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Spiroxatrine

From Wikipedia, the free encyclopedia
Spiroxatrine
Names
IUPAC name
8-(2,3-Dihydro-1,4-benzodioxin-2-ylmethyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
MeSHSpiroxatrine
UNII
  • InChI=1S/C22H25N3O3/c26-21-22(25(16-23-21)17-6-2-1-3-7-17)10-12-24(13-11-22)14-18-15-27-19-8-4-5-9-20(19)28-18/h1-9,18H,10-16H2,(H,23,26) checkY
    Key: JVGBTTIJPBFLTE-UHFFFAOYSA-N checkY
  • O=C2NCN(c1ccccc1)C23CCN(CC3)CC4Oc5ccccc5OC4
Properties
C22H25N3O3
Molar mass379.460 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Spiroxatrine (Spiroxamide,R5188) is a drug which acts as a selectiveantagonist at both the5-HT1A receptor and theα2Cadrenergic receptor.[1] It is ananalog ofspiperone and also has somedopamine antagonist effects and a relatively weakopioid action.[2][3]

References

[edit]
  1. ^Terrón, J. A.; Ibarra, M; Ransanz, V; Hong, E; Villalón, C. M. (1993). "The alpha-antiadrenergic properties of spiroxatrine, a ligand of serotonergic 5-HT1A receptors".Archivos del Instituto de Cardiología de México.63 (4):289–95.PMID 8105762.
  2. ^Niemegeers, CJ; Verbruggen, FJ; Vannueten, JM; Janssen, PA (Dec 1963). "Spiroxamide (R 5188) : A new compound producing morphine-like and chlorpromazine-like effects in animals".Int J Neuropharmacol.2 (6):349–54.doi:10.1016/0028-3908(63)90010-8.PMID 14119495.
  3. ^Leysen, J; Tollenaere, JP; Koch, MHJ; Laduron, P (1977). "Differentiation of opiate and neuroleptic receptor binding in rat brain".European Journal of Pharmacology.43 (3):253–267.doi:10.1016/0014-2999(77)90025-5.PMID 194781.
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
D1-like
Agonists
PAMs
Antagonists
D2-like
Agonists
Antagonists
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
CARTooltip Constitutive androstane receptor
PXRTooltip Pregnane X receptor


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