| Literature DB >> 35839126 |
Duy Dinh Do Pham1, Viktor Mojr1, Michaela Helusová2, Gabriela Mikušová1,2, Radek Pohl1, Eva Dávidová1, Hana Šanderová3, Dragana Vítovská3, Kateřina Bogdanová4, Renata Večeřová4, Miroslava Htoutou Sedláková4, Radovan Fišer2, Petra Sudzinová3, Jiří Pospíšil3, Oldřich Benada3, Tomáš Křížek5, Adéla Galandáková6, Milan Kolář4, Libor Krásný3, Dominik Rejman1.
Abstract
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.Entities:
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Year: 2022 PMID: 35839126 PMCID: PMC9580004 DOI: 10.1021/acs.jmedchem.2c00684
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 8.039