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Nav1.7-IN-13

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Catalog No. T209439Cas No. 2776235-57-3

Nav1.7-IN-13 (compound 3g) is a sodium channel inhibitor that notably suppresses Veratridine-induced neuronal activity. It inhibits the total Na+ current in DRG neurons in a concentration-dependent manner and delays the activation of Navs. Nav1.7-IN-13 significantly alleviates mechanical pain behavior in a rat model of nerve injury (SNI), exhibiting analgesic properties.

Nav1.7-IN-13

Nav1.7-IN-13

🥰Excellent
Catalog No. T209439Cas No. 2776235-57-3
Nav1.7-IN-13 (compound 3g) is a sodium channel inhibitor that notably suppresses Veratridine-induced neuronal activity. It inhibits the total Na+ current in DRG neurons in a concentration-dependent manner and delays the activation of Navs. Nav1.7-IN-13 significantly alleviates mechanical pain behavior in a rat model of nerve injury (SNI), exhibiting analgesic properties.
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Product Introduction

Bioactivity
Description
Nav1.7-IN-13 (compound 3g) is a sodium channel inhibitor that notably suppresses Veratridine-induced neuronal activity. It inhibits the total Na+ current in DRG neurons in a concentration-dependent manner and delays the activation of Navs. Nav1.7-IN-13 significantly alleviates mechanical pain behavior in a rat model of nerve injury (SNI), exhibiting analgesic properties.
In vitro
Nav1.7-IN-13 (compound 3g) effectively blocks open sodium channels in an over-excited state. At concentrations of 50-150 μM over 16 hours, it inhibits sodium channel activation in rat DRG neurons in a dose-dependent manner and exhibits safety by not affecting hERG channel current at 150 μM.
Chemical Properties
Molecular Weight472.33
FormulaC23H22BrNO5
Cas No.2776235-57-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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