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Pyk2-IN-2
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Catalog No. T87280Cas No. 1271418-15-5
Pyk2-IN-2 (compound 13j) acts as a Pyk2 inhibitor, exhibiting an IC 50 value of 0.608 μM for FAK kinase [1].
Pyk2-IN-2
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Catalog No. T87280Cas No. 1271418-15-5
Pyk2-IN-2 (compound 13j) acts as a Pyk2 inhibitor, exhibiting an IC 50 value of 0.608 μM for FAK kinase [1].
| 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
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Pyk2-IN-2 (compound 13j) acts as a Pyk2 inhibitor, exhibiting an IC 50 value of 0.608 μM for FAK kinase [1]. |
| In vitro | Pyk2-IN-2 (compound 13j) has an IC₅₀ value of 55 nM against PYK2 cells [1]. |
| In vivo | The HLM blood clearance rate of Pyk2-IN-2 (compound 13j) is 31 mL/min/kg [1]. In pharmacokinetic studies on male Wistar-Han rats [1], the following data was observed: For intravenous administration at a dose of 1 mg/kg, the half-life (t 1/2) was 2.0 hours, plasma clearance (Cl p) was 2.0 mL/min/kg, and steady-state volume of distribution (Vd ss) was 0.15 L/kg. For the oral administration at a dose of 30 mg/kg, the maximum concentration (C max) was 61324 nM, calculated free maximum concentration (Calc C max free) was 184 nM, with a bioavailability (%F) of 47, and plasma protein binding (PPB, fu) of 0.003. |
| Molecular Weight | 465.55 |
| Formula | C27H27N7O |
| Cas No. | 1271418-15-5 |
| Smiles | N(C(NC=1C=C(NN1)C2=CC3=C(C=C2)N=CC=C3)=O)C=4N(N=C(C(C)(C)C)C4)C5=CC=C(C)C=C5 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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
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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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