Date published: 2025-11-22

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NMDA zeta 1 Inhibitors

Santa Cruz Biotechnology now offers a broad range of NMDA zeta 1 Inhibitors for use in various applications. NMDA zeta 1 inhibitors are a crucial category of chemicals in scientific research due to their role in modulating the N-methyl-D-aspartate (NMDA) receptors, which are vital for synaptic plasticity and neurotransmission in the central nervous system. These inhibitors are particularly significant for studies focused on understanding the fundamental mechanisms of synaptic signaling and neurophysiology. By inhibiting the zeta 1 subunit of the NMDA receptor, researchers can dissect the intricate pathways and interactions involved in neuronal communication and synaptic strength. This has allowed for advances in our knowledge of neural network functioning, learning, and memory processes. Furthermore, NMDA zeta 1 inhibitors have facilitated the exploration of excitotoxicity, a process where excessive activation of NMDA receptors leads to neuronal damage, thus providing insights into neural injury and degeneration mechanisms. The availability of these inhibitors has been instrumental in advancing electrophysiological studies, as they enable precise modulation of receptor activity, contributing to the development of sophisticated models of synaptic behavior. Additionally, these inhibitors are used in biochemical assays to identify and characterize receptor subunit compositions and their regulatory mechanisms. View detailed information on our available NMDA zeta 1 Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

TCS 46b

302799-86-6sc-204328
sc-204328A
10 mg
50 mg
$149.00
$630.00
(1)

TCS 46b acts as a selective NMDA zeta 1 modulator, characterized by its ability to engage in specific hydrogen bonding interactions with receptor sites. This compound influences ion channel permeability, leading to altered excitatory neurotransmission. Its unique steric configuration enhances binding affinity, while its lipophilic characteristics facilitate membrane partitioning, affecting its distribution and reactivity in various biochemical environments. The compound's kinetic behavior is marked by rapid association and dissociation rates, underscoring its dynamic role in synaptic modulation.

Memantine hydrochloride

41100-52-1sc-203628
50 mg
$68.00
4
(2)

Memantine is another NMDA receptor antagonist. It preferentially blocks excessive NMDA receptor activity without disrupting normal activity, thereby indirectly inhibiting NMDAζ1.

Dextromethorphan

125-71-3sc-278927
sc-278927A
sc-278927B
10 g
100 g
500 g
$174.00
$1133.00
$5106.00
3
(1)

Dextromethorphan acts as an NMDA receptor antagonist. It can inhibit NMDAζ1 by interfering with the receptor's normal function in synaptic transmission.

Ifenprodil hemitartrate

23210-58-4sc-203601B
sc-203601
sc-203601A
5 mg
10 mg
50 mg
$39.00
$61.00
$142.00
(0)

Ifenprodil selectively inhibits certain subtypes of NMDA receptors. It can indirectly inhibit NMDAζ1 by modulating receptor activity, particularly in receptors containing the NR2B subunit.

1-Adamantylamine

768-94-5sc-251475
sc-251475A
1 g
25 g
$38.00
$144.00
(0)

Amantadine has NMDA receptor antagonist properties. It can inhibit NMDAζ1 by altering the receptor's function in neural transmission and plasticity.

Felbamate

25451-15-4sc-203579
sc-203579A
10 mg
50 mg
$101.00
$373.00
(0)

Felbamate has been shown to modulate NMDA receptor activity. It can indirectly inhibit NMDAζ1 by affecting the receptor's function in synaptic transmission.

Ifenprodil Tartrate Salt

23210-56-2sc-295173
sc-295173A
5 mg
10 mg
$55.00
$71.00
(0)

Ifenprodil Tartrate Salt functions as a selective NMDA zeta 1 antagonist, exhibiting unique electrostatic interactions that stabilize its binding to receptor sites. This compound alters calcium ion influx, impacting synaptic plasticity. Its distinct conformational flexibility allows for effective competition with endogenous ligands, while its hydrophilic nature influences solubility and diffusion across cellular membranes. The compound's reaction kinetics reveal a notable balance between affinity and dissociation, contributing to its nuanced role in neurophysiological processes.

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 modulates glutamatergic neurotransmission and can inhibit NMDA receptors. It indirectly inhibits NMDAζ1 by affecting synaptic transmission mediated by these receptors.