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VU0606170

Chemical Structure : VU0606170

CAS No.: 879054-55-4

VU0606170 (VU 0606170)

Catalog No.: PC-73240Not For Human Use, Lab Use Only.

VU 0606170 is a selective sodium-activated potassium channel KNa1.1 (Slack, Slo2.2) inhibitor with EC50 of 1.84 and 1.16 uM for WT Slack and A934T Slack, repectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    VU 0606170 is a selective sodium-activated potassium channel KNa1.1 (Slack, Slo2.2) inhibitor with EC50 of 1.84 and 1.16 uM for WT Slack and A934T Slack, repectively.
    VU0606170 did not modulate HEK293 channels expressing Slick, Slo1 α1/β1, Slo1 α1/β2, Slo1 α1/β3, Slo1 α1/β4, or Slo3 channels. also potently inhibits G288S and R428Q Slack channels.
    VU0606170 also proved effective at significantly decreasing the firing rate in overexcited, spontaneously firing cortical neuron cultures.

    Physicochemical Properties

    M.Wt 444.975
    Formula C19H29ClN4O4S
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20°C 12 Months; 4°C 6 Months
    In Solvent
    -80°C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    N-(5-chloro-2-methoxyphenyl)-2-(4-((4-methylpiperidin-1-yl)sulfonyl)piperazin-1-yl)acetamide

    References

    1. Brittany D Spitznagel, et al. ACS Chem Neurosci. 2020 Nov 4;11(21):3658-3671.

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