SCH 23390
From Infogalactic: the planetary knowledge core
Names | |
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IUPAC name
7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol
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Identifiers | |
87075-17-0 | |
ChEBI | CHEBI:73297 |
ChEMBL | ChEMBL62 |
943 | |
Jmol 3D model | Interactive image |
PubChem | 5018 |
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Properties | |
C17H18ClNO | |
Molar mass | 287.78 g/mol |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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
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Categories:
- Chemical pages without ChemSpiderID
- Articles without KEGG source
- Articles without InChI source
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- Chemical articles using a fixed chemical formula
- D1 antagonists
- Benzazepines
- Chloroarenes
- Nervous system drug stubs