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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 1035072-16-2 Chemical Structure| 1035072-16-2

Structure of ML162
CAS No.: 1035072-16-2

Chemical Structure| 1035072-16-2

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ML162 is a covalent GPX4 inhibitor that selectively kills cell lines expressing mutant RAS oncogenes.

Synonyms: ML162

4.5 *For Research Use Only !

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Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

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Product Details of ML162

CAS No. :1035072-16-2
Formula : C23H22Cl2N2O3S
M.W : 477.40
SMILES Code : O=C(N(C1=CC=C(OC)C(Cl)=C1)C(C2=CC=CS2)C(NCCC3=CC=CC=C3)=O)CCl
Synonyms :
ML162
MDL No. :MFCD03450805

Safety of ML162

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:8
UN#:3261
Packing Group:

Related Pathways of ML162

ferroptosis

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
COS-7 cells 0.001 to 8 μM 24 hours Evaluate the effect of ML-162 on the viability of COS-7 cells, results showed that WT cells overexpressing CYP2E1 were less sensitive to ML-162 than Mock cells Res Sq [Preprint]. 2023 Mar 22:rs.3.rs-2702878.
SH-SY5Y neuroblastoma cells 10 µm 24 hours Ferroptosis was induced by the addition of 10 µM (final concentration) of RSL3 or ML162. Antioxidants (Basel). 2024 Feb 17;13(2):242.
A673 cells 10 µM 30 minutes To evaluate the inhibitory effect of ML162 on P-gp-mediated rhodamine 123 transport. Results showed that ML162 significantly increased intracellular rhodamine 123 fluorescence in P-gp-expressing cells. Cancer Drug Resist. 2023 Jul 27;6(6):468-480.
Human chondrocytes 5 µM 24, 48, 72 hours Induced ferroptosis, significantly reduced chondrocyte metabolic activity and DNA content J Clin Med. 2024 Jan 18;13(2):559.
A549 cells 0.5 μM or higher 4 hours Evaluate the inhibitory effect of ML162 on TXNRD1 enzymatic activity Redox Biol. 2023 Jun;62:102703.
BHT101 cells 2 μM 24 hours Inducing ferroptosis, SIRT6 overexpression enhanced the lethal effect of ML162 Am J Cancer Res. 2023 Feb 15;13(2):464-474.
CAL62 cells 2 μM 24 hours Inducing ferroptosis, SIRT6 overexpression enhanced the lethal effect of ML162 Am J Cancer Res. 2023 Feb 15;13(2):464-474.
RPMI-8226 8.181 μM 24 hours Evaluate the cytotoxicity of ML162 on RPMI-8226 cells, results showed that ML162 has synergistic effects when combined with bortezomib or lenalidomide Front Oncol. 2023 Feb 10;13:999688.

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

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10 mM

2.09mL

0.42mL

0.21mL

10.47mL

2.09mL

1.05mL

20.95mL

4.19mL

2.09mL

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