Date published: 2026-4-5

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mGluR Substrates

Santa Cruz Biotechnology now offers a broad range of mGluR Substrates for use in various applications. Metabotropic glutamate receptors (mGluRs) are a class of G-protein-coupled receptors that are pivotal in modulating synaptic transmission and neural plasticity in the central nervous system. Unlike ionotropic receptors that mediate rapid synaptic responses, mGluRs are involved in slower, modulatory processes that influence a wide array of neurological functions, including cognition, memory formation, and sensory perception. mGluR Substrates are essential tools in scientific research, providing the necessary components to study the enzymatic activities and signal transduction pathways associated with these receptors. By using these substrates, researchers can investigate how mGluRs contribute to the regulation of neurotransmitter release, synaptic plasticity, and the overall balance of excitatory and inhibitory signals within neural circuits. These substrates are extensively employed in studies aimed at understanding the molecular mechanisms underlying various neurological conditions, such as schizophrenia, autism, and neurodegenerative diseases, where mGluR signaling is often altered. Additionally, mGluR Substrates are valuable in the development of pharmacological agents that target specific mGluR pathways, offering potential scientific approaches for modulating glutamatergic signaling in the brain. The availability of these substrates has significantly advanced research in neuroscience, offering critical insights into the complex regulatory functions of mGluRs and their broader implications for brain health and disease. View detailed information on our available mGluR Substrates by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

TCN 238

125404-04-8sc-362803
sc-362803A
10 mg
50 mg
$155.00
$620.00
(0)

TCN 238 is a selective modulator of metabotropic glutamate receptors, distinguished by its unique structural features that promote targeted interactions with receptor domains. This compound exhibits a distinct mechanism of action, influencing receptor conformations and enhancing downstream signaling cascades. Its reaction kinetics suggest a nuanced engagement with the receptor, allowing for precise modulation of synaptic activity. TCN 238's ability to stabilize specific receptor states further underscores its role in fine-tuning neural communication.

(1S,3S)-homo-ACPD

194785-78-9sc-206307
5 mg
$315.00
(0)

(1S,3S)-homo-ACPD is a potent allosteric modulator of metabotropic glutamate receptors, characterized by its ability to selectively bind to specific receptor sites, thereby altering their functional dynamics. This compound engages in unique molecular interactions that facilitate the activation of intracellular signaling pathways, leading to enhanced synaptic plasticity. Its distinct reaction kinetics allow for a finely-tuned modulation of receptor activity, contributing to the regulation of excitatory neurotransmission.

LY 487379 hydrochloride

353229-59-1sc-204065
sc-204065A
10 mg
50 mg
$145.00
$615.00
(0)

LY 487379 hydrochloride is a selective allosteric modulator of metabotropic glutamate receptors, exhibiting unique binding properties that influence receptor conformation. This compound interacts with specific allosteric sites, promoting distinct signaling cascades that modulate neuronal excitability. Its kinetic profile allows for precise temporal control over receptor activation, enhancing the understanding of synaptic mechanisms and providing insights into glutamatergic transmission dynamics.

VU 0357121

433967-28-3sc-364645
sc-364645A
10 mg
50 mg
$145.00
$615.00
(0)

VU 0357121 is a potent allosteric modulator of metabotropic glutamate receptors, characterized by its ability to stabilize specific receptor conformations. This compound engages with unique binding sites, facilitating selective signaling pathways that influence intracellular calcium levels and neurotransmitter release. Its distinct interaction dynamics contribute to a nuanced understanding of synaptic plasticity and receptor desensitization, offering insights into the modulation of excitatory neurotransmission.

CBiPES hydrochloride

856702-40-4sc-358830
sc-358830A
10 mg
50 mg
$145.00
$645.00
(0)

CBiPES hydrochloride acts as a selective modulator of metabotropic glutamate receptors, exhibiting unique binding affinities that alter receptor dynamics. Its interactions promote distinct conformational changes, influencing downstream signaling cascades and intracellular responses. The compound's kinetic profile reveals rapid association and dissociation rates, allowing for fine-tuning of synaptic responses. This specificity in receptor engagement enhances our understanding of glutamatergic signaling mechanisms.

BINA

866823-73-6sc-361121
sc-361121A
10 mg
50 mg
$134.00
$756.00
1
(0)

BINA functions as a selective modulator of metabotropic glutamate receptors, characterized by its ability to stabilize specific receptor conformations. This stabilization leads to altered G-protein coupling efficiency, impacting intracellular calcium signaling pathways. The compound exhibits unique allosteric properties, enhancing receptor sensitivity to endogenous ligands. Its distinct interaction kinetics facilitate nuanced regulation of synaptic plasticity, providing insights into glutamate-mediated neurotransmission.

VU 0361737

1161205-04-4sc-301976
sc-301976A
10 mg
50 mg
$115.00
$440.00
(0)

VU 0361737 acts as a selective modulator of metabotropic glutamate receptors, exhibiting unique binding dynamics that influence receptor activation states. Its distinct molecular interactions promote a shift in receptor conformational landscape, enhancing downstream signaling cascades. The compound's ability to fine-tune G-protein interactions allows for precise modulation of synaptic responses, contributing to a deeper understanding of glutamate's role in neural communication and plasticity.

L-γ-Carboxyglutamic acid

53861-57-7sc-295277
sc-295277A
10 mg
50 mg
$402.00
$1047.00
(0)

L-γ-Carboxyglutamic acid serves as a potent allosteric modulator of metabotropic glutamate receptors, engaging in specific hydrogen bonding and ionic interactions that stabilize receptor conformations. This compound influences the kinetics of receptor activation, facilitating nuanced signaling pathways. Its unique structural features enable selective engagement with G-proteins, thereby altering intracellular calcium dynamics and impacting synaptic efficacy and neuronal excitability.