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-000511 |
CAS: 180268-82-0 |
Molecular Formula: C3[13C]6H11NO2 |
Molecular Weight: 171.146 |
Chemical Structure |
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Description | L-Phenylalanine [Ring-13C6] is a labelled L-Phenylalanine. Phenylalanine is an α-amino acid essential for humans that is found in breast milk of mammals. It is commonly used as a dietary supplement. |
Synonyms | L-Phenylalanine-13C6; L-Phenyl-13C6-alanine; (S)-(-)-Phenylalanine-13C6; (S)-|A-Aminohydrocinmic Acid-13C6; (S)-|A-Amino-benzenepropanoic Acid-13C6 |
IUPAC Name | 2-amino-3-((1,2,3,4,5,6-13C6)cyclohexatrienyl)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/i1+1,2+1,3+1,4+1,5+1,7+1 |
InChI Key | COLNVLDHVKWLRT-KILZIXFTSA-N |
Melting Point | 266-267°C (dec.) |
Purity | 95% by HPLC; 98% atom 13C |
Appearance | White to Off-white Solid |
L-Phenylalanine [Ring-13C6], a stable isotope-labeled compound extensively utilized in bioscience research, offers diverse applications. Here are the key applications of L-Phenylalanine [Ring-13C6]:
Metabolic Flux Analysis: Employing L-Phenylalanine [Ring-13C6] for metabolic flux analysis illuminates the journey of phenylalanine through intricate metabolic pathways. By tracing the labeled carbon atoms, researchers unveil insights into amino acid metabolism and pinpoint regulatory hotspots critical for comprehending metabolic disorders and fine-tuning metabolic engineering strategies.
Protein Structure and Function Studies: Within the realm of protein biochemistry, the incorporation of L-Phenylalanine [Ring-13C6] into proteins unlocks a treasure trove of knowledge about their structure, dynamics, and interactions. Mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy serve as trusty companions in dissecting these labeled proteins, offering a profound understanding of protein folding, stability, and function.
Pharmacokinetics and Drug Development: Unraveling the mysteries of pharmacokinetics, the labeled version of phenylalanine is a linchpin in tracking the journey of drugs through absorption, distribution, metabolism, and excretion pathways. Integrating L-Phenylalanine [Ring-13C6] into drug candidates enables researchers to monitor their metabolic fate and behavior within the body, facilitating the development of potent and safer pharmaceutical agents.
Nutritional Studies: In the realm of nutritional science, L-Phenylalanine [Ring-13C6] acts as a beacon for exploring the metabolism of phenylalanine under various dietary scenarios. This exploration sheds light on the role of this amino acid in growth, development, and overall well-being. Furthermore, it serves as a key tool in investigating phenylalanine metabolism in individuals grappling with metabolic disorders like phenylketonuria (PKU), offering insights into personalized nutrition interventions.
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