Date published: 2025-12-24

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Contactin 3 Inhibitors

Chemical inhibitors of Contactin 3 are diverse in their modes of action, primarily affecting the protein's role in the nervous system by targeting various ion channels with which it interacts. Tetrodotoxin and saxitoxin, for instance, are neurotoxic compounds that exert their inhibitory effects by binding to and blocking voltage-gated sodium channels. These sodium channels are integral to the initiation and propagation of electrical signals in neurons, and their blockade by these toxins can disrupt the functional role of Contactin 3 in modulating neuronal excitability. Similarly, phenytoin and lamotrigine act upon these sodium channels, though their mechanism stabilizes the channels in an inactive state, thus dampening the excitation of neurons and indirectly limiting the action of Contactin 3 in maintaining neuronal connectivity and plasticity. In addition to sodium channel blockers, other inhibitors target different ion channels that are also critical for the functions attributed to Contactin 3. Conotoxins and ω-conotoxin GVIA, found in marine snails, specifically inhibit calcium channels, while agatoxin, which acts on the same type of channels, impedes the calcium influx necessary for synaptic vesicle release. This inhibition can affect the role of Contactin 3 in synaptic function and plasticity. Tetraethylammonium and dendrotoxin selectively block potassium channels, which are essential for the repolarization phase of the action potential, thereby influencing Contactin 3's modulation of nerve impulse propagation. Bungarotoxin targets nicotinic acetylcholine receptors, leading to an indirect inhibition of Contactin 3's involvement in synapse formation and maintenance due to the disruption of cholinergic neurotransmission. Lastly, riluzole interacts with glutamatergic neurotransmission and also blocks sodium channels, which can influence Contactin 3's function in the organization of neuronal networks and the modulation of synapses, highlighting the complex interplay between Contactin 3 and various ion channels in the nervous system.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

α-Bungarotoxin

11032-79-4sc-202897
1 mg
$344.00
5
(1)

Bungarotoxin, particularly α-bungarotoxin, binds irreversibly to nicotinic acetylcholine receptors, inhibiting synaptic transmission. Contactin 3's role in synapse formation and maintenance may be indirectly inhibited by the disruption of cholinergic neurotransmission.

ω-Agatoxin IVA

145017-83-0sc-302015
100 µg
$454.00
(0)

Agatoxin targets calcium channels, impeding the calcium influx required for synaptic vesicle release. As Contactin 3 is associated with synaptic function, the attenuation of calcium-mediated neurotransmission can inhibit the protein's involvement in synaptic plasticity.

5,5-Diphenyl Hydantoin

57-41-0sc-210385
5 g
$70.00
(0)

Phenytoin is known to stabilize the inactive state of sodium channels, reducing repetitive neuronal firing. The stabilization of these channels can indirectly inhibit Contactin 3's role in modulating neuronal connectivity and plasticity.

Lamotrigine

84057-84-1sc-201079
sc-201079A
10 mg
50 mg
$118.00
$476.00
1
(1)

Lamotrigine acts to inhibit voltage-sensitive sodium channels, which can dampen the excitation of neurons. By affecting these channels, lamotrigine can indirectly inhibit the action of Contactin 3 on neuronal communication.

Riluzole

1744-22-5sc-201081
sc-201081A
sc-201081B
sc-201081C
20 mg
100 mg
1 g
25 g
$20.00
$189.00
$209.00
$311.00
1
(1)

Riluzole interferes with glutamatergic neurotransmission and can also block sodium channels. Its action on glutamate signaling can impede Contactin 3's function in the organization of neuronal networks and synapse modulation.