Design and Synthesis of Small Molecules as Potent Staphylococcus aureus Sortase A Inhibitors

被引:27
|
作者
Ha, Min Woo [1 ,2 ]
Yi, Sung Wook [3 ]
Paek, Seung-Mann [4 ,5 ]
机构
[1] Jeju Natl Univ, Coll Pharm, 102 Jejudaehak Ro, Jeju 63243, Jeju Do, South Korea
[2] Jeju Natl Univ, Interdisciplinary Grad Program Adv Convergence Te, 102 Jejudaehak Ro, Jeju 63243, Jeju Do, South Korea
[3] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[4] Gyeongsang Natl Univ, Coll Pharm, Jinju Daero 501, Jinju 52828, Gyeongsangnam D, South Korea
[5] Gyeongsang Natl Univ, Res Inst Pharmaceut Sci, Jinju Daero 501, Jinju 52828, Gyeongsangnam D, South Korea
来源
ANTIBIOTICS-BASEL | 2020年 / 9卷 / 10期
基金
新加坡国家研究基金会;
关键词
drug resistant; sortase A; Staphylococcus aureus; sortase A inhibitor; small organic molecule; synthetic chemistry; SORTING SIGNAL BINDING; SURFACE-PROTEINS; CELL-WALL; ANTIBIOTIC-RESISTANCE; BIOLOGICAL EVALUATION; TRANSPEPTIDASE SRTA; DRUG DISCOVERY; MANNICH-BASES; MECHANISM; DERIVATIVES;
D O I
10.3390/antibiotics9100706
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The widespread and uncontrollable emergence of antibiotic-resistant bacteria, especially methicillin-resistant Staphylococcus aureus, has promoted a wave of efforts to discover a new generation of antibiotics that prevent or treat bacterial infections neither as bactericides nor bacteriostats. Due to its crucial role in virulence and its nonessentiality in bacterial survival, sortase A has been considered as a great target for new antibiotics. Sortase A inhibitors have emerged as promising alternative antivirulence agents against bacteria. Herein, the structural and preparative aspects of some small synthetic organic compounds that block the pathogenic action of sortase A have been described.
引用
收藏
页码:1 / 16
页数:16
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