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Synonyms: RG7907


| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $98 | In Stock | In Stock | |
| 5 mg | $263 | In Stock | In Stock | |
| 10 mg | $378 | In Stock | In Stock | |
| 25 mg | $612 | In Stock | In Stock | |
| 50 mg | $818 | - | In Stock | |
| 100 mg | $1,090 | - | In Stock | |
| 200 mg | $1,480 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $347 | In Stock | In Stock |
| Description | Linvencorvir (RG7907) belongs to HBV core protein allosteric modulators (CpAM) and is an orally active HBV core protein inhibitor with potent anti-HBV activity, low CYP3A4 induction, and good metabolic stability. This compound is used for the treatment of chronic hepatitis B virus infection. |
| Targets & IC50 | HepG2.2.15 cells:6 nM (EC50) |
| In vitro | Methods: In HepG2.2.15 cells, treatment with different concentrations of Linvencorvir was performed to detect HBV DNA replication levels. Results: Linvencorvir inhibited HBV DNA replication with an EC50 of 62 nM. [1] Methods: In HepG2.117 cells, treatment with different concentrations of Linvencorvir was performed to detect HBV DNA production levels. Results: Linvencorvir inhibited HBV DNA production with an EC50 of 64 nM. [2] |
| In vivo | Methods: In the AAV-HBV mouse model, oral administration of Linvencorvir (20 mg/kg, once daily) was given for 70 consecutive days, and serum and liver virological indicators as well as liver injury markers were detected. Results: Linvencorvir significantly reduced serum HBsAg, HBeAg, and liver AAV-HBV episome levels, induced hepatocyte apoptosis and proliferation, accompanied by transient ALT elevation.[2] Methods: In the AAV-HBV mouse model, oral administration of Linvencorvir (6-20 mg/kg, once daily) was given for 8 consecutive weeks, and serum HBV DNA, HBsAg, and HBeAg levels were detected. Results: Linvencorvir dose-dependently reduced serum HBV DNA, HBsAg, and HBeAg levels.[3] |
| Synonyms | RG7907 |
| Molecular Weight | 598.69 |
| Formula | C29H35FN6O5S |
| Cas No. | 1808248-05-6 |
| Smiles | C(OCC)(=O)C=1[C@@H](NC(=NC1CN2C[C@@]3(N(CC2)C(=O)N(CC(C(O)=O)(C)C)C3)[H])C4=NC=CS4)C5=C(C)C(F)=CC=C5 |
| 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: 128.8 mg/mL (215.14 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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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