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Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $1,980 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $2,500 | 6-8 weeks | 6-8 weeks |
| Description | Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia. |
| Targets&IC50 | D2 receptor:8.83 (pKi), 5-HT1A receptor:6.37(pEC50), 5-HT1A receptor:7.19 (pKi) |
| In vitro | Bifeprunox has a pKi of 8 at h5-HT1A receptors (Emax: 70%) [1]. |
| In vivo | Bifeprunox (0.001-2.5 mg/kg) reduces marble burying in mice [2] and (4-250 μg/kg) alters nicotine-seeking behavior in response to drug-associated stimuli in rats [3]. |
| Molecular Weight | 385.46 |
| Formula | C24H23N3O2 |
| Cas No. | 350992-10-8 |
| Smiles | O=C1NC2=CC=CC(N3CCN(CC4=CC=CC(=C4)C4=CC=CC=C4)CC3)=C2O1 |
| Relative Density. | 1.247g/cm3 |
| 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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