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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)

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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