舒巴坦钠
抗生素
β-内酰胺酶抑制剂
克拉维酸
他唑巴坦
可药性
广谱
微生物学
抗生素耐药性
医学
生物
化学
亚胺培南
阿莫西林
生物化学
组合化学
基因
作者
Jiao Chen,Xianwen Shang,Feng Hu,Xingzhen Lao,Xiangdong Gao,Heng Zheng,Wenbing Yao
出处
期刊:Mini-reviews in Medicinal Chemistry
[Bentham Science]
日期:2013-10-01
卷期号:13 (13): 1846-1861
被引量:40
标识
DOI:10.2174/13895575113139990074
摘要
β-lactamase-mediated resistance to β-lactam antibiotics is an increasing threat to clinical antimicrobial chemotherapy. The combinations of β-lactam antibiotics and β-lactamase inhibitors (such as sulbactam, tazobactam and clavulanic acid) have been successfully used for overcoming class A β-lactamase-mediated resistance. However, none of the inhibitors effective against class B, C or D β-lactamases are available in the clinic, which alarms an urgent need to discover/design broad-spectrum β-lactamase inhibitors or new β-lactam antibiotics capable of evading bacterial enzymatic inactivation. In recent years, inhibitors targeted to serine β-lactamases have been developed rapidly with a few of them under clinical trials. In contrast, none promising class B β-lactamase (metallo-β-lactamase) inhibitors with good druggability have been discovered, despite the increasing number of active molecules reported. In this review, we summarized the potential β-lactamase inhibitors reported in recent years and updated the current status of β-lactamase inhibitor discovery. Keywords: Antibiotic resistance, β-lactam antibiotics, β-lactamases, inhibitors, broad spectrum, drug discovery.
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