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S5321

Sigma-Aldrich

S15535

≥98% (HPLC), solid

Sinonimo/i:

1-(2,3-Dihydro-1,4-benzodioxin-5-yl)-4-(2,3-dihydro-1h-inden-2-yl)-piperazine

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25 MG
CHF 529.00

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25 MG
CHF 529.00

About This Item

Formula empirica (notazione di Hill):
C21H24N2O2
Numero CAS:
146998-34-7
Peso molecolare:
336.43
Numero MDL:
MFCD00911672
Codice UNSPSC:
12352200
ID PubChem:
329824452
NACRES:
NA.77

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Saggio

≥98% (HPLC)

Stato

solid

Colore

white

Solubilità

DMSO: ~6 mg/mL
H2O: insoluble

Temperatura di conservazione

2-8°C

Stringa SMILE

C1COc2c(O1)cccc2N3CCN(CC3)C4Cc5ccccc5C4

InChI

1S/C21H24N2O2/c1-2-5-17-15-18(14-16(17)4-1)22-8-10-23(11-9-22)19-6-3-7-20-21(19)25-13-12-24-20/h1-7,18H,8-15H2
QJPPEMXOOWNICQ-UHFFFAOYSA-N

Applicazioni

S15535 has been used as a serotonin 1A receptor (5-HT1A) agonist in zebrafish.[1]
S15535 may be used in histamine 5-HT1A-medaited cell signaling studies.

Azioni biochim/fisiol

Potent, orally active, partial 5-HT1A receptor agonist
S15535, a benzodioxane, is a selective but partial agonist of histamine serotonin 1A (5-HT1A) receptor. It activates presynaptic 5-HT1A receptors and suppresses the release of hippocampal 5-HT. It acts as an anxiolytic agent and modulates the cholinergic and cognitive function in rodents.[2]

Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273 - P391 - P501

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
016K46151
017K4619
017K4609
016K4615

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Jasmin M Dao et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 36(7), 1319-1331 (2011-03-18)
Epidemiological studies have shown that adolescent smoking is associated with health risk behaviors, including high-risk sexual activity and illicit drug use. Using rat as an animal model, we evaluated the behavioral and biochemical effects of a 4-day, low-dose nicotine pretreatment
A Dekeyne et al.
Psychopharmacology, 152(1), 55-66 (2000-10-21)
The benzodioxane, S15535, possesses low intrinsic activity and marked selectivity at 5-HT1A receptors, hippocampal populations of which are implicated in anxious states. Herein, we examined its potential anxiolytic actions in relation to its influence upon extracellular levels of 5-HT in
Parallel evaluation of 5-HT1A receptor localization and functionality: autoradiographic studies with [35S]-GTP gamma S and the novel, selective radioligand, [3H]-S 15535.
A Newman-Tancredi et al.
Annals of the New York Academy of Sciences, 861, 263-264 (1999-02-03)
B J van der Vegt et al.
Physiology & behavior, 74(1-2), 205-211 (2001-09-21)
Individual differences in aggressive behaviour have been linked to variability in central serotonergic activity, both in humans and animals. A previous experiment in mice, selectively bred for high or low levels of aggression, showed an up-regulation of postsynaptic serotonin-1A (5-HT(1A))
M J Millan et al.
The Journal of pharmacology and experimental therapeutics, 282(1), 148-161 (1997-07-01)
In these studies, we characterized the influence of the novel benzodioxopiperazine serotonin (5-HT)1A ligand, S 15535, on the release of 5-HT in rat hippocampus and compared its potential anxiolytic properties with those of the 5-HT1A receptor partial agonist, buspirone, the
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