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Syk Inhibitor II

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Catalog No. T4348Cas No. 726695-51-8

Syk inhibitor II, a cell-permeable, ATP-competitive, pyrimidine-carboxamide compound, selectively and reversibly inhibits Syk (IC50 = 41 nM).

Syk Inhibitor II

Syk Inhibitor II

😃Good
Purity: 97.63%
Catalog No. T4348Cas No. 726695-51-8
Syk inhibitor II, a cell-permeable, ATP-competitive, pyrimidine-carboxamide compound, selectively and reversibly inhibits Syk (IC50 = 41 nM).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$40-In Stock
1 mL x 10 mM (in DMSO)$86-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:97.63%
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Product Introduction

Bioactivity
Description
Syk inhibitor II, a cell-permeable, ATP-competitive, pyrimidine-carboxamide compound, selectively and reversibly inhibits Syk (IC50 = 41 nM).
Targets&IC50
ZAP70:11.2 μM, Syk:41 nM, ITK:22.6 μM, PKCε:5.1 μM, 5-HT:460 nM, BTK:15.5 μM, PKCβ2:11 μM
In vitro
In mice,Syk inhibitor II prevents FcεRI-mediated 5-HT release in RBL-2H3 cells in vitro (IC50 = 460 nM) and inhibits passive cutaneous anaphylaxis reactions (ID50 = 13.2 mg/kg, s.c.).
Chemical Properties
Molecular Weight340.3
FormulaC14H15F3N6O
Cas No.726695-51-8
SmilesNCCNc1ncc(C(N)=O)c(Nc2cccc(c2)C(F)(F)F)n1
Relative Density.1.455 g/cm3 (Predicted)
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: 100 mg/mL (293.86 mM), Sonication is recommended.
H2O: 25 mg/mL (73.46 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.9386 mL14.6929 mL29.3858 mL146.9292 mL
5 mM0.5877 mL2.9386 mL5.8772 mL29.3858 mL
10 mM0.2939 mL1.4693 mL2.9386 mL14.6929 mL
20 mM0.1469 mL0.7346 mL1.4693 mL7.3465 mL
50 mM0.0588 mL0.2939 mL0.5877 mL2.9386 mL
DMSO
1mg5mg10mg50mg
100 mM0.0294 mL0.1469 mL0.2939 mL1.4693 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

Keywords

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