药代动力学
蛋白酶抑制剂(药理学)
虚拟筛选
病毒学
药理学
2019年冠状病毒病(COVID-19)
体内
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
加药
离体
医学
大流行
抗病毒药物
药物发现
冠状病毒
药效学
药品
病毒载量
病毒
生物
疾病
生物信息学
传染病(医学专业)
内科学
遗传学
抗逆转录病毒疗法
作者
Yuto Unoh,Shota Uehara,Kenji Nakahara,Haruaki Nobori,Yukiko Yamatsu,Shiho Yamamoto,Yuki Maruyama,Yoshiyuki Taoda,Koji Kasamatsu,Takahiro Suto,Kensuke Kouki,Atsufumi Nakahashi,Sho Kawashima,Takao Sanaki,Shinsuke Toba,Kentaro Uemura,Tohru Mizutare,Shigeru Ando,Michihito Sasaki,Yasuko Orba
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2022-01-26
被引量:28
标识
DOI:10.1101/2022.01.26.477782
摘要
Abstract The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in millions of deaths and threatens public health and safety. Despite the rapid global spread of COVID-19 vaccines, effective oral antiviral drugs are urgently needed. Here, we describe the discovery of S-217622, the first oral non-covalent, non-peptidic SARS-CoV-2 3CL protease inhibitor clinical candidate. S-217622 was discovered via virtual screening followed by biological screening of an in-house compound library, and optimization of the hit compound using a structure-based drug-design strategy. S-217622 exhibited antiviral activity in vitro against current outbreaking SARS-CoV-2 variants and showed favorable pharmacokinetic profiles in vivo for once-daily oral dosing. Furthermore, S-217622 dose-dependently inhibited intrapulmonary replication of SARS-CoV-2 in mice, indicating that this novel non-covalent inhibitor could be a potential oral agent for treating COVID-19.
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