Date published: 2026-5-28

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Na+ CP type X alpha Inhibitors

Santa Cruz Biotechnology now offers a broad range of Na+ CP type X alpha Inhibitors for use in various applications. Sodium channels are critical components of excitable cells, such as neurons and muscle cells, where they are responsible for the initiation and propagation of action potentials. The Na+ CP type X alpha subunit is a specific isoform of voltage-gated sodium channels that plays a unique role in modulating the electrical activity of cells, particularly in specialized tissues such as the brain and heart. Inhibitors targeting this specific sodium channel subtype are invaluable tools in scientific research, allowing for the selective inhibition of Na+ CP type X alpha channels to study their function in cellular signaling and electrical excitability. Researchers use these inhibitors to explore how the Na+ CP type X alpha channels contribute to the regulation of neuronal firing patterns, muscle contractions, and other vital physiological processes. These inhibitors are also critical in investigations into the molecular mechanisms underlying neurological disorders, cardiac arrhythmias, and other conditions where abnormal sodium channel activity is implicated. Additionally, Na+ CP type X alpha Inhibitors are essential in the development of new therapeutic approaches aimed at modulating sodium channel activity to treat diseases associated with disrupted electrical signaling. The availability of these inhibitors has significantly advanced research in neuroscience, cardiology, and cellular biology, providing crucial insights into the complex regulatory mechanisms of sodium channel function. View detailed information on our available Na+ CP type X alpha Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

A-803467

944261-79-4sc-201068
sc-201068B
sc-201068A
10 mg
25 mg
50 mg
$89.00
$188.00
$349.00
1
(1)

A-803467 acts as a selective modulator of sodium channels, particularly influencing the gating mechanisms associated with the inactivated state. Its unique molecular architecture enables it to interact with specific binding sites, altering the conformational dynamics of the channel. This modulation affects the kinetics of sodium ion permeability, resulting in distinct electrophysiological responses. The compound's lipophilic characteristics contribute to its membrane partitioning, enhancing its interaction with lipid bilayers.

Tetracaine hydrochloride

136-47-0sc-251166
sc-251166A
5 g
25 g
$52.00
$95.00
(0)

Tetracaine hydrochloride functions as a potent sodium channel blocker, exhibiting a unique affinity for the inactivated state of these channels. Its structural features facilitate specific interactions with channel proteins, leading to altered gating kinetics. The compound's hydrophobic regions promote effective integration into lipid membranes, influencing ion flow and channel dynamics. Additionally, its ability to stabilize certain conformations of the channel enhances its impact on sodium ion conductance, resulting in distinctive biophysical properties.