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Ruzotolimod (RO7020531) is an orally active Toll-like receptor 7 agonist that suppresses WHV replication and, in combination with RO-7049389, significantly reduces AAV-HBV viral load, while also serving as an experimental immunomodulatory agent for studying antiviral innate immune responses and therapeutic strategies relevant to SARS-CoV-2 and COVID-19 infection models.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $1,980 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $2,500 | 6-8 weeks | 6-8 weeks |
| Description | Ruzotolimod (RO7020531) is an orally active Toll-like receptor 7 agonist that suppresses WHV replication and, in combination with RO-7049389, significantly reduces AAV-HBV viral load, while also serving as an experimental immunomodulatory agent for studying antiviral innate immune responses and therapeutic strategies relevant to SARS-CoV-2 and COVID-19 infection models. |
| In vivo | In animal models of hepatitis B, Ruzotolimod exhibits antiviral activity and the potential for seroconversion. In AAV-HBV transduced mice, oral administration of Ruzotolimod (100 mg/kg, every 2 days) in combination with RO-7049389 results in sustained suppression of the viral load and a reduction of Hepatitis B surface antigen (HBsAg) levels. In the woodchuck model chronically infected with Woodchuck Hepatitis Virus (WHV), treatment with Ruzotolimod (30-120 mg/kg, p.o., every other day) as monotherapy or in combination with Entecavir leads to the suppression of viral replication. These studies observed the loss of viral antigens and the appearance of anti-surface antibodies (seroconversion), representing a sustained antiviral response after treatment cessation [3][4]. |
| Synonyms | RO7020531, RO 7020531, RG7854, RG 7854 |
| Molecular Weight | 354.38 |
| Formula | C14H18N4O5S |
| Cas No. | 1948241-60-8 |
| Smiles | O=C1N(C=2C(S1)=CN=C(N)N2)[C@@H]3O[C@]([C@@H](OC(C)=O)CC)(C[C@H]3O)[H] |
| Storage | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 100 mg/mL (282.18 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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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