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SU 4313

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Catalog No. T3568Cas No. 186611-55-2

SU 4313 is a bioactive chemical.

SU 4313

SU 4313

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Purity: 99.89%
Catalog No. T3568Cas No. 186611-55-2
SU 4313 is a bioactive chemical.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$30In StockIn Stock
5 mg$64In StockIn Stock
10 mg$98In StockIn Stock
25 mg$179In StockIn Stock
50 mg$263In StockIn Stock
100 mg$392In StockIn Stock
200 mg$575-In Stock
1 mL x 10 mM (in DMSO)$71In 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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Batch Information

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Purity:99.89%
Appearance:Solid
Color:White to Yellow
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Product Introduction

SU 4313 AI Summary
SU 4313 exhibits inhibitory activity against multiple receptors and enzymes. It inhibits vascular endothelial growth factor receptor 2 (VEGFR2 or FLK1) with an IC50 value of 5248.07 nM. Additionally, it inhibits tyrosine phosphorylation on several receptors, including human Platelet-derived growth factor receptor beta (IC50 = 24200.0 nM), murine VEGF receptor (IC50 = 5200.0 nM), human Epidermal growth factor receptor (IC50 = 18500.0 nM), human Her-2 receptor tyrosine kinase (IC50 = 16900.0 nM), and human Insulin-like growth factor I receptor (IC50 = 10000.0 nM). SU 4313 also shows significant inhibitory activity against AmpC beta-Lactamase with an IC50 of 6000.0 nM, and against beta-Lactamase, displaying 95.0% inhibition at 20 uM in the absence of detergent Triton X-100, which drops to 27.0% in the presence of 0.01% Triton X-100. It further inhibits chymotrypsinogen, cloned Dihydrofolate reductase (cDHFR), and Beta-galactosidase, with IC50 values of 30000.0 nM, 30000.0 nM, and 55000.0 nM respectively. Notably, the compound forms aggregates as observed by dynamic light scattering at a concentration of 10.0 uM, and its inhibitory activity is influenced by varying potassium phosphate buffer concentrations, with IC50 values ranging from 3000.0 nM to 7000.0 nM. SU 4313 also shows improved inhibitory activity against beta-lactamase when preincubated, leading to a fold decrease in IC50..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
SU 4313 is a bioactive chemical.
Targets&IC50
PDGFR:14.5 μM, IGF-1R:8.0 μM, FLK1:18.8 μM, EGFR:11 μM, HER2:16.9 μM
Chemical Properties
Molecular Weight263.33
FormulaC18H17NO
Cas No.186611-55-2
SmilesC(=C1C=2C(NC1=O)=CC=CC2)C3=CC=C(C(C)C)C=C3
Relative Density.no data available
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: 65 mg/mL (246.84 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 5 mg/mL (18.99 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.7975 mL18.9876 mL37.9752 mL189.8758 mL
5 mM0.7595 mL3.7975 mL7.5950 mL37.9752 mL
10 mM0.3798 mL1.8988 mL3.7975 mL18.9876 mL
20 mM0.1899 mL0.9494 mL1.8988 mL9.4938 mL
50 mM0.0760 mL0.3798 mL0.7595 mL3.7975 mL
100 mM0.0380 mL0.1899 mL0.3798 mL1.8988 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

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