ebselen and meropenem

ebselen has been researched along with meropenem in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Chan, EWC; Chan, KF; Chan, TH; Chen, S; Cheng, Q; Gao, W; Jin, WB; Leung, YC; Qi, XL; Wong, KY; Xu, C; Zheng, Z1
Bai, W; Cheng, K; Gao, Y; Guo, H; He, W; Li, C; Li, Z; Wu, C1
Chan, EW; Chan, KF; Chan, TH; Chen, S; Chiou, J; He, D; So, PK; Tao, J; Wan, S; Wong, KY1

Other Studies

3 other study(ies) available for ebselen and meropenem

ArticleYear
Investigation of synergistic antimicrobial effects of the drug combinations of meropenem and 1,2-benzisoselenazol-3(2H)-one derivatives on carbapenem-resistant Enterobacteriaceae producing NDM-1.
    European journal of medicinal chemistry, 2018, Jul-15, Volume: 155

    Topics: Anti-Bacterial Agents; beta-Lactamases; Carbapenem-Resistant Enterobacteriaceae; Cell Line, Tumor; Cell Survival; Dose-Response Relationship, Drug; HeLa Cells; Humans; Meropenem; Molecular Structure; Organoselenium Compounds; Structure-Activity Relationship; Thienamycins

2018
A novel potent metal-binding NDM-1 inhibitor was identified by fragment virtual, SPR and NMR screening.
    Bioorganic & medicinal chemistry, 2020, 05-01, Volume: 28, Issue:9

    Topics: Anti-Bacterial Agents; beta-Lactamases; Coordination Complexes; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Enzyme Inhibitors; Klebsiella pneumoniae; Magnetic Resonance Spectroscopy; Microbial Sensitivity Tests; Molecular Structure; Structure-Activity Relationship; Surface Plasmon Resonance; Zinc

2020
Ebselen as a potent covalent inhibitor of New Delhi metallo-β-lactamase (NDM-1).
    Chemical communications (Cambridge, England), 2015, Jun-11, Volume: 51, Issue:46

    Topics: Ampicillin; Anti-Bacterial Agents; Azoles; beta-Lactamase Inhibitors; beta-Lactamases; Escherichia coli; Isoindoles; Meropenem; Microbial Sensitivity Tests; Organoselenium Compounds; Thienamycins

2015