Number of the records: 1
LEGO-Lipophosphonoxins: A Novel Approach in Designing Membrane Targeting Antimicrobials
- 1.0559721 - ÚOCHB 2023 RIV US eng J - Journal Article
Do Pham, Duy Dinh - Mojr, Viktor - Helusová, M. - Mikušová, Gabriela - Pohl, Radek - Dávidová, Eva - Šanderová, Hana - Vítovská, Dragana - Bogdanová, K. - Večeřová, R. - Sedláková, M. H. - Fišer, R. - Sudzinová, Petra - Pospíšil, Jiří - Benada, Oldřich - Křížek, T. - Galandáková, A. - Kolář, M. - Krásný, Libor - Rejman, Dominik
LEGO-Lipophosphonoxins: A Novel Approach in Designing Membrane Targeting Antimicrobials.
Journal of Medicinal Chemistry. Roč. 65, č. 14 (2022), s. 10045-10078. ISSN 0022-2623. E-ISSN 1520-4804
R&D Projects: GA MZd(CZ) NV17-29680A; GA MŠMT(CZ) 8F19006; GA ČR(CZ) GA22-08857S; GA MŠMT(CZ) LX22NPO5103; GA ČR(CZ) GA22-12023S
Institutional support: RVO:61388963 ; RVO:61388971
Keywords : small molecules * antibacterial * resistant
OECD category: Microbiology; Medicinal chemistry (MBU-M)
Impact factor: 7.3, year: 2022
Method of publishing: Open access
https://doi.org/10.1021/acs.jmedchem.2c00684
The alarming rise of bacterial antibiotic resistance requires the development of new compounds. Such compounds, lipophosphonoxins (LPPOs), were previously reported to be active against numerous bacterial species, but serum albumins abolished their activity. Here we describe the synthesis and evaluation of novel antibacterial compounds termed LEGO-LPPOs, loosely based on LPPOs, consisting of a central linker module with two attached connector modules on either side. The connector modules are then decorated with polar and hydrophobic modules. We performed an extensive structure-activity relationship study by varying the length of the linker and hydrophobic modules. The best compounds were active against both Gram-negative and Gram-positive species including multiresistant strains and persisters. LEGO-LPPOs act by first depleting the membrane potential and then creating pores in the cytoplasmic membrane. Importantly, their efficacy is not affected by the presence of serum albumins. Low cytotoxicity and low propensity for resistance development demonstrate their potential for therapeutic use.
Permanent Link: https://hdl.handle.net/11104/0332930
File Download Size Commentary Version Access acs.jmedchem.2c00684.pdf 5 6.8 MB Publisher’s postprint open-access
Number of the records: 1