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-004301 |
Molecular Formula: C5[13C]6H12N2O2 |
Molecular Weight: 210.18 |
Chemical Structure |
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Description | L-Tryptophan (Ring-[13C6]) is the labelled form of L-Tryptophan, which is an essential amino acid. |
Synonyms | L-Tryptophan (Ring-13C6); L-Tryptophan-13C6; (2S)-2-amino-3-(1H-indol-3-yl)propanoic acid-13C6 |
IUPAC Name | (2S)-3-[(3a,4,5,6,7,7a-13C6)-1H-indol-3-yl]-2-aminopropanoic acid |
Related CAS | 73-22-3 (unlabelled) |
Purity | 98% by CP |
L-Tryptophan (Ring-[13C6]), an isotopically labeled amino acid widely utilized in biochemical research and analysis, finds versatile applications in various fields. Here are key applications of L-Tryptophan (Ring-[13C6]) presented with high perplexity and burstiness:
Metabolic Tracing: Delving into metabolic tracing studies, researchers employ L-Tryptophan (Ring-[13C6]) to investigate the intricate pathways of tryptophan metabolism. By meticulously tracking the 13C-labeled carbon atoms, they unravel the complex metabolic destiny of tryptophan in cells and tissues. This exploration sheds light on disorders like tryptophan malabsorption and unveils the pivotal role of tryptophan in neurotransmitter synthesis.
Structural Biology: Within the realm of structural biology, L-Tryptophan (Ring-[13C6]) serves as a cornerstone for NMR (nuclear magnetic resonance) spectroscopy studies. The isotopic enrichment offers a window into the detailed examination of tryptophan residues within proteins, aiding in unraveling the intricacies of protein structure and dynamics. By leveraging this tool, researchers glean insights into protein folding, conformational changes, and interactions with other biomolecules.
Protein-Protein Interaction Studies: In the realm of protein-protein interactions, L-Tryptophan (Ring-[13C6]) plays a pivotal role by integrating the labeled amino acid into target proteins. This labeled tryptophan serves as a discerning reporter, pinpointing interaction sites and binding interfaces through techniques such as fluorescence spectroscopy and mass spectrometry. These studies are instrumental in unraveling cellular pathways and laying the groundwork for designing targeted therapeutic interventions.
Nutritional Research: In the domain of nutritional research, L-Tryptophan (Ring-[13C6]) emerges as a valuable tool for assessing the bioavailability and digestion of dietary tryptophan. Researchers delve into understanding how the body metabolizes and utilizes tryptophan from diverse dietary sources by quantifying the 13C isotopic enrichment in biological samples. This knowledge plays a pivotal role in shaping dietary recommendations and deepening our understanding of the nutritional implications of tryptophan intake.
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