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AZD9362
Catalog No. T213765 Copy Product Info
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AZD9362 is a reversible, ATP-competitive inhibitor of the insulin-like growth factor 1 receptor (IGF-1R) and the insulin receptor (insulin receptor) with oral bioavailability. It inhibits IGF-1R enzyme activity with an IC50 value of 14 nM. AZD9362 enhances the antitumor effects of AZD5363 and can be applied in cancer research, including studies on breast cancer.
AZD9362
Copy Product Info🥰Excellent
Catalog No. T213765
AZD9362 is a reversible, ATP-competitive inhibitor of the insulin-like growth factor 1 receptor (IGF-1R) and the insulin receptor (insulin receptor) with oral bioavailability. It inhibits IGF-1R enzyme activity with an IC50 value of 14 nM. AZD9362 enhances the antitumor effects of AZD5363 and can be applied in cancer research, including studies on breast cancer.
AZD9362
Cas No. 1905412-80-7
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | AZD9362 is a reversible, ATP-competitive inhibitor of the insulin-like growth factor 1 receptor (IGF-1R) and the insulin receptor (insulin receptor) with oral bioavailability. It inhibits IGF-1R enzyme activity with an IC50 value of 14 nM. AZD9362 enhances the antitumor effects of AZD5363 and can be applied in cancer research, including studies on breast cancer. |
| In vivo | Administered orally at 25 mg/kg, AZD9362 enhanced the antitumor efficacy of AZD5363 in both MCF-7/LTED cells and MCF-7 xenografts in ovariectomized mice without estrogen supplementation. |
| Molecular Weight | 494.98 |
| Formula | C24H27ClN8O2 |
| Cas No. | 1905412-80-7 |
| Smiles | ClC=1C(C2=C3N(N=C2)C=CC=C3)=NC(NC4=C(C)N(N=C4C)C5CCN(C([C@@H](C)O)=O)CC5)=NC1 |
| 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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
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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