Synthesis and biological evaluation of 2-benzylaminoquinazolin-4(3H)-one derivatives as a potential treatment for SARS-CoV-2

被引:8
|
作者
Lee, Jun Young [1 ]
Shin, Young Sup [1 ]
Jeon, Sangeun [2 ]
Lee, Se In [1 ]
Cho, Jung-Eun [1 ]
Myung, Subeen [1 ,3 ]
Jang, Min Seong [4 ]
Kim, Seungtaek [2 ]
Song, Jong Hwan [1 ]
Kim, Hyoung Rae [1 ]
Park, Chul Min [1 ,3 ]
机构
[1] Korea Res Inst Chem Technol, Ctr Convergent Res Emerging Virus Infect CEVI, 141 Gajeong Ro, Daejeon 34114, South Korea
[2] Inst Pasteur Korea, Zoonot Virus Lab, Seongnam Si, Gyeonggi Do, South Korea
[3] Korea Univ Sci & Technol, Med Chem & Pharmacol, Daejeon, South Korea
[4] Korea Inst Toxicol, Dept Nonclin Studies, Daejeon, South Korea
关键词
2-benzylaminoquinazolin-4(3H)-ones; antiviral activity; coronaviruses; COVID-19;
D O I
10.1002/bkcs.12470
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the continuing global crisis caused by coronavirus disease 2019 (COVID-19), there is still no effective treatment. Therefore, we designed and synthesized a novel series of 2-benzylaminoquinazolin-4(3H)-one derivatives and demonstrated that they are effective against SARS-CoV-2. Among the synthesized derivatives, 7-chloro-2-(((4-chlorophenyl)(phenyl)methyl)amino)quinazolin-4(3H)-one (Compound 39) showed highest anti-SARS-CoV-2 activity, with a half-maximal inhibitory concentration value greater than that of remdesivir (IC50 = 4.2 mu M vs. 7.6 mu M, respectively), which gained urgent approval from the U.S. Food and Drug Administration. In addition, Compound 39 showed good results in various assays measuring metabolic stability, human ether a-go-go, Cytochromes P450 (CYPs) inhibition, and plasma protein binding (PPB), and showed better solubility and pharmacokinetics than our previous work.
引用
收藏
页码:412 / 416
页数:5
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