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- W4308055892 abstract "Riboswitches are 5'-untranslated mRNA regions mostly found in bacteria. They are promising drug targets to overcome emerging bacterial resistance against commonly used antibiotics. The glmS riboswitch is unique among the family of riboswitches as it is a ribozyme that undergoes self-cleavage upon binding to glucosamine-6-phosphate (GlcN6P). Previously, we showed that carba glucosamine-6-phosphate (carba-GlcN6P) induces self-cleavage of the riboswitch with a potency similar to that of GlcN6P. Here, we report a synthetic approach to a new class of carba-GlcN6P derivatives with an alkoxy substituent in the carba position. Key features of the synthesis are a ring closing metathesis followed by a hydroboration. The strategy gives access to libraries of carba-GlcN6P derivatives. Ribozyme cleavage assays unraveled new activators for the glmS riboswitch from Listeria monocytogenes and Clostridium difficile." @default.
- W4308055892 created "2022-11-07" @default.
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- W4308055892 date "2022-11-27" @default.
- W4308055892 modified "2023-10-14" @default.
- W4308055892 title "Carba‐Sugar Analogs of Glucosamine‐6‐Phosphate: New Activators for the <i>glmS</i> Riboswitch" @default.
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- W4308055892 doi "https://doi.org/10.1002/chem.202202378" @default.
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