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-009890 |
CAS: 1356016-86-8 |
Molecular Formula: C5H6D3NO3 |
Molecular Weight: 134.15 |
Chemical Structure |
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Description | Trans-4-Hydroxy-L-proline-[2,5,5-d3] is a labelled trans-4-Hydroxy-L-proline. Trans-4-Hydroxy-L-proline is a hydroxylated derivative of amino acid proline in the class of non-proteinogenic amino acids. |
Synonyms | (2S,4R)-4-Hydroxy-2-pyrrolidinecarboxylic acid-d3; H-L-Hyp-OH-d3 |
Related CAS | 51-35-4 (unlabelled) |
Purity | 95% by HPLC; 98% atom D |
trans-4-Hydroxy-L-proline-[2,5,5-d3], an isotopically labeled derivative of hydroxyproline, plays a vital role in biochemical and medical research. Here are the key applications of trans-4-Hydroxy-L-proline-[2,5,5-d3]:
Protein Structure Studies: Deuterium-labeled trans-4-Hydroxy-L-proline emerges as a pivotal tool for unraveling the intricacies of protein structure and dynamics using NMR spectroscopy. By incorporating this specialized amino acid into proteins, researchers can delve deep into hydrogen-deuterium exchange and the complex processes of protein folding. This nuanced approach illuminates the stability, functionality, and intricate interactions of proteins, enhancing our understanding of molecular mechanisms.
Collagen Research: Investigating collagen synthesis and metabolism, trans-4-Hydroxy-L-proline-[2,5,5-d3] assumes a critical role due to the significance of hydroxyproline in collagen composition. Through the use of this labeled compound, researchers can meticulously track and quantify collagen turnover and degradation within biological systems. This capability proves invaluable for unraveling the pathophysiology of conditions like osteoarthritis and fibrosis, characterized by disturbances in collagen metabolism.
Metabolic Pathway Analysis: Driving the exploration of proline and hydroxyproline pathways in metabolic studies, this isotopically labeled compound enables researchers to trace the incorporation and conversion processes within cellular and tissue models. This detailed insight into the metabolism of trans-4-Hydroxy-L-proline-[2,5,5-d3] assists in deciphering metabolic fluxes and enzyme kinetics, shedding light on the pathogenesis of metabolic disorders and facilitating the development of precisely targeted therapeutic interventions.
Drug Development: Positioned at the forefront of drug discovery endeavors, trans-4-Hydroxy-L-proline-[2,5,5-d3] plays a crucial role in developing novel therapeutics tailored to address collagen-related disorders. Leveraging this labeled compound, researchers delve into drug-proline interactions and their effects on hydroxyproline metabolism, a pivotal aspect in designing effective and selective therapeutics. This application holds particular relevance in fields such as fibrosis, cancer, and dermatological disorders where collagen-related processes exert significant influence.
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