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  • DC Chemicals Limited
  • China
  • Product Name: RS 39604
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

167710-87-4

167710-87-4 structure
167710-87-4 structure
  • Name: RS 39604 hydrochloride
  • Chemical Name: N-[2-[4-[3-[4-amino-5-chloro-2-[(3,5-dimethoxyphenyl)methoxy]phenyl]-3-oxopropyl]piperidin-1-yl]ethyl]methanesulfonamide,hydrochloride
  • CAS Number: 167710-87-4
  • Molecular Formula: C26H37Cl2N3O6S
  • Molecular Weight: 590.55900
  • Catalog: Signaling Pathways GPCR/G Protein 5-HT Receptor
  • Create Date: 2018-02-14 08:00:00
  • Modify Date: 2024-01-15 15:22:50
  • RS 39604 is a potent, selective, and orally active 5-HT4 receptor antagonist with a pKi of 9.1 in guinea pig striatal membranes. RS 39604 displays a low affinity (pKi<6.5) for 5-HT1A, 5-HT2C, 5-HT3, α1c, D1, D2, M1, M2, AT1, B1 and opioid mu receptors and moderate affinity for δ1, (pKi=6.8) and δ2 (pKi=7.8) sites[1].

Name N-[2-[4-[3-[4-amino-5-chloro-2-[(3,5-dimethoxyphenyl)methoxy]phenyl]-3-oxopropyl]piperidin-1-yl]ethyl]methanesulfonamide,hydrochloride
Synonyms GNF-Pf-5475
Description RS 39604 is a potent, selective, and orally active 5-HT4 receptor antagonist with a pKi of 9.1 in guinea pig striatal membranes. RS 39604 displays a low affinity (pKi<6.5) for 5-HT1A, 5-HT2C, 5-HT3, α1c, D1, D2, M1, M2, AT1, B1 and opioid mu receptors and moderate affinity for δ1, (pKi=6.8) and δ2 (pKi=7.8) sites[1].
Related Catalog
Target

5-HT4 Receptor:9.1 (pKi)

References

[1]. Hegde SS, et al. RS 39604: a potent, selective and orally active 5-HT4 receptor antagonist. Br J Pharmacol. 1995;115(6):1087-1095.

Boiling Point 746.9ºC at 760 mmHg
Molecular Formula C26H37Cl2N3O6S
Molecular Weight 590.55900
Flash Point 405.5ºC
Exact Mass 589.17800
PSA 128.57000
LogP 6.53530
Vapour Pressure 1.25E-22mmHg at 25°C