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Cat.No.S7243
| Related Targets | Dehydrogenase HSP Transferase P450 (e.g. CYP17) PDE phosphatase PPAR Vitamin Carbohydrate Metabolism Mitochondrial Metabolism |
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| Other Ferroptosis Inhibitors | Liproxstatin-1 Erastin Imidazole Ketone Erastin (IKE) FIN56 iFSP1 UAMC-3203 SRS11-92 SRS16-86 icFSP1 N6F11 |
| Cell Lines | Assay Type | Concentration | Incubation Time | Formulation | Activity Description | PMID |
|---|---|---|---|---|---|---|
| human IMR32 neuroblastoma cells | Function assay | 13 h | Antiferroptotic activity in human IMR32 neuroblastoma cells assessed as inhibition of erastin-induced cell death preincubated for 1 hr before erastin stimulation and measured after 13 hrs by fluorescence plate reader method, IC50=0.018 μM | 26696014 | ||
| HT1080 cells | Function assay | Antiferroptotic activity in human HT1080 cells assessed as inhibition of erastin-induced cell death by Alamar blue assay, IC50=0.095 μM | 26696014 | |||
| HRE cells | Cell viability assay | 1 μM | 48-72 hours | Induction of cell apoptosis | 30794682 | |
| U57810 and C2C12 cells | Cell viability assay | 10 μM | 24, 48, and 72 h | Administration of ferrostatin-1 almost completely prevented the ferroptotic cell death. | 29971532 | |
| Leishmania major Friedlin clone V1 | Antileishmanial assay | 72 h | LD50 = 28.75 μM | 26410073 | ||
| IMR32 | Function assay | 1 h | IC50 = 0.033 μM | 30354101 | ||
| Click to View More Cell Line Experimental Data | ||||||
| Molecular Weight | 262.35 | Formula | C15H22N2O2 |
Storage (From the date of receipt) | |
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| CAS No. | 347174-05-4 | Download SDF | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CCOC(=O)C1=CC(=C(C=C1)NC2CCCCC2)N | ||
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In vitro |
DMSO
: 55 mg/mL
(209.64 mM)
Ethanol : 55 mg/mL Water : Insoluble |
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In vivo |
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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
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| Targets/IC50/Ki |
Ferroptosis
(HT-1080 cells) 60 nM(EC50)
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| In vitro |
Ferrostatin-1 (Fer-1) (2 μM) prevents erastin-induced ferroptosis in cancer cells, as well as glutamate-induced cell death in postnatal rat brain slices. It is a lipid ROS scavenger, with the N-cyclohexyl moiety serving as a lipo-philic anchor within biological membranes. This compound does not inhibit extracellular signal -regulated kinase (ERK) phos-phorylation or arrest the proliferation of HT-1080 cells, suggesting that it does not inhibit the MEK/ERK pathway, chelate iron, or inhibit protein synthesis. It does, however, prevent erastin-induced accumulation of cytosolic and lipid ROS. Ferrostatin-1 readily oxidizes the stable radical 2,2-diphenyl-1-picrylhydrazyl (DPPH) under cell-free conditions. |
| In vivo |
Ferrostatin-1 (Fer-1), a synthetic antioxidant, is a potent and selective inhibitor of ferroptosis. It acts via a reductive mechanism to prevent damage to membrane lipids and thereby inhibits cell death. |
References |
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| Methods | Biomarkers | Images | PMID |
|---|---|---|---|
| Western blot | Nrf2 / Gpx4 / β-Actin gp91 phox / β-actin KIM-1 / NGAL / β-actin Collagen I / β-actin cleaved caspase-3 / β-actin |
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31571665 |
| Growth inhibition assay | Cell viability Cell viability |
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31899616 |
| Immunofluorescence | γH2AX morphological features of HT-22 cells renal apoptosis ROS formation |
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31899616 |
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