Table 2.
The anti-SARS-CoV-2 3CLpro activity of baicalein analogue flavonoids.
Compound | Chemical structure | IC50 (μM) | % Inhibition at 50 μM |
---|---|---|---|
Scutellarein |
![]() |
5.80 ± 0.22 | – |
Dihydromyricetin |
![]() |
1.20 ± 0.09 | – |
Quercetagetin |
![]() |
1.24 ± 0.14 | – |
Myricetin |
![]() |
2.86 ± 0.23 | – |
Scutellarin |
![]() |
– | 28.9 ± 1.6 |
5,6-Dihydroxyflavone |
![]() |
– | 26.6 ± 0.4 |
6,7-Dihydroxyflavone |
![]() |
– | 56.7 ± 2.0 |
Chrysin |
![]() |
– | 2.6 ± 1.1 |
Myricetin |
![]() |
– | 30.8 ± 4.6 |
Herbacetin |
![]() |
– | 59.1 ± 1.9 |