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Tpl2 Kinase Inhibitor 1 hydrochloride
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Catalog No. T211946Cas No. 2934185-09-6
Tpl2 Kinase Inhibitor 1 hydrochloride is a selective Tpl2 inhibitor with an IC50 value of 50 nM. Tpl2 encompasses COT kinase and MAP3K8, and this inhibitor is applicable for research related to inflammatory responses and certain types of cancer.
Tpl2 Kinase Inhibitor 1 hydrochloride
Copy Product Info😃Good
Catalog No. T211946Cas No. 2934185-09-6
Tpl2 Kinase Inhibitor 1 hydrochloride is a selective Tpl2 inhibitor with an IC50 value of 50 nM. Tpl2 encompasses COT kinase and MAP3K8, and this inhibitor is applicable for research related to inflammatory responses and certain types of cancer.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
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Chemical Properties
Storage & Solubility Information
| Description | Tpl2 Kinase Inhibitor 1 hydrochloride is a selective Tpl2 inhibitor with an IC50 value of 50 nM. Tpl2 encompasses COT kinase and MAP3K8, and this inhibitor is applicable for research related to inflammatory responses and certain types of cancer. |
| Targets&IC50 | p38:180 μM |
| In vitro | Tpl2 (Cot/MAP3K8) is a serine/threonine kinase within the MAP3K family, acting upstream of MEK in the ERK pathway. The Cancer Osaka thyroid (COT) kinase (Tpl2) plays a critical role as a regulator of pro-inflammatory cytokines in macrophages. Tpl2 Kinase Inhibitor 1 (Compound 2p) hydrochloride also inhibits MK2 and p38 with IC₅₀ values of 110 μM and 180 μM in A431 cells, respectively. This inhibitor suppresses the production of TNF-a in lipopolysaccharide-induced human primary monocytes and human whole blood, with IC₅₀ values of 0.7 μM and 8.5 μM, respectively. |
| Molecular Weight | 441.29 |
| Formula | C21H15Cl2FN6 |
| Cas No. | 2934185-09-6 |
| Smiles | Cl.N#CC=1C=NC2=CN=C(C=C2C1NC3=CC=C(F)C(Cl)=C3)NCC=4C=NC=CC4 |
| 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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