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Synonyms: RO-0529, AK0529


| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 2 mg | $97 | In Stock | In Stock | |
| 5 mg | $162 | In Stock | In Stock | |
| 10 mg | $247 | In Stock | In Stock | |
| 25 mg | $397 | In Stock | In Stock | |
| 50 mg | $569 | In Stock | In Stock | |
| 100 mg | $786 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $178 | In Stock | In Stock |
| Description | Ziresovir (RO-0529/AK0529) belongs to small molecule inhibitors and is a respiratory syncytial virus (RSV) fusion protein (F protein) inhibitor (EC50 = 3 nM) with oral activity and selectivity. This compound is used in research on respiratory syncytial virus infection, significantly alleviating bronchitis symptoms and reducing viral load. |
| Targets & IC50 | D486N (RSV,Mutant strain):2.1 μM (EC50), RSV (WT):0.003 μM (EC50), D489A (RSV,Mutant strain):> 10μM (EC50), RSV F:3 nM (EC50) |
| In vitro | Methods: In HEp-2 cells, Ziresovir (0.003–0.004 μM) was administered for 5 days, and cytopathic effect assay was used for detection. Results: The EC50 of Ziresovir against RSV Long, A2, B18537 laboratory strains and clinical isolates was 0.002–0.004 μM.[1] Methods: In HEp-2 cells, Ziresovir (0.03–3 nM) was co-incubated with RSV-Luc for 48 hours, and antiviral activity was determined by luciferase activity assay. Results: Ziresovir inhibited viral replication in a concentration-dependent manner, with an IC50 of approximately 0.2 nM, and no cytotoxicity was observed.[2] |
| In vivo | Methods: In a female BALB/c mouse RSV infection model, Ziresovir was administered orally at doses of 12.5 mg/kg and 50 mg/kg twice daily for 4 consecutive days. Results: Viral titers were reduced by more than 1 log at the 12.5 mg/kg dose, and decreased to 1.9 log at the 50 mg/kg dose.[1] |
| Synonyms | RO-0529, AK0529 |
| Molecular Weight | 439.53 |
| Formula | C22H25N5O3S |
| Cas No. | 1422500-60-4 |
| Smiles | Cc1ccc2nc(nc(NCC3(N)COC3)c2c1)N1CCS(=O)(=O)c2ccccc2C1 |
| Relative Density. | 1.390 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. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 38 mg/mL (86.46 mM), Sonication and heating are recommended. | ||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.55 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | |||||||||||||||||||||||||||||||
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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