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ML162

Product Name
ML162
CAS No.
1035072-16-2
Chemical Name
ML162
Synonyms
ML162;ML162, 10 mM in DMSO;2-Thiopheneacetamide, α-[(2-chloroacetyl)(3-chloro-4-methoxyphenyl)amino]-N-(2-phenylethyl)-;2-Chloro-N-(3-chloro-4-methoxyphenyl)-N-(2-oxo-2-(phenethylamino)-1-(thiophen-2-yl)ethyl)acetamide;2-Chloro-N-(3-chloro-4-methoxyphenyl)-N-{2-oxo-2-[(2-phenylethyl)amino]-1-(2-thienyl)ethyl}acetamide;p62,Glutathione Peroxidase,GPX4,ML-162,Nrf2,anticancer,HRAS,Ferroptosis,Inhibitor,inhibit,ML 162,ML162
CBNumber
CB04203599
Molecular Formula
C23H22Cl2N2O3S
Formula Weight
477.40338
MOL File
1035072-16-2.mol
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ML162 Property

Boiling point:
699.3±55.0 °C(Predicted)
Density 
1.342±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMF:10.0(Max Conc. mg/mL);20.95(Max Conc. mM)
DMSO:25.0(Max Conc. mg/mL);52.37(Max Conc. mM)
Ethanol:1.0(Max Conc. mg/mL);2.09(Max Conc. mM)
form 
A crystalline solid
pka
13.84±0.46(Predicted)
color 
Off-white to light yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML2561
Product name
ML162
Purity
≥98% (HPLC)
Packaging
5MG
Price
$100
Updated
2025/07/31
Sigma-Aldrich
Product number
SML2561
Product name
ML162
Purity
≥98% (HPLC)
Packaging
25MG
Price
$406
Updated
2025/07/31
Cayman Chemical
Product number
20455
Product name
ML-162
Purity
≥95%
Packaging
1mg
Price
$46
Updated
2024/03/01
Cayman Chemical
Product number
20455
Product name
ML-162
Purity
≥95%
Packaging
500μg
Price
$31
Updated
2023/06/20
Cayman Chemical
Product number
20455
Product name
ML-162
Purity
≥95%
Packaging
5mg
Price
$92
Updated
2024/03/01
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ML162 Chemical Properties,Usage,Production

Description

ML-162 is an inhibitor of glutathione peroxidase 4 (GPX4) and decreases GPX4 levels in MDA-MB-231 breast cancer cells, as well as the viability of BT-549 breast cancer cells.

Uses

ML162 is a covalent glutathione peroxidase 4 (GPX4) inhibitor. ML162 has a selective lethal effect on mutant RAS oncogene-expressing cell lines[1][2]

storage

Store at -20°C

References

[1] Michel We?wer, et al. Development of small-molecule probes that selectively kill cells induced to express mutant RAS. Bioorg Med Chem Lett. 2012 Feb 15;22(4):1822-6. DOI:10.1016/j.bmcl.2011.09.047
[2] Daiha Shin, et al. Nrf2 inhibition reverses resistance to GPX4 inhibitor-induced ferroptosis in head and neck cancer. Free Radic Biol Med. 2018 Dec;129:454-462. DOI:10.1016/j.freeradbiomed.2018.10.426

ML162 Preparation Products And Raw materials

Raw materials

Preparation Products

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ML162 Suppliers

Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354;
Email
support@targetmol.com
Country
United States
ProdList
39035
Advantage
58
EBRATOR BIOCHEMICALS,INC.
Tel
--
Fax
--
Email
sales@ebtbio.com
Country
United States
ProdList
577
Advantage
58
Abcam Limited
Tel
--
Fax
--
Email
us.orders@abcam.com
Country
United States
ProdList
6001
Advantage
50
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81

1035072-16-2, ML162Related Search:


  • 2-Chloro-N-(3-chloro-4-methoxyphenyl)-N-{2-oxo-2-[(2-phenylethyl)amino]-1-(2-thienyl)ethyl}acetamide
  • ML162
  • p62,Glutathione Peroxidase,GPX4,ML-162,Nrf2,anticancer,HRAS,Ferroptosis,Inhibitor,inhibit,ML 162,ML162
  • 2-Thiopheneacetamide, α-[(2-chloroacetyl)(3-chloro-4-methoxyphenyl)amino]-N-(2-phenylethyl)-
  • 2-Chloro-N-(3-chloro-4-methoxyphenyl)-N-(2-oxo-2-(phenethylamino)-1-(thiophen-2-yl)ethyl)acetamide
  • ML162, 10 mM in DMSO
  • 1035072-16-2