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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
CAL62 cells 2 μM 24 hours Inducing ferroptosis, SIRT6 overexpression enhanced the lethal effect of ML162 PMC9989618
A549 cells 0.5 μM or higher 4 hours Evaluate the inhibitory effect of ML162 on TXNRD1 enzymatic activity PMC10149367
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 PMC10055644
SH-SY5Y neuroblastoma cells 10 µm 24 hours Ferroptosis was induced by the addition of 10 µM (final concentration) of RSL3 or ML162. PMC10886092
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. PMC10571053
Human chondrocytes 5 µM 24, 48, 72 hours Induced ferroptosis, significantly reduced chondrocyte metabolic activity and DNA content PMC10816407
BHT101 cells 2 μM 24 hours Inducing ferroptosis, SIRT6 overexpression enhanced the lethal effect of ML162 PMC9989618
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 PMC9950937

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.09mL

0.42mL

0.21mL

10.47mL

2.09mL

1.05mL

20.95mL

4.19mL

2.09mL

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