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T3SS-IN-5
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Catalog No. T209790
T3SS-IN-5 (Compound F9) is a specific inhibitor of the type III secretion system (T3SS), a virulence factor. By suppressing the expression of genes associated with T3SS, T3SS-IN-5 reduces the pathogenicity of bacteria without affecting their viability.
T3SS-IN-5
T3SS-IN-5
Copy Product Info😃Good
Catalog No. T209790
T3SS-IN-5 (Compound F9) is a specific inhibitor of the type III secretion system (T3SS), a virulence factor. By suppressing the expression of genes associated with T3SS, T3SS-IN-5 reduces the pathogenicity of bacteria without affecting their viability.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | T3SS-IN-5 (Compound F9) is a specific inhibitor of the type III secretion system (T3SS), a virulence factor. By suppressing the expression of genes associated with T3SS, T3SS-IN-5 reduces the pathogenicity of bacteria without affecting their viability. |
| In vitro | T3SS-IN-5 does not have a statistically significant effect on the survival of Xcc. When used at 200 μM for 5 days, T3SS-IN-5 significantly reduces the hypersensitive response (HR) induced by Xcc-jx-6 in Nicotiana benthamiana. At the same concentration over 4-7 days, it alleviates canker symptoms in Orah orange more effectively than bismerthiazol. Treatment with T3SS-IN-5 at 200 μM for 16 hours significantly lowers the relative incidence of disease caused by Xcc. However, T3SS-IN-5 (200 μM for 48 hours to 5 days) does not affect other virulence factors of Xcc, such as extracellular enzyme activity, EPS activity, motility, and biofilm formation. Additionally, the combination of T3SS-IN-5 (100-200 μM for 4 days) with Burkholderia anthina hN-8 enhances the inhibitory effect on Xcc. |
| Formula | C16H14N2OS2 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
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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