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-006996 |
Molecular Formula: C5[13C]H11DO6 |
Molecular Weight: 182.16 |
Chemical Structure |
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Synonyms | D-[1-13C,2-2H]mannose; D-mannose-1-13C,2-d |
IUPAC Name | (3S,4S,5S,6R)-6-(hydroxymethyl)tetrahydro-2H-pyran-2-13C-3-d-2,3,4,5-tetraol |
Related CAS | 3458-28-4 (unlabelled) |
Solubility | Soluble in Methanol, Water |
Appearance | White to Off-white Solid |
Storage | Store at -20°C |
D-mannose-[1-13C,2-d], a specialized sugar molecule with isotopic labeling, finds diverse applications in scientific research. Here are the key applications of this compound:
Metabolic Flux Analysis: Delving into metabolic pathways, scientists utilize D-mannose-[1-13C,2-d] to track the flow of carbon in carbohydrate metabolism. By following the labeled carbon's journey through metabolic reactions, researchers uncover insights into the fluxes across various pathways. This approach aids in unraveling the intricate web of metabolic networks and pinpointing critical regulatory nodes.
Glycoprotein Synthesis Studies: In the realm of glycosylation research, D-mannose-[1-13C,2-d] emerges as a crucial tool for investigating glycoprotein synthesis and function. The incorporation of labeled mannose into glycoproteins enables a meticulous exploration of glycosylation patterns and dynamics. This meticulous analysis sheds light on the roles of glycoproteins in cellular processes and disease mechanisms, offering a deeper understanding of these complex biological phenomena.
NMR Spectroscopy: Employed in nuclear magnetic resonance (NMR) spectroscopy, D-mannose-[1-13C,2-d] stands as a valuable resource for studying carbohydrate structure and dynamics. With its dual labeling, this compound generates unique NMR signals that aid in detailed characterization of mannose-containing molecules. Researchers leverage this information to investigate carbohydrate-protein interactions and molecular conformations, unlocking the secrets of molecular architectures.
Diabetes Research: Pioneering studies in glucose metabolism and diabetes employ D-mannose-[1-13C,2-d] to explore the intricate connection between altered glucose handling and diabetic conditions. By utilizing labeled mannose in metabolic assays, scientists monitor the impact of disrupted glucose metabolism on overall carbohydrate metabolic processes in diabetic contexts. This investigative approach helps identify metabolic changes and potential targets for therapeutic interventions in diabetes management, paving the way for innovative treatment strategies.
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