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TNIK-IN-1 (Compound 1) is a potent inhibitor of Traf2 and Nck-interacting kinase (TNIK), with an IC50 of 65 nM. TNIK is a pivotal effector in the Wnt/beta-catenin signaling pathway, essential for the maintenance of cancer stem cell properties and cellular proliferation. As a lead molecule based on the 4-phenyl-2-phenylaminopyridine scaffold, TNIK-IN-1 demonstrates significant antitumor activity by blocking TNIK kinase function and disrupting oncogenic signaling cascades, making it a valuable tool for researching Wnt-driven malignancies.

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | - | In Stock | |
| 50 mg | $1,980 | - | In Stock | |
| 100 mg | $2,500 | 6-8 weeks | 6-8 weeks |
| Description | TNIK-IN-1 (Compound 1) is a potent inhibitor of Traf2 and Nck-interacting kinase (TNIK), with an IC50 of 65 nM. TNIK is a pivotal effector in the Wnt/beta-catenin signaling pathway, essential for the maintenance of cancer stem cell properties and cellular proliferation. As a lead molecule based on the 4-phenyl-2-phenylaminopyridine scaffold, TNIK-IN-1 demonstrates significant antitumor activity by blocking TNIK kinase function and disrupting oncogenic signaling cascades, making it a valuable tool for researching Wnt-driven malignancies. |
| Targets&IC50 | TNIK:65 nM |
| In vitro | In kinase activity assays, TNIK-IN-1 exhibits high affinity for TNIK, functioning as an ATP-competitive inhibitor that binds to the kinase domain. It effectively suppresses the proliferation of tumor cell lines dependent on Wnt signaling, particularly in models of colorectal cancer. Furthermore, as TNIK is involved in cytoskeletal reorganization, TNIK-IN-1 serves as an ideal probe for investigating the molecular drivers of tumor cell migration and invasion [1]. |
| Synonyms | TNIK-inhibitor-1, TNIK inhibitor 1 |
| Molecular Weight | 395.43 |
| Formula | C19H17N5O3S |
| Cas No. | 933886-36-3 |
| Smiles | O=C(N)C=1N=C(SC1NC(=O)C2=CC=C(C=C2)NC(=O)C)NC=3C=CC=CC3 |
| Relative Density. | 1.470 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (202.31 mM), Sonication is recommmended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | ||||||||||||||||||||||||||||||||||||
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.
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.
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