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Description
GX 201 is a potent and selective Nav1.7 blocker (IC50 = 3.2 nM). Exhibits 10x selectivity for Nav1.7 over Nav1.1, Nav1.2, and Nav1.6 channels. Displays prolonged residency time on the Nav1.7 channel. Chronic dosing increases compound potency ∽10-fold and provides efficacy that persists after the compound has cleared from plasma. Suppresses neuropathic pain in a mouse diabetic neuropathy model. Analgesic.
Specifications
Specifications
| Chemical Name or Material | 4-[[1-[[2-Chloro-5-(trifluoromethyl)phenyl]methyl]-4-piperidinyl]methoxy]-5-cyclopropyl-2-fluoro-N-(methylsulfonyl)benzamide |
| CAS | 1788071-27-1 |
| Quantity | 10 mg |
| Target | Voltage-gated Sodium Channel Blockers |
| Molecular Formula | C25H27ClF4N2O4S |
| Purity | 0.98 |
Product Title
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