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Tegobuvir

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Catalog No. T17029Cas No. 1000787-75-6
Alias GS-9190, GS 333126

Tegobuvir (GS 333126) is a specific and covalent HCV NS5B polymerase inhibitor.

Tegobuvir

Tegobuvir

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Purity: 99.21%
Catalog No. T17029Alias GS-9190, GS 333126Cas No. 1000787-75-6
Tegobuvir (GS 333126) is a specific and covalent HCV NS5B polymerase inhibitor.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$81In StockIn Stock
5 mg$197In StockIn Stock
10 mg$328In StockIn Stock
25 mg$559In StockIn Stock
50 mg$790In StockIn Stock
100 mg$1,090In StockIn Stock
1 mL x 10 mM (in DMSO)$225In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.21%
Appearance:solid
Color:White
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Product Introduction

Tegobuvir AI Summary
Tegobuvir exhibits notable antiviral activity and enzyme inhibition properties. Specifically, it demonstrates potent antiviral efficacy against Hepatitis C virus (HCV) genotype 1b in human HuH5.2 cells with an EC50 of 0.7 nM after 72 hours, as assessed via a luciferase reporter gene assay. Additionally, it shows antiviral activity against HCV genotype 1b in human HuH7 cells with an EC50 of 5.0 nM after 48 hours and inhibits HCV genotype 1b NS5B RNA-dependent-RNA polymerase with an EC50 of approximately 2.908-2.9 nM. The compound also exhibits inhibitory effects on human ERG expressed in CHO cells with an IC50 of 794.33 nM, and it inhibits human HDAC6 enzyme activity by 24.72% using a commercial peptide substrate. Furthermore, Tegobuvir demonstrates antiviral effects against SARS-CoV-2, inhibiting the virus-induced cytotoxicity of Caco-2 cells at 10 µM after 48 hours with an inhibition rate of 4.14%. It also inhibits SARS-CoV-2 3CL-Pro protease activity at 20 µM with inhibition percentages of 7.92% and 7.017%. However, inhibition of SARS-CoV-2 induced cytotoxicity in VERO-6 cells was relatively minimal, with percentages of 0.18% and -0.23%..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Tegobuvir (GS 333126) is a specific and covalent HCV NS5B polymerase inhibitor.
SynonymsGS-9190, GS 333126
Chemical Properties
Molecular Weight517.4
FormulaC25H14F7N5
Cas No.1000787-75-6
SmilesFc1ccccc1-c1nc2ccn(Cc3ccc(nn3)-c3ccc(cc3C(F)(F)F)C(F)(F)F)cc2n1
Relative Density.1.46 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 50 mg/mL (96.64 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.87 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9327 mL9.6637 mL19.3274 mL96.6370 mL
5 mM0.3865 mL1.9327 mL3.8655 mL19.3274 mL
10 mM0.1933 mL0.9664 mL1.9327 mL9.6637 mL
20 mM0.0966 mL0.4832 mL0.9664 mL4.8319 mL
50 mM0.0387 mL0.1933 mL0.3865 mL1.9327 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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