Enterovirus

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Enterovirus Products

  • All (4)
  • Enterovirus Inhibitors (4)
  • New Enterovirus Products
Catalog No. Product Name Information Product Use Citations Product Validations
S9018 Luteoloside Luteoloside (Cynaroside, Luteolin 7-β-D-Glucopyranoside) is a member of the flavonoids family that exhibits several bioactivities including anti-microbial and anti-cancer activities. It is an inhibitor of 3C Protease of Enterovirus 71 with an IC50 value of 0.36 mM.
Histol Histopathol, 2025, 18922
Pharmaceuticals (Basel), 2023, 16(4)548
S5183 PD 169316 PD 169316 is a potent, selective and cell-permeable p38 MAP kinase inhibitor with IC50 of 89 nM. PD169316 abrogates signaling initiated by both TGFbeta and Activin A. PD169316 shows antiviral activity against Enterovirus71.
PLoS One, 2021, 16(5):e0252541
E1741New Rupintrivir Rupintrivir (AG7088) is an irreversible, selective, and potent inhibitor of human rhinovirus (HRV) 3C protease. In H1-HeLa and MRC-5 cell protection assays, it demonstrates antiviral activity against 48 HRV serotypes, exhibiting a mean EC50 of 0.023 μM. Additionally, rupintrivir exhibits immunomodulatory properties.
S0436 Pleconaril Pleconaril (APO-P001, Picovir, VP 63843, WIN 63843) is a capsid inhibitor used previously to treat enterovirus infections. Pleconaril is effective in inhibiting replication with IC50 of < 0.050 μM.
S9018 Luteoloside Luteoloside (Cynaroside, Luteolin 7-β-D-Glucopyranoside) is a member of the flavonoids family that exhibits several bioactivities including anti-microbial and anti-cancer activities. It is an inhibitor of 3C Protease of Enterovirus 71 with an IC50 value of 0.36 mM.
Histol Histopathol, 2025, 18922
Pharmaceuticals (Basel), 2023, 16(4)548
S5183 PD 169316 PD 169316 is a potent, selective and cell-permeable p38 MAP kinase inhibitor with IC50 of 89 nM. PD169316 abrogates signaling initiated by both TGFbeta and Activin A. PD169316 shows antiviral activity against Enterovirus71.
PLoS One, 2021, 16(5):e0252541
E1741New Rupintrivir Rupintrivir (AG7088) is an irreversible, selective, and potent inhibitor of human rhinovirus (HRV) 3C protease. In H1-HeLa and MRC-5 cell protection assays, it demonstrates antiviral activity against 48 HRV serotypes, exhibiting a mean EC50 of 0.023 μM. Additionally, rupintrivir exhibits immunomodulatory properties.
S0436 Pleconaril Pleconaril (APO-P001, Picovir, VP 63843, WIN 63843) is a capsid inhibitor used previously to treat enterovirus infections. Pleconaril is effective in inhibiting replication with IC50 of < 0.050 μM.
E1741New Rupintrivir Rupintrivir (AG7088) is an irreversible, selective, and potent inhibitor of human rhinovirus (HRV) 3C protease. In H1-HeLa and MRC-5 cell protection assays, it demonstrates antiviral activity against 48 HRV serotypes, exhibiting a mean EC50 of 0.023 μM. Additionally, rupintrivir exhibits immunomodulatory properties.

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