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NUN82647

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Catalog No. T8331Cas No. 16082-64-7
Alias CU-242

NUN82647 (CU-242) is an Inhibitor of cell cycle at G2 phase, and apoptosis inducer.

NUN82647

NUN82647

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Purity: 98.91%
Catalog No. T8331Alias CU-242Cas No. 16082-64-7
NUN82647 (CU-242) is an Inhibitor of cell cycle at G2 phase, and apoptosis inducer.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$39In StockIn Stock
5 mg$89In StockIn Stock
10 mg$143In StockIn Stock
25 mg$263In StockIn Stock
50 mg$396In StockIn Stock
100 mg$579In StockIn Stock
200 mg$783-In Stock
1 mL x 10 mM (in DMSO)$88In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.91%
Appearance:Solid
Color:White
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Product Introduction

NUN82647 AI Summary
NUN82647 exhibits a range of bioactivities. It stabilizes human IkappaBalpha in OCI-Ly3 cells with an EC50 of 11000.0 nM and achieves 300.0% efficacy relative to control. It effectively inhibits TNF-alpha-stimulated human NF-kappaB p65 RelA subunit nuclear translocation in HUVEC with an efficacy greater than 90.0% and an IC50 of 2000.0 nM. Additionally, it inhibits TNFalpha-stimulated human NF-kappaB-mediated beta-lactamase gene expression in HUVEC with an IC50 of 13500.0 nM and shows cytotoxicity against NF-kappaB overexpressing OCI-Ly3 cells with an IC50 exceeding 57000.0 nM. Beyond NF-kappaB inhibition, NUN82647 inhibits a variety of enzymatic and protein-protein interactions, including those involving TDP1, ROR gamma, menin-MLL in leukemias, and several others related to infectious diseases like Giardia Lamblia and viruses like Lassa and Marburg. Importantly, it has an IC50 value greater than 10420.0 nM when tested against Human African Trypanosomiasis (HAT) and shows antagonist activity by inhibiting hepcidin-induced ferroportin internalization in MDCK cells with an IC50 of 20800.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
NUN82647 (CU-242) is an Inhibitor of cell cycle at G2 phase, and apoptosis inducer.
SynonymsCU-242
Chemical Properties
Molecular Weight299.35
FormulaC15H13N3O2S
Cas No.16082-64-7
SmilesNc1ccccc1S(=O)(=O)Nc1cccc2cccnc12
Relative Density.1.437 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: 25 mg/mL (83.51 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.3406 mL16.7029 mL33.4057 mL167.0286 mL
5 mM0.6681 mL3.3406 mL6.6811 mL33.4057 mL
10 mM0.3341 mL1.6703 mL3.3406 mL16.7029 mL
20 mM0.1670 mL0.8351 mL1.6703 mL8.3514 mL
50 mM0.0668 mL0.3341 mL0.6681 mL3.3406 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

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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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