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Tizoxanide

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Catalog No. T2279Cas No. 173903-47-4
Alias TIZ, Desacetyl-nitazoxanide

Tizoxanide (Desacetyl-nitazoxanide) is a metabolite of lamivudine. Lamivudine (2', 3'-dideoxy-3'-thiacytidine, commonly called 3TC) is a potent nucleoside analog reverse transcriptase inhibitor (nRTI).

Tizoxanide

Tizoxanide

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Purity: 99.28%
Catalog No. T2279Alias TIZ, Desacetyl-nitazoxanideCas No. 173903-47-4
Tizoxanide (Desacetyl-nitazoxanide) is a metabolite of lamivudine. Lamivudine (2', 3'-dideoxy-3'-thiacytidine, commonly called 3TC) is a potent nucleoside analog reverse transcriptase inhibitor (nRTI).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$46In StockIn Stock
10 mg$72In StockIn Stock
25 mg$148In StockIn Stock
50 mg$233In StockIn Stock
100 mg$346In StockIn Stock
1 mL x 10 mM (in DMSO)$54In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.28%
Color:White
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Product Introduction

Tizoxanide AI Summary
Tizoxanide exhibits a broad spectrum of bioactivities, including antimicrobial, antiviral, antiprotozoan, and antitumor properties. It inhibits Giardia lamblia recombinant nitroreductase 1 in Escherichia coli with more than 75% inhibition at 5 μM, and shows activity against Clostridium difficile with MIC50 of 0.06 μg/mL and MIC90 of 0.125 μg/mL. Against Mycobacterium tuberculosis H37Rv, it has a Minimum Inhibitory Concentration (MIC) of 16.0 μg/mL in liquid medium after 7 days. It demonstrates antiviral efficacy against HCV genotypes 1a and 1b with EC50 values ranging from 150.0 nM to 2.0 μM and cytotoxicity in human cells with CC50 values of 14,000.0 nM to 92,000.0 nM, along with high selectivity indices. It also exhibits potent antiviral activity against HBV with EC50 values of 150.0 nM and 460.0 nM and low toxicity (CC50 > 100,000.0 nM). For HBV-infected HepG2(2.2.15) cells, it inhibits extracellular and intracellular viral DNA with EC90 values of 0.58 μM and 1.2 μM respectively. Against Trichomonas vaginalis, it has an IC50 of 211.0 nM and displays antiprotozoan activity against various pathogens, including Giardia intestinalis and Leishmania mexicana. The compound shows antimicrobial activity against Mycobacterium tuberculosis in both replicating and non-replicating states with a MIC of 60,380.0 nM, and against Staphylococcus epidermidis with a MIC of 8.0 μg/mL. It has been reported to exert antitumor growth inhibition across multiple human cancer cell lines with GI50 values ranging from 3,000 nM to 40,000 nM. Additionally, Tizoxanide inhibits IL-6 induced STAT3 transcriptional activity in HEK-Blue IL-6 cells, showing 60% inhibition at 10 μM and an IC50 of 8,900.0 nM, while exhibiting 12.7% cytotoxicity in HeLa cells. In animal models, it has a rapid elimination half-life of 0.7 hours in Sprague-Dawley rats when administered via oral gavage. Furthermore, it demonstrates binding affinity with human plasma proteins at 97.5% and a favorable selectivity index, indicating potential therapeutic applications across various medical conditions..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Tizoxanide (Desacetyl-nitazoxanide) is a metabolite of lamivudine. Lamivudine (2', 3'-dideoxy-3'-thiacytidine, commonly called 3TC) is a potent nucleoside analog reverse transcriptase inhibitor (nRTI).
SynonymsTIZ, Desacetyl-nitazoxanide
Chemical Properties
Molecular Weight265.25
FormulaC10H7N3O4S
Cas No.173903-47-4
SmilesOc1ccccc1C(=O)Nc1ncc(s1)[N+]([O-])=O
Relative Density.1.644 g/cm3 (Predicted)
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: 20 mg/mL (75.4 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.7700 mL18.8501 mL37.7003 mL188.5014 mL
5 mM0.7540 mL3.7700 mL7.5401 mL37.7003 mL
10 mM0.3770 mL1.8850 mL3.7700 mL18.8501 mL
20 mM0.1885 mL0.9425 mL1.8850 mL9.4251 mL
50 mM0.0754 mL0.3770 mL0.7540 mL3.7700 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:
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2 Enter the in vivo formulation:
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