ML 210 GPX4 Inhibitor

Cat.No.S0788

ML-210 (CID 49766530) is a selective covalent inhibitor of cellular glutathione peroxidase 4 (GPX4) with EC50 of 0.04 μM and induces ferroptosis. ML-210 can selectively kill cells induced to express mutant RAS. ML-210 exhibits anti-cancer activity.
ML 210 Peroxidases inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 475.32

Quality Control

Cell Culture, Treatment & Working Concentration

Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
BJeLR Cytotoxicity assay 48 hrs Cytotoxicity against human BJeLR cells expressing HRAS G12V mutant after 48 hrs by alamar blue assay, IC50 = 0.071 μM. 22297109
BJ Cytotoxicity assay 48 hrs Cytotoxicity against human BJ cells expressing HRAS G12V mutant with alternative oncogenic constructs after 48 hrs by alamar blue assay, IC50 = 0.107 μM. 22297109
BJeH-LT Cytotoxicity assay 48 hrs Cytotoxicity against human BJeH-LT cells after 48 hrs by alamar blue assay, IC50 = 0.272 μM. 22297109
BJeH Cytotoxicity assay 48 hrs Cytotoxicity against human BJeH cells after 48 hrs by alamar blue assay, IC50 = 0.628 μM. 22297109
Click to View More Cell Line Experimental Data

Chemical Information, Storage & Stability

Molecular Weight 475.32 Formula

C22H20Cl2N4O4

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 1360705-96-9 -- Storage of Stock Solutions

Synonyms CID 49766530 Smiles CC1=C(C(=NO1)C(=O)N2CCN(CC2)C(C3=CC=C(C=C3)Cl)C4=CC=C(C=C4)Cl)[N+](=O)[O-]

Solubility

In vitro
Batch:

DMSO : 24 mg/mL (50.49 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 3 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

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%
% Tween 80
% ddH2O
% DMSO
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Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
RAS [1]
GPX4 [2]
(Cell-free assay)
0.04 μM(EC50)
In vitro

ML-210 has IC50s of 71 nM, 272 nM and 107nM for BJeLR (HRASV12), BJeH-LT (without HRASV12) and DRD cell lines, respectively[2].[1]

References

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