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SCH-23390

From Wikipedia, the free encyclopedia
SCH-23390
Names
IUPAC name
7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
UNII
  • CN1CCC2=CC(=C(C=C2C(C1)C3=CC=CC=C3)O)Cl
Properties
C17H18ClNO
Molar mass287.78 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

SCH-23390, also known ashalobenzazepine, is a synthetic compound that acts as adopamineD1 receptorantagonist with either minimal or negligible effects on theD2 receptor.

In a 1990 study in rats SCH-23390 offered significant protection from death indextroamphetamine overdose, without providing protection from death bymethamphetamine overdose. The compound provided significant protection from cocaine overdose in rats only at the lowest dose tested in the measurement series. This suggested that dextroamphetamine and methamphetamine at high (lethal) doses have different mechanisms of toxicity in rats.[1]

See also

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References

[edit]
  1. ^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.


D1-like
Agonists
PAMs
Antagonists
D2-like
Agonists
Antagonists
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