Description
A competitive antagonist of the nucleotide receptor P2X7 (pIC50 = 6.9); inhibits both calcium flux and IL-1β release mediated by P2X7 while not affecting the activity of other P2X receptors; used to evaluate the role of P2X7 in nociception, oxidative stress, and apoptosis in cells and animals
Formal name: 3-[[5-(2,3-dichlorophenyl)-1H-tetrazol-1-yl]methyl]-pyridine, monohydrochloride
Synonyms:
Molecular weight: 342.6
CAS: 899431-18-6
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Ion Channel Modulation|Blockers||Product Type|Biochemicals|Nucleotides/Nucleosides||Research Area|Cell Biology|Cell Death|Apoptosis||Research Area|Neuroscience|Pain Research