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Sulfanitran

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Catalog No. T1248Cas No. 122-16-7

Sulfanitran is a sulfonamide antibiotic used in the poultry industry.

Sulfanitran

Sulfanitran

Copy Product Info
🥰Excellent
Purity: 99.60%
Catalog No. T1248Cas No. 122-16-7
Sulfanitran is a sulfonamide antibiotic used in the poultry industry.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$31In StockIn Stock
100 mg$51In StockIn Stock
500 mg$92In StockIn Stock
1 g$133In Stock-
1 mL x 10 mM (in DMSO)$29In 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:99.60%
Appearance:Solid
Color:White
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Product Introduction

Sulfanitran AI Summary
Sulfanitran has demonstrated varied bioactivity across multiple biological targets and assays. It significantly influences human MRP2-mediated estradiol-17-beta-glucuronide transport in Sf9 cells inverted membrane vesicles with an activity level of 116.0%. Additionally, it acts as an inhibitor in assays involving several proteins such as human JMJD2E, TDP1, ALDH1A1, Menin-MLL interaction in leukemia, HPGD, ROR gamma transcriptional activity, Cytochrome P450 3A4, N370S glucocerebrosidase, and S16 Schwann cell PMP22 intronic element. The compound also showed efficacy in antiviral assays against Foot and Mouth Disease Virus and Ebola Virus entry. In transport assays, Sulfanitran inhibits sodium fluorescein uptake in OATP1B1-transfected CHO cells by 61.58% and in OATP1B3-transfected CHO cells by 88.89% at 10 µM concentration. However, it does not significantly inhibit human BSEP, MRP3, and MRP4 as indicated by the high IC50 values (> 133,000.0 nM) in the respective membrane vesicle transport assays. Concerning its antiviral activity, Sulfanitran inhibits SARS-CoV-2 induced cytotoxicity in Caco-2 and VERO-6 cells. At a 10 µM concentration, it shows modest inhibition rates of 5.41% and -0.21%, respectively, after 48 hours. Nevertheless, the IC50 values suggest it may require higher concentrations for significant activity against SARS-CoV-2 (> 20000.0 nM and 19952.62 nM). The compound also inhibits SARS-CoV-2 3CL-Pro protease by 6.588% at a concentration of 20 µM. Additionally, Sulfanitran exhibits inhibitory activity against human HDAC6 in enzymatic assays, showing inhibition percentages of 17.7% and 5.02% with commercial and custom peptide substrates, respectively, indicating its potential HDAC6 inhibitory bioactivity..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Sulfanitran is a sulfonamide antibiotic used in the poultry industry.
Chemical Properties
Molecular Weight335.34
FormulaC14H13N3O5S
Cas No.122-16-7
SmilesCC(=O)Nc1ccc(cc1)S(=O)(=O)Nc1ccc(cc1)[N+]([O-])=O
Relative Density.1.5g/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: 55 mg/mL (164.01 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.96 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 mM2.9820 mL14.9102 mL29.8205 mL149.1024 mL
5 mM0.5964 mL2.9820 mL5.9641 mL29.8205 mL
10 mM0.2982 mL1.4910 mL2.9820 mL14.9102 mL
20 mM0.1491 mL0.7455 mL1.4910 mL7.4551 mL
50 mM0.0596 mL0.2982 mL0.5964 mL2.9820 mL
100 mM0.0298 mL0.1491 mL0.2982 mL1.4910 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

You can also refer to dose conversion for different animals. More Dose Conversion

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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