Experimental Therapeutics Centre, Agency for Science, Technology and Research (A*STAR), 31 Biopolis Way, Nanos #03-01, Singapore 138669, Singapore.
Eur J Med Chem. 2013 Oct;68:72-80. doi: 10.1016/j.ejmech.2013.07.028. Epub 2013 Aug 9.
Murray Valley encephalitis is an infectious disease spread by a mosquito-borne virus endemic in Papua New Guinea and northern Australia. In the past decade, it has spread to various regions of Australia and there is currently no therapeutic treatment against this disease. An attractive drug target is the viral serine protease NS2B/NS3, a critical enzyme involved in viral replication. Herein, we report the inhibitory activities of 37 C-terminal agmatine peptidomimetic inhibitors which led to the design of a novel structurally-constrained competitive inhibitor 38 possessing a Ki of 2.5±0.5 μM. We believe our data provides crucial insights into the viral protease active site specificity which could be used to facilitate drug design against Murray Valley encephalitis viral infections.
默里谷脑炎是一种传染病,由一种流行于巴布亚新几内亚和澳大利亚北部的蚊子传播的病毒引起。在过去的十年中,它已经传播到澳大利亚的各个地区,目前还没有针对这种疾病的治疗方法。一种有吸引力的药物靶点是病毒丝氨酸蛋白酶 NS2B/NS3,这是一种参与病毒复制的关键酶。在此,我们报告了 37 个 C 末端胍基肽拟肽抑制剂的抑制活性,这导致了设计具有 Ki 值为 2.5±0.5 μM 的新型结构约束竞争性抑制剂 38。我们相信,我们的数据提供了对病毒蛋白酶活性位点特异性的重要见解,这可以用于促进针对默里谷脑炎病毒感染的药物设计。