| Name | 2-[(2,6-Dimethylphenyl)amino]-N,N,N-trimethyl-2-oxoethanaminium c hloride |
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| Description | QX-222 chloride, a trimethyl analogue of Lignocaine (HY-B0185), is a potent Na+ channel blocker[1][2][3]. |
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| Related Catalog | |
| In Vitro | Twelve minutes after external application of 500 μM QX222 chloride, μ1 IP-Loop to Heart Sequence (μ1-Y401C) results in a significant block compared with μ1-WT (WT, 14.2±1.6% block, n = 8; Y401C, 45.2±3.6% block, n = 9; P < 0.001)[1]. |
| In Vivo | QX-222 (10 mg/kg; intravenous infusion 7 days) chloride reverses spinal nerve ligation (SNL)-induced thermal hypersensitivity and induced antinociception in sham-operated rats[2]. |
| References |
| Molecular Formula | C13H21ClN2O |
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| Molecular Weight | 256.77200 |
| Exact Mass | 256.13400 |
| PSA | 35.42000 |
| LogP | 3.27210 |
| Hazard Codes | Xi |
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