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-009316 |
CAS: 160033-95-4 |
Molecular Formula: C3[13C]H7NO4 |
Molecular Weight: 134.10 |
Chemical Structure |
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Description | L-Aspartic acid-[2-13C] is a labelled L-Aspartic acid. Aspartic Acid is an α-amino acid used in the biosythesis of proteins. It is a non-essential amino acid for humans. |
IUPAC Name | (2S)-2-amino(2-13C)butanedioic acid |
Related CAS | 56-84-8 (unlabelled) |
Canonical SMILES | C(C(C(=O)O)N)C(=O)O |
InChI | InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1/i2+1 |
InChI Key | CKLJMWTZIZZHCS-JACJRKFSSA-N |
Melting Point | >300°C (dec.) (lit.) |
Purity | 98% by HPLC; 99% atom 13C |
Storage | Store at RT |
L-Aspartic acid-[2-13C], a stable isotope-labeled compound, finds extensive utility across diverse scientific domains. Here are the key applications of L-Aspartic acid-[2-13C]:
Metabolic Tracing: Delving into metabolic tracing studies, L-Aspartic acid-[2-13C] serves as a crucial tool for unraveling intricate metabolic pathways and fluxes within cellular ecosystems. By meticulously tracking the incorporation of labeled carbon into metabolic intermediates, researchers unearth profound insights into cellular metabolism. This application stands as a cornerstone for deciphering diseases linked to metabolic dysregulation and for refining industrial bioprocesses with precision.
Proteomics Research: Within the domain of proteomics, L-Aspartic acid-[2-13C] emerges as a pivotal player in probing protein synthesis dynamics and turnover phenomena. Through integration of the labeled amino acid into newly synthesized proteins, researchers embark on a quantitative analysis of protein dynamics using cutting-edge mass spectrometry techniques. This methodology aids in identifying nuanced changes in protein expression levels under diverse physiological contexts or in response to therapeutic interventions.
Structural Biology: Navigating the intricate realms of structural biology, L-Aspartic acid-[2-13C] unveils its potential in NMR spectroscopy applications aimed at unraveling protein structure intricacies and dynamic behaviors. The 13C label acts as a versatile probe, shedding light on the local nuances of aspartic acid residues within proteins. This detailed information forms the bedrock for deciphering protein folding processes, intermolecular interactions, and functional attributes at the molecular scale, driving forward our comprehension of biological complexities.
Drug Metabolism Studies: In the realm of pharmacokinetics, L-Aspartic acid-[2-13C] stands at the forefront as a vital tracer, facilitating in-depth investigations into drug and xenobiotic metabolism dynamics. By scrutinizing the metabolic fate and excretion patterns of the labeled compound within biological milieus, researchers gain crucial insights into the pharmacodynamics and toxicity profiles of therapeutic agents. This pivotal knowledge streamlines drug design processes.
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