Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Pipamperone acts as an antagonist of the 5-HT2A, 5-HT2B, 5-HT2C D2, D3, D4, α1-adrenergic, and α2-adrenergic receptors. It shows much higher affinity for the 5-HT2A and D4 receptors over the D2 receptor (15-fold in the case of the D4 receptor, and even higher in the case of the 5-HT2A receptor), being regarded as "highly selective" for the former two sites at low doses. Pipamperone has low and likely insignificant affinity for the H1 and mACh receptors, as well as for other serotonin and dopamine receptors.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 mg | 6-8 weeks | $ 1,520.00 | |
50 mg | 6-8 weeks | $ 1,980.00 | |
100 mg | 6-8 weeks | $ 2,500.00 |
Description | Pipamperone acts as an antagonist of the 5-HT2A, 5-HT2B, 5-HT2C D2, D3, D4, α1-adrenergic, and α2-adrenergic receptors. It shows much higher affinity for the 5-HT2A and D4 receptors over the D2 receptor (15-fold in the case of the D4 receptor, and even higher in the case of the 5-HT2A receptor), being regarded as "highly selective" for the former two sites at low doses. Pipamperone has low and likely insignificant affinity for the H1 and mACh receptors, as well as for other serotonin and dopamine receptors. |
Synonyms | fluoropipamide, floropipamide hydrochloride, carpiperone, floropipamide, R4050, Pipamperone |
Molecular Weight | 411.95 |
Formula | C21H31ClFN3O2 |
CAS No. | 2448-68-2 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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Pipamperone HCl 2448-68-2 fluoropipamide floropipamide Hydrochloride floropipamide hydrochloride carpiperone R-4050 floropipamide R4050 R 4050 Pipamperone inhibitor inhibit