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3-Chloro-L-tyrosine-[13C6]

General Information
Catalog: BLP-008285
Molecular Formula: C3[13C]6H10ClNO3
Molecular Weight: 221.59
Chemical Structure
3-Chloro-L-tyrosine-[13C6]
Description 3-chloro-L-Tyrosine (RING-13C6) is a labelled 3-chloro-L-Tyrosine. 3-chloro-L-Tyrosine is a derivative of tyrosine potentially used for proteomics studies.
Synonyms 3-Chloro-L-tyrosine (ring-13C6); Monochlorotyrosine-13C6; 3-Chlorotyrosine-13C6; (S)-2-Amino-3-(3-chloro-4-hydroxyphenyl)propanoic acid-13C6; 3-chloro-4-hydroxy-L-phenylalanine-13C6; CLY-13C6; H-Tyr(3-Cl)-OH-13C6
IUPAC Name (S)-2-amino-3-(3-chloro-4-hydroxyphenyl-1,2,3,4,5,6-13C6)propanoic acid
Related CAS 7423-93-0 (unlabelled)
Purity 95%; 99% atom 13C
Solubility Slightly soluble in Chloroform, Methanol, Water
Appearance Off-white Solid
Storage Store at 2-8°C under inert atmosphere

3-Chloro-L-tyrosine-[13C6] is a labeled amino acid used in various scientific research and analytical applications. Here are some key applications of 3-Chloro-L-tyrosine-[13C6]:

Stable Isotope Labeling: 3-Chloro-L-tyrosine-[13C6] is employed as a stable isotope-labeled amino acid in proteomics and metabolic research. By incorporating this compound into proteins, researchers can trace metabolic pathways and quantitatively analyze protein dynamics using mass spectrometry. This technique is invaluable for understanding protein turnover and metabolic fluxes in complex biological systems.

Analytical Chemistry: In analytical chemistry, 3-Chloro-L-tyrosine-[13C6] serves as an internal standard for quantitative analyses of amino acids and related compounds. Its incorporation helps in correcting for matrix effects and ensuring precision in measurements. This enhances the accuracy and reliability of analytical methods used in environmental, food, and clinical sample assessments.

Pharmaceutical Research: 3-Chloro-L-tyrosine-[13C6] is used in pharmaceutical research to study drug metabolism and pharmacokinetics. By incorporating the labeled compound into drugs, researchers can track and analyze the distribution, absorption, and breakdown of pharmaceuticals within the body. This information is crucial for drug development and optimizing therapeutic regimens.

Biochemical Pathway Analysis: Researchers use 3-Chloro-L-tyrosine-[13C6] to investigate the biochemical pathways involving chlorinated tyrosine derivatives. Its presence allows scientists to study enzyme kinetics and substrate specificities in reactions involving halogenated amino acids. This contributes to a deeper understanding of biochemical transformations and the influence of halogenation on enzyme activity.

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