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L-Tryptophan-[d8,15N2]

General Information
Catalog: BLP-009538
Molecular Formula: C11H4D8[15N]2O2
Molecular Weight: 214.26
Chemical Structure
L-Tryptophan-[d8,15N2]
Description L-Tryptophan-[d8,15N2] is a deuterium & 15N labelled L-Tryptophan. L-Tryptophan is an essential amino acid that is the precursor of serotonin, melatonin, and vitamin B3.
Synonyms H-Trp-OH-d8,15N2; (2S)-2-amino-3-(1H-indol-3-yl)propanoic acid-d8,15N2
Related CAS 73-22-3 (unlabelled)
InChI InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m1/s1/i1D,2D,3D,4D,5D2,6D,9D,12+1,13+1
InChI Key QIVBCDIJIAJPQS-DESWZXJHSA-N
Purity 98% by CP; 98% atom D; 98% atom 15N
Appearance White Solid

L-Tryptophan-[d8,15N2] is an isotopically labeled amino acid used in biochemical and clinical research. Here are some key applications of L-Tryptophan-[d8,15N2]:

Metabolic Tracing: L-Tryptophan-[d8,15N2] is used in metabolic tracing studies to track tryptophan metabolism and its conversion into various metabolites within biological systems. By measuring the incorporation of isotopically labeled tryptophan into metabolites like serotonin and kynurenine, researchers can gain insights into metabolic pathways and alterations in disease states. This application helps in understanding metabolic disorders and the effects of therapeutic interventions.

Protein Structure Elucidation: The incorporation of L-Tryptophan-[d8,15N2] into proteins enables detailed nuclear magnetic resonance (NMR) and mass spectrometry studies. By observing the labeled tryptophan residues, scientists can determine protein folding dynamics and interactions with other molecules. This is particularly valuable in structural biology for elucidating protein function and in drug design to identify binding sites.

Nutritional Studies: L-Tryptophan-[d8,15N2] is employed in nutritional research to study tryptophan absorption, bioavailability, and its role in human health. By tracking the labeled amino acid in dietary studies, researchers can assess the impact of different diets on tryptophan metabolism. This information is crucial for developing dietary recommendations and understanding the nutritional impact on health conditions like mood disorders and sleep.

Pharmacokinetics: The use of L-Tryptophan-[d8,15N2] in pharmacokinetic studies allows scientists to analyze the distribution, metabolism, and elimination of tryptophan in the body. By using the labeled tryptophan, researchers can determine the kinetics of tryptophan metabolism in various physiological and pathological conditions. This assists in the development of therapeutic strategies and understanding the interactions between tryptophan metabolism and drug efficacy.

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