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P2Y2R antagonist 1 is a selective P2Y2R antagonist with a pIC50 of 7.78 and is utilized in glioma research.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | P2Y2R antagonist 1 is a selective P2Y2R antagonist with a pIC50 of 7.78 and is utilized in glioma research. |
| In vitro | P2Y2R antagonist 1 (Compound 32g) shows no activity against hP2Y1, hP2Y4, and hP2Y11 receptors in 1321N1 cells (pIC 50 < 5), and exhibits a 0% inhibition rate for the P2Y11 receptor at a concentration of 10 μM. It has a LogD 7.4 value of 4.57, indicating high lipophilicity. When administered at 0.1-10 μM for 1-72 hours, P2Y2R antagonist 1 demonstrates significant cytotoxicity in 1321N1 cells at 10 μM, with the peak effect occurring at 48 hours, while CHO cells exhibit lower sensitivity to this P2Y2R antagonist. |
| 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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