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15 janv. 2023
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Synthesis and structure-activity relationship studies of original cyclic diadenosine derivatives as nanomolar inhibitors of NAD kinase from pathogenic bacteria.
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Structure-based design, synthesis and biological evaluation of a NAD+ analogue targeting Pseudomonas aeruginosa NAD kinase.
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From Substrate to Fragments to Inhibitor Active In Vivo against Staphylococcus aureus.
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