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Gaboxadol HCl

SKU: orb2655501

Description

Gaboxadol (hydrochloride) is a GABAA receptor agonist.(In Vitro):Gaboxadol hydrochloride (0.34, 3.5 and 7.0 μM) decreses permeability across Caco-2 cell monolayers with a dose dependent manner, shows the mean Papp values with 8.1 × 10-6 cm·s-1, 6.1 × 10-1 cm·s-6 and 5.6 × 10-6 cm·s-1 for 0.34, 3.5 and 7 μM gaboxadol, respectively.(In Vivo):Gaboxadol hydrochloride (intraperitoneal injection; 0.5, 1, 1.5, 2, 3, 4, or 5 mg/kg; once daily; three-day interval) normalizes the distance traveled by Fmr1 KO2 mice to WT activity levels at 0.5 mg/kg, additionally, this compound has no effect on locomotor activity in Fmr1 KO2 mice.

Research Area

Neuroscience

Images & Validation

Key Properties

CAS Number85118-33-8
MW176.60
Purity>98%
FormulaC6H8N2O2 · HCl
SMILESCl.O=c1[nH]oc2c1CCNC2
TargetGABAA receptor
SolubilitySoluble in DMSO (up to 20 mg/ml) or in Ethanol (up to 20 mg/ml).

Bioactivity

In Vivo
Gaboxadol hydrochloride (intraperitoneal injection; 0.5, 1, 1.5, 2, 3, 4, or 5 mg/kg; once daily; three-day interval) normalizes the distance traveled by Fmr1 KO2 mice to WT activity levels at 0.5 mg/kg, additionally, this compound has no effect on locomotor activity in Fmr1 KO2 mice. Animal model: Fmr1 KO2 mice (deletion of the promoter and first exon of Fmr1 resulting in mRNA and protein null mice). Dosage: 0.5, 1, 1.5, 2, 3, 4, or 5 mg/kg. Administration: Intraperitoneal injection. Result: Normalized Hyperactivity Observed in Fmr1 KO2 mice.
In Vitro
Gaboxadol hydrochloride (0.34, 3.5 and 7.0 μM) decreses permeability across Caco-2 cell monolayers with a dose dependent manner, shows the mean Papp values with8.1 x 10-6 cm·s-1, 6.1 x 10-1 cm·s-6 and 5.6 x 10-6 cm·s-1 for 0.34, 3.5 and 7 μM gaboxadol, respectively.

Storage & Handling

StorageRT
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

THIP HCl
Quality Guarantee

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Protocol Information

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25 mg
$ 190.00
100 mg
$ 310.00
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