KV9.3 Inhibitors are a chemical class of compounds that target and modulate the activity of the KV9.3 protein, also known as KCNB3 or the voltage-gated potassium channel subunit Kv2.3. KV9.3 is a member of the voltage-gated potassium channel family, which plays a crucial role in the regulation of membrane potential and neuronal excitability. Structurally, KV9.3 forms functional potassium channels by interacting with other subunits, typically forming heterotetrameric complexes. These channels are integral components of the plasma membrane and play a pivotal role in controlling the flow of potassium ions across the membrane in response to changes in membrane voltage
The functions of KV9.3 are diverse and context-dependent, contributing to the electrical properties of various cell types, including neurons, muscle cells, and other excitable cells. KV9.3 channels participate in the repolarization phase of action potentials, helping restore the resting membrane potential after depolarization. Additionally, they influence the duration and frequency of action potentials, which can impact neurotransmitter release, muscle contraction, and neuronal excitability. Furthermore, KV9.3 channels have been implicated in synaptic plasticity, where they can modulate the strength of synaptic transmission and participate in learning and memory processes. Dysregulation of KV9.3 channel activity has been associated with various neurological disorders and cardiac conditions. KV9.3 Inhibitors are meticulously designed as small molecules or compounds engineered to interfere with the channel activity, ion conduction, or interactions of KV9.3, potentially influencing membrane excitability, cellular signaling, and neuronal function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-Aminopyridine | 504-24-5 | sc-202421 sc-202421B sc-202421A | 25 g 1 kg 100 g | $38.00 $1155.00 $122.00 | 3 | |
4-Aminopyridine blocks voltage-gated potassium channels, potentially preventing the outward flow of potassium ions, which can alter membrane excitability. It might inhibit Kv9.3 by affecting its pore region or by affecting its voltage-sensing mechanism. | ||||||
Tetraethylammonium chloride | 56-34-8 | sc-202834 | 25 g | $45.00 | 2 | |
TEA is a classic potassium channel blocker that plugs the channel's open pore. If Kv9.3 forms part of a functioning channel, TEA might inhibit it by occluding the pore. | ||||||
Quinidine | 56-54-2 | sc-212614 | 10 g | $104.00 | 3 | |
Quinidine may inhibit Kv9.3 by binding to the channel's pore region, thus preventing potassium ion flow and modifying cellular excitability. | ||||||
Charybdotoxin | 95751-30-7 | sc-200979 | 100 µg | $401.00 | 9 | |
Charybdotoxin binds to the outer vestibule of certain potassium channels, blocking ion conduction. It might inhibit Kv9.3 if the toxin interacts with its extracellular regions. | ||||||
Glyburide (Glibenclamide) | 10238-21-8 | sc-200982 sc-200982A sc-200982D sc-200982B sc-200982C | 1 g 5 g 25 g 100 g 500 g | $46.00 $61.00 $117.00 $173.00 $530.00 | 36 | |
Glibenclamide blocks ATP-sensitive potassium channels by binding to the sulfonylurea receptor. If Kv9.3 interacts with similar regulatory proteins, Glibenclamide might affect its activity. | ||||||
Amiodarone | 1951-25-3 | sc-480089 | 5 g | $318.00 | ||
Amiodarone affects various ion channels by altering their biophysical properties. It could inhibit Kv9.3 by affecting its gating mechanism or ion conduction pathway. | ||||||