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对苄叉丙烯酰肼抗病毒骨架的合理修饰、合成及其对基孔肯雅病毒的生物活性评估

Rational modifications on a benzylidene-acrylohydrazide antiviral scaffold, synthesis and evaluation of bioactivity against Chikungunya virus.

作者信息

Giancotti Gilda, Cancellieri Michela, Balboni Andrea, Giustiniano Mariateresa, Novellino Ettore, Delang Leen, Neyts Johan, Leyssen Pieter, Brancale Andrea, Bassetto Marcella

机构信息

Cardiff School of Pharmacy and Pharmaceutical Sciences, Cardiff, King Edward VII Avenue, Cardiff, CF103NB, UK.

Department of Pharmacy, University of Naples 'Federico II', Naples, 80131, Italy.

出版信息

Eur J Med Chem. 2018 Apr 10;149:56-68. doi: 10.1016/j.ejmech.2018.02.054. Epub 2018 Feb 23.

Abstract

Chikungunya virus is a re-emerging arbovirus transmitted to humans by Aedes mosquitoes, responsible for an acute febrile illness associated with painful and debilitating arthralgia, which can persist for several months or become chronic. Over the past few years, infection with this virus has spread worldwide with a previously unknown virulence. No specific antiviral treatments nor vaccines are currently available against this important pathogen. Starting from the structure of a class of selective anti-CHIKV agents previously identified in our research group, different modifications to this scaffold were rationally designed, and 69 novel small-molecule derivatives were synthesised and evaluated for their inhibition of Chikungunya virus replication in Vero cells. Further structure-activity relationships associated with this class of antiviral agents were elucidated for the original scaffolds, and novel antiviral compounds with EC values in the low micromolar range were identified. This work provides the foundation for further investigation of these new structures as antivirals against Chikungunya virus.

摘要

基孔肯雅病毒是一种再度出现的虫媒病毒,通过伊蚊传播给人类,可引发一种伴有疼痛且使人衰弱的关节痛的急性发热疾病,这种关节痛可持续数月或转为慢性。在过去几年里,该病毒感染已在全球范围内传播,其毒力前所未知。目前尚无针对这种重要病原体的特异性抗病毒治疗方法或疫苗。从我们研究小组先前鉴定出的一类选择性抗基孔肯雅病毒(CHIKV)药物的结构出发,合理设计了对该骨架的不同修饰,并合成了69种新型小分子衍生物,评估了它们对基孔肯雅病毒在Vero细胞中复制的抑制作用。针对原始骨架阐明了这类抗病毒药物的进一步构效关系,并鉴定出了具有低微摩尔范围EC值的新型抗病毒化合物。这项工作为进一步研究这些新结构作为抗基孔肯雅病毒的抗病毒药物奠定了基础。

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