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严重急性呼吸综合征冠状病毒2 3CL蛋白酶大环共价抑制剂的发现

Discovery of macrocyclic covalent inhibitors for severe acute respiratory syndrome coronavirus 2 3CL protease.

作者信息

Tang Xiubo, Hou Kai, Chen Xiaowu, Fan Wenyuan, Wu Hao, Lu Changliang, He Gong-Xin

机构信息

Shanghai CureGene Pharmaceutical Co., Ltd, 2nd floor, Building C1, No. 1976 middle Gaoke Road, ZhangJiang Hitech Park, Pudong, Shanghai 201210, China.

Shanghai CureGene Pharmaceutical Co., Ltd, 2nd floor, Building C1, No. 1976 middle Gaoke Road, ZhangJiang Hitech Park, Pudong, Shanghai 201210, China.

出版信息

Bioorg Med Chem. 2024 Sep 1;111:117846. doi: 10.1016/j.bmc.2024.117846. Epub 2024 Jul 22.

Abstract

The coronavirus disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been spread worldwide for more than 3 years. Although the hospitalization rate and mortality have decreased dramatically due to wide vaccination effort and improved treatment options, the disease is still a global health issue due to constant viral mutations, causing negative impact on social and economic activities. In addition, long COVID and complications arising from COVID-19 weeks after infection have become a concern for public health experts. Therefore, better treatments for COVID-19 are still needed. Herein, we describe a class of macrocyclic peptidomimetic compounds that are potent inhibitors of SARS-Cov-2 3CL protease (3CL). Significantly, some of the compounds showed a higher stability against human liver microsomes (HLM t > 180 min) and may be suitable for oral administration without the need for a pharmacokinetic (PK) boosting agent such as ritonavir.

摘要

由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的冠状病毒病已在全球传播了3年多。尽管由于广泛的疫苗接种努力和改进的治疗方案,住院率和死亡率大幅下降,但由于病毒不断变异,该疾病仍是一个全球健康问题,对社会和经济活动造成负面影响。此外,感染新冠病毒数周后的长期新冠症状和并发症已成为公共卫生专家关注的问题。因此,仍需要更好的新冠治疗方法。在此,我们描述了一类大环肽模拟化合物,它们是SARS-CoV-2 3CL蛋白酶(3CL)的有效抑制剂。值得注意的是,其中一些化合物对人肝微粒体表现出更高的稳定性(HLM t>180分钟),可能适合口服给药,无需使用如利托那韦等药代动力学(PK)增强剂。

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