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A2A/A3 agonist-1 serves as a dual A2A/A3 adenosine receptor agonist. It has a Ki value greater than 2.9 nM and an EC50 of 0.51 nM for hA2AAR. For hA3AR, the Ki is 0.8 nM and the EC50 is less than 0.10 nM. A2A/A3 agonist-1 exhibits anti-inflammatory properties and is applicable in the research of inflammatory diseases.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | A2A/A3 agonist-1 serves as a dual A2A/A3 adenosine receptor agonist. It has a Ki value greater than 2.9 nM and an EC50 of 0.51 nM for hA2AAR. For hA3AR, the Ki is 0.8 nM and the EC50 is less than 0.10 nM. A2A/A3 agonist-1 exhibits anti-inflammatory properties and is applicable in the research of inflammatory diseases. |
| In vitro | A2A/A3 agonist-1 (10-50 nM; 24 hours) demonstrates significant inhibitory effects on IL-12/IL-23p40 and IL-6 in LPS-stimulated bone marrow-derived dendritic cells (BMDCs). Additionally, A2A/A3 agonist-1 (1 μM; 0-60 minutes) exhibits good metabolic stability in human liver microsomes and plasma, with no evident hERG inhibition. |
| 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.
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