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N-Acetyl-L-leucine-[d10]

General Information
Catalog: BLP-009048
Molecular Formula: C8H5D10NO3
Molecular Weight: 183.3
Chemical Structure
N-Acetyl-L-leucine-[d10]
Description N-Acetyl-L-leucine-[d10] is a labelled N-acetyl-L-Leucine. N-acetyl-L-Leucine is a derivative of leucine and is used as a drug for the treatment of vertigo.
Synonyms N-Acetyl-L-leucine d10
Related CAS 1188-21-2 (unlabelled)
Purity 98% by CP; 98% atom D
Storage Store at RT

N-Acetyl-L-leucine-[d10], a deuterated analog of N-Acetyl-L-leucine, finds extensive use in diverse biochemical and pharmacological investigations. Here are the key applications of N-Acetyl-L-leucine-[d10]:

Metabolic Tracing: Delving into metabolic intricacies, N-Acetyl-L-leucine-[d10] serves as a stable isotope tracer in metabolic explorations, offering insights into leucine metabolism. By integrating this deuterated compound into metabolic pathways, researchers can meticulously monitor its conversions and destiny within biological frameworks. This endeavor enhances comprehension of amino acid metabolism dynamics and protein turnover kinetics.

Pharmacokinetic Studies: A cornerstone of pharmacokinetic scrutiny, N-Acetyl-L-leucine-[d10] plays a pivotal role in investigating the absorption, distribution, metabolism, and excretion (ADME) patterns of leucine derivatives. The deuterium label facilitates precise quantitation and differentiation from endogenous leucine, furnishing essential data for optimizing dosing strategies and elucidating drug synergies and antagonisms.

Proteomics: Within the realm of mass spectrometry-based proteomics, N-Acetyl-L-leucine-[d10] emerges as a potent tool for quantitative protein analysis. By integrating deuterated leucine into proteins, scientists can discern protein turnover dynamics and differential expression across diverse settings. This methodology aids in pinpointing biomarkers and unraveling disease pathways at the proteome level, offering profound insights into cellular behavior.

Stable Isotope Labeling: Revolutionizing stable isotope labeling techniques (SILAC) for quantitative proteomics, N-Acetyl-L-leucine-[d10] facilitates precise analyses of protein synthesis and degradation dynamics. Substituting natural leucine with its deuterated variant in cell cultures enables the quantification of cellular responses to different stimuli and the conduct of comparative proteomic investigations. This technique stands as a cornerstone for deciphering intricate cellular responses and unraveling molecular complexities.

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