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A438079

Chemical Structure : A438079

CAS No.: 899507-36-9

A438079 (A 438079)

Catalog No.: PC-21903Not For Human Use, Lab Use Only.

A438079 is a selective, competitive P2X7 receptor antagonist with pIC50 of 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

A438079 is a selective, competitive P2X7 receptor antagonist with pIC50 of 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line.
A438079 hows little to no activity at other P2 receptors (IC50 > 10 μM).
A438079 inhibits methamphetamine-induced microglial migration and phagocytosis in vitro.
A438079 possesses antinociceptive activity in models of neuropathic pain in vivo.

Physicochemical Properties

M.Wt 306.15
Formula C13H9Cl2N5
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-[[5-(2,3-dichlorophenyl)tetrazol-1-yl]methyl]pyridine

References

1. Tsukimoto M, et al. Biochem Biophys Res Commun. 2009 Jul 10;384(4):512-8.

2. Nelson DW, et al. J Med Chem. 2006 Jun 15;49(12):3659-66. doi: 10.1021/jm051202e.

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