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SR-57227

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
SR-57227
Identifiers
  • 1-(6-chloropyridin-2-yl)piperidin-4-amine
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
CompTox Dashboard(EPA)
ECHA InfoCard100.163.915Edit this at Wikidata
Chemical and physical data
FormulaC10H14ClN3
Molar mass211.69 g·mol−1
3D model (JSmol)
  • ClC1=CC=CC(N2CCC(N)CC2)=N1
  • InChI=1S/C10H14ClN3/c11-9-2-1-3-10(13-9)14-6-4-8(12)5-7-14/h1-3,8H,4-7,12H2
  • Key:WPVVMKYQOMJPIN-UHFFFAOYSA-N

SR-57227 is a potent and selectiveagonist at the5HT3 receptor, with high selectivity over otherserotonin receptor subtypes and goodblood–brain barrier penetration.[1][2][3][4]

References

[edit]
  1. ^Bachy A, Héaulme M, Giudice A, Michaud JC, Lefevre IA, Souilhac J, et al. (June 1993). "SR 57227A: a potent and selective agonist at central and peripheral 5-HT3 receptors in vitro and in vivo".European Journal of Pharmacology.237 (2–3):299–309.doi:10.1016/0014-2999(93)90282-M.PMID 7689975.
  2. ^Maksay G, Simonyi M, Bikádi Z (October 2004). "Subunit rotation models activation of serotonin 5-HT3AB receptors by agonists".Journal of Computer-Aided Molecular Design.18 (10):651–64.doi:10.1007/s10822-004-6259-0.PMID 15849995.S2CID 10510254.
  3. ^Yoo JH, Cho JH, Yu HS, Lee KW, Lee BH, Jeong SM, et al. (November 2006)."Involvement of 5-HT receptors in the development and expression of methamphetamine-induced behavioral sensitization: 5-HT receptor channel and binding study".Journal of Neurochemistry.99 (3):976–88.doi:10.1111/j.1471-4159.2006.04137.x.PMID 16942594.S2CID 38685481.
  4. ^Li Y, Raaby KF, Sánchez C, Gulinello M (November 2013). "Serotonergic receptor mechanisms underlying antidepressant-like action in the progesterone withdrawal model of hormonally induced depression in rats".Behavioural Brain Research.256:520–8.doi:10.1016/j.bbr.2013.09.002.PMID 24016840.S2CID 45617581.
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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