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Medchemexpress LLC N-[4-[2-(5-chloro-2-methoxy-4-pyrimidinyl)ethyl]-2-thiazolyl]-2-(trifluoromethyl)-4-pyridinesulfonam | 1788872-06-9 | >98.0% | 430.95 g/mol | C17H20ClFN4O2S2 | 50 MG
SDP

Catalog No. 5000248666
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Nav1.7-IN-3 is a selective, orally bioavailable small-molecule inhibitor of the voltage-gated sodium channel Nav1.7 (IC50 ≈ 8 nM) developed for neuroscience research into pain mechanisms. It shows limited central nervous system penetration and is supplied as a research reagent for in vivo and in vitro studies.

  • Selective Nav1.7 inhibition with IC50 ≈ 8 nM.
  • Orally bioavailable, suitable for oral dosing studies.
  • Limited central nervous system penetration.
  • Provided as a solid for formulation and dosing flexibility.
  • Characterized by CAS 1788872-06-9 and molecular weight 430.95 g/mol.

Catalog No. 50-002-48666 Supplier Medchemexpress LLC Supplier No. HY10178950MG
May include imposed supplier surcharges.
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Nav1.7-IN-3 is a selective, orally bioavailable small-molecule inhibitor of the voltage-gated sodium channel Nav1.7 (IC50 ≈ 8 nM) developed for neuroscience research into pain mechanisms. It shows limited central nervous system penetration and is supplied as a research reagent for in vivo and in vitro studies.

  • Selective Nav1.7 inhibition with IC50 ≈ 8 nM.
  • Orally bioavailable, suitable for oral dosing studies.
  • Limited central nervous system penetration.
  • Provided as a solid for formulation and dosing flexibility.
  • Characterized by CAS 1788872-06-9 and molecular weight 430.95 g/mol.

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