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Bay 41-4109, a potent HBV inhibitor with an IC50 of 53 nM, exhibits greater activity compared to its less active enantiomer.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
5 mg | $293 | Backorder | |
10 mg | $443 | Backorder | |
50 mg | $1,323 | Backorder | |
100 mg | $1,850 | Backorder | |
200 mg | Inquiry | Backorder | |
500 mg | Inquiry | Backorder | |
1 mL x 10 mM (in DMSO) | $256 | Backorder |
Description | Bay 41-4109, a potent HBV inhibitor with an IC50 of 53 nM, exhibits greater activity compared to its less active enantiomer. |
Targets&IC50 | HBV:53 nM |
In vivo | BAY 41-4109 exhibits dose-dependent reductions in viral DNA levels in both the liver and plasma, demonstrating effectiveness commensurate with 3TC. It also diminishes the hepatitis B virus core antigen (HBcAg) in the livers of HBV-transgenic mice. Pharmacokinetic analyses reveal swift absorption, a 30% bioavailability in mice, and dose-proportional plasma concentrations, reaching approximately 60% in rats and dogs [1]. Furthermore, BAY41-4109 disrupts in vivo virus production through a mechanism that interacts with the viral capsid [2]. |
Molecular Weight | 395.76 |
Formula | C18H13ClF3N3O2 |
Cas No. | 476617-51-3 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||
Solubility Information | DMSO: 37 mg/mL (93.49 mM) | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
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