Date published: 2026-5-1

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SCNM1 Activators

SCNM1 activators are compounds known to modulate the activity of sodium channels indirectly. These activators exert their influence by binding to various sites on the sodium channel, either stabilizing the active state, altering gating kinetics, or affecting the inactivation process. Such modulation of sodium channel dynamics is crucial as it underlies the excitability of neurons and other excitable cells. The persistent activity of sodium channels induced by these compounds leads to sustained depolarization or altered electrical signaling patterns within the cells. This, in turn, affects the function of proteins associated with or regulated by sodium channel activity, such as SCNM1.

The actions of these activators range from prolonging the open state of the channels, as seen with veratridine and batrachotoxin, to modulating the gating kinetics, as observed with phenytoin and lacosamide. These effects can lead to increased intracellular sodium concentrations or altered cellular excitability, conditions that are known to regulate the activity of sodium channel-associated proteins. While not directly interacting with SCNM1, the impact of these compounds on sodium channel physiology creates a cellular context in which SCNM1 function is indirectly modulated.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Veratridine

71-62-5sc-201075B
sc-201075
sc-201075C
sc-201075A
5 mg
10 mg
25 mg
50 mg
$82.00
$104.00
$201.00
$379.00
3
(1)

An alkaloid that targets voltage-gated sodium channels, causing persistent activation by preventing inactivation. This prolongation of the sodium influx can indirectly upregulate SCNM1 activity by maintaining the depolarized state of the membrane.

Aconitine

302-27-2sc-202441
sc-202441A
sc-202441B
sc-202441C
sc-202441D
25 mg
50 mg
100 mg
250 mg
500 mg
$306.00
$459.00
$663.00
$1277.00
$2091.00
(1)

A neurotoxin that binds to the open state of voltage-gated sodium channels, stabilizing their active form. The continued sodium current can modulate SCNM1 indirectly through sustained excitatory signaling.