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E/Z-FETPY
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Catalog No. T210127Cas No. 3056250-97-3
E/Z-FETPY is an organic diiron (I) complex with significant cytotoxicity in cancer cell lines, capable of inducing ferroptosis in poorly differentiated cell lines, such as A2780 cells.
E/Z-FETPY
E/Z-FETPY
Copy Product Info😃Good
Catalog No. T210127Cas No. 3056250-97-3
E/Z-FETPY is an organic diiron (I) complex with significant cytotoxicity in cancer cell lines, capable of inducing ferroptosis in poorly differentiated cell lines, such as A2780 cells.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | E/Z-FETPY is an organic diiron (I) complex with significant cytotoxicity in cancer cell lines, capable of inducing ferroptosis in poorly differentiated cell lines, such as A2780 cells. |
| In vitro | E/Z-FETPY demonstrates cytotoxic potential by inhibiting the growth of HCT 116, MCF7, and A2780 cells, with IC50 values of 4 μM, 2.1 μM, and 2.5 μM, respectively. At a concentration of 2.5 μM over 24-48 hours, E/Z-FETPY increases iron uptake in A2780 cells over time. It inhibits hydrogen peroxide (H2O2) and peroxynitrite (O═NOO-), while enhancing the production of superoxide anions (O2-) and nitric oxide (NO). Additionally, FETPY at 5 μM induces significant morphological changes in murine B16-F1 and B16-F10 melanoma cells, leading to senescence and/or transdifferentiation into Schwann-like cells, thereby significantly diminishing their tumorigenic potential. |
| In vivo | Administered at 4 mg/kg via intraperitoneal injection once daily for three weeks, FETPY significantly reduces growth rates and tumor volume in both models. |
| Molecular Weight | 628.24 |
| Formula | C22H23F3Fe2N2O5S2 |
| Cas No. | 3056250-97-3 |
| Smiles | O#C[Fe+4]123456([C-2](=O)[Fe+4]789%102(=[C-3]1SC)([N]=%11C=CC(=CC%11)N(C)C)[CH]=%12[CH]%10=[CH]9[CH-]8[CH]%127)[CH]=%13[CH]6=[CH]5[CH-]4[CH]%133.O=S(=O)([O-])C(F)(F)F |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
Dissolve 2 mg of the compound in 100 μL DMSO to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
Preparation of the In Vivo Formulation:
1) Add 100 μL of the DMSO stock solution to 400 μL PEG300 and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O and mix thoroughly until a homogeneous solution is obtained.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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