Fragment-based Drug Discovery Strategy and its Application to the Design of SARS-CoV-2 Main Protease Inhibitor

被引:0
|
作者
Jiang, Yu [1 ,2 ]
Wu, Yingnan [2 ]
Wang, Jing [2 ]
Ma, Yuheng [2 ]
Yu, Hui [3 ,4 ]
Wang, Zhanli [1 ,5 ]
机构
[1] Baotou Med Coll, Affiliated Hosp 2, Inner Mongolia Key Lab Dis Related Biomarkers, Baotou, Peoples R China
[2] Inner Mongolia Med Univ, Coll Pharm, Hohhot, Peoples R China
[3] Baotou Med Coll, Sch Basic Med, Baotou, Peoples R China
[4] Baotou Med Coll, Sch Basic Med, 31 Jianshe Rd, Baotou 014060, Peoples R China
[5] Baotou Med Coll, Affiliated Hosp 2, 30 Hudemulin Ave, Baotou 014030, Inner Mongolia, Peoples R China
基金
中国国家自然科学基金;
关键词
SARS-CoV-2; main protease; inhibitor; fragment-based drug discovery; covaxi; ritonavir; SURFACE-PLASMON RESONANCE; LEAD DISCOVERY; RECEPTOR INTERACTIONS; FUNCTIONAL RECEPTOR; HIT IDENTIFICATION; PRACTICAL ASPECTS; SARS CORONAVIRUS; GAS-DETECTION; LIBRARIES; LIGANDS;
D O I
10.2174/0109298673294251240229070740
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Severe Acute Respiratory Syndrome Coronavirus Type 2 (SARS-CoV-2) emerged at the end of 2019, causing a highly infectious and pathogenic disease known as 2019 coronavirus disease. This disease poses a serious threat to human health and public safety. The SARS-CoV-2 main protease (Mpro) is a highly sought-after target for developing drugs against COVID-19 due to its exceptional specificity. Its crystal structure has been extensively documented. Numerous strategies have been employed in the investigation of Mpro inhibitors. This paper is primarily concerned with Fragment-based Drug Discovery (FBDD), which has emerged as an effective approach to drug design in recent times. Here, we summarize the research on the approach of FBDD and its application in developing inhibitors for SARS-CoV-2 Mpro.
引用
收藏
页码:6204 / 6226
页数:23
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