| Literature DB >> 30838850 |
Zhi Meng1, Mei-Lin Tang1,2, Liting Yu1, Yongxi Liang1, Jilai Han1, ChenChen Zhang1, Fupin Hu3, Jian-Ming Yu1, Xun Sun1.
Abstract
The emergence and worldwide prevalence of New Delhi metallo-β-lactamase 1 (NDM-1) expressing Gram-negative bacteria with resistance against most β-lactam antibiotics pose a serious threat to human health. However, no NDM-1 inhibitors are clinically approved at present. Herein, based on the lead compound captopril, a series of compounds were designed, synthesized, and evaluated for NDM-1 inhibitory activities. All designed compounds showed single digit micromolar or submicromolar NDM-1 inhibitory activities, which were much more potent than that of captopril. Among them, compounds 14a and 14m exhibited excellent NDM-1 inhibitory activities, with IC50 values of 0.10 and 0.12 μM, respectively. Further studies demonstrated that compound 14m displayed low cytotoxicity, good water solubility, high metabolic stability, and low acute toxicity in mice. Importantly, compound 14m exhibited potent synergistic antimicrobial activities with Meropenem (MEM) for the treatment of clinically isolated NDM-1-expressing strains.Entities:
Keywords: Gram-negative bacteria; Meropenem; NDM-1; captopril; inhibitors; inhibitory activities; resistance
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Year: 2019 PMID: 30838850 DOI: 10.1021/acsinfecdis.8b00366
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084