Antiviral drugs specific for coronaviruses in preclinical development

被引:69
作者
Adedeji, Adeyemi O. [1 ]
Sarafianos, Stefan G. [2 ,3 ,4 ]
机构
[1] Univ Calif Davis, Sch Vet Med, Vet Med Teaching Hosp, Davis, CA 95616 USA
[2] Univ Missouri, Christopher Bond Life Sci Ctr, Columbia, MO 65211 USA
[3] Univ Missouri, Sch Med, Dept Mol Microbiol & Immunol, Columbia, MO 65211 USA
[4] Univ Missouri, Dept Biochem, Columbia, MO 65211 USA
基金
美国国家卫生研究院;
关键词
ACUTE RESPIRATORY SYNDROME; ANGIOTENSIN-CONVERTING ENZYME-2; IMMUNODEFICIENCY-VIRUS TYPE-1; PAPAIN-LIKE PROTEASE; 3CL PROTEASE; SPIKE GLYCOPROTEIN; SYNCYTIAL VIRUS; INHIBITOR T-20; FUSION PROTEIN; VIRAL ENTRY;
D O I
10.1016/j.coviro.2014.06.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Coronaviruses are positive stranded RNA viruses that cause respiratory, enteric and central nervous system diseases in many species, including humans. Until recently, the relatively low burden of disease in humans caused by few of these viruses impeded the development of coronavirus specific therapeutics. However, the emergence of severe acute respiratory syndrome coronavirus (SARS-CoV), and more recently, Middle East respiratory syndrome coronavirus (MERS-CoV), has impelled the development of such drugs. This review focuses on some newly identified SARS-CoV inhibitors, with known mechanisms of action and their potential to inhibit the novel MERS-CoV. The clinical development of optimized versions of such compounds could be beneficial for the treatment and control of SARS-CoV, the current MERS-CoV and other future SARS-like epidemics.
引用
收藏
页码:45 / 53
页数:9
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