Small molecule inhibitors of ebola virus infection

被引:54
|
作者
Picazo, Edwige [1 ]
Giordanetto, Fabrizio [1 ]
机构
[1] Taros Chem GmbH & Co KG, Med Chem, D-44227 Dortmund, Germany
关键词
ACUTE RESPIRATORY SYNDROME; NIEMANN-PICK C1; T-705; FAVIPIRAVIR; ANTIVIRAL ACTIVITY; HOST-CELLS; IN-VITRO; ENTRY; IDENTIFICATION; MARBURG; METABOLISM;
D O I
10.1016/j.drudis.2014.12.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ebola viruses are extremely virulent and highly transmissible. They are responsible for sporadic outbreaks of severe hemorrhagic fevers with human mortality rates of up to 90%. No prophylactic or therapeutic treatments in the form of vaccine, biologicals or small molecule, currently exist. Yet, a wealth of antiviral research on ebola virus is being generated and potential inhibitors have been identified in biological screening and medicinal chemistry programs. Here, we detail the state-of-the-art in small molecule inhibitors of ebola virus infection, with >60 examples, including approved drugs, compounds currently in clinical trials, and more exploratory leads, and summarize the associated in vitro and in vivo evidence for their effectiveness.
引用
收藏
页码:277 / 286
页数:10
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