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SU5408

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Catalog No. T4026Cas No. 15966-93-5
Alias VEGFR2 Kinase Inhibitor I

SU5408 (VEGFR2 Kinase Inhibitor I) is a potent, cell-permeable inhibitor of the VEGFR2 kinase.

SU5408

SU5408

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Purity: 99.35%
Catalog No. T4026Alias VEGFR2 Kinase Inhibitor ICas No. 15966-93-5
SU5408 (VEGFR2 Kinase Inhibitor I) is a potent, cell-permeable inhibitor of the VEGFR2 kinase.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$64In StockIn Stock
5 mg$197In StockIn Stock
10 mg$297In StockIn Stock
25 mg$546In StockIn Stock
50 mg$737In StockIn Stock
100 mg$953In StockIn Stock
500 mg$1,880-In Stock
1 mL x 10 mM (in DMSO)$217In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.35%
Appearance:Solid
Color:orange
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Product Introduction

SU5408 AI Summary
SU5408 inhibits tyrosine phosphorylation of murine VEGF receptor (FLK-1 RTK) with an IC50 of 70.0 nM and shows significant inhibition of VEGFR with an IC50 of 70.0 nM. It exhibits no significant inhibition on human Platelet-derived growth factor receptor beta (PDGF RTK), human Epidermal growth factor receptor (EGF RTK), human Her-2 receptor tyrosine kinase (HER-2 RTK), and human Insulin-like growth factor I receptor at concentrations up to 100,000.0 nM. In addition, SU5408 inhibits bPDGFR in human PAC1 cells with an IC50 of 4000.0 nM. It also targets FLT3 with an IC50 of 4300.0 nM, ABL with an IC50 of 19000.0 nM, ALK with an IC50 of 5400.0 nM, and inhibits human recombinant His-tagged RET expressed in Sf9 insect cells with an IC50 of 760.0 nM. Moreover, it inhibits the growth of mouse BA/F3 cells with an IC50 of 2600.0 nM and mouse BaPTC2 cells with an IC50 of 25.0 nM. Different kinases and proteins exhibit various degrees of thermal melting changes upon binding with SU5408..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
SU5408 (VEGFR2 Kinase Inhibitor I) is a potent, cell-permeable inhibitor of the VEGFR2 kinase.
Targets&IC50
VEGFR2:70 nM.
SynonymsVEGFR2 Kinase Inhibitor I
Chemical Properties
Molecular Weight310.35
FormulaC18H18N2O3
Cas No.15966-93-5
SmilesCCOC(=O)c1c(C)[nH]c(\C=C2\C(=O)Nc3ccccc23)c1C
Relative Density.1.271 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: 5 mg/mL (16.11 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.2222 mL16.1108 mL32.2217 mL161.1084 mL
5 mM0.6444 mL3.2222 mL6.4443 mL32.2217 mL
10 mM0.3222 mL1.6111 mL3.2222 mL16.1108 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:
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μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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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