体内
中东呼吸综合征冠状病毒
化学
铅化合物
病毒学
蛋白酶
化学型
冠状病毒
蛋白酵素
药物发现
离体
药代动力学
药理学
抗病毒药物
体外
蛋白酶抑制剂(药理学)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
冠状病毒感染
病毒
结构-活动关系
2019年冠状病毒病(COVID-19)
细胞病变效应
酶
病毒进入
半胱氨酸蛋白酶
病毒复制
中东呼吸综合征
药品
作者
Luca Lizzadro,Jiapeng Li,Taha Y. Taha,Gilles Degotte,Tyler C. Detomasi,Francisco J. Zapatero-Belinchon,Eric R. Hantz,Sijie Huang,Yusuke Matsui,W H Henderson,Jack T. McCann,Mauricio Montaño,Julia Rosecrans,Daniel F. Torres Pomares,Briana L McGovern,Randy Diaz-Tapia,Jared Benjamin,M. Trenholme Gordon,Isidora D. Suazo,Nicholas S. Settineri
标识
DOI:10.1021/acs.jmedchem.5c03015
摘要
The main proteases (M Pro ) of coronaviruses are clinically validated targets for antiviral discovery. Herein, we detail the in vivo optimization of uracil-core M Pro inhibitors derived from AVI-4516, an in vivo active lead bearing an unactivated propargyl warhead. To expand the anticoronaviral spectrum, we introduced diverse C6 substitution to target the S1’ pocket in M Pro and observed enhanced cellular activity against various nirmatrelvir-resistant mutants. Pharmacokinetic profiling of 12 analogs revealed overall inferior exposure of the C6 aryl analogs. However, PK profiling across three species identified the improved atropisomeric lead ( M )-AVI-4773 (5-(5,6-difluoro-1 H -benzo[ d ][1,2,3]triazol-1-yl)-3-(( M )-isoquinolin-4-yl)-6-methyl-1-(prop-2-yn-1-yl)pyrimidine-2,4(1 H,3 H )-dione), which exhibits rapid-onset oral efficacy in both SARS-CoV-2 and Middle East respiratory syndrome (MERS) mouse models, highlighting a promising chemotype with the potential to deliver anticoronaviral development candidates.
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