Date published: 2025-10-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

SCH 23390 (CAS 125941-87-9)

5.0(1)
Write a reviewAsk a question

See product citations (2)

Alternate Names:
R-(+)-7-Chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine•HCl
Application:
SCH 23390 is a selective and highly effective D1DR and D5DR antagonist
CAS Number:
125941-87-9
Purity:
98%
Molecular Weight:
324.2
Molecular Formula:
C17H18ClNO•HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

SCH-23390 (SCH) is a highly selective dopamine D1 receptor antagonist with a rich history of over 30 years in scientific research. Renowned as one of the most extensively investigated dopamine antagonists, it has played a pivotal role in numerous studies exploring the impact of dopamine in the brain and its behavioral effects. By delving into the central nervous system, SCH has contributed to our understanding of dopamine′s influence on various diseases and conditions. SCH-23390 exhibits a diverse range of biochemical and physiological effects. These include inhibiting dopamine reuptake and release, as well as suppressing the activity of phosphodiesterase enzymes and adenylyl cyclase. Through studies utilizing SCH-23390, researchers have investigated the effects of dopamine on behavior, cognition, and neurophysiology. Moreover, they have examined its potential implications in disorders such as Parkinson′s disease, Huntington′s disease, schizophrenia, and depression. Furthermore, SCH-23390 has shed light on the impact of dopamine on essential biochemical processes, encompassing gene expression, signal transduction, and neurotransmitter release. Studies have encompassed various cell types, from neurons to glial cells, to comprehensively explore the effects of SCH-23390. By binding to the dopamine D1 receptor, which belongs to the G-protein coupled receptor family, SCH-23390 elicits a reduction in receptor activity, ultimately leading to diminished dopamine signaling.


SCH 23390 (CAS 125941-87-9) References

  1. Stimulus properties of 7-OH-DPAT versus auto- and postsynaptic receptor-specific doses of quinpirole.  |  Zuch, CL. and Cory-Slechta, DA. 2001. Pharmacol Biochem Behav. 68: 469-79. PMID: 11325401
  2. SCH 23390: the first selective dopamine D1-like receptor antagonist.  |  Bourne, JA. 2001. CNS Drug Rev. 7: 399-414. PMID: 11830757
  3. Pharmacological identification of inward current evoked by dopamine in rat subthalamic neurons in vitro.  |  Zhu, ZT., et al. 2002. Neuropharmacology. 42: 772-81. PMID: 12015203
  4. Excitatory effects of dopamine on subthalamic nucleus neurons: in vitro study of rats pretreated with 6-hydroxydopamine and levodopa.  |  Zhu, Z., et al. 2002. Brain Res. 945: 31-40. PMID: 12113949
  5. Hippocampal dopamine receptors modulate the motor activation and the increase in dopamine levels in the rat nucleus accumbens evoked by chemical stimulation of the ventral hippocampus.  |  Zornoza, T., et al. 2005. Neuropsychopharmacology. 30: 843-52. PMID: 15689964
  6. Hippocampal dopamine receptors modulate cFos expression in the rat nucleus accumbens evoked by chemical stimulation of the ventral hippocampus.  |  Zornoza, T., et al. 2005. Neuropharmacology. 49: 1067-76. PMID: 16040065
  7. NMDA and dopamine interactions in the nucleus accumbens modulate cortical acetylcholine release.  |  Zmarowski, A., et al. 2005. Eur J Neurosci. 22: 1731-40. PMID: 16197513
  8. Design and discovery of 1,3-benzodiazepines as novel dopamine antagonists.  |  Zhu, Z., et al. 2009. Bioorg Med Chem Lett. 19: 5218-21. PMID: 19643610
  9. D1 receptors play a major role in the dopamine modulation of mouse ileum contractility.  |  Zizzo, MG., et al. 2010. Pharmacol Res. 61: 371-8. PMID: 20138148
  10. Galantamine ameliorates the impairment of recognition memory in mice repeatedly treated with methamphetamine: involvement of allosteric potentiation of nicotinic acetylcholine receptors and dopaminergic-ERK1/2 systems.  |  Noda, Y., et al. 2010. Int J Neuropsychopharmacol. 13: 1343-54. PMID: 20219155
  11. Pharmacological Enhancement of Regeneration-Dependent Regulatory T Cell Recruitment in Zebrafish.  |  Zwi, SF., et al. 2019. Int J Mol Sci. 20: PMID: 31635133
  12. The D1 receptor-mediated effects of the ergoline derivative LEK-8829 in rats with unilateral 6-hydroxydopamine lesions.  |  Zivin, M., et al. 1996. Br J Pharmacol. 119: 1187-96. PMID: 8937722
  13. Antiparkinsonian potential of interaction of LEK-8829 with bromocriptine.  |  Zivin, M., et al. 1998. Eur J Pharmacol. 349: 151-7. PMID: 9671092

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

SCH 23390, 5 mg

sc-200408
5 mg
$175.00

SCH 23390, 25 mg

sc-200408A
25 mg
$719.00