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Dexrazoxane

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Catalog No. T22305Cas No. 24584-09-6
Alias ICRF-187

Dexrazoxane (ICRF-187) is an anticancer drug used to block mitosis and arrest dividing cells. It is an iron chelator and provides cardioprotection against anthracycline toxicity.

Dexrazoxane

Dexrazoxane

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Purity: 99.88%
Catalog No. T22305Alias ICRF-187Cas No. 24584-09-6
Dexrazoxane (ICRF-187) is an anticancer drug used to block mitosis and arrest dividing cells. It is an iron chelator and provides cardioprotection against anthracycline toxicity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$39In StockIn Stock
50 mg$57In StockIn Stock
100 mg$81In StockIn Stock
500 mg$200In StockIn Stock
1 mL x 10 mM (in DMSO)$45In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.88%
Appearance:Solid
Color:White to Yellow
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Product Introduction

Dexrazoxane AI Summary
Dexrazoxane is a multifaceted compound studied for its pharmacokinetics, bioactivity, and potential therapeutic applications. It has a total body clearance of 3.1 mL/min/kg and a renal clearance of 1.4 mL/min/kg, indicating how it is processed and eliminated. With a volume of distribution at steady state of 0.55 L/kg and a half-life of 2.5 hours, it distributes well in the body and remains active for a moderate duration. The compound shows involvement in various liver enzyme activities but exhibits no bioactivities related to drug-induced liver injury. It demonstrates inhibitory effects in NCI human tumor cell line growth assays and has antiviral activity against SARS-CoV-2. Additionally, Dexrazoxane has moderate antimalarial activity against Plasmodium species and impacts epirubicin pharmacokinetics in dogs. In terms of toxicity, it exhibits elevated serum enzyme activities indicative of moderate liver toxicity, but no severe liver conditions were reported. The compound shows metal chelation capability and possesses cardioprotective, antiproliferative, and specific enzyme inhibitory activities, though with generally low potency. It also induces DNA damage in human HCT15 cells and demonstrates minimal activity against certain viral infections in VERO-6 cells. Despite these diverse properties, it exhibits low binding affinity and inhibitory activity in various in vitro assays..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Dexrazoxane (ICRF-187) is an anticancer drug used to block mitosis and arrest dividing cells. It is an iron chelator and provides cardioprotection against anthracycline toxicity.
SynonymsICRF-187
Chemical Properties
Molecular Weight268.27
FormulaC11H16N4O4
Cas No.24584-09-6
SmilesC[C@@H](CN1CC(=O)NC(=O)C1)N1CC(=O)NC(=O)C1
Relative Density.1.333 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 57 mg/mL (212.47 mM), Sonication is recommended.
Methanol: 1.25 mg/mL (4.66 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (7.46 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
Methanol/DMSO
1mg5mg10mg50mg
1 mM3.7276 mL18.6379 mL37.2759 mL186.3794 mL
DMSO
1mg5mg10mg50mg
5 mM0.7455 mL3.7276 mL7.4552 mL37.2759 mL
10 mM0.3728 mL1.8638 mL3.7276 mL18.6379 mL
20 mM0.1864 mL0.9319 mL1.8638 mL9.3190 mL
50 mM0.0746 mL0.3728 mL0.7455 mL3.7276 mL
100 mM0.0373 mL0.1864 mL0.3728 mL1.8638 mL

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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:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 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 DMSOTargetMol | reagent 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 DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent 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.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

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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