Chemical Structure : ICA604025
货号: PC-26899Not For Human Use, Lab Use Only.
ICA604025 is a potent, selective sodium channel Nav1.9 subtype inhibitor, inhibits human Nav1.9 in a state dependent manner with EC50s of 9 nM and 1.1 μM for the activated/inactivated state versus resting closed state.
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ICA604025 is a potent, selective sodium channel Nav1.9 subtype inhibitor, inhibits human Nav1.9 in a state dependent manner with EC50s of 9 nM and 1.1 μM for the activated/inactivated state versus resting closed state.
ICA604025 exhibits a similar potency for inhibition of cynomolgus monkey Nav1.9 but ∼50-fold lower potency for inhibition of rodent Nav1.9.
ICA604025 is a 300- to 1800-fold more potent inhibitor of human Nav1.9 compared with other human Nav1.x family members.
Nav1.9 is a voltage-gated sodium channel genetically associated with human pain disorders and thus is a key target for new analgesics.
| 分子量 | 378.30 | |
| 分子式 | C16H15F5N2O3 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. Potet F, et al. Mol Pharmacol. 2026 May 5;108(5-6):100125.
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