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Medchemexpress LLC Nav1.7-IN-3 | 1788872-06-9 | 98.2% | 430.95 g·mol⁻¹ | C17H20ClFN4O2S2 | 25 MG
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Catalog No. 5000246764
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Nav1.7-IN-3 is a selective, orally bioavailable inhibitor of the voltage-gated sodium channel Nav1.7, showing potent activity (IC50 8 nM). The compound is reported to have limited central nervous system penetration and is supplied for research use only.

  • Potent Nav1.7 inhibition (IC50 8 nM).
  • Orally bioavailable profile suitable for in vivo studies.
  • Limited CNS penetration, supporting peripheral pain models.
  • High analytical purity (98.21%).
  • Well-characterized composition (MW 430.95 g·mol⁻¹; formula C17H20ClFN4O2S2).
  • Provided for research use only.

Catalog No. 50-002-46764 Supplier Medchemexpress LLC Supplier No. HY10178925MG
May include imposed supplier surcharges.
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Nav1.7-IN-3 is a selective, orally bioavailable inhibitor of the voltage-gated sodium channel Nav1.7, showing potent activity (IC50 8 nM). The compound is reported to have limited central nervous system penetration and is supplied for research use only.

  • Potent Nav1.7 inhibition (IC50 8 nM).
  • Orally bioavailable profile suitable for in vivo studies.
  • Limited CNS penetration, supporting peripheral pain models.
  • High analytical purity (98.21%).
  • Well-characterized composition (MW 430.95 g·mol⁻¹; formula C17H20ClFN4O2S2).
  • Provided for research use only.

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