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J Med Chem ; 63(11): 5990-6002, 2020 06 11.
Article in English | MEDLINE | ID: mdl-32420736

ABSTRACT

Treatment of multidrug-resistant Gram-negative bacterial pathogens represents a critical clinical need. Here, we report a novel γ-lactam pyrazolidinone that targets penicillin-binding proteins (PBPs) and incorporates a siderophore moiety to facilitate uptake into the periplasm. The MIC values of γ-lactam YU253434, 1, are reported along with the finding that 1 is resistant to hydrolysis by all four classes of ß-lactamases. The druglike characteristics and mouse PK data are described along with the X-ray crystal structure of 1 binding to its target PBP3.


Subject(s)
Anti-Bacterial Agents/pharmacology , Drug Resistance, Multiple, Bacterial/drug effects , Lactams/chemistry , Siderophores/chemistry , Animals , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/metabolism , Anti-Bacterial Agents/pharmacokinetics , Bacterial Proteins/antagonists & inhibitors , Bacterial Proteins/metabolism , Binding Sites , Catalytic Domain , Crystallography, X-Ray , Gram-Negative Bacteria/drug effects , Half-Life , Lactams/metabolism , Lactams/pharmacokinetics , Lactams/pharmacology , Mice , Microbial Sensitivity Tests , Molecular Docking Simulation , Penicillin-Binding Proteins/antagonists & inhibitors , Penicillin-Binding Proteins/metabolism , Pseudomonas aeruginosa/metabolism , Siderophores/metabolism
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