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Flavivirus Entry Inhibitors
被引:24
|作者:
Wang, Qing-Yin
[1
]
Shi, Pei-Yong
[1
]
机构:
[1] Novartis Inst Trop Dis, 10 Biopolis Rd,Chromos Bldg, Singapore 138670, Singapore
来源:
关键词:
flavivirus;
virus entry;
antivirals;
DENGUE VIRUS-INFECTION;
BORNE ENCEPHALITIS-VIRUS;
ENVELOPE PROTEIN;
CRYSTAL-STRUCTURE;
JAPANESE ENCEPHALITIS;
YELLOW-FEVER;
DOMAIN-III;
IN-VITRO;
SULFATED POLYSACCHARIDE;
PEPTIDE INHIBITORS;
D O I:
10.1021/acsinfecdis.5b00066
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Many flaviviruses are significant human pathogens that are transmitted by mosquitoes and ticks. Although effective vaccines are available for yellow fever virus, Japanese encephalitic virus, and tick-borne encephalitis virus, these and other flaviviruses still cause thousands of human deaths and millions of illnesses each year. No clinically approved antiviral therapy is available for flavivirus treatment. To meet this unmet medical need, industry and academia have taken multiple approaches to develop antiflavivirus therapy, among which targeting viral entry has been actively pursued in the past decade. Here we review the current knowledge of flavivirus entry and its use for small molecule drug discovery. Inhibitors of two major steps of flaviviral entry have been reported: (i) molecules that block virus-receptor interaction; (ii) compounds that prevent conformational change of viral envelope protein during virus-host membrane fusion. We also discuss the advantages and disadvantages of targeting viral entry for treatment of flavivirus infection as compared to targeting viral replication proteins.
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页码:428 / 434
页数:7
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