Therapeutically effective covalent spike protein inhibitors in treatment of SARS-CoV-2

被引:8
作者
Vikram Choudhary
Amisha Gupta
Rajesh Sharma
Hamendra Singh Parmar
机构
[1] Devi Ahilya Vishwavidyalaya,School of Pharmacy
[2] Takshila Campus,School of Biotechnology
[3] Devi Ahilya Vishwavidyalaya,undefined
[4] Takshila Campus,undefined
关键词
Spike protein; COVID-19; SARS-CoV-2; Drug repurposing; Arbidol; Transmembrane protease serine-type 2;
D O I
10.1007/s42485-021-00074-x
中图分类号
学科分类号
摘要
COVID-19 [coronavirus disease 2019] has resulted in over 204,644,849 confirmed cases and over 4,323,139 deaths throughout the world as of 12 August 2021, a total of 4,428,168,759 vaccine doses have been administered. The lack of potentially effective drugs against the virus is making the situation worse and dangerous. Numerous forces are working on finding an effective treatment against the virus but it is believed that a de novo drug would take several months even if huge financial support is provided. The only solution left with is drug repurposing that would not only provide effective therapy with the already used clinical drugs, but also save time and cost of the de novo drug discovery. The initiation of the COVID-19 infection starts with the attachment of spike glycoprotein of SARS-CoV-2 to the host receptor. Hence, the inhibition of the binding of the virus to the host membrane and the entry of the viral particle into the host cell are one of the main therapeutic targets. This paper not only summarizes the structure and the mechanism of spike protein, but the main focus is on the potential covalent spike protein inhibitors.
引用
收藏
页码:257 / 270
页数:13
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