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Description
C 101248 is a selective and potent inhibitor of both mouse and human tandem pore domain halothane-inhibited K+ channel 1 (THIK-1, IC50 = 50 nM); it exhibits no activity against K2P family members, TREK-1 and TWIK-2, and Kv2.1. C 101248 blocks both tonic and ATP-evoked THIK-1 K+ currents in whole-cell patch-clamp recordings of mouse hippocampal microglia. C 101248 reduces neuroinflammation by preventing NLRP3-dependent release of IL-1β in isolated microglia.
Specifications
Specifications
| Chemical Name or Material | 4-[1-(4-Pyridinylmethyl)-1 H-benzimidazol-2-yl]-1,2,5-oxadiazol-3-amine |
| CAS | 361368-24-3 |
| Quantity | 50 mg |
| Target | Two-P Potassium Channels Blockers |
| Molecular Formula | C15H12N6O |
| Purity | 0.98 |
Product Title
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