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-009898 |
CAS: 1202359-57-6 |
Molecular Formula: C11H7D5N2O2 |
Molecular Weight: 209.26 |
Chemical Structure |
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Description | D-Tryptophan-[indole-d5] is a labelled D-Tryptophan. Tryptophan is an essential amino acid obtained from diet. Tryptophan is also a precursor of the neurotransmitter serotonin and the hormone melatonin. |
Synonyms | (R)-2-Amino-3-(3-indoyl)propionic Acid-d5; H-D-Trp-OH-d5 |
IUPAC Name | (2R)-2-amino-3-(2,4,5,6,7-pentadeuterio-1H-indol-3-yl)propanoic acid |
Related CAS | 153-94-6 (unlabelled) |
Isomeric SMILES | [2H]C1=C(C(=C2C(=C1[2H])C(=C(N2)[2H])C[C@H](C(=O)O)N)[2H])[2H] |
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)/t9-/m1/s1/i1D,2D,3D,4D,6D |
InChI Key | QIVBCDIJIAJPQS-BZVPBINISA-N |
Purity | 95% by HPLC; 98% atom D |
D-Tryptophan-[indole-d5], an amino acid enriched with stable isotopes, is a cornerstone in bioscience research .Here are some key applications:
Protein Structure Analysis: Navigating the realm of NMR spectroscopy, D-Tryptophan-[indole-d5] emerges as a beacon for unveiling intricate protein architectures. With its isotopic illuminations enhancing signal clarity, researchers can seamlessly chart protein folding dynamics and conformational metamorphoses. These revelations unlock profound insights into protein functionality and intermolecular liaisons.
Metabolic Flux Analysis: Embarking on metabolic explorations, D-Tryptophan-[indole-d5] serves as a strategic guide, tracing metabolic pathways as a vigilant sentinel. Its isotopic identity facilitates the monitoring and dissection of tryptophan’s journey through biochemical labyrinths. This strategy empowers a deeper comprehension of metabolic orchestration and the identification of pivotal regulatory nodes within metabolic networks.
Isotope-Dilution Mass Spectrometry: In the realm of quantitative mass spectrometry, D-Tryptophan-[indole-d5] emerges as a steadfast ally, meticulously gauging the concentrations of tryptophan and its metabolites in biological realms. Its isotopic signature acts as a reliable compass, refining the precision and fidelity of measurements. This precision is indispensable for scrutinizing tryptophan metabolism intricacies in health and disease landscapes.
Pharmacokinetics Studies: Embarking on pharmacokinetic odysseys, D-Tryptophan-[indole-d5] emerges as a beacon, shedding light on the absorption, distribution, metabolism, and excretion (ADME) of tryptophan-based compounds. By harnessing its labeled essence, researchers can shadow the metabolic destiny of drugs entwined with the tryptophan lineage. This knowledge is pivotal for decoding drug dynamics and optimizing therapeutic blueprints.
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