Targeting SARS-CoV-2 Polymerase with New Nucleoside Analogues

被引:10
作者
Daikopoulou, Vasiliki [1 ]
Apostolou, Panagiotis [1 ]
Mourati, Sofia [1 ]
Vlachou, Ioanna [1 ]
Gougousi, Maria [1 ]
Papasotiriou, Ioannis [2 ]
机构
[1] Res Genet Canc Ctr SA Ind Area Florina, GR-53100 Florina, Greece
[2] Res Genet Canc Ctr Int GmbH, Baarerstr 95, CH-6301 Zug, Switzerland
关键词
nucleoside derivatives; COVID-19; quinazoline moiety; QUINAZOLINE DERIVATIVES; REPLICATION; DRUGS;
D O I
10.3390/molecules26113461
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
Despite the fact that COVID-19 vaccines are already available on the market, there have not been any effective FDA-approved drugs to treat this disease. There are several already known drugs that through drug repositioning have shown an inhibitory activity against SARS-CoV-2 RNA-dependent RNA polymerase. These drugs are included in the family of nucleoside analogues. In our efforts, we synthesized a group of new nucleoside analogues, which are modified at the sugar moiety that is replaced by a quinazoline entity. Different nucleobase derivatives are used in order to increase the inhibition. Five new nucleoside analogues were evaluated with in vitro assays for targeting polymerase of SARS-CoV-2.
引用
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页数:12
相关论文
共 43 条
[1]   Analysis of SARS-CoV-2 RNA-dependent RNA polymerase as a potential therapeutic drug target using a computational approach [J].
Aftab, Syed Ovais ;
Ghouri, Muhammad Zubair ;
Masood, Muhammad Umer ;
Haider, Zeshan ;
Khan, Zulqurnain ;
Ahmad, Aftab ;
Munawar, Nayla .
JOURNAL OF TRANSLATIONAL MEDICINE, 2020, 18 (01)
[2]  
[Anonymous], WHO CORONAVIRUS COVI
[3]   Novel Nucleoside Analogues as Effective Antiviral Agents for Zika Virus Infections [J].
Bassetto, Marcella ;
Cima, Cecilia M. ;
Basso, Mattia ;
Salerno, Martina ;
Schwarze, Frank ;
Friese, Daniela ;
Bugert, Joachim J. ;
Brancale, Andrea .
MOLECULES, 2020, 25 (20)
[4]  
Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases, LIVERTOX CLIN RES IN
[5]   Inhibition of hepatitis C virus RNA replication by 2′-modified nucleoside analogs [J].
Carroll, SS ;
Tomassini, JE ;
Bosserman, M ;
Getty, K ;
Stahlhut, MW ;
Eldrup, AB ;
Bhat, B ;
Hall, D ;
Simcoe, AL ;
LaFemina, R ;
Rutkowski, CA ;
Wolanski, B ;
Yang, ZC ;
Migliaccio, G ;
De Francesco, R ;
Kuo, LC ;
MacCoss, M ;
Olsen, DB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (14) :11979-11984
[6]  
Chien MC, 2020, J PROTEOME RES, V19, P4690, DOI [10.1021/acs.jproteome.0c00392, 10.1101/2020.03.18.997585]
[7]   Nucleoside anticancer drugs: the role of nucleoside transporters in resistance to cancer chemotherapy [J].
Damaraju, VL ;
Damaraju, S ;
Young, JD ;
Baldwin, SA ;
Mackey, J ;
Sawyer, MB ;
Cass, CE .
ONCOGENE, 2003, 22 (47) :7524-7536
[8]   Approved Antiviral Drugs over the Past 50 Years [J].
De Clercq, Erik ;
Li, Guangdi .
CLINICAL MICROBIOLOGY REVIEWS, 2016, 29 (03) :695-747
[9]  
El-Sherbeny MA, 2003, ARZNEIMITTELFORSCH, V53, P206
[10]  
Eyer Ludek, 2018, Antiviral Chemistry & Chemotherapy, V26, DOI 10.1177/2040206618761299