Table 2.
In-Vitro Study of QS Against SARS-CoV-2
Cells | Type of Virus | Result | Reference |
---|---|---|---|
Vero B4 cells | The virus strain SARS-CoV-2 PR1 | Quinine exerts antiviral activity against SARS-CoV-2 that at 10 μM was even stronger than that of HCQ or CQ. With 10μM QS viral replication can be reduced by 90%, while HCQ is only reduced by 50% | [6] |
Vero B4 cells | The virus strain SARS-CoV-2 PR1 | Quinine exerts antiviral activity against SARS-CoV-2 that at 10 μM was even stronger than that of HCQ or CQ. With 10μM QS viral replication can be reduced by 90%, while HCQ is only reduced by 50% | [34] |
TMPRSS2+ Human Colon Cells | The recombinant SARS-CoV-2 infectious clone, icSARS-CoV-2-mNG, expressing mNeonGreen as a reporter gene | Quinine treatment in doses of 50 μM and above inhibited SARS-CoV-2 infection at this high MOI setting nearly completely, with a with a dose dependent effect down to 2 μM | |
Human Transgenic Lung Cancer Cells | The virus strain SARS-CoV-2 PR1 | Quinine exhibits antiviral activity against SARS-CoV-2 in A549 lung cancer cell lines and that its antiviral activity might be modulated but not abrogated by the expression of TMPRSS2 | |
Calu-3 lung cell | icSARS-CoV-2 mNG | Quinine excerted antiviral activity with IC50 27 μM | |
Vero E6 cells | SARS-CoV-2 strain (IHUMI-3) | Quinine showed medium antiviral in vitro activity with EC50 of 10.7 ± 3.0 µM and EC90 of 38.8 ± 34 µM | [35] |
Abbreviation: TMPRSS2+, Transmembrane Serine Protease 2; MOI, Multiplicity of Infection; IC, Inhibition Concentration; EC, Effective Concentration.