tcsc1292 A 438079 (hydrochloride)

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Product Description

A 438079 (hydrochloride) is a potent, and selective P2X7 receptor antagonist with pIC50 of 6.9.

IC50 & Target: pIC50: 6.9

In Vitro: In 1321N1 cells stably expressing rat P2X7 receptors, A 438079 blocks BzATP-(10 μM) evoked changes in intracellular calcium concentrations with an IC50 of 321 nM. A 438079 is also selective for the P2X7 receptor, at concentrations up to 100 μM[1].

In Vivo: A 438079 (80 μmol/kg, i.v.) reduces noxious and innocuous evoked activity of different classes of spinal neurons in neuropathic rats. A 438079 (100 and 300 μmol/kg, i.p.) significantly raises withdrawal thresh-olds in both the SNL and CCI models[1]. Intraperitoneal injection of A 438079 (5 and 15 mg/kg) 60 min after triggering seizures reduces seizure severity and neuronal death within the hippocampus. A 438079 has superior neuroprotective effects compared with an equally dose of phenobarbital (25 mg/kg)[2]. A 438079 partially but significantly prevents the 6-OHDA-induced depletion of striatal DA stores[3]. Pretreatment with A 438079 reduces nociceptive behaviour scores in the HC model[4]

Information

CAS No899431-18-6
FormulaC13H10Cl3N5
Clinical Informationclinicalinformation
PathwayMembrane Transporter/Ion Channel
TargetP2X Receptor

Specifications

Purity / Grade>98%
SolubilityH2O : ≥ 350 mg/mL (1021.57 mM)
Smilessmiles

Misc Information

Observed Molecular Weight342.61
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