Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-009557 |
CAS: 71939-39-4 |
Molecular Formula: C9H8D3NO3 |
Molecular Weight: 184.21 |
Chemical Structure |
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Description | L-Tyrosine-[d3] is a deuterium labelled analogue of L-Tyrosine. L-Tyrosine is a non-essential amino acid and one of the 22 amino acids used in the synthesis of protein. It is derived from phenylalanine in human body and abundant in high-protein food products. |
Synonyms | L-4-Hydroxyphenyl-2,6-d2-alanine-2-d1; L-4-hydroxyphenyl-(ring-2,6-d2)-2-d |
IUPAC Name | (2S)-2-amino-2-deuterio-3-(2,6-dideuterio-4-hydroxyphenyl)propanoic acid |
Related CAS | 60-18-4 (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-/m0/s1/i1D,2D,8D |
InChI Key | OUYCCCASQSFEME-JAGVNIBFSA-N |
Purity | 98% by CP; 30% atom D |
Appearance | White Solid |
L-Tyrosine-[d3], a labeled isotope of the amino acid L-tyrosine, finds diverse applications in scientific research. Here are the key applications of L-Tyrosine-[d3]:
Metabolic Tracing Studies: Delving into metabolic intricacies, L-Tyrosine-[d3] serves as a valuable tool for tracing the pathways and fate of tyrosine within biological systems. By integrating this isotope into metabolic networks, researchers can meticulously monitor its conversion into downstream metabolites, shedding light on metabolic fluxes and the intricate role of tyrosine in various physiological and pathological contexts.
Protein Synthesis Research: Unraveling the complexities of protein synthesis, L-Tyrosine-[d3] enables scientists to closely observe the incorporation of tyrosine into newly synthesized proteins. This application is pivotal for exploring protein turnover rates and the dynamic processes of protein synthesis within cells. Furthermore, it offers insights into how external factors such as stress or disease influence protein production dynamics.
Quantitative Mass Spectrometry: Positioned as an internal standard in quantitative mass spectrometry analyses, L-Tyrosine-[d3] plays a critical role in ensuring precise quantification of tyrosine and its associated metabolites. By incorporating this labeled isotope into samples, researchers can obtain highly accurate measurements essential for diagnostic assays and advancing biochemical research methodologies.
Neurotransmitter Dynamics: Serving as a key precursor to neurotransmitters like dopamine, norepinephrine, and epinephrine, tyrosine plays a pivotal role in neurotransmitter dynamics. Through the utilization of L-Tyrosine-[d3], researchers can delve into the biosynthesis and degradation pathways of these crucial neurotransmitters within the brain. This application holds significant value in elucidating neurotransmitter dynamics in the context of neurological disorders and exploring the effects of various drugs on neurotransmitter function.
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