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Ziresovir

(Synonyms: RO-0529, AK0529) Copy Product Info
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Synonyms: RO-0529, AK0529

Catalog No. T13401 Copy Product Info
Purity: 99.98%
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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.
Ziresovir
Cas No. 1422500-60-4
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Pack SizePriceUSA StockGlobal StockQuantity
2 mg$97In StockIn Stock
5 mg$162In StockIn Stock
10 mg$247In StockIn Stock
25 mg$397In StockIn Stock
50 mg$569In StockIn Stock
100 mg$786-In Stock
1 mL x 10 mM (in DMSO)$178In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.98%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
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]
SynonymsRO-0529, AK0529
Chemical Properties
Molecular Weight439.53
FormulaC22H25N5O3S
Cas No.1422500-60-4
SmilesCc1ccc2nc(nc(NCC3(N)COC3)c2c1)N1CCS(=O)(=O)c2ccccc2C1
Relative Density.1.390 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -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
1mg5mg10mg50mg
1 mM2.2752 mL11.3758 mL22.7516 mL113.7579 mL
5 mM0.4550 mL2.2752 mL4.5503 mL22.7516 mL
10 mM0.2275 mL1.1376 mL2.2752 mL11.3758 mL
20 mM0.1138 mL0.5688 mL1.1376 mL5.6879 mL
50 mM0.0455 mL0.2275 mL0.4550 mL2.2752 mL
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.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Keywords

Related Tags: Ziresovir chemical structure | Ziresovir in vivo | Ziresovir in vitro | Ziresovir formula | Ziresovir molecular weight