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N-Ethylmaleimide

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Catalog No. T3088Cas No. 128-53-0
Alias NEM, Ethylmaleimide, 1-Ethyl-1H-pyrrole-2,5-dione

N-Ethylmaleimide (NEM) is a reagent for alkylation of free sulfhydryl groups, a cysteine protease inhibitor used in experimental biochemistry. N-Ethylmaleimide is also a deubiquitinating enzyme inhibitor that specifically inhibits phosphate transport in mitochondria.

N-Ethylmaleimide

N-Ethylmaleimide

🥰Excellent
Purity: 99.50%
Catalog No. T3088Alias NEM, Ethylmaleimide, 1-Ethyl-1H-pyrrole-2,5-dioneCas No. 128-53-0
N-Ethylmaleimide (NEM) is a reagent for alkylation of free sulfhydryl groups, a cysteine protease inhibitor used in experimental biochemistry. N-Ethylmaleimide is also a deubiquitinating enzyme inhibitor that specifically inhibits phosphate transport in mitochondria.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$39In StockIn Stock
25 mg$62In StockIn Stock
100 mg$82In StockIn Stock
200 mg$98In StockIn Stock
500 mg$158In StockIn Stock
1 g$236In StockIn Stock
1 mL x 10 mM (in DMSO)$43In 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:99.50%
Color:White
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Product Introduction

Bioactivity
Description
N-Ethylmaleimide (NEM) is a reagent for alkylation of free sulfhydryl groups, a cysteine protease inhibitor used in experimental biochemistry. N-Ethylmaleimide is also a deubiquitinating enzyme inhibitor that specifically inhibits phosphate transport in mitochondria.
Targets&IC50
prolyl endopeptidase:6.3 μM, COS-7 cells:43.7 μM (EC50), KB-3-1 cells:0.03 mM, SF-268 cells:6.5 μg/mL (GL50), KB-V1 cells:0.016 mM, MCF-7 cells:9.9 μg/mL (GL50), NCI-H4 cells:6.7 μg/mL (GL50)
In vitro
METHODS: Growth-arrested VSMC cells were treated with N-Ethylmaleimide (20 µM) and PDGF-BB (20 ng/mL) for 5 min - 2 h, and the expression levels of target proteins were detected by Western Blot.
RESULTS: N-Ethylmaleimide inhibited PDGF BB-stimulated Akt phosphorylation. [1]
METHODS: Jurkat T cells were treated with N-Ethylmaleimide (3-100 µM) for 1-20 min, and target protein expression levels were detected by immunoblots.
RESULTS: Treatment of intact cells with 50-100 µM N-Ethylmaleimide for 5-10 min resulted in a significant increase in tyrosine residue phosphorylation. [2]
In vivo
METHODS: To examine the potential enhancement of sleep properties induced by alprazolam (Alp), N-Ethylmaleimide (1 mg/kg, 1% CMC-Na) and Alp (1.84 mg/kg, 1% CMC-Na) were administered by gavage to C57BL/6J mice.
RESULTS: Combined administration of Alp and NEM significantly reduced sleep latency and prolonged sleep duration compared with Alp alone. This effect was characterized by a significant increase in REM duration. [3]
SynonymsNEM, Ethylmaleimide, 1-Ethyl-1H-pyrrole-2,5-dione
Chemical Properties
Molecular Weight125.13
FormulaC6H7NO2
Cas No.128-53-0
SmilesC(C)N1C(=O)C=CC1=O
Relative Density.1.207 g/cm3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 237.5 mg/mL (1898.03 mM), Sonication is recommended.
H2O: 50 mg/mL (399.58 mM), Sonication and heating are recommended.
In Vivo Formulation
5% DMSO+95% Saline: 1.2 mg/mL (9.59 mM), Solution.
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
H2O/DMSO
1mg5mg10mg50mg
1 mM7.9917 mL39.9584 mL79.9169 mL399.5844 mL
5 mM1.5983 mL7.9917 mL15.9834 mL79.9169 mL
10 mM0.7992 mL3.9958 mL7.9917 mL39.9584 mL
20 mM0.3996 mL1.9979 mL3.9958 mL19.9792 mL
50 mM0.1598 mL0.7992 mL1.5983 mL7.9917 mL
100 mM0.0799 mL0.3996 mL0.7992 mL3.9958 mL

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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:
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%
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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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