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P2X Receptor
| 货号 | 产品名 | CAS号 | 信息 |
|---|---|---|---|
| CSN21970 | PSB-12062 | 55476-47-6 | PSB-12062 is a potent and selective P2X4 antagonist with IC50 of 1.38 μM for human P2X4. |
| CSN21352 | BzATP Triethylammonium Salt | 112898-15-4 | Prototypic P2X7 receptor agonist that exhibits 5 - 10 fold greater potency than ATP (EC50 = 0.7 μM in HEK 293 cells; EC50 values are 3.6 and 285 μM for rat and mouse receptors respectively). Exhibits partial agonist activity at P2X1 (pEC50 = 8.7) and P2Y1 receptors and can be used as a photoaffinity label for ATPase. |
| CSN21404 | BzATP | 81790-82-1 | Prototypic P2X7 receptor agonist that exhibits 5 - 10 fold greater potency than ATP (EC50 = 0.7 μM in HEK 293 cells; EC50 values are 3.6 and 285 μM for rat and mouse receptors respectively). Exhibits partial agonist activity at P2X1 (pEC50 = 8.7) and P2Y1 receptors and can be used as a photoaffinity label for ATPase. |
| CSN16004 | NF449 | 627034-85-9 | NF449 is a potent purinergic receptor antagonist that displays high selectivity for P2X1 (IC50 values are 0.28, 0.69, 120, 1820, 47000 and > 300000 nM for rP2X1, rP2X1+5, rP2X2+3, rP2X3, rP2X2 and P2X4 receptors respectively). Provides antithrombotic protection in vivo. Also acts as a Gsα-selective antagonist. |
| CSN20323 | NF023 | 104869-31-0 | NF023, a subtype-selective, competitive and reversible P2X1 receptor antagonist, displays IC50 values of 0.21, 28.9, > 50 and > 100 μM for human P2X1, P2X3, P2X2, and P2X4-mediated responses respectively. |
| CSN11254 | KN-62 | 127191-97-3 | KN-62 is a selective and potent inhibitor of calmodulin-dependent protein kinase II (CaMK-II) with IC50 of 0.9 μM, KN-62 also displays noncompetitive antagonism at P2X7 receptors in HEK293 cells, with an IC50 value of approximately 15 nM.. |
| CSN19839 | JNJ 47965567 | 1428327-31-4 | JNJ 47965567 is a potent and selective P2X7 antagonist (pIC50 values are 8.3, 7.5 and 7.2 for human, mouse and rat receptors respectively). |
| CSN18197 | GW791343 3HCl | 309712-55-8 | GW791343 3HCl is a P2X7 allosteric modulator and exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). |
| CSN10731 | CTP Disodium Dihydrate | 81012-87-5 | CTP Disodium Dihydrate is a P2X4 purinergic receptor agonist. |
| CSN25312 | BX430 | 688309-70-8 | BX430 is selective P2X4 allosteric antagonist with IC50 of 0.54 μM. |
| CSN19020 | A-804598 | 1125758-85-1 | A-804598 is a competitive, and selective P2X7 receptor antagonist with IC50 of 10 nM, 9 nM and 11 nM in rat, mouse and human P2X7 receptors respectively. |
| CSN13107 | A-740003 | 861393-28-4 | A-740003 is potent, selective and competitive P2X7 receptor antagonist (IC50 values are 18 and 40 nM for rat and human receptors respectively). |
