Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Ropinirole (SKF 101468) is a selective D2-like family receptor agonist whereas it has no affinity for the D1 receptors. It is an orally active, potent D3/D2 receptor agonist with a Ki of 29 nM for D2 receptor, which also has pEC50s of 7.4, 8.4 and 6.8 for hD2, hD3 and hD4 receptors, respectively. Ropinirole has the potential for the treatment of Parkinson's disease[1] [2].
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 | Ropinirole (SKF 101468) is a selective D2-like family receptor agonist whereas it has no affinity for the D1 receptors. It is an orally active, potent D3/D2 receptor agonist with a Ki of 29 nM for D2 receptor, which also has pEC50s of 7.4, 8.4 and 6.8 for hD2, hD3 and hD4 receptors, respectively. Ropinirole has the potential for the treatment of Parkinson's disease[1] [2]. |
In vitro | Ropinirole has 10-20 times higher affinity for D 3 receptors than for D 2 and D 4 receptors. It is weakly active at α2-adrenoceptors and 5-HT2 receptors but inactive at 5-HT1, benzodiazepine and gamma-aminobu acid receptors or α1 and β-adrenoceptors [1] [2]. |
In vivo | Ropinirole, administered intraperitoneally at doses ranging from 0.1 to 10 mg/kg, effectively reduces intracranial self-stimulation thresholds and exhibits anxiolytic- and antidepressant-like properties, without impacting motor function or spatial memory [2]. |
Molecular Weight | 260.37 |
Formula | C16H24N2O |
CAS No. | 91374-21-9 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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Ropinirole 91374-21-9 inhibitor inhibit