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-009045 |
CAS: 80134-83-4 |
Molecular Formula: C5[13C]H13[15N]O2 |
Molecular Weight: 133.16 |
Chemical Structure |
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Description | L-Leucine-[1-13C,15N] is the labelled analogue of L-Leucine. Leucine is a non-glucogenic, essential amino acid. It is a branched-chain amino acid that is a structural component of proteins. Leucine positively influences insulin release to eliminate toxic sugars out of the blood. |
Synonyms | L-Leucine-1-13C,15N |
IUPAC Name | (2S)-2-(15N)azanyl-4-methyl(1-13C)pentanoic acid |
Related CAS | 61-90-5 (unlabelled) |
Isomeric SMILES | CC(C)C[C@@H]([13C](=O)O)[15NH2] |
Canonical SMILES | CC(C)CC(C(=O)O)N |
InChI | InChI=1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t5-/m0/s1/i6+1,7+1 |
InChI Key | ROHFNLRQFUQHCH-XAAHKOKXSA-N |
Purity | 98% by CP; 99% atom 13C; 98% atom 15N |
Storage | Store at 2-8°C |
L-Leucine-[1-13C,15N], a stable isotope-labeled amino acid, finds extensive use in biochemical and physiological studies. Here are the key applications of L-Leucine-[1-13C,15N]:
Metabolic Flux Analysis: Delving into metabolic pathways, L-Leucine-[1-13C,15N] serves as a powerful tool for tracing the incorporation and conversion of the labeled isotope in metabolic intermediates. This method sheds light on the dynamics and control of metabolic networks, providing insights into how various metabolic conditions or perturbations influence leucine metabolism.
Protein Turnover Studies: By harnessing L-Leucine-[1-13C,15N], researchers can gauge the rates of protein synthesis and degradation within cells and tissues. The labeled amino acid becomes part of newly formed proteins, allowing for quantification of turnover. This capability is crucial for investigating conditions related to protein balance, such as muscle atrophy and neurodegenerative diseases.
NMR Spectroscopy: Widely employed in NMR spectroscopy, L-Leucine-[1-13C,15N] contributes to determining protein structure and dynamics. The isotope labeling enriches the resolution and sensitivity of NMR signals, facilitating detailed exploration of protein folding, interactions, and conformational changes. This technique plays a pivotal role in structural biology and pharmaceutical development.
Nutritional Studies: In the realm of nutritional research, L-Leucine-[1-13C,15N] serves as a valuable asset for probing amino acid utilization and metabolism in diverse physiological states like fasting, exercise, and disease. By monitoring the labeled leucine, researchers can evaluate how dietary factors and metabolic states impact leucine kinetics, aiding in the formulation of dietary guidelines and enhancing understanding of metabolic wellness.
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