Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2

被引:21
|
作者
Shin, Young Sup [1 ]
Lee, Jun Young [1 ]
Noh, Soojin [1 ]
Kwak, Yoonna [1 ]
Jeon, Sangeun [2 ]
Kwon, Sunoh [3 ]
Jin, Young-hee [4 ]
Jang, Min Seong [5 ]
Kim, Seungtaek [2 ]
Song, Jong Hwan [1 ]
Kim, Hyoung Rae [1 ]
Park, Chul Min [1 ]
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 13488, Gyeonggi Do, South Korea
[3] Korea Inst Oriental Med, Herbal Med Res Div, Daejeon 34054, South Korea
[4] Korea Inst Oriental Med, KM Applicat Ctr, Daegu 41062, South Korea
[5] Korea Inst Toxicol, Dept Nonclin Studies, Daejeon 34114, South Korea
基金
新加坡国家研究基金会;
关键词
SARS-CoV-2; Cyclic sulfonamide; Coronavirus; Inhibitor; Structure activity relationship;
D O I
10.1016/j.bmcl.2020.127667
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) continues to spread worldwide, with 25 million confirmed cases and 800 thousand deaths. Effective treatments to target SARS-CoV-2 are urgently needed. In the present study, we have identified a class of cyclic sulfonamide derivatives as novel SARS-CoV-2 inhibitors. Compound 13c of the synthesized compounds exhibited robust inhibitory activity (IC50 = 0.88 mu M) against SARS-CoV-2 without cytotoxicity (CC50 > 25 mu M), with a selectivity index (SI) of 30.7. In addition, compound 13c exhibited high oral bioavailability (77%) and metabolic stability with good safety profiles in hERG and cytotoxicity studies. The present study identified that cyclic sulfonamide derivatives are a promising new template for the development of anti-SARS-CoV-2 agents.
引用
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页数:5
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