New developments in flavivirus drug discovery

被引:48
作者
Kok, W. Mei [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Div Chem & Struct Biol, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
Antiviral; dengue; flavivirus; inhibitor; nucleoside; peptide; small molecule; WEST-NILE-VIRUS; HEPATITIS-C VIRUS; TICK-BORNE ENCEPHALITIS; ANTIBODY-DEPENDENT ENHANCEMENT; ADENOSINE NUCLEOSIDE INHIBITOR; DENGUE-VIRUS; NS2B-NS3; PROTEASE; CRYSTAL-STRUCTURE; NS3; PROTEIN; NONSTRUCTURAL PROTEIN;
D O I
10.1517/17460441.2016.1160887
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Flaviviruses are major causes of infectious disease. The vast global, social and economic impact due to morbidity and mortality associated with diseases caused by these viruses urgently demands effective therapeutic interventions. There is currently no specific antiviral therapy available for the effective clinical treatment of infections by any of the flaviviridae. Development of more effective vaccines and antiviral agents for the prevention and treatment of most flavivirus infections remains a clear public health priority in the 21st century.Areas covered: This review describes some of the recent discoveries in the field of flavivirus inhibitor development, with a particular focus on targeting viral proteins. Emphasis is placed on the advances published during the 2012-2015 period.Expert opinion: The field of drug discovery targeting viral proteins has progressed slowly in recent years. New information, particularly on structures, location and mechanisms of action of established protein targets have been reported. There have also been studies on repurposing known drugs as templates for targeting flavivirus proteins and these hits could be promising templates for developing new more potent inhibitors. Further research should be conducted to improve in vitro assays that better reflect the conditions found in cellular environments.
引用
收藏
页码:433 / 445
页数:13
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