Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty

Pevonedistat hydrochloride

Catalog No. T16117Cas No. 1160295-21-5
Alias MLN-4924 hydrochloride, MLN4924 hydrochloride, MLN 4924 hydrochloride

Pevonedistat hydrochloride (MLN4924 hydrochloride) is a selective and potent NEDD8 activating enzyme inhibitor (IC50: 4.7 nM) that induces apoptosis and cell cycle inhibition in cancer cells, and is used in the study of acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). Pelubiprofen has been used in the study of AML and MDS.)

Pevonedistat hydrochloride

Pevonedistat hydrochloride

Purity: 99.19%
Catalog No. T16117Alias MLN-4924 hydrochloride, MLN4924 hydrochloride, MLN 4924 hydrochlorideCas No. 1160295-21-5
Pevonedistat hydrochloride (MLN4924 hydrochloride) is a selective and potent NEDD8 activating enzyme inhibitor (IC50: 4.7 nM) that induces apoptosis and cell cycle inhibition in cancer cells, and is used in the study of acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). Pelubiprofen has been used in the study of AML and MDS.)
Pack SizePriceAvailabilityQuantity
1 mg$485 days
Bulk & Custom
Add to Cart
Questions
View More
Select Batch
Purity:99.19%
Contact us for more batch information
Resource Download
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.

Product Introduction

Bioactivity
Description
Pevonedistat hydrochloride (MLN4924 hydrochloride) is a selective and potent NEDD8 activating enzyme inhibitor (IC50: 4.7 nM) that induces apoptosis and cell cycle inhibition in cancer cells, and is used in the study of acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). Pelubiprofen has been used in the study of AML and MDS.)
Targets&IC50
NAE:4.7 nM
In vitro
METHODS: To determine the effects of Pevonedistat hydrochloride on cell viability and clonogenic survival in four gastric cancer cell lines, cells were treated with different concentrations of Pevonedistat hydrochloride (0.01-4 μM) for 72 hours, followed by viability assays based on the ATP-lite assay.
RESULTS: Three of the gastric cancer cell lines were more sensitive to the growth inhibitory effects of Pevonedistat hydrochloride than GES-1 cells [3].
In vivo
METHODS: To investigate the mechanism and therapeutic effects ofPevonedistat hydrochloride as an effective and selective NAE inhibitor.
RESULTS: Pevonedistat hydrochloride disrupted cullin-RING ligase-mediated protein turnover, leading to apoptosis in human tumor cells and inhibition of human tumor xenograft growth in mice[1].
AliasMLN-4924 hydrochloride, MLN4924 hydrochloride, MLN 4924 hydrochloride
Chemical Properties
Molecular Weight479.98
FormulaC21H26ClN5O4S
Cas No.1160295-21-5
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 80 mg/mL (166.67 mM), Sonication is recommended.
H2O: 8 mg/mL (16.67 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.0834 mL10.4171 mL20.8342 mL104.1710 mL
5 mM0.4167 mL2.0834 mL4.1668 mL20.8342 mL
10 mM0.2083 mL1.0417 mL2.0834 mL10.4171 mL
DMSO
1mg5mg10mg50mg
20 mM0.1042 mL0.5209 mL1.0417 mL5.2086 mL
50 mM0.0417 mL0.2083 mL0.4167 mL2.0834 mL
100 mM0.0208 mL0.1042 mL0.2083 mL1.0417 mL

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
%Tween 80
%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
Related Tags: buy Pevonedistat hydrochloride | purchase Pevonedistat hydrochloride | Pevonedistat hydrochloride cost | order Pevonedistat hydrochloride | Pevonedistat hydrochloride chemical structure | Pevonedistat hydrochloride in vivo | Pevonedistat hydrochloride in vitro | Pevonedistat hydrochloride formula | Pevonedistat hydrochloride molecular weight