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Medchemexpress LLC Nav1.7-IN-3 (N-linked arylsulfonamide) | 1788872-06-9 | 98.2% | 430.95 g/mol | C17H20ClFN4O2S2 | 5 MG
SDP

Catalog No. 5000247169
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Nav1.7-IN-3 is a selective, orally bioavailable inhibitor of the voltage-gated sodium channel Nav1.7 (IC50 = 8 nM). It exhibits limited central nervous system penetration and has demonstrated pain-relief activity in preclinical studies. Supplied as a research chemical with reported analytical data for use in pharmacology and mechanistic studies.

  • Selective Nav1.7 inhibition (IC50 = 8 nM).
  • Orally bioavailable in preclinical models.
  • Limited CNS penetration, suitable for peripheral pain research.
  • High reported purity (≈98.2%).
  • Molecular weight 430.95 g/mol; formula C17H20ClFN4O2S2.
  • Available in small research quantities for laboratory use.

Catalog No. 50-002-47169 Supplier Medchemexpress LLC Supplier No. HY1017895MG
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Nav1.7-IN-3 is a selective, orally bioavailable inhibitor of the voltage-gated sodium channel Nav1.7 (IC50 = 8 nM). It exhibits limited central nervous system penetration and has demonstrated pain-relief activity in preclinical studies. Supplied as a research chemical with reported analytical data for use in pharmacology and mechanistic studies.

  • Selective Nav1.7 inhibition (IC50 = 8 nM).
  • Orally bioavailable in preclinical models.
  • Limited CNS penetration, suitable for peripheral pain research.
  • High reported purity (≈98.2%).
  • Molecular weight 430.95 g/mol; formula C17H20ClFN4O2S2.
  • Available in small research quantities for laboratory use.

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