OD1
This small molecule is a potent and selective activator of Nav1.7, Nav1.4, and Nav1.6 sodium channels, inhibiting fast inactivation. It is a valuable research tool for studying channel biophysics, pain mechanisms in vitro, and has been shown to induce spontaneous pain in vivo models.
Product Specifications
Field of Research
Pharmacology & Drug Discovery
Molecular Weight
7206.1
Storage Conditions
-20°C
Notes
For research use only.
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