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L-Dopa-[2,5,6,α,β,β-d6]

General Information
Catalog: BLP-009874
CAS: 713140-75-1
Molecular Formula: C9H5D6NO4
Molecular Weight: 203.23
Chemical Structure
L-Dopa-[2,5,6,α,β,β-d6]
Description L-Dopa-[2,5,6,α,β,β-d6] is a labelled L-Dopa. L-Dopa is an amino acid that can be biosynthesized from L-tyrosine. L-Dopa is the precursor of dopamine, norepinephrine and epinephrine. It can be used as a psychoactive drug and the treatment of Parkinson's disease as well as dopamine-responsive dystonia.
Synonyms 3-(3,4-Dihydroxyphenyl)-L-alanine-d6; L-3-Hydroxytyrosine-d6; Levodopa-d6
Related CAS 59-92-7 (unlabelled)
Purity 95% by HPLC; 98% atom D

L-Dopa-[2,5,6,α,β,β-d6] is a labeled form of L-Dopa commonly used in research and medical applications. Here are some key applications of L-Dopa-[2,5,6,α,β,β-d6]:

Parkinson’s Disease Research: L-Dopa-[2,5,6,α,β,β-d6] is employed in Parkinson’s disease research to study the metabolic pathways and mechanisms of L-Dopa metabolism. The deuterated analog allows for precise tracking and quantification of metabolic products in biological samples using techniques such as mass spectrometry. This aids in understanding the in vivo metabolism of L-Dopa and optimizing therapeutic regimens.

Pharmacokinetics Studies: Researchers use L-Dopa-[2,5,6,α,β,β-d6] to investigate the pharmacokinetics of L-Dopa in various biological systems. The labeled compound provides detailed insights into absorption, distribution, metabolism, and excretion (ADME) processes. These studies help in improving drug formulations and dosing strategies for better patient outcomes.

Biomarker Discovery: L-Dopa-[2,5,6,α,β,β-d6] serves as a valuable tool in the discovery and validation of biomarkers for neurological diseases. By analyzing its metabolic pathways, scientists can identify potential biomarkers related to disease progression and treatment response. This can lead to the development of more accurate diagnostic and monitoring tools.

Neurochemistry: In neurochemical research, L-Dopa-[2,5,6,α,β,β-d6] is used to study the synthesis and turnover of neurotransmitters such as dopamine. The labeled form allows for precise measurement of neurotransmitter production and degradation rates. This contributes to a deeper understanding of neurochemical dynamics in various physiological and pathological conditions.

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