Small molecule inhibitors of anthrax edema factor

被引:7
|
作者
Jiao, Guan-Sheng [1 ]
Kim, Seongjin [1 ]
Moayeri, Mahtab [2 ]
Thai, April [1 ]
Cregar-Hernandez, Lynne [1 ]
McKasson, Linda [1 ]
O'Malley, Sean [1 ]
Leppla, Stephen H. [2 ]
Johnson, Alan T. [1 ]
机构
[1] Hawaii Biotech, 650 Iwilei Rd,Suite 204, Honolulu, HI 96817 USA
[2] NIAID, Lab Parasit Dis, NIH, Bethesda, MD 20892 USA
关键词
Anthrax; Edema factor; Covalent inhibitor; SULFONYL FLUORIDES; LETHAL FACTOR; TOXIN; CALMODULIN; COVALENT; CYCLASE; KINASE; ACID; ACTIVATION; TARGETS;
D O I
10.1016/j.bmcl.2017.11.040
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Anthrax is a highly lethal disease caused by the Gram-(+) bacteria Bacillus anthracis. Edema toxin (ET) is a major contributor to the pathogenesis of disease in humans exposed to B. anthracis. ET is a bipartite toxin composed of two proteins secreted by the vegetative bacteria, edema factor (EF) and protective antigen (PA). Our work towards identifying a small molecule inhibitor of anthrax edema factor is the subject of this letter. First we demonstrate that the small molecule probe 50-Fluorosulfonylbenzoyl 50-adenosine (FSBA) reacts irreversibly with EF and blocks enzymatic activity. We then show that the adenosine portion of FSBA can be replaced to provide more drug-like molecules which are up to 1000-fold more potent against EF relative to FSBA, display low cross reactivity when tested against a panel of kinases, and are nanomolar inhibitors of EF in a cell-based assay of cAMP production. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:134 / 139
页数:6
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