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WAY-181187

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
WAY-181187
Clinical data
ATC code
  • none
Identifiers
  • 2-(1-{6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonyl}-1H-indol-3-yl)ethan-1-amine
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H13ClN4O2S2
Molar mass380.87 g·mol−1
3D model (JSmol)
  • NCCc1cn(c2ccccc12)S(=O)(=O)c1c(Cl)nc2sccn12
  • InChI=1S/C15H13ClN4O2S2/c16-13-14(19-7-8-23-15(19)18-13)24(21,22)20-9-10(5-6-17)11-3-1-2-4-12(11)20/h1-4,7-9H,5-6,17H2
  • Key:RYBOXBBYCVOYNO-UHFFFAOYSA-N

WAY-181187 is a highaffinity andselective5-HT6 receptorfull agonist.[1][2] It induces robust increases inextracellularGABA levels in thefrontal cortex,hippocampus,striatum, andamygdala of rats without affecting concentrations in thenucleus accumbens orthalamus, and has modest to no effects onnorepinephrine,serotonin,dopamine, orglutamate levels in these areas.[1][3] WAY-181187 has demonstrated preclinical efficacy in rodent models ofdepression,anxiety, and notablyobsessive-compulsive disorder,[1][4] though it has also been shown to impaircognition andmemory.[3][5]

See also

[edit]

References

[edit]
  1. ^abcSchechter LE, Lin Q, Smith DL, et al. (May 2008)."Neuropharmacological profile of novel and selective 5-HT6 receptor agonists: WAY-181187 and WAY-208466".Neuropsychopharmacology.33 (6):1323–35.doi:10.1038/sj.npp.1301503.PMID 17625499.
  2. ^Cole DC, Stock JR, Lennox WJ, et al. (November 2007). "Discovery of N1-(6-chloroimidazo[2,1-b][1,3]thiazole-5-sulfonyl)tryptamine as a potent, selective, and orally active 5-HT(6) receptor agonist".Journal of Medicinal Chemistry.50 (23):5535–8.doi:10.1021/jm070521y.PMID 17948978.
  3. ^abWest PJ, Marcy VR, Marino MJ, Schaffhauser H (December 2009). "Activation of the 5-HT(6) receptor attenuates long-term potentiation and facilitates GABAergic neurotransmission in rat hippocampus".Neuroscience.164 (2):692–701.doi:10.1016/j.neuroscience.2009.07.061.PMID 19660530.S2CID 207246603.
  4. ^Carr GV, Schechter LE, Lucki I (March 2010)."Antidepressant and anxiolytic effects of selective 5-HT(6) receptor agonists in rats".Psychopharmacology.213 (2–3):499–507.doi:10.1007/s00213-010-1798-7.PMC 2910165.PMID 20217056.
  5. ^Loiseau F, Dekeyne A, Millan MJ (January 2008). "Pro-cognitive effects of 5-HT6 receptor antagonists in the social recognition procedure in rats: implication of the frontal cortex".Psychopharmacology.196 (1):93–104.doi:10.1007/s00213-007-0934-5.PMID 17922111.S2CID 35795618.
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
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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