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Synonyms:
A2AAR antagonist 2
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | 3′-Methoxyfurano[4″,5″:3,4]chalcone (Compound 2) is a selective A2AAR antagonist with an IC50 of 33.5 nM, indicating it has a high affinity. This compound is a natural product that can be extracted from the skins of Allium cepa L. Additionally, 3′-Methoxyfurano[4″,5″:3,4]chalcone is capable of promoting T cell activation and is useful in cancer immunology research. |
| Targets & IC50 | A2a adenosine receptor:33.5 nM |
| Formula | C18H14O3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
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.
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.
| Size | Quantity | Unit Price | Amount | Operation |
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