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具有抗冠状病毒(包括 SARS-CoV-2)活性的氘代 S-217622(恩赛特韦)的合成。

Synthesis of deuterated S-217622 (Ensitrelvir) with antiviral activity against coronaviruses including SARS-CoV-2.

机构信息

Department of Chemistry, College of Science, Academy for Advanced Interdisciplinary Studies, and Medi-X Pingshan, Southern University of Science and Technology, Shenzhen, Guangdong, 518000, China.

Centre for Infection and Immunity Studies (CIIS), School of Medicine, Sun Yat-sen University, Shenzhen, Guangdong, 518107, China.

出版信息

Antiviral Res. 2023 May;213:105586. doi: 10.1016/j.antiviral.2023.105586. Epub 2023 Mar 28.

Abstract

S-217622 (Ensitrelvir) is a reversible severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 3-chymotrypsin-like protease (3CL) inhibitor which obtained emergency regulatory approval in Japan for the treatment of SARS-CoV-2 infection on Nov 22, 2022. Herein, analogs of S-271622 with deuterium-for-hydrogen replacement were synthesized for comparison of the antiviral activities and pharmacokinetic (PK) profiles. Compared to the parent compound, C11-d2-S-217622 compound YY-278 retained in vitro activity against 3CL and SARS-CoV-2. X-ray crystal structural studies showed similar interactions of SARS-CoV-2 3CL with YY-278 and S-271622. The PK profiling revealed the relatively favorable bioavailability and plasma exposure of YY-278. In addition, YY-278, as well as S-217622, displayed broadly anti-coronaviral activities against 6 other coronaviruses that infect humans and animals. These results laid the foundation for further research on the therapeutic potential of YY-278 against COVID-19 and other coronaviral diseases.

摘要

S-217622(恩赛特韦)是一种可逆转的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)3-糜蛋白酶样蛋白酶(3CL)抑制剂,于 2022 年 11 月 22 日在日本获得紧急监管批准,用于治疗 SARS-CoV-2 感染。在此,合成了 S-271622 的氘代类似物,用于比较抗病毒活性和药代动力学(PK)特征。与母体化合物相比,C11-d2-S-217622 化合物 YY-278 对 3CL 和 SARS-CoV-2 保持体外活性。X 射线晶体结构研究表明,SARS-CoV-2 3CL 与 YY-278 和 S-271622 具有相似的相互作用。PK 分析显示,YY-278 具有相对较好的生物利用度和血浆暴露量。此外,YY-278 以及 S-217622 对感染人类和动物的其他 6 种冠状病毒均表现出广泛的抗冠状病毒活性。这些结果为进一步研究 YY-278 治疗 COVID-19 和其他冠状病毒病的潜力奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbab/10043954/f7212d4da64c/gr1_lrg.jpg

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