Author: Aktaş, Ahmet; Tüzün, Burak; Aslan, Rukiye; Sayin, Koray; Ataseven, Hilmi
Title: New anti-viral drugs for the treatment of COVID-19 instead of favipiravir Cord-id: 4ci12ex9 Document date: 2020_8_12
ID: 4ci12ex9
Snippet: 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 R
Document: 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
Search related documents:
Co phrase search for related documents- acceptor hydrogen and active site: 1, 2, 3, 4, 5
- acceptor hydrogen and adme excretion: 1
- acceptor hydrogen and adme excretion metabolism: 1
- acceptor hydrogen and adme excretion metabolism distribution: 1
- acceptor hydrogen and adme excretion metabolism distribution absorption: 1
- acceptor hydrogen and adme excretion toxicity metabolism distribution: 1
- acceptor hydrogen and adme excretion toxicity metabolism distribution absorption: 1
- acceptor hydrogen bond and active site: 1, 2, 3, 4
- acceptor hydrogen bond and adme excretion: 1
- acceptor hydrogen bond and adme excretion metabolism: 1
- acceptor hydrogen bond and adme excretion metabolism distribution: 1
- acceptor hydrogen bond and adme excretion metabolism distribution absorption: 1
- acceptor hydrogen bond and adme excretion toxicity metabolism distribution: 1
- acceptor hydrogen bond and adme excretion toxicity metabolism distribution absorption: 1
- active site and adme excretion: 1, 2, 3
- active site and adme excretion metabolism: 1, 2, 3
- active site and adme excretion metabolism distribution: 1, 2, 3
- active site and adme excretion metabolism distribution absorption: 1, 2, 3
- active site and adme property: 1
Co phrase search for related documents, hyperlinks ordered by date