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ABT-072 potassium trihydrate

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Catalog No. T38510Cas No. 1132940-31-8

ABT-072, also known as potassium trihydrate, is a highly effective non-nucleoside inhibitor of the HCV NS5B polymerase, administered orally. This compound exhibits potent activity against HCV GT1a (with an EC50 of 1 nM) and HCV GT1b (with an EC50 of 0.3 nM).

ABT-072 potassium trihydrate

ABT-072 potassium trihydrate

🥰Excellent
Catalog No. T38510Cas No. 1132940-31-8
ABT-072, also known as potassium trihydrate, is a highly effective non-nucleoside inhibitor of the HCV NS5B polymerase, administered orally. This compound exhibits potent activity against HCV GT1a (with an EC50 of 1 nM) and HCV GT1b (with an EC50 of 0.3 nM).
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Product Introduction

Bioactivity
Description
ABT-072, also known as potassium trihydrate, is a highly effective non-nucleoside inhibitor of the HCV NS5B polymerase, administered orally. This compound exhibits potent activity against HCV GT1a (with an EC50 of 1 nM) and HCV GT1b (with an EC50 of 0.3 nM).
In vitro
ABT-072 (potassium trihydrate) is a non-nucleoside inhibitor of NS5B polymerase, exhibiting nanomolar potency in vitro against genotype 1a and 1b hepatitis C virus polymerases[1].
In vivo
ABT-072, administered intravenously or orally at dosages of 5 and/or 30 mg/kg (potassium trihydrate), exhibited favorable pharmacokinetic (PK) properties in rats, with outcomes indicating good PK characteristics. Similarly, at dosages of 2.5 and/or 30 mg/kg (potassium trihydrate), ABT-072 showed low plasma clearance and high oral bioavailability in dogs. These results, from pharmacokinetic analyses, highlight ABT-072's potential, suggesting it has efficient systemic absorption and retention, with varying impacts observed across different animal models (rats and dogs).
Chemical Properties
Molecular Weight561.69
FormulaC24H32KN3O8S
Cas No.1132940-31-8
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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
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