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-009888 |
CAS: 133519-78-5 |
Molecular Formula: C11H9D3N2O2 |
Molecular Weight: 207.25 |
Chemical Structure |
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Description | L-Tryptophan-[2,3,3-d3] is a labelled L-Tryptophan. Tryptophan is an essential amino acid obtained from diet. Tryptophan is also a precursor of the neurotransmitter serotonin and the hormone melatonin. |
Synonyms | (S)-2-Amino-3-(3-indolyl)propionic Acid-d3; H-L-Trp-OH-d3 |
IUPAC Name | 2-amino-3-(1H-indol-3-yl)propanoic acid |
Related CAS | 73-22-3 (unlabelled) |
Canonical SMILES | C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N |
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) |
InChI Key | QIVBCDIJIAJPQS-UHFFFAOYSA-N |
Purity | 95% by HPLC; 98% atom D |
L-Tryptophan-[2,3,3-d3], a stable isotope-labeled amino acid, finds diverse applications in research. Explore the key applications of L-Tryptophan-[2,3,3-d3]:
Metabolic Studies: Delving into metabolic intricacies, researchers utilize L-Tryptophan-[2,3,3-d3] to unravel the biosynthesis, degradation, and pathways of tryptophan within organisms. This labeled amino acid offers precise insights into metabolic flux through advanced isotopic labeling techniques like NMR and mass spectrometry. By deciphering tryptophan metabolism, researchers gain profound understanding of its roles in diverse physiological and pathological states.
Protein Synthesis Research: In the exploration of protein synthesis, L-Tryptophan-[2,3,3-d3] integrates into proteins, tracing their synthesis and breakdown. The deuterium labeling facilitates detailed examination of protein turnover and dynamics using cutting-edge mass spectrometry. This enables researchers to probe protein life cycles, unveiling the influence of diverse conditions on protein stability and functionality.
Pharmacokinetics: For pharmacokinetic inquiries, L-Tryptophan-[2,3,3-d3] serves to probe the absorption, distribution, metabolism, and excretion (ADME) of tryptophan-containing compounds. The stable isotope labeling yields precise quantitative data, enriching comprehension of the pharmacokinetic properties of drugs derived from tryptophan. This knowledge is pivotal in drug development and optimizing therapeutic protocols.
Neuroscience Research: Within neuroscience, L-Tryptophan-[2,3,3-d3] emerges as a vital tool for investigating the synthesis and metabolism of serotonin, a crucial neurotransmitter originating from tryptophan. By tracing the labeled amino acid, researchers unravel the intricate pathways governing serotonin production and its impact on brain function and behavior. This application proves invaluable in exploring the mechanisms underlying neurological and psychiatric disorders, offering deeper insights into brain-related complexities.
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