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Medchemexpress LLC TC-N 1752 | 1211866-85-1 | MFCD22123242 | >98.0% | 516.52 g·mol⁻¹ | C25H27F3N6O3 | 50 MG
Supplier: Medchemexpress LLC HY10740550MG
A small-molecule research compound that functions as a potent, orally active inhibitor of Nav1.7 voltage-gated sodium channels. It shows activity across multiple Nav subtypes and has demonstrated analgesic efficacy in preclinical pain models. It is provided as a high-purity solid for use in in vitro and in vivo pharmacology and electrophysiology studies.
- Potent Nav1.7 inhibition (hNav1.7 IC50 ≈ 0.17 μM).
- Activity across multiple Nav channel subtypes.
- Demonstrated analgesic efficacy in preclinical pain models.
- High purity suitable for pharmacology and electrophysiology studies.
- Soluble in DMSO for in vitro testing.
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