The Development of New Small-molecule Inhibitors Targeting Bacterial Metallo-β-lactamases

被引:7
作者
Wang, Ping [1 ,2 ]
Cheng, Jing [1 ,2 ]
Liu, Cong-Cong [1 ,2 ]
Tang, Kai [1 ,2 ]
Xu, Feng [1 ,2 ]
Yu, Zhiqiang [3 ]
Yu, Bin [1 ,2 ,3 ,4 ]
Chang, Junbiao [1 ,4 ]
机构
[1] Coinnovat Ctr Henan Prov New Drug R&D & Preclin S, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Henan, Peoples R China
[3] Guangdong Prov Key Lab New Drug Screening, Guangzhou 510033, Guangdong, Peoples R China
[4] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Henan, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Metallo-beta-lactamases; thiol derivatives; dicarboxylic acid derivatives; cyclic Boronates; triazoles; natural products; peptide inhibitors; BROAD-SPECTRUM INHIBITORS; POTENT INHIBITORS; ACID-DERIVATIVES; IN-VITRO; BIOLOGICAL EVALUATION; CAPTOPRIL ANALOGS; STRUCTURAL BASIS; NDM-1; SCAFFOLD; ASPERGILLOMARASMINE;
D O I
10.2174/1568026618666180518101028
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Metallo-beta-lactamases (MBLs) are a family of Zn(II)-dependent enzymes that can hydrolyze almost all beta-lactam antibiotics. Horizontal transfer of the genes encoding MBLs among Gram-negative bacteria pathogens has led to the emergence of extensively drug-resistant pathogens, which now represent a major threat to human health. As there is not to date yet a clinically available MBL inhibitor, the discovery of new MBL inhibitors has great urgency. This review highlights the recent developments in the discovery of small-molecule MBL inhibitors.
引用
收藏
页码:834 / 843
页数:10
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