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GPX4-IN-19

CAT: 0804-HY-178364-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-178364-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
GPX4-IN-19 is an effective GPX4 inhibitor (IC50 = 0.311 μM), covalently binds to the Sec 46 site of GPX4. GPX4-IN-19 shows strong anti-proliferative activity with high ferroptosis selectivity. GPX4-IN-19 causes intracellular Fe²⁺ accumulation, leading to increased levels of lipid peroxides (LPOs) and reactive oxygen species (ROS), which induces ferroptosis and subsequently results in DNA damage. GPX4-IN-19 can be used for the study of Triple-Negative Breast Cancer (TNBC) [1].
CAS Number
3102894-57-2
UNSPSC
12352005
Target
DNA/RNA Synthesis; Ferroptosis; Glutathione Peroxidase; Lipoxygenase; Reactive Oxygen Species (ROS)
Related Pathways
Apoptosis; Cell Cycle/DNA Damage; Immunology/Inflammation; Metabolic Enzyme/Protease; NF-κB
Applications
Cancer-programmed cell death
Field of Research
Cancer
Concentration
10mM
Purity
99.45
Solubility
DMSO : 50 mg/mL (ultrasonic)
Smiles
COC1=CC(N(C(CCl)=O)CC2=CC3=C(OCCO3)C=C2)=CC(OC)=C1F
Molecular Formula
C19H19ClFNO5
Molecular Weight
395.81
References & Citations
[1]Ning M, et al. Discovery of novel benzylaniline derivatives containing chloroacetamide as GPX4 inhibitors with potential efficacy in triple-negative breast cancer. Eur J Med Chem. 2025 Dec 15;300:118189.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported

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