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RS-56812

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
RS-56812
Identifiers
  • N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-2-(1-methyl-1H-indol-3-yl)-2-oxoacetamide
CAS Number
PubChemCID
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H21N3O2
Molar mass311.385 g·mol−1
3D model (JSmol)
  • c14ccccc4n(C)cc1C(=O)C(=O)NC2CN3CCC2CC3
  (verify)

RS-56812 is a potent and selectivepartial agonist at the5HT3 receptor.[1] It has been shown to improve performance on animal tests of memory. Its use in humans is not well documented.[2]

References

[edit]
  1. ^Van Hooft JA, Vijverberg HP (March 1997). "RS-056812-198: partial agonist on native and antagonist on cloned 5-HT3 receptors".European Journal of Pharmacology.322 (2–3):229–33.doi:10.1016/s0014-2999(96)00993-4.PMID 9098692.
  2. ^Terry AV, Buccafusco JJ, Prendergast MA, Jackson WJ, Fontana DL, Wong EH, et al. (December 1996). "The 5-HT3 receptor antagonist, RS-56812, enhances delayed matching performance in monkeys".NeuroReport.8 (1):49–54.doi:10.1097/00001756-199612200-00011.PMID 9051751.S2CID 42903427.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7


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