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D-4-Hydroxyphenylalanine-[3,3-d2]

General Information
Catalog: BLP-009852
CAS: 1202064-22-9
Molecular Formula: C9H9D2NO3
Molecular Weight: 183.2
Chemical Structure
D-4-Hydroxyphenylalanine-[3,3-d2]
Description D-4-Hydroxyphenylalanine-[3,3-d2] is a labelled D-tyrosine. Tyrosine is a non-essential amino acid synthesized from phenylalanine. It is the precursor of some neurotransmitters.
Synonyms D-Tyrosine-d2; p-Hydroxyphenyl-D-alanine-d2; H-D-Tyr-OH-d2
IUPAC Name (2R)-2-amino-3,3-dideuterio-3-(4-hydroxyphenyl)propanoic acid
Related CAS 556-02-5 (unlabelled)
Canonical SMILES C1=CC(=CC=C1CC(C(=O)O)N)O
InChI InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m1/s1/i5D2
InChI Key OUYCCCASQSFEME-JZAVKUPRSA-N
Purity 95% by HPLC; 98% atom D

D-4-Hydroxyphenylalanine-[3,3-d2] (DOPA-d2), a deuterium-labeled variant of the amino acid D-4-Hydroxyphenylalanine, is extensively utilized in bioscience research. Here are the key applications of D-4-Hydroxyphenylalanine-[33-d2]:

Neurotransmitter Studies: Delving into neurochemical intricacies, DOPA-d2 plays a pivotal role in investigating the synthesis and metabolism of dopamine, a vital neurotransmitter in the brain. The deuterated composition enables precise pathway tracing through cutting-edge techniques like Mass Spectrometry (MS) or Nuclear Magnetic Resonance (NMR) spectroscopy. This empowers researchers to delve into neurological disorders such as Parkinson’s disease and schizophrenia with unparalleled precision.

Pharmacokinetic Studies: Positioned at the forefront of pharmaceutical exploration, DOPA-d2 serves as a key tool in unraveling the pharmacokinetics of L-DOPA, the dopamine precursor crucial in Parkinson’s disease treatment. By meticulously monitoring the labeled compound, scientists gain profound insights into absorption, distribution, metabolism, and excretion (ADME) dynamics. This knowledge is instrumental in refining drug formulations and therapeutic approaches, marking a milestone in precision medicine.

Enzyme Kinetics: Unveiling the mysteries of enzyme activity in catecholamine biosynthesis, including key players like tyrosine hydroxylase and aromatic L-amino acid decarboxylase, DOPA-d2 emerges as an indispensable asset. The presence of deuterium facilitates clear differentiation between the labeled substrate and its natural counterpart, streamlining kinetic investigations. This aids in unraveling enzyme mechanisms and crafting enzyme inhibitors as potential therapeutic marvels, pushing the boundaries of biomedical research.

Isotope Dilution Assays: In the realm of quantitative analysis, DOPA-d2 shines as a trusted internal standard for isotope dilution assays, enabling precise quantification of L-DOPA and its metabolites in biological samples. This cutting-edge technique finds particular relevance in clinical diagnostics and metabolic explorations, offering unparalleled accuracy and reproducibility in data. By ensuring superior diagnostic precision and research reliability, this application propels the field of bioscience forward with unwavering certainty.

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