New anti-viral drugs for the treatment of COVID-19 instead of favipiravir

被引:50
作者
Aktas, Ahmet [1 ]
Tuzun, Burak [2 ]
Aslan, Rukiye [3 ]
Sayin, Koray [2 ,4 ]
Ataseven, Hilmi [5 ,6 ]
机构
[1] Sivas Cumhuriyet Univ, Fac Med, Dept Internal Med, Sivas, Turkey
[2] Sivas Cumhuriyet Univ, Fac Sci, Dept Chem, Sivas, Turkey
[3] Sivas Cumhuriyet Univ, Vocat Sch Hlth Serv, Med Serv & Tech Dept, Sivas, Turkey
[4] Sivas Cumhuriyet Univ, Adv Technol Res & Applicat Ctr, Sivas, Turkey
[5] Sivas Cumhuriyet Univ, Fac Med, Dept Gastroenterol, Sivas, Turkey
[6] Gen Directorate Publ Hosp, Minist Hlth Republ Turkey, Ankara, Turkey
关键词
COVID19; RNA polymerase; favipiravir; MM-PBSA; ADME; MOLECULAR DOCKING; SOLUBILITY; EXPRESSION; GLIDE;
D O I
10.1080/07391102.2020.1806112
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
The SARS-CoV-2 virus is a major problem in the world right now. Currently, all the attention of research centers and governments globally are focused on the investigation of vaccination studies and the discovery of small molecules that inhibit the SARS-CoV-2 virus in the treatment of patients. The goal of this study was to locate small molecules to be used against COVID19 instead of favipiravir. Favipiravir analogues were selected as drug candidates from the PubChem web tool. The RNA dependent RNA polymerase (RdRp) protein was selected as the target protein as favipiravir inhibits this protein in the human body. Initially, the inhibition activity of the studied compounds against RdRp of different virus types was investigated. Then, the inhibition properties of selected drug candidates and favipiravir were examined in detail against SARS-CoV-2 RdRp proteins. It was found that 2-oxo-1H-pyrazine-3-carboxamide performed better than favipiravir in the results of molecular docking, molecular mechanics Poisson-Boltzmann surface area (MM-PSBA) calculations, and ADME analyses. Communicated by Ramaswamy H. Sarma
引用
收藏
页码:7263 / 7273
页数:11
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