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Influenza A virus-IN-1, a dihydropyrrolidones derivative, is a highly effective inhibitor of various subtypes of influenza A virus (IAV) with IC 50 values ranging from 3.11 μM to 7.13 μM. It effectively suppresses IAV replication and enhances the expression of key antiviral cytokines, such as IFN-β, and the antiviral protein MxA.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $970 | Inquiry | Inquiry |
| Description | Influenza A virus-IN-1, a dihydropyrrolidones derivative, is a highly effective inhibitor of various subtypes of influenza A virus (IAV) with IC 50 values ranging from 3.11 μM to 7.13 μM. It effectively suppresses IAV replication and enhances the expression of key antiviral cytokines, such as IFN-β, and the antiviral protein MxA. |
| Targets&IC50 | A/FM-1/1/47 (H1N1):3.58 μM (IC50), Influenza A virus 690 (H3):7.13 μM (IC50), A/PR/8/34 (H1N1) with NA-H274Y:6.48 μM (IC50), A/Aichi/2/68 (H3N2):5.26 μM (IC50), A/Puerto Rico/8/34 (H1N1):3.11 μM (IC50) |
| In vitro | Treatment with Influenza A virus-IN-1 (compound 5-2; concentrations ranging from 5-40 μM; for 24 hours; in MDCK cells) notably diminishes the yield of influenza viral nucleoprotein (NP) and the expression level of NP protein in a dose-dependent manner. Additionally, this compound lowers influenza hemagglutinin (HA) mRNA expression at all assessed time points. It effectively hampers Influenza A virus (IAV) replication and curtails the production of NDAPH oxidase NOX1 in MDCK cells. Western Blot analysis conducted on IAV-infected MDCK cells treated with varying concentrations (5 μM, 10 μM, 20 μM, 40 μM) for 24 hours corroborates the significant reduction in influenza viral NP yields, evidencing a dose-responsive effect. |
| Molecular Weight | 534.458 |
| Formula | C27H20F6N2O3 |
| Cas No. | 2250313-14-3 |
| Smiles | CCOC(=O)C1=C(Nc2ccc(cc2)C(F)(F)F)C(=O)N(C1c1ccccc1)c1ccc(cc1)C(F)(F)F |c:5| |
| Relative Density. | 1.406 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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