A review of potential suggested drugs for coronavirus disease (COVID-19) treatment

被引:93
作者
Tarighi, Parastoo [1 ]
Eftekhari, Samane [1 ]
Chizari, Milad [1 ]
Sabernavaei, Mahsa [2 ]
Jafari, Davod [1 ]
Mirzabeigi, Parastoo [3 ]
机构
[1] Iran Univ Med Sci, Fac Allied Med, Dept Med Biotechnol, Tehran, Iran
[2] Iran Univ Med Sci, Sch Pharm, Dept Pharmacognosy & Pharmaceut Biotechnol, Tehran, Iran
[3] Iran Univ Med Sci, Sch Pharm, Dept Clin Pharm, Tehran, Iran
基金
英国科研创新办公室;
关键词
COVID-19; SARS-CoV-2; Drug repositioning; Outbreak; 2019-nCoV; Review; CLINICAL CHARACTERISTICS; MECHANICAL VENTILATION; SARS; AZITHROMYCIN; REPLICATION; SARS-COV-2; PNEUMONIA; ENTRY; HYPERINFLAMMATION; INHIBITION;
D O I
10.1016/j.ejphar.2021.173890
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The latest pandemic, coronavirus disease-2019 (COVID-19), is associated with high prevalence and easy transmission, which is expanding globally with no conventional treatment or vaccine. The new virus revealed 79% and 50% genomic similarities with severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV), respectively. Accordingly, since the disease resists testing and adopting new therapeutics, repositioning pre-existing drugs may present a fast and attractive strategy with known safety, characteristics, and dosage used. However, they are not specific and targeted. Therefore, several drugs have been investigated for their efficacy and safety in the treatment of COVID-19; most of them are undergoing clinical trials. This article summarizes clinical investigations of potential therapeutic drugs used as COVID-19 therapy. Subsequently, it prepares a pattern of results and therapeutic targets to help further experiment designs. We have investigated drugs as classified in the following three groups; 1) The drugs which computationally showed effectiveness (in silico) but needed further lab confirmations; 2) Emetine, Teicoplanin, and Nelfinavir have shown effectiveness in vitro; 3) The drugs currently under clinical trial.
引用
收藏
页数:21
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