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IKK2-IN-4

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Catalog No. T36524Cas No. 354811-10-2
Alias IKK2 Inhibitor IV, 5-Phenyl-2-ureidothiophene-3-carboxylic Acid Amide

IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.

IKK2-IN-4

IKK2-IN-4

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Purity: 99.83%
Catalog No. T36524Alias IKK2 Inhibitor IV, 5-Phenyl-2-ureidothiophene-3-carboxylic Acid AmideCas No. 354811-10-2
IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 μg$79-In Stock
1 mg$116-In Stock
5 mg$291-In Stock
10 mg$446-In Stock
25 mg$691-In Stock
50 mg$931-In Stock
100 mg$1,250-In Stock
200 mg$1,670-In 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:99.83%
Appearance:Solid
Color:Yellow
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Product Introduction

IKK2-IN-4 AI Summary
IKK2-IN-4 exhibits significant bioactivity as an inhibitor of multiple enzymes, including IKK-beta with an IC50 value of approximately 13.0 nM, JAK2 with an IC50 of 61.0 nM, and JAK3 with an IC50 of 2000.0 nM. It demonstrates potential anti-inflammatory and immune response modulation by inhibiting the human IKKbeta enzyme. Additionally, IKK2-IN-4 has shown activity against the SARS-CoV-2 virus, inhibiting the 3CL-Pro protease by 18.53% at a concentration of 20µM and reducing virus-induced cytotoxicity in VERO-6 cells by 0.37% at 10 µM after 48 hours of exposure. For its physicochemical properties, it has a LogD7.4 value of 2.42, indicating its lipophilicity, and an intrinsic clearance rate of 21.0 mL.min-1.g-1 in human liver microsomes, reflecting its metabolic stability. Lastly, IKK2-IN-4 exhibits cytotoxicity against human HepG2 cells, with an IC50 value of 7900.0 nM as determined by the CellTiter-Glo luminescent cell viability assay..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.
Targets&IC50
IKKβ:25 nM
SynonymsIKK2 Inhibitor IV, 5-Phenyl-2-ureidothiophene-3-carboxylic Acid Amide
Chemical Properties
Molecular Weight261.3
FormulaC12H11N3O2S
Cas No.354811-10-2
SmilesN(C(N)=O)C=1SC(=CC1C(N)=O)C2=CC=CC=C2
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
Ethanol: 2 mg/mL (7.65 mM), Sonication is recommended.
DMSO: 30 mg/mL (114.81 mM), Sonication is recommended.
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM3.8270 mL19.1351 mL38.2702 mL191.3509 mL
5 mM0.7654 mL3.8270 mL7.6540 mL38.2702 mL
DMSO
1mg5mg10mg50mg
10 mM0.3827 mL1.9135 mL3.8270 mL19.1351 mL
20 mM0.1914 mL0.9568 mL1.9135 mL9.5675 mL
50 mM0.0765 mL0.3827 mL0.7654 mL3.8270 mL
100 mM0.0383 mL0.1914 mL0.3827 mL1.9135 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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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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