Date published: 2026-4-1

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EAAT4 Inhibitors

EAAT4 inhibitors represent a class of chemical compounds that have garnered interest in scientific research due to their interactions with the Excitatory Amino Acid Transporter 4 (EAAT4). This transporter is a member of the family of excitatory amino acid transporters and plays a critical role in regulating the levels of neurotransmitters like glutamate in neuronal synapses. The intricate balance of neurotransmitter concentrations is essential for normal neuronal communication and overall brain function. EAAT4 inhibitors are designed to interact with the EAAT4 protein and modulate its activity, affecting the reuptake of glutamate from the synaptic cleft into neurons. By doing so, these inhibitors could influence the delicate balance of neurotransmitter signaling and contribute to our understanding of neuronal processes. Neuronal communication is a complex process that relies on the precise release and reception of neurotransmitters at synapses, the junctions between nerve cells. Glutamate, an excitatory neurotransmitter, plays a central role in transmitting signals between neurons. After release, glutamate needs to be efficiently cleared from the synaptic cleft to ensure proper signaling.This is where EAAT4, a subtype of the excitatory amino acid transporter family, comes into play. EAAT4 is predominantly expressed in the cerebellum, a brain region crucial for motor coordination and balance. Its primary function is to uptake glutamate from the synapse back into neurons, effectively terminating the signaling process and resetting the synapse for the next transmission. However, in situations where there is dysfunction in glutamate clearance, such as in certain neurological conditions, the balance of neurotransmission can be disrupted, contributing to disorders like epilepsy, neurodegenerative diseases, and movement disorders. Understanding and modulating the activity of EAAT4 could provide insights into these conditions. EAAT4 inhibitors, as a chemical class, hold the promise of influencing the glutamate uptake process mediated by EAAT4. By binding to specific sites on the EAAT4 protein, these inhibitors could alter its function, affecting the reuptake of glutamate. This, in turn, could impact the overall levels of glutamate in the synapse, leading to modifications in synaptic transmission. Research into EAAT4 inhibitors could shed light on the intricacies of glutamate regulation and its implications for neurological health.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

L-(-)-threo-3-Hydroxyaspartic acid

7298-99-9sc-204033
10 mg
$218.00
1
(0)

L-(-)-threo-3-Hydroxyaspartic acid acts as a selective modulator of excitatory amino acid transporters (EAAT4), distinguished by its hydroxyl group that enhances hydrogen bonding interactions. This compound influences the transporter's activity through specific conformational changes, promoting efficient glutamate transport. Its unique stereochemistry contributes to distinct binding affinities, affecting synaptic transmission and neuronal excitability in a nuanced manner.

L-trans-Pyrrolidine-2,4-dicarboxylic acid

64769-66-0sc-200477
sc-200477A
5 mg
25 mg
$66.00
$419.00
8
(1)

L-trans-Pyrrolidine-2,4-dicarboxylic acid serves as a potent modulator of excitatory amino acid transporters (EAAT4), characterized by its dual carboxylate groups that facilitate strong ionic interactions. This compound induces specific conformational shifts in the transporter, enhancing substrate affinity and transport kinetics. Its unique cyclic structure allows for distinct steric effects, influencing the dynamics of glutamate uptake and contributing to the regulation of synaptic activity.

(±)-threo-3-Methylglutamic acid

63088-04-0sc-204344
sc-204344A
5 mg
50 mg
$318.00
$1570.00
(0)

(±)-threo-3-Methylglutamic acid acts as a selective modulator of excitatory amino acid transporter 4 (EAAT4), distinguished by its branched side chain that introduces steric hindrance, affecting binding dynamics. This compound exhibits unique electrostatic interactions due to its asymmetric configuration, which can alter the transporter’s conformational landscape. Its presence influences the rate of glutamate transport, thereby impacting neuronal excitability and synaptic plasticity.

UCPH 101

1118460-77-7sc-361391
sc-361391A
10 mg
50 mg
$388.00
$908.00
3
(1)

UCPH-101 is a compound that has shown inhibitory effects on glutamate transporters, including EAAT4, in some studies. It's an example of a small molecule inhibitor that could potentially interfere with the function of EAAT4 by binding to specific sites on the transporter and blocking its activity.

L-4-Thiazolidinecarboxylic acid

34592-47-7sc-255234
10 g
$35.00
(0)

Some thiazolidine-4-carboxylic acid derivatives have been investigated for their potential to inhibit EAATThese compounds have shown to modulate glutamate uptake by targeting the transporters. The exact mechanisms of inhibition might vary based on the specific compound and its interactions with EAAT4.