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Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
Structure-Directed Optimization of Ebselen Derivatives as Potent NDM-1 Inhibitors Reverses Meropenem Resistance
Yan Guo1, Chenyu Liu2, Wandong Liu3
1State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun 130062, China.
Abstract:
"Superbugs" harboring the New Delhi metallo-β-lactamase-1 (NDM-1) have disseminated globally, posing a severe threat to the clinical efficacy of β-lactam antibiotics. Developing NDM-1 inhibitors to restore the efficacy of β-lactam antibiotics against resistant bacteria is critically important. Using ebselen as a lead, we designed and synthesized 59 novel derivatives to develop potent NDM-1 inhibitors. Among them, compound 27k demonstrated the most potent NDM-1 inhibitory activity with an IC50 value of 1.12 μM. The combination of 27k and Mem reduced the minimum inhibitory concentration (MIC) of Mem by 4-16-fold in NDM-1-producing isolates. Importantly, the combination of 27k and Mem effectively suppressed the bacterial loads in mice. Mechanistically, 27k effectively inhibits the activity of NDM-1 by forming a Se-S covalent bond with the NDM-1 protein. Collectively, these findings confirm that compound 27k is an excellent NDM-1 covalent inhibitor, offering a promising lead compound for addressing bacterial resistance driven by NDM-1.
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