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Bay 41-4109 (less active enantiomer)

Catalog No. T10480Cas No. 476617-51-3

Bay 41-4109, a potent HBV inhibitor with an IC50 of 53 nM, exhibits greater activity compared to its less active enantiomer.

Bay 41-4109 (less active enantiomer)

Bay 41-4109 (less active enantiomer)

Catalog No. T10480Cas No. 476617-51-3
Bay 41-4109, a potent HBV inhibitor with an IC50 of 53 nM, exhibits greater activity compared to its less active enantiomer.
Pack SizePriceAvailabilityQuantity
5 mg$293Backorder
10 mg$443Backorder
50 mg$1,323Backorder
100 mg$1,850Backorder
200 mgInquiryBackorder
500 mgInquiryBackorder
1 mL x 10 mM (in DMSO)$256Backorder
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Product Introduction

Bioactivity
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].
Chemical Properties
Molecular Weight395.76
FormulaC18H13ClF3N3O2
Cas No.476617-51-3
Storage & Solubility Information
StoragePowder: -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
1mg5mg10mg50mg
1 mM2.5268 mL12.6339 mL25.2678 mL126.3392 mL
5 mM0.5054 mL2.5268 mL5.0536 mL25.2678 mL
10 mM0.2527 mL1.2634 mL2.5268 mL12.6339 mL
20 mM0.1263 mL0.6317 mL1.2634 mL6.3170 mL
50 mM0.0505 mL0.2527 mL0.5054 mL2.5268 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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