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-009865 |
CAS: 1994265-09-6 |
Molecular Formula: C5H6D3NO2 |
Molecular Weight: 118.15 |
Chemical Structure |
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Description | D-Proline-[2,5,5-d3] is a labelled D-Proline. Proline is the only proteinogenic amino acid with a secondary amine. It can be used as an asymmetric catalyst in proline organocatalysis reactions. |
Synonyms | (R)-2-Pyrrolidinecarboxylic Acid-d3; H-D-Pro-OH-d3 |
Related CAS | 344-25-2 (unlabelled) |
Purity | 95% by HPLC; 98% atom D |
D-Proline-[2,5,5-d3] is a deuterated form of the amino acid proline widely used in various scientific research fields. Here are some key applications of D-Proline-[2,5,5-d3]:
Metabolic Tracing: D-Proline-[2,5,5-d3] is employed in metabolic studies as a tracer to understand the dynamics of proline metabolism. By incorporating this compound into metabolic pathways, researchers can track the biochemical fate of proline in cells and tissues. This application is crucial for elucidating metabolic disorders and optimizing nutritional interventions.
NMR Spectroscopy: In structural biology and biochemistry, D-Proline-[2,5,5-d3] is used in NMR spectroscopy to study protein structures. The deuterium atoms provide enhanced spectral resolution, allowing for more precise identification of protein conformations and interactions. This application is essential for drug design and understanding protein function at the atomic level.
Peptide Synthesis: D-Proline-[2,5,5-d3] is used in the synthesis of labeled peptides for use in various biochemical assays. The incorporation of deuterium-labeled proline can aid in the identification and quantification of these peptides in mass spectrometry studies. This application is valuable for proteomics research and the development of peptide-based therapeutics.
Isotope Effect Studies: Researchers utilize D-Proline-[2,5,5-d3] to investigate kinetic isotope effects in enzymatic reactions involving proline. By comparing the reaction rates of deuterated and non-deuterated proline, scientists can gain insights into the reaction mechanisms and transition states. This application helps in understanding enzyme catalysis and designing more effective enzyme inhibitors.
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