Date published: 2026-3-16

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GABA Receptor Inhibitors

Santa Cruz Biotechnology now offers a broad range of GABA Receptor Inhibitors for use in various applications. GABA Receptor Inhibitors are vital tools in the field of neuroscience research, specifically targeting gamma-aminobutyric acid (GABA) receptors, which are crucial for inhibitory neurotransmission in the central nervous system. By inhibiting GABA receptors, these compounds help researchers understand the mechanisms of synaptic transmission and neuronal communication. Scientists utilize GABA Receptor Inhibitors to explore the balance between neuronal excitation and inhibition, shedding light on the fundamental processes that regulate neural activity. These inhibitors are essential for investigating the structural and functional properties of GABA receptors, including their subunit composition, binding sites, and the conformational changes that occur upon inhibition. By employing these inhibitors, researchers can study the impact of reduced GABAergic activity on neuronal circuits, synaptic plasticity, and overall brain function. GABA Receptor Inhibitors also facilitate the detailed characterization of receptor subtypes and their specific roles in various physiological processes, enhancing our understanding of receptor biology. Additionally, these inhibitors are used in electrophysiological experiments to measure changes in membrane potential and ion flux, providing insights into the biophysical properties of GABA receptor channels. The data derived from these studies are crucial for advancing knowledge in neural network dynamics and the regulatory mechanisms that govern inhibitory neurotransmission. GABA Receptor Inhibitors are indispensable tools for neurobiologists and biochemists aiming to uncover the complexities of neuronal signaling and the modulation of neural activity. View detailed information on our available GABA Receptor Inhibitors by clicking on the product name.

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Items 31 to 34 of 34 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Droperidol

548-73-2sc-211382
1 g
$190.00
(1)

Droperidol functions as a GABA receptor modulator, exhibiting unique allosteric properties that enhance receptor sensitivity to GABA. Its molecular structure facilitates specific interactions with the receptor's allosteric sites, promoting conformational changes that influence chloride ion permeability. This modulation alters synaptic transmission dynamics, with a distinctive profile of receptor activation and desensitization. The compound's kinetics reveal a complex interplay between binding affinity and receptor response, contributing to its nuanced effects on neural signaling pathways.

DMCM hydrochloride

82499-00-1sc-205295
sc-205295A
10 mg
50 mg
$208.00
$832.00
2
(0)

DMCM hydrochloride acts as a GABA receptor antagonist, uniquely disrupting the receptor's normal function. Its molecular interactions involve competitive binding at the GABA site, leading to altered chloride ion flow and reduced inhibitory neurotransmission. This compound exhibits distinctive kinetics, characterized by rapid onset and a short duration of action, which influences synaptic plasticity. The resulting changes in neuronal excitability highlight its role in modulating central nervous system activity.

Imidazole-4-acetic acid sodium salt

56368-58-2sc-252900
sc-252900A
500 mg
1 g
$214.00
$318.00
(0)

Imidazole-4-acetic acid sodium salt functions as a GABA receptor modulator, engaging in allosteric interactions that enhance receptor sensitivity. Its unique structure allows for specific binding to auxiliary sites, facilitating increased chloride ion conductance. The compound exhibits a gradual onset of action, promoting sustained effects on synaptic transmission. This modulation of receptor dynamics can influence neuronal signaling pathways, contributing to the fine-tuning of excitatory and inhibitory balance in neural circuits.

Xli 093

646066-59-3sc-264494
5 mg
$134.00
(0)

Xli 093 acts as a GABA receptor modulator, characterized by its ability to selectively bind to distinct allosteric sites, thereby altering receptor conformation. This interaction promotes enhanced chloride ion influx, leading to a pronounced effect on neuronal excitability. The compound exhibits unique reaction kinetics, with a rapid onset followed by a prolonged modulation of synaptic activity, influencing neurotransmitter release and receptor desensitization in neural networks.