Inhibition of Dengue virus and West Nile virus proteases by click chemistry-derived benz[d]isothiazol-3(2H)-one derivatives.

Inhibition of Dengue virus and West Nile virus proteases by click chemistry-derived benz[d]isothiazol-3(2H)-one derivatives.
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DOI:
10.1016/j.bmc.2011.12.047
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发表时间:
2012-02-01
影响因子:
3.5
通讯作者:
Groutas, William C.
Groutas, William C.
中科院分区:
医学3区
文献类型:
--
作者:
Tiew, Kok-Chuan;Dou, Dengfeng;Teramoto, Tadahisa;Lai, Huiguo;Alliston, Kevin R.;Lushington, Gerald H.;Padmanabhan, R.;Groutas, William C.

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合成了两个基于 benz[d]isothiazol-3(2H)-one 支架的点击化学衍生的聚焦文库,并针对登革热病毒和西尼罗河病毒 NS2B-NS3 蛋白酶进行筛选。在添加洗涤剂的情况下,几种化合物 (4l, 7j-n) 对登革热病毒 NS2B-NS3 蛋白酶表现出显着的抑制活性。这些化合物有可能成为“从命中到先导”优化活动的启动平台。
Two click chemistry-derived focused libraries based on the benz[d]isothiazol-3(2H)-one scaffold were synthesized and screened against Dengue virus and West Nile virus NS2B-NS3 proteases. Several compounds (4l, 7j-n) displayed noteworthy inhibitory activity toward Dengue virus NS2B-NS3 protease in the absence and presence of added detergent. These compounds could potentially serve as a launching pad for a hit-to-lead optimization campaign.
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