Investigational antiviral therapies for the treatment of influenza

被引:15
|
作者
Yang, Jie [1 ]
Huang, Yingna [1 ]
Liu, Shuwen [1 ,2 ]
机构
[1] Southern Med Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Screening, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Guangdong Prov Inst Nephrol, State Key Lab Organ Failure Res, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Baloxavir; influenza virus; inhibitor; vRNPs; VIRUS-RNA-POLYMERASE; PROTEIN-PROTEIN INTERACTION; A VIRUS; SMALL-MOLECULE; UNCOMPLICATED INFLUENZA; BIOLOGICAL EVALUATION; STRUCTURAL BASIS; PB2; SUBUNIT; CAP-BINDING; IN-VITRO;
D O I
10.1080/13543784.2019.1606210
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Influenza viral ribonucleoprotein complexes (vRNPs) play a key role in viral transcription and replication; hence, the recent development of novel anti-influenza drugs targeting vRNPs has garnered widespread interest.Areas covered: We discuss the function of the constituents of vRNPs and summarize those vRNPs-targeted synthetic drugs that are in preclinical and early clinical development.Expert opinion: vRNPs contain high-value drug targets; such targets include the subunits PA, PB1, PB2, and NP. Developing a new generation of antiviral therapies with strategies that utilize existing drugs, natural compounds originated from new resources and novel drug combinations may open up new therapeutic approaches to influenza.
引用
收藏
页码:481 / 488
页数:8
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