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• W4291281067 endingPage "106087" @default.
• W4291281067 startingPage "106087" @default.
• W4291281067 abstract "Novel bacterial topoisomerase inhibitors (NBTIs) are an important new class of antibacterials targeting bacterial type II topoisomerases (DNA gyrase and topoisomerase IV). Notwithstanding their potent antibacterial activity, they suffer from a detrimental class-related hERG blockage. In this study, we designed and synthesized an optimized library of NBTIs comprising different linker moieties that exhibit reduced hERG inhibition and retain inhibitory potencies on DNA gyrase and topoisomerase IV of Staphylococcus aureus and Escherichia coli, respectively, as well as potent antibacterial activities. Substitution of the linker's tertiary amine with polar groups outcome in diminished hERG inhibition. Compound 17 expresses nanomolar enzyme inhibitory potency and antibacterial activity against both Gram-positive and Gram-negative bacteria as well as reduced hERG inhibition relative to our previously published NBTI analogs. Here, we point to some important NBTI's structural features that influence their hERG inhibitory activity." @default.
• W4291281067 created "2022-08-14" @default.
• W4291281067 creator A5009319775 @default.
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• W4291281067 date "2022-11-01" @default.
• W4291281067 modified "2023-10-18" @default.
• W4291281067 title "Diminishing hERG inhibitory activity of aminopiperidine-naphthyridine linked NBTI antibacterials by structural and physicochemical optimizations" @default.
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• W4291281067 doi "https://doi.org/10.1016/j.bioorg.2022.106087" @default.
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