Selected article for: "antiviral activity and binding pocket"

Author: Raj, Vinit; Park, Jae Gyu; Cho, Kiu-Hyung; Choi, Pilju; Kim, Taejung; Ham, Jungyeob; Lee, Jintae
Title: Assessment of antiviral potencies of cannabinoids against SARS-CoV-2 using computational and in vitro approaches
  • Cord-id: vadaxbsr
  • Document date: 2021_1_31
  • ID: vadaxbsr
    Snippet: Effective treatment choices to the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) are limited because of the absence of effective target-based therapeutics. The main object of the current research was to estimate the antiviral activity of cannabinoids (CBDs) against the human coronavirus SARS-CoV-2. In the presented research work, we performed in silico and in vitro experiments to aid the sighting of lead CBDs for treating the viral infections of SARS-CoV-2. Virtual screening was c
    Document: Effective treatment choices to the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) are limited because of the absence of effective target-based therapeutics. The main object of the current research was to estimate the antiviral activity of cannabinoids (CBDs) against the human coronavirus SARS-CoV-2. In the presented research work, we performed in silico and in vitro experiments to aid the sighting of lead CBDs for treating the viral infections of SARS-CoV-2. Virtual screening was carried out for interactions between 32 CBDs and the SARS-CoV-2 M(pro) enzyme. Afterward, in vitro antiviral activity was carried out of five CBDs molecules against SARS-CoV-2. Interestingly, among them, two CBDs molecules namely Δ(9) -tetrahydrocannabinol (IC(50) = 10.25 μM) and cannabidiol (IC(50) = 7.91 μM) were observed to be more potent antiviral molecules against SARS-CoV-2 compared to the reference drugs lopinavir, chloroquine, and remdesivir (IC(50) ranges of 8.16–13.15 μM). These molecules were found to have stable conformations with the active binding pocket of the SARS-CoV-2 M(pro) by molecular dynamic simulation and density functional theory. Our findings suggest cannabidiol and Δ(9) -tetrahydrocannabinol are possible drugs against human coronavirus that might be used in combination or with other drug molecules to treat COVID-19 patients.

    Search related documents:
    Co phrase search for related documents
    • absorption profile and active site: 1, 2, 3, 4
    • absorption profile and adme profile: 1, 2
    • acceptable range and adme profile: 1
    • acid motif and active site: 1, 2, 3, 4, 5, 6
    • acid motif and acute respiratory distress: 1
    • active site and acute respiratory distress: 1, 2, 3
    • active site and adme profile: 1
    • active site and lpv lopinavir: 1, 2, 3
    • acute respiratory distress and low respiratory: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
    • acute respiratory distress and low respiratory tract: 1, 2
    • acute respiratory distress and lpv lopinavir: 1, 2, 3, 4