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Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) is an inducer of ferroptosis.1 It induces ferroptosis, but not apoptosis or necroptosis, in NB1 cancer cells when used at a concentration of 3 μM.1 Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) inhibits proliferation of BJAB, NALM-6, Jurkat, MelHO, and MCF-7 cancer cells (IC50s = 0.07, 2.5, 1.5, 3, and 5 μM, respectively), as well as NALM-6 cells resistant to daunorubicin and vincristine when used at concentrations ranging from 0.04 to 0.125 μM.2
![Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III)](https://cdn.targetmol.com/group3/M00/03/88/CgoaEWY7Tu-EOm1KAAAAAMYBAbA153.png)
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $137 | 35 days | 35 days | |
| 10 mg | $232 | 35 days | 35 days | |
| 50 mg | $862 | 35 days | 35 days | |
| 100 mg | $1,580 | 35 days | 35 days |
| Description | Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) is an inducer of ferroptosis.1 It induces ferroptosis, but not apoptosis or necroptosis, in NB1 cancer cells when used at a concentration of 3 μM.1 Chlorido[N,N'-disalicylidene-1,2-phenylenediamine]iron(III) inhibits proliferation of BJAB, NALM-6, Jurkat, MelHO, and MCF-7 cancer cells (IC50s = 0.07, 2.5, 1.5, 3, and 5 μM, respectively), as well as NALM-6 cells resistant to daunorubicin and vincristine when used at concentrations ranging from 0.04 to 0.125 μM.2 |
| Molecular Weight | 405.64 |
| Formula | C20H14ClFeN2O2 |
| Cas No. | 39916-28-4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO: 14 mg/mL (34.51 mM), Sonication is recommended. DMF: 20 mg/mL (49.3 mM), Sonication is recommended. PBS (pH 7.2): Partially Soluble Ethanol: 0.3 mg/mL (0.74 mM), Sonication is recommended. |
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