作者
Vadim A Shiryaev, Eugene V Radchenko, Vladimir A Palyulin, Nikolay S Zefirov, Nikolay I Bormotov, Olga A Serova, Larisa N Shishkina, Marat R Baimuratov, Kseniya M Bormasheva, Yulia A Gruzd, Elena A Ivleva, Marina V Leonova, Anton V Lukashenko, Dmitry V Osipov, Vitaliy A Osyanin, Alexander N Reznikov, Vera A Shadrikova, Anastasia E Sibiryakova, Ilya M Tkachenko, Yuri N Klimochkin
发表日期
2018/10/5
期刊
European Journal of Medicinal Chemistry
卷号
158
页码范围
214-235
出版商
Elsevier Masson
简介
The hepatitis C caused by the hepatitis C virus (HCV) is an acute and/or chronic liver disease ranging in severity from a mild brief ailment to a serious lifelong illness that affects up to 3% of the world population and imposes significant and increasing social, economic, and humanistic burden. Over the past decade, its treatment was revolutionized by the development and introduction into clinical practice of the direct acting antiviral (DAA) agents targeting the non-structural viral proteins NS3/4A, NS5A, and NS5B. However, the current treatment options still have important limitations, thus, the development of new classes of DAAs acting on different viral targets and having better pharmacological profile is highly desirable. The hepatitis C virus p7 viroporin is a relatively small hydrophobic oligomeric viral ion channel that plays a critical role during virus assembly and maturation, making it an attractive and validated target …
引用总数
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