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BzATP triethylammonium salt functions primarily as a potent agonist of the P2X7 receptor, demonstrating a notably higher efficacy in receptor activation compared to ATP, suggesting it to be between five to ten times more potent. This enhanced potency makes BzATP useful in the study of P2X7 receptor dynamics and its role in cellular signaling. Beyond its primary action, BzATP has partial agonist activity at other purinergic receptor sites, such as P2X1 and P2Y1 receptors, with a reported pEC50 value of 8.7 at P2X1 receptors. This capability to interact with multiple receptor types adds a layer of complexity to its utility in purinergic signaling research. BzATP has been utilized in biochemical studies as a photoaffinity label for ATPase enzymes, aiding in the elucidation of binding sites and mechanistic insights into ATPase function and regulation. This multifaceted application across different receptor interactions and enzyme studies underlines its importance in molecular and cellular biology research, particularly in the exploration of ATP-mediated processes and signaling pathways.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
BzATP triethylammonium salt, 5 mg | sc-203862 | 5 mg | $153.00 |