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SKF 81297 hydrobromide (CAS 71636-61-8)

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Alternate Names:
(±)-6-Chloro-PB hydrobromide
Application:
SKF 81297 hydrobromide is an agonist of the D1DR
CAS Number:
71636-61-8
Purity:
≥98%
Molecular Weight:
370.67
Molecular Formula:
C16H16ClNO2•HBr
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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SKF 81297 hydrobromide is a full D1-like dopamine receptor agonist with diverse applications in scientific research, particularly in neuroscience. It serves as useful for investigating the effects of d-amphetamine and has shown remarkable efficacy in stimulating adenylate cyclase, an enzyme responsible for cAMP synthesis from ATP, exhibiting a 25-fold greater efficacy compared to other compounds. Furthermore, SKF 81297 hydrobromide acts as a selective and potent partial agonist of the human 5-HT2A serotonin receptor, contributing to its significance in the field of neuroscience. This compound′s broad range of applications encompasses in vitro and in vivo studies, allowing researchers to explore its mechanism of action, biological activity, biochemical and physiological effects, pharmacodynamics, and future directions. By binding to the 5-HT2A receptor and activating it to a certain extent, SKF 81297 hydrobromide demonstrates its partial agonist activity. This feature underlies its impact on behavior and cardiovascular function. With its ability to selectively modulate the 5-HT2A receptor, SKF 81297 hydrobromide presents an invaluable resource for understanding the mechanisms of serotonin receptor agonists and antagonists.


SKF 81297 hydrobromide (CAS 71636-61-8) References

  1. Effects of D1 dopamine receptor agonists on oral ethanol self-administration in rats: comparison with their efficacy to produce grooming and hyperactivity.  |  Cohen, C., et al. 1999. Psychopharmacology (Berl). 142: 102-10. PMID: 10102789
  2. Pharmacological characterization of the discriminative stimulus properties of the dopamine D1 agonist, SKF 81297.  |  Reavill, C., et al. 1993. Behav Pharmacol. 4: 135-146. PMID: 11224180
  3. Dopamine D1 receptor activation in the medial prefrontal cortex prevents the expression of cocaine sensitization.  |  Sorg, BA., et al. 2001. J Pharmacol Exp Ther. 297: 501-8. PMID: 11303036
  4. Partial and full dopamine D1 receptor agonists in mice and rats: relation between behavioural effects and stimulation of adenylate cyclase activity in vitro.  |  Arnt, J., et al. 1992. Eur J Pharmacol. 213: 259-67. PMID: 1355737
  5. Activation of dopamine D1 receptors in the medial prefrontal cortex produces bidirectional effects on cocaine-induced locomotor activity in rats: effects of repeated stress.  |  Sorg, BA., et al. 2004. Neuroscience. 127: 187-96. PMID: 15219681
  6. Locomotor hyperactivity and alterations in dopamine neurotransmission are associated with overexpression of A53T mutant human alpha-synuclein in mice.  |  Unger, EL., et al. 2006. Neurobiol Dis. 21: 431-43. PMID: 16230020
  7. Dopamine receptor agonists: selectivity and dopamine D1 receptor efficacy.  |  Andersen, PH. and Jansen, JA. 1990. Eur J Pharmacol. 188: 335-47. PMID: 1973652
  8. The effects of dopamine D1 and D2 receptor agonists and antagonists in monkeys withdrawn from long-term neuroleptic treatment.  |  Peacock, L., et al. 1990. Eur J Pharmacol. 186: 49-59. PMID: 1980891
  9. AMPA receptor-mediated miniature EPSCs have heterogeneous time courses in orexin neurons.  |  Alberto, CO. and Hirasawa, M. 2010. Biochem Biophys Res Commun. 400: 707-12. PMID: 20816937
  10. Amphetamine discrimination: effects of dopamine receptor agonists.  |  Nielsen, EB., et al. 1989. Eur J Pharmacol. 160: 253-62. PMID: 2569406
  11. The serotonin 5-HT₁A receptor agonist tandospirone improves executive function in common marmosets.  |  Baba, S., et al. 2015. Behav Brain Res. 287: 120-6. PMID: 25804359
  12. Monitoring Behaviorally Induced Biochemical Changes Using Fluorescence Lifetime Photometry.  |  Lee, SJ., et al. 2019. Front Neurosci. 13: 766. PMID: 31417343
  13. Effect of dopamine receptor-related compounds on naïve common marmosets for auditory steady-state response.  |  Iwamura, Y., et al. 2022. J Neurophysiol. 128: 229-238. PMID: 35583977
  14. Cellular responses to psychomotor stimulant and neuroleptic drugs are abnormal in mice lacking the D1 dopamine receptor.  |  Moratalla, R., et al. 1996. Proc Natl Acad Sci U S A. 93: 14928-33. PMID: 8962158
  15. Evidence for the involvement of dopamine receptors in ethanol-induced hyperactivity in mice.  |  Cohen, C., et al. 1997. Neuropharmacology. 36: 1099-108. PMID: 9294975

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

SKF 81297 hydrobromide, 5 mg

sc-204283B
5 mg
$128.00

SKF 81297 hydrobromide, 10 mg

sc-204283
10 mg
$198.00

SKF 81297 hydrobromide, 25 mg

sc-204283C
25 mg
$280.00

SKF 81297 hydrobromide, 50 mg

sc-204283A
50 mg
$890.00

Please share the mu agonist catagory

Asked by: Midnight raven
Thank you for your question. We do not have any information about your question. This chemical is for research use only. Not intended for diagnostic or therapeutic use.
Answered by: Technical Support
Date published: 2019-10-29
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Rated 5 out of 5 by from GangarossaGangarossa, G. et al. (25044816) found that repeated stimulation of dopamine D1-like receptor by SKF 81297 and hyperactivation of mTOR signaling lead to generalized seizures, altered dentate gyrus plasticity, and memory deficits in mice. -SCBT Publication Review
Date published: 2015-06-23
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SKF 81297 hydrobromide is rated 5.0 out of 5 by 1.
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