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GPX

Glutathione peroxidase (GPx) is an important peroxide disintegrating enzyme widely present in the organism.The active center of GSx is selenocysteine, and the amount of its activity can reflect the selenium level of the organism. Selenium is a component of the GSx enzyme system, which catalyzes the change of GSH to GSSG and the reduction of toxic peroxides to non-toxic hydroxyl compounds, thus protecting the structure and function of cell membranes from the interference and damage caused by peroxides.The reduction of NADPH is linearly correlated with the activity of glutathione peroxidase.

  • RSL3
    T36461219810-16-8
    RSL3 (RSL3 1S) is an inhibitor of GPX4, and inhibits system xc- that blocks GSH synthesis (IC50=100 nM). RSL3 is a VDAC-independent activator of ferroptosis that is selective for tumor cells carrying oncogenic RAS.
    • $33
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  • JKE-1674
    T373142421119-60-8
    JKE-1674 is an orally active glutathione peroxidase 4 (GPX4) inhibitor and the active metabolite of ML-210, which is converted to butyronitrile oxide JKE-1777. JKE-1674 kills LOX-IMVI cells in the same manner as ML-210 and is completely rescued by ferroptosis inhibitors.
    • $48
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  • ML162
    T89701035072-16-2
    ML162 is a covalent glutathione peroxidase 4 (GPX4) inhibitor that induces ferroptosis. ML162 has antitumor activity and selectively inhibits cell lines expressing mutant RAS oncogenes.
    • $91
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    TargetMol | Citations Cited
  • PKUMDL-LC-101-D04
    T369352143896-83-5
    PKUMDL-LC-101-D04 is a potent allosteric activator of glutathione peroxidase 4 (GPX4), a regulator of ferroptosis. GPX4 activity was increased to 150% of control levels when used at a concentration of 20 μM in a cell-free assay, and at a concentration of 61 μM in wild-type, but not Gpx4-/-, mouse embryonic fibroblast (MEF) extracts.PKUMDL-LC-101-D04 (200 μM) reduced cholesterol peroxide-induced MEF death.
    • $80
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  • N6F11
    T77745851398-76-0
    N6F11 is a novel, selective and potent inducer of ferroptosis with anticancer and antitumour activity that promotes GPX4 degradation by binding to TRIM25 in cancer cells.N6F11 can be used to study pancreatic cancer.
    • $195
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  • ML-210
    T83751360705-96-9
    ML-210 (CID 49766530) is a glutathione peroxidase 4 (GPX4) inhibitor (EC50=30 nM) that is covalent and selective. ML-210 has antitumor activity and induces ferroptosis.
    • $34
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    TargetMol | Citations Cited
  • Misonidazole
    T2189913551-87-6
    Misonidazole as a novel GPX inhibitors to cause oxidative stress in chemotherapy-resistant tumors.
    • $42
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  • 3-Deoxyglucosone
    T191174084-27-9
    3-Deoxyglucosone(3-Deoxy-D-glucosone) is synthesized by the intermediate pathway of the melad and polyol reactions.3-Deoxyglucosone reacts rapidly with protein amino groups to form advanced glycosylated end proteins (AGEs).3-Deoxyglucosone inactivates glutathione peroxidase and synergizes with low glucose to enhance GLP-1 secretion.3-Deoxyglucosone is used as a biomarker for diabetes mellitus.3-Deoxyglucosone has been shown to be an inhibitor of GLP-1 secretion in the presence of low glucose. 3-Deoxyglucosone inactivates glutathione oxidase, synergizes with low glucose to enhance GLP-1 secretion, and can be used as a biologic marker for diabetes.
    • $188
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  • GPX4-IN-6
    T777592922824-07-3
    GPX4-IN-6 is a small molecule covalent GPX4 inhibitor (IC50: 0.12 μM) with antitumour activity.GPX4-IN-6 induces ferroptosis and is used for the treatment= and prevention of triple negative breast cancer (TNBC).
    • $64
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  • GPX4-IN-5
    T777552922824-09-5
    GPX4-IN-5 is a small molecule covalent GPX4 inhibitor (IC50: 0.12 μM) with antitumour activity.GPX4-IN-5 induces ferroptosis and can be used for the prevention and treatment of triple-negative breast cancer (TNBC).
    • $63
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  • BCP-T.A
    T628272786829-70-5
    BCP-T.A is an ferroptosis inducer that acts by binding to GPX4.
    • $78
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