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L-Glutamic acid-[2,3,3,4,4-d5]

General Information
Catalog: BLP-009903
CAS: 2784-50-1
Molecular Formula: C5H4D5NO4
Molecular Weight: 152.16
Chemical Structure
L-Glutamic acid-[2,3,3,4,4-d5]
Description L-Glutamic acid-[2,3,3,4,4-d5] is a labelled L-Glutamic acid. Glutamic acid is a non-essential amino acid that acts as an excitatory neurotransmitter in the CNS.
Synonyms Glutamicol-d5; L-Glutamic Acid-d5; Glutamidex-d5
IUPAC Name (2S)-2-amino-2,3,3,4,4-pentadeuteriopentanedioic acid
Related CAS 56-86-0 (unlabelled)
Isomeric SMILES [2H][C@@](C(=O)O)(C([2H])([2H])C([2H])([2H])C(=O)O)N
Canonical SMILES C(CC(=O)O)C(C(=O)O)N
InChI InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1/i1D2,2D2,3D
InChI Key WHUUTDBJXJRKMK-NKXUJHECSA-N
Purity 98% by HPLC; 98% atom D

L-Glutamic acid-[2,3,3,4,4-d5], a deuterated variant of L-Glutamic acid with five deuterium atoms replacing hydrogen atoms, finds diverse applications in scientific research. Here are the key applications:

Metabolic Flux Analysis: Employing L-Glutamic acid-[2,3,3,4,4-d5] in metabolic flux analysis allows researchers to delve into cellular metabolic pathways. By tracing the integration of deuterium-labeled glutamic acid into various metabolic products, scientists can meticulously delineate and quantify metabolic processes. This methodology aids in the comprehension of cellular metabolism and the identification of potential targets for metabolic manipulation, paving the way for innovative therapeutic strategies.

NMR Spectroscopy: Within the realm of nuclear magnetic resonance (NMR) spectroscopy, L-Glutamic acid-[2,3,3,4,4-d5] emerges as a critical stable isotope-labeled compound, providing sharper signals and in-depth insights into molecular structures. The deuterium atoms play a pivotal role in diminishing background interference and signal overlap, facilitating precise structural analysis. Researchers can leverage this technique to explore intricate protein-ligand interactions, amino acid dynamics, and more, unlocking new dimensions in structural biology.

Neurochemistry Research: Positioned as a fundamental neurotransmitter in the central nervous system, L-Glutamic acid is pivotal for neurochemistry investigations. The deuterated iteration, L-Glutamic acid-[2,3,3,4,4-d5], serves as an invaluable tool in elucidating glutamate metabolism and functions within neurochemical processes. By utilizing this compound, scientists can meticulously track glutamate turnover and pathways in the brain, shedding light on glutamate's roles in neurotransmission, neuroplasticity, and neurological disorders. This research is indispensable for deciphering complex conditions like Alzheimer's disease and schizophrenia, driving advancements in neuroscience.

Pharmacokinetics Studies: In the realm of pharmacokinetics, L-Glutamic acid-[2,3,3,4,4-d5] emerges as a potent asset for exploring drug and nutrient absorption, distribution, metabolism, and excretion dynamics. The distinct deuterium labeling provides a discernible marker, streamlining the monitoring of glutamic acid within biological systems. This data serves as a crucial foundation for enhancing drug formulations and unraveling the metabolic destinies of amino acid supplements, paving the way for optimized therapeutic interventions.

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