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-009355 |
Molecular Formula: C10[13C]H12N2O2 |
Molecular Weight: 205.22 |
Chemical Structure |
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Description | L-Tryptophan-[indole-4-13C] 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 | L-Tryptophan-(indole ring-4-13C) |
Related CAS | 73-22-3 (unlabelled) |
Melting Point | 280-285°C (dec.) (lit.) |
Purity | 98% by HPLC; 98% atom 13C |
L-Tryptophan-[indole-4-13C] is a stable isotope-labeled amino acid commonly used in biochemical and pharmaceutical research. Here are some key applications of L-Tryptophan-[indole-4-13C]:
Metabolic Pathway Tracing: L-Tryptophan-[indole-4-13C] is employed in metabolic studies to trace the fate of tryptophan through various biochemical pathways. By using this labeled compound, researchers can monitor and identify metabolic intermediates and products. This application provides insights into the metabolism of tryptophan and its role in physiological and pathological conditions.
Protein Structure and Dynamics: By incorporating L-Tryptophan-[indole-4-13C] into proteins, scientists can utilize NMR spectroscopy to study protein structure and dynamics. The labeled tryptophan serves as a reporter, allowing researchers to explore protein folding, conformational changes, and protein-protein interactions. This helps in understanding the molecular mechanisms underlying protein function and stability.
Pharmacokinetics: L-Tryptophan-[indole-4-13C] is used in pharmacokinetic studies to evaluate the absorption, distribution, metabolism, and excretion (ADME) of tryptophan-containing drugs. The labeled compound enables precise tracking of the drug within the body. This information is vital for drug development and optimizing therapeutic regimens.
Neurotransmitter Research: L-Tryptophan-[indole-4-13C] plays a significant role in studying the biosynthesis and regulation of neurotransmitters such as serotonin and melatonin. By tracing the conversion of labeled tryptophan in neuronal systems, researchers can elucidate the pathways involved in neurotransmitter production. This aids in understanding the biochemical basis of mood disorders and developing targeted treatments.
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