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Pharmacology » Ion Channels » Ligand-gated Ion Channels » GABAA and GABAC Receptors » GABAA Receptors » Zolpidem
Zolpidem
Cat No. 0655
Price and Availability
Special Conditions
This product is a Controlled Substance and may have associated conditions of supply.
Chemical Name: N,N,6-Trimethyl-2-(4-methylphenyl)imidazo[1,2-a]pyridine -3-acetamide
Biological Activity
Benzodiazepine agonist with high selectivity for α1-subunit-containing GABAA receptors (BZ/ω 1 site) and very high intrinsic activity. Ki values are 20, 400 and ≥ 5000 nM for α1-, α 2-/α3-, and α5-containing GABAA receptors respectively. Hypnotic that does not induce physical dependence.Technical Data
M.Wt:307.39
Formula:C19H21N3O
Solubility:Soluble to 100 mM in 1eq. NaOH and to 100 mM in Ethanol
Purity: >99 %
Storage:Store at RT
CAS No:[82626-48-0]
Resources
Certificate of Analysis / MSDS
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References
Arbilla et al (1986) High affinity [3H]zolpidem binding in the rat brain: an imidazopyridine with agonist properties at central benzodiazepine receptors. Eur.J.Pharmacol. 130 257. Depoortere et al (1986) Zolpidem, a novel nonbenzodiazepine hypnotic. 1. Neuropharmacological and behavioural effects. J.Pharmacol.Exp.Ther. 237 649. Perrault et al (1992) Lack of tolerance and physical dependence upon repeated treatment with the novel hypnotic zolpidem. J.Pharmacol.Exp.Ther. 263 298. Crestani et al (2000) Mechanism of action of the hypnotic zolpidem in vivo. Br.J.Pharmacol. 131 1251.
Keywords: Zolpidem, Benzodiazepine, GABAA
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