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-009539 |
Molecular Formula: C11H12[15N]NO2 |
Molecular Weight: 205.22 |
Chemical Structure |
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Description | L-Tryptophan-[indole-15N] is a 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 (indole-15N); (2S)-2-amino-3-(1H-indol-3-yl)propanoic acid (indole-15N) |
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-/m0/s1/i13+1 |
InChI Key | QIVBCDIJIAJPQS-DQOKOWHWSA-N |
Purity | 98% by CP; 98% atom 15N; 98% atom D |
Appearance | White Solid |
L-Tryptophan-[indole-15N], an isotopically labeled amino acid, finds diverse applications in scientific research. Here are the key applications of L-Tryptophan-[indole-15N]:
Protein Structure Analysis: Delving into the realm of protein dynamics and structures, L-Tryptophan-[indole-15N] serves as a pivotal tool in NMR spectroscopy. The inclusion of the labeled nitrogen atom significantly boosts the sensitivity and resolution of NMR signals, enabling a meticulous examination of protein folding and interactions. This deepens our comprehension of protein functionalities at the atomic scale, unraveling the intricate choreography of biomolecules.
Metabolic Tracing: In the intricate web of metabolic pathways, L-Tryptophan-[indole-15N] emerges as a crucial tracer for dissecting tryptophan-related metabolisms. By meticulously tracking the incorporation and transformation of this labeled amino acid, researchers illuminate the metabolic fluxes, shedding light on alterations observed in pathological conditions. This scrutiny offers invaluable insights into metabolic control mechanisms and unveils potential targets for therapeutic interventions.
Neuroscience Research: At the forefront of brain exploration, L-Tryptophan-[indole-15N] plays a pivotal role in unraveling the intricate world of neurotransmitter biosynthesis and metabolism. By harnessing this labeled precursor, scientists can quantify the rates of neurotransmitter genesis and degradation in the brain, offering a window into the dynamics of neuronal signaling. This knowledge is instrumental in dissecting neurological disorders and crafting tailored therapeutic modalities to address them.
Microbial Physiology: Venturing into the microbial realm, L-Tryptophan-[indole-15N] unlocks the door to understanding tryptophan metabolism in bacteria and fungi. By integrating the labeled amino acid, researchers can trace the labyrinthine pathways of microbial metabolism, unearthing novel avenues of metabolic processes. This research not only enhances our grasp of microbial physiology but also steers the development of innovative antimicrobial strategies, paving the way for combating microbial challenges effectively.
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