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Adenosine receptor antagonist 4
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Catalog No. T21620Cas No. 133240-06-9
Adenosine receptor antagonist 4 is an adenosine receptor antagonist.
Adenosine receptor antagonist 4
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Purity: 99.65%
Catalog No. T21620Cas No. 133240-06-9
Adenosine receptor antagonist 4 is an adenosine receptor antagonist.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 50 mg | $41 | In Stock | In Stock | |
| 100 mg | $68 | In Stock | In Stock | |
| 500 mg | $158 | - | In Stock | |
| 1 g | $237 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $29 | In Stock | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Batch Information
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Purity:99.65%
Appearance:Solid
Color:White to Yellow
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Product Introduction
Adenosine receptor antagonist 4 AI Summary
Adenosine receptor antagonist 4 exhibits a multifaceted range of bioactivities across different assays and targets. It shows 8.0% inhibition in displacing [3H]ZM241385 from the human adenosine A2A receptor and 49.0% inhibition in displacing [125I]AB-MECA from the human adenosine A3 receptor, both at a 1 μM concentration. Additionally, Adenosine receptor antagonist 4 has a Ki value of 101.0 nM for displacing [3H]DPCPX from the human adenosine A1 receptor expressed in CHO cells. It has a basic pKa value (pKa B1) of 5.5, determined through absorption and potentiometric titration methods. In cell viability assays, it affects growth rates with values ranging from 0.2 to 0.96 in human fibroblast, U2OS, and HEK293T cells, indicating potential impacts on cell proliferation and viability. Thermal shift assays reveal that Adenosine receptor antagonist 4 can both stabilize and destabilize various protein domains, indicating diverse influences on protein structure. It also demonstrates modulation of GPCR signaling pathways with varying potency in GPCR beta-arrestin recruitment assays, exhibiting both inhibitory and activating effects across multiple targets..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Adenosine receptor antagonist 4 is an adenosine receptor antagonist. |
| Molecular Weight | 175.23 |
| Formula | C10H13N3 |
| Cas No. | 133240-06-9 |
| Smiles | CCc1nc2c(C)cc(C)nc2[nH]1 |
| Relative Density. | 1.18 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 55 mg/mL (313.87 mM), Sonication is recommended.  | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween-80+45% Saline: 5 mg/mL (28.53 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 | ||||||||||||||||||||||||||||||||||||
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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
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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