funding programme:OTKA
Project number:2018-2.1.11-TÉT-SI-2018-00005

Funder:ARRS - Slovenian Research Agency
Project number:P1-0208
Name:Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin

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