Repurposing cefuroxime for treatment of COVID-19: a scoping review ofin silicostudies

被引:44
作者
Durojaiye, Ashimiyu B. [1 ]
Clarke, John-Ross D. [1 ]
Stamatiades, George A. [1 ]
Wang, Can [1 ]
机构
[1] Yale New Haven Hlth Bridgeport Hosp, Dept Internal Med, Bridgeport, CT 06610 USA
关键词
SARS-CoV-2; COVID-19; in silico; drug repurposing; cefuroxime; CORONAVIRUS; PROTEIN; BINDING; DOCKING; TARGET; AXETIL; ICM;
D O I
10.1080/07391102.2020.1777904
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 2 (SARS-CoV-2), the causative agent of Coronavirus disease 19 (COVID-19), is a novel human Coronavirus that is responsible for about 300,000 deaths worldwide. To date, there is no confirmed treatment or vaccine prevention strategy against COVID-19. Due to the urgent need for effective treatment, drug repurposing is regarded as the immediate option. Potential drugs can often be identified viain silicodrug screening experiments. Consequently, there has been an explosion ofin silicoexperiments to find drug candidates or investigate anecdotal claims. One drug with several anecdotal accounts of benefit is Cefuroxime. The aim of this study was to identify and summarizein silicoevidence for possible activity of Cefuroxime against SARS-CoV-2.To this end, we performed a scoping review of literature ofin silicodrug repurposing experiments for SARS-CoV-2 using PRISMA-ScR. We searched Medline, Embase, Scopus, Web of Knowledge, and Google Scholar for original studies published between 1st Feb, 2020 and 15th May, 2020 that screened drug libraries, and identified Cefuroxime as a top-ranked potential inhibitor drug against SARS-CoV-2 proteins. Six studies were identified. These studies reported Cefuroxime as a potential inhibitor of 3 key SARS-CoV-2 proteins; main protease, RNA dependent RNA polymerase, and ACE2-Spike complex. We provided a summary of the methodology and findings of the identified studies. Our scoping review identified significantin silicoevidence that Cefuroxime may be a potential multi-target inhibitor of SARS-CoV-2. Furtherin vitroandin vivostudies are required to evaluate the potential of Cefuroxime for COVID-19. Communicated by Ramaswamy H. Sarma
引用
收藏
页码:4547 / 4554
页数:8
相关论文
共 76 条
[1]   ICM - A NEW METHOD FOR PROTEIN MODELING AND DESIGN - APPLICATIONS TO DOCKING AND STRUCTURE PREDICTION FROM THE DISTORTED NATIVE CONFORMATION [J].
ABAGYAN, R ;
TOTROV, M ;
KUZNETSOV, D .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1994, 15 (05) :488-506
[2]  
ABAGYAN R, 2020, ICM PROUSER GUIDE V
[3]   Identification of Ezetimibe and Pranlukast as Pharmacological Chaperones for the Treatment of the Rare Disease Mucopolysaccharidosis Type IVA [J].
Almeciga-Diaz, Carlos J. ;
Hidalgo, Oscar A. ;
Olarte-Avellaneda, Sergio ;
Rodriguez-Lopez, Alexander ;
Guzman, Esteban ;
Garzon, Rafael ;
Natalia Pimentel-Vera, Luisa ;
Alejandra Puentes-Tellez, Maria ;
Felipe Rojas-Rodriguez, Andres ;
Gorshkov, Kirill ;
Li, Rong ;
Zheng, Wei .
JOURNAL OF MEDICINAL CHEMISTRY, 2019, 62 (13) :6175-6189
[4]  
AlmecigaDiaz CJ, 2020, VIRTUAL SCREENING PO
[5]   Rapid Identification of Potential Inhibitors of SARS-CoV-2 Main Protease by Deep Docking of 1.3 Billion Compounds [J].
Anh-Tien Ton ;
Gentile, Francesco ;
Hsing, Michael ;
Ban, Fuqiang ;
Cherkasov, Artem .
MOLECULAR INFORMATICS, 2020, 39 (08)
[6]  
[Anonymous], 2020, infants. Vaccine, V38, P101, DOI [10.1016/j, DOI 10.1080/19427867.2023.2237736]
[7]   Potential Drugs Targeting Early Innate Immune Evasion of SARS-Coronavirus 2 via 2'-O-Methylation of Viral RNA [J].
Antonio Encinar, Jose ;
Menendez, Javier A. .
VIRUSES-BASEL, 2020, 12 (05)
[8]  
AQUINO MC, 2020, JUST WANT SHARE I HA
[9]  
BARRETO P, 2020, DAY 13 ISOLATION TEM
[10]   Predicting commercially available antiviral drugs that may act on the novel coronavirus (SARS-CoV-2) through a drug-target interaction deep learning model [J].
Beck, Bo Ram ;
Shin, Bonggun ;
Choi, Yoonjung ;
Park, Sungsoo ;
Kang, Keunsoo .
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2020, 18 :784-790