Date published: 2026-1-28

1-800-457-3801

SCBT Portrait Logo
Seach Input

GluR Inhibitors

Santa Cruz Biotechnology now offers a broad range of GluR Inhibitors for use in various applications. Glutamate receptors (GluRs) are critical components of the excitatory neurotransmission system in the central nervous system, playing a key role in synaptic plasticity, learning, and memory. These receptors are activated by the neurotransmitter glutamate, the primary excitatory neurotransmitter in the brain, and are classified into different subtypes, including AMPA, NMDA, and kainate receptors, each contributing to different aspects of neural communication. GluR Inhibitors are essential tools in scientific research, enabling the study of how blocking these receptors can influence neural activity, synaptic strength, and the overall functioning of neural networks. By inhibiting GluRs, researchers can explore the underlying mechanisms of excitotoxicity, a process where excessive glutamate activity leads to neuronal damage, which is implicated in various neurodegenerative diseases. These inhibitors are widely used in electrophysiological studies and behavioral experiments to dissect the roles of different GluR subtypes in brain function and to understand how their dysregulation may contribute to conditions such as epilepsy, Alzheimer's disease, and schizophrenia. Additionally, GluR Inhibitors are valuable in research aimed at developing new strategies for managing excitatory signaling disorders. The availability of these inhibitors has significantly advanced research in neurobiology, offering critical insights into the modulation of excitatory neurotransmission and its implications for brain health. View detailed information on our available GluR Inhibitors by clicking on the product name.

SEE ALSO...

Items 21 to 22 of 22 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

γ-D-Glutamylaminomethylsulfonic acid

90237-02-8sc-295005
sc-295005A
1 mg
5 mg
$92.00
$306.00
(0)

γ-D-Glutamylaminomethylsulfonic acid acts as a selective antagonist of glutamate receptors, characterized by its unique sulfonic acid group that enhances solubility and interaction with receptor sites. Its molecular structure promotes specific ionic interactions, which modulate receptor conformational states. The compound demonstrates a distinctive reaction profile, exhibiting a rapid onset of action and a prolonged duration of receptor engagement, thereby influencing synaptic dynamics and neurotransmitter release.

Kynurenic acid sodium salt

492-27-3 (non-salt)sc-358835
100 mg
$103.00
(1)

Kynurenic acid sodium salt serves as a modulator of glutamate receptors, distinguished by its dual role as an antagonist and agonist depending on the receptor subtype. Its unique carboxylate and aromatic structures facilitate specific hydrogen bonding and hydrophobic interactions, influencing receptor activation pathways. The compound exhibits notable stability in aqueous environments, allowing for sustained interactions that can alter synaptic signaling and neuronal excitability over time.