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Antitumor agent-145
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Catalog No. T85706Cas No. 2983120-65-4
Compound Ir5 (Antitumor agent-145) serves as a tumor inhibitor characterized by significant fluorescence and mitochondrial targeting. It promotes anti-cancer activity by inducing necroptosis and stimulating the necroptosis-related immune response [1].
Antitumor agent-145
Antitumor agent-145
Copy Product Info😃Good
Catalog No. T85706Cas No. 2983120-65-4
Compound Ir5 (Antitumor agent-145) serves as a tumor inhibitor characterized by significant fluorescence and mitochondrial targeting. It promotes anti-cancer activity by inducing necroptosis and stimulating the necroptosis-related immune response [1].
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
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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 | Compound Ir5 (Antitumor agent-145) serves as a tumor inhibitor characterized by significant fluorescence and mitochondrial targeting. It promotes anti-cancer activity by inducing necroptosis and stimulating the necroptosis-related immune response [1]. |
| In vitro | Antitumor agent-145 (Compound Ir5) has an IC 50 value of 0.49 μM against BEL-7402/DDP cells over 48 hours with a resistance factor (RF) of 1.04, and it exhibits no significant cytotoxicity [1]. |
| In vivo | Antitumor agent-145 (Compound Ir5), administered intravenously at doses of 1.5 or 3.0 mg/kg every other day for 21 days, effectively reduces tumor volume in BALB/c mice without causing significant liver or kidney dysfunction [1]. In the BEL-7402/DDP tumor xenograft model, Ir5 significantly inhibits the growth and metastasis of CDDP-resistant tumors, displaying an inhibition rate of tumor growth (IRT) of 40.0% at 1.5 mg/kg and 58.1% at 3 mg/kg, compared to 10.1% in the CDDP group, without inducing notable tissue damage [1]. |
| Molecular Weight | 873.06 |
| Formula | C44H34IrN5OS |
| Cas No. | 2983120-65-4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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.
Dose Conversion
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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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