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AZ 5704
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Catalog No. T35942Cas No. 1941214-06-7
Alias AZ-5704, AZ5704, ATM Inhibitor-10
AZ 5704 (compound 74) is a selective and orally active ATM inhibitor (IC50 = 0.6 nM), which can enhance the anti-tumor activity of irinotecan in the SW620 xenograft model.
AZ 5704
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Purity: 99.69%
Catalog No. T35942Alias AZ-5704, AZ5704, ATM Inhibitor-10Cas No. 1941214-06-7
AZ 5704 (compound 74) is a selective and orally active ATM inhibitor (IC50 = 0.6 nM), which can enhance the anti-tumor activity of irinotecan in the SW620 xenograft model.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $109 | - | In Stock | |
| 5 mg | $267 | - | In Stock | |
| 10 mg | $393 | - | In Stock | |
| 25 mg | $676 | - | In Stock | |
| 50 mg | $952 | - | In Stock | |
| 100 mg | $1,280 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.69%
Appearance:Solid
Color:White
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | AZ 5704 (compound 74) is a selective and orally active ATM inhibitor (IC50 = 0.6 nM), which can enhance the anti-tumor activity of irinotecan in the SW620 xenograft model. |
| Targets&IC50 | DNAPK:370 nM, ATM:0.6 nM, PI3Kα:0.445 μM, mTOR:1.48 μM |
| In vivo | Method: In immunodeficient SW620 (colorectal cell line) tumor-bearing mice, administer Irinotecan (50 mg/kg, intraperitoneal injection, once daily on Day 1) and AZ 5704 (50 mg/kg, oral, twice daily on Days 2 and 4; no dosing on Days 5 and 7). Results: AZ 5704 monotherapy showed no significant efficacy. However, after 3 weeks of combination therapy with Irinotecan, tumor growth in the SW620 xenograft model was markedly reduced, with greater efficacy than Irinotecan monotherapy. |
| Synonyms | AZ-5704, AZ5704, ATM Inhibitor-10 |
| Molecular Weight | 434.47 |
| Formula | C23H23FN6O2 |
| Cas No. | 1941214-06-7 |
| Smiles | N([C@@H](C)C1=NN(C)C=C1)C=2C3=C(C=C(F)C(=C3)C=4C=CC(COC)=NC4)N=CC2C(N)=O |
| Relative Density. | 1.36 g/cm3 (Predicted) |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO: Soluble, Sonication is recommended. |
Calculator
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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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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