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. 2022 Sep 6;8:86. doi: 10.1038/s41421-022-00450-x

Fig. 4. Anti-SARS-CoV-2 activity of TMPyP4 in cell-based assays.

Fig. 4

ac Vero E6 cells infected with SARS-CoV-2 (103 TCID50 virus/mL) were pretreated with different concentrations of TMPyP4, TMPyP2, PDP or remdesivir. At 72 h post infection, viral RNA copies in cell lysates (a) and in cell culture supernatants (b) were detected by qRT-PCR. Viral titers (log10TCID50/mL) (c) were quantified by TCID50. Lower limit of detection for viral titers is indicated with a red dotted line. TCID50, median tissue culture infectious dose. d Fitting viral loads (viral RNA copies/mL) and cell viability under increasing concentration of TMPyP4 to determine the EC50 and CC50 of TMPyP4, PDP and remdesivir. The drugs cytotoxicity was detected by SRB assays. EC50, half-maximal effective doses. EC90, 90% maximal effective doses. CC10, 10% cytotoxic concentration. CC50, half-cytotoxic concentration. Data are shown as means ± SEM of three independent experiments, two-tailed Student’s t-test. **P < 0.01, ***P < 0.001, ****P < 0.0001.