Molecular Formula | C24H25FN4O2 |
Molar Mass | 420.48 |
Melting Point | 180.0 to 184.0 °C |
Appearance | powder to crystal |
Color | White to Light yellow |
Storage Condition | 2-8°C |
In vitro study | Ocaperidone has high affinify at 5-HT 2 and dopamine D 2 , with K i s of 0.14 nM, 0.46 nM, 0.75 nM, 1.6 nM and 5.4 nM for 5HT 2 , a 1 -adrenergic, dopamine D 2 , histamine H 1 and a 2 -adrenergic, respectively. Ocaperidone shows 5-HT 1A receptor agonist activity, with a pEC 50 and pK i of 7.60 and 8.08. |
In vivo study | Ocaperidone shows a potent occupation of 5HT 2 receptor via in vivo binding in the frontal cortex of rats with an ED 50 of 0.04 mg/kg, and 0.1 4-0.1 6 mg/kg for D 2 receptor in the striatum and the nucleus accumbens. Ocaperidone (R 79598) antagonizes dopamine D 2 and 5-HT 2 , and shows a a partial generalization to buspirone with an ED 50 of 0.163 mg/kg. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.378 ml | 11.891 ml | 23.782 ml |
5 mM | 0.476 ml | 2.378 ml | 4.756 ml |
10 mM | 0.238 ml | 1.189 ml | 2.378 ml |
5 mM | 0.048 ml | 0.238 ml | 0.476 ml |