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-009083 |
CAS: 136056-01-4 |
Molecular Formula: C8[13C]H11NO2 |
Molecular Weight: 166.18 |
Chemical Structure |
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Description | L-Phenylalanine-[2-13C] is the isotope form of L-phenylalanine. L-Phenylalanine is an essential amino acid that is important for the biosynthesis of other amino acids including melanin, dopamine, noradrenalin and thyroxine. |
Synonyms | L-Phenylalanine-2-13C |
IUPAC Name | (2S)-2-amino-3-phenyl(2-13C)propanoic acid |
Related CAS | 63-91-2 (unlabelled) |
Canonical SMILES | C1=CC=C(C=C1)CC(C(=O)O)N |
InChI | InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1/i8+1 |
InChI Key | COLNVLDHVKWLRT-IDMPRHEVSA-N |
Purity | 98% by CP; 99% atom 13C |
Solubility | Soluble in DMSO, Water |
Appearance | White to Off-white Solid |
Storage | Store at -20°C |
L-Phenylalanine-[2-13C], an isotopically labeled version of the amino acid phenylalanine, finds extensive use in diverse scientific research applications. Here are the key applications of L-Phenylalanine-[2-13C]:
Metabolic Tracing: Delving into metabolic tracing studies, L-Phenylalanine-[2-13C] unlocks insights into the intricate pathways governing phenylalanine catabolism and anabolism. By meticulously tracking the 13C label, researchers unravel the processing and utilization of phenylalanine across varied biological systems. This exploration sheds light on amino acid metabolism, disease states, and potential therapeutic strategies, offering a deeper understanding of physiological processes.
Nutritional Studies: In the realm of nutritional research, L-Phenylalanine-[2-13C] serves as a critical tool for investigating the digestion, absorption, and utilization of phenylalanine within the human body. Through the administration of this labeled compound, scientists monitor its integration into proteins and other biomolecules, enriching our knowledge of dietary requirements and the repercussions of nutritional imbalances. This exploration aids in comprehending the complexities of human nutrition and metabolic health.
Protein Synthesis Research: Unlocking the realms of protein synthesis, L-Phenylalanine-[2-13C] emerges as a valuable asset for scrutinizing the rates of synthesis and turnover within diverse tissues. By incorporating this labeled amino acid into cell cultures or animal models, researchers uncover the kinetics of protein generation and breakdown, offering insights into cellular dynamics, growth processes, and responses to external stimuli. This investigation enhances our grasp of fundamental biological processes and the intricacies of protein regulation.
Medical Diagnostics: In the domain of medical diagnostics, L-Phenylalanine-[2-13C] plays a pivotal role, particularly in advanced imaging techniques like Magnetic Resonance Spectroscopy (MRS). Through the introduction of labeled phenylalanine, practitioners gain a window into metabolic processes, enabling the detection of anomalies in tissues such as the brain. This diagnostic capability proves invaluable in identifying metabolic disorders, monitoring disease progression, and guiding personalized treatment approaches, showcasing the convergence of cutting-edge science and clinical practice.
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