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PZ-1129 is a selective ligand for the 5-HT7 receptor (5-HT7 receptor) with a Ki value of 7 nM. It exhibits Ki values of 159 nM for the 5-HT1A receptor and 24 nM for the D2 receptor. PZ-1129 inhibits constitutive cyclic adenosine monophosphate (cAMP) production mediated by the Gs signaling pathway, with an EC50 of 13.7 nM. This compound is applicable for research into affective disorders such as depression and bipolar disorder.
| 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 |
| Description | PZ-1129 is a selective ligand for the 5-HT7 receptor (5-HT7 receptor) with a Ki value of 7 nM. It exhibits Ki values of 159 nM for the 5-HT1A receptor and 24 nM for the D2 receptor. PZ-1129 inhibits constitutive cyclic adenosine monophosphate (cAMP) production mediated by the Gs signaling pathway, with an EC50 of 13.7 nM. This compound is applicable for research into affective disorders such as depression and bipolar disorder. |
| Targets&IC50 | 5-HT7 receptor:7 nM (Ki) |
| Molecular Weight | 454.56 |
| Formula | C25H27FN2O3S |
| Cas No. | 1919029-61-0 |
| Smiles | O=S(=O)(NC1CCN(CCOC=2C=CC=CC2C=3C=CC=CC3)CC1)C4=CC=C(F)C=C4 |
| 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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