SCH 23390
 | |
| Names | |
|---|---|
| IUPAC name
7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol | |
| Identifiers | |
87075-17-0  | |
| ChEBI | CHEBI:73297  |
| ChEMBL | ChEMBL62 |
| IUPHAR ligand | 943 |
| Jmol-3D images | Image |
| PubChem | 5018 |
| |
| Properties | |
| C17H18ClNO | |
| Molar mass | 287.78 g/mol |
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| verify (what is: /?) | |
| Infobox references | |
SCH 23390 is a synthetic compound that acts as a D1 receptor antagonist and has either minimal or negligible effects on the D2 receptor.
In a 1990 study in rats SCH 23390 offered significant protection from death in dextroamphetamine overdosage, without providing protection from death by methamphetamine overdose. The compound provided significant protection from cocaine overdose in rats only at the lowest dose tested in the measurement series. This suggested that d-amphetamine and methamphetamine at high (lethal) doses have different mechanisms of toxicity in rats.[1]
References
- ↑ Derlet, R. W.; Albertson, T. E.; Rice, P. (1990). "The Effect of SCH 23390 Against Toxic Doses of Cocaine, d-Amphetamine and Methamphetamine". Life Sciences 47 (9): 821–827. doi:10.1016/0024-3205(90)90555-6. PMID 2215083.