2020
DOI: 10.1016/j.jep.2020.112671
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Anti-influenza virus phytochemicals from Radix Paeoniae Alba and characterization of their neuraminidase inhibitory activities

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Cited by 32 publications
(11 citation statements)
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“…It has been shown that it affects mainly the virus' replication cycle by interacting with the active sites of caspase or protein synthesis. In the case of curcumin [60,69,100], gallic acid [101,102] and catechin [103,104], examples of an inhibitory effect on the influenza virus are shown. Those publications point out the different methods of inhibition for each compound.…”
Section: Mechanism Of Antiviral Activitymentioning
confidence: 99%
See 1 more Smart Citation
“…It has been shown that it affects mainly the virus' replication cycle by interacting with the active sites of caspase or protein synthesis. In the case of curcumin [60,69,100], gallic acid [101,102] and catechin [103,104], examples of an inhibitory effect on the influenza virus are shown. Those publications point out the different methods of inhibition for each compound.…”
Section: Mechanism Of Antiviral Activitymentioning
confidence: 99%
“…EGCG HCV suppressing by blocking virus entry via viral envelope proteins and inhibiting cell-to-cell transmission [25] HBV inhibition of DNA synthesis during virus replication [29] the duck Tembusu virus (DTMUV) reduction of the viral infection in BHK-21 cells, expressions of the viral E protein and virus titers. EGCG affects the adsorption step of the infection and replication stage of the virus in BHK-21 cells [106] chlorogenic acid infectious bursal disease virus inhibiting histamine production, NF-kB activation, which affects the production of the pro-inflammatory cytokines TNF-a and IL-1b [105] HBV inhibiting DNA of the virus by binding to HepG2.2.15 and HepG2.A64 [107] catechin influenza A virus binding to functional sites PHE47A and LEU43A, which inhibits M2 viral mRNA synthesis as well as M2 protein expression [103] dengue virus interaction with NS5 protein, by binding to amino acids Asn609, Asp663, His798 [104] gallic acid influenza A virus inhibition of replication of the virus, by binding to Arg152 of neuraminidase protein [101] paramyxoviruses affects replication cycle of the virus by inhibiting ribonucleotide reductase enzyme [102]…”
Section: Polyphenolmentioning
confidence: 99%
“…Three tannins in the aqueous extract of Paeonia lactiflora were found to inhibit the replication of influenza A virus in MDCK cells, and all three compounds significantly reduced the activity of neuraminidase (Zhang, Lo, et al. 2020 ). Recent studies have shown that porcine jujube exhibits antiviral activity against DENV-2 in Vero cells, and its anti-dengue properties are most likely attributable to its tannin compounds (Pong et al.…”
Section: Antiviral Constituents In Traditional Chinese Medicinesmentioning
confidence: 99%
“…6,7 Previous studies showed that PRA could be used for anti-inflammatory effects, 8 immune regulation, 9 treatment of depression 10,11 and anemia, 12 promotion of peripheral nerve regeneration, 13 and treatment of viral infections. 14 Modern studies of pharmacological mechanisms have found that the main active components of PRA include paeoniflorin, paeonol, paeonin, benzoylpaeoniflorin, albiflorin, oxypaeoniflorin, paeoniflorigenone, benzoic acid, β-sitosterol, and gal-lotannin. Paeoniflorin is the main pharmacological component of PRA.…”
Section: Pharmacological Studies On the Active Ingredients Of The Sixmentioning
confidence: 99%