TABLE 3.
Compound | Mechanism | References |
---|---|---|
Quercetin | Shows strong binding abilities to NA from H1N1 (A/PR/8/34) comparable with zanamivir | Liu et al. (2016) |
Quercetin‐7‐O‐glucoside | Blocks RNA polymerase of influenza viruses A and B and completely inhibits or reduces AVO formation | Gansukh et al. (2016) |
Quercetin‐3‐O‐α‐L‐rhamnopyranoside | Decreases the H1N1 viral titer by 6 logs (p < 0.01) in MDCK cells with IC50 25 μg/ml, decreases NP and M2 genes copy numbers and the expression of cytokines | Mehrbod et al. (2018) |
Quercetin | Molecular docking exhibit relatively high potential for binding quercetin to the active site of neuraminidase N1 | Sadati et al. (2019) |
Quercetin derivates | Show high binding activity on cap‐binding site of the PB2 of influenza viral RNA polymerase | Gansukh et al. (2021) |
Note: AVO, acidic vesicular organelles; IC50, half‐maximal inhibitory concentration; M2, matrix 2 ion channel; MDCK, Madin–Darby canine kidney; NA, neuroamminidase; PB2, polymerase basic 2.