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-012737 |
Molecular Formula: C6H12O5[18O] |
Molecular Weight: 182.16 |
Chemical Structure |
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Description | D-Mannose-[1-18O] is the labelled analogue of D-Mannose, which is a monosaccharide involved in glycosylation of some molecules in various cellular processes. Nutritional supplement in health care products. |
Synonyms | D-[1-18O]mannose; D-mannose-1-18O; Carubinose-1-18O; Seminose-1-18O; NSC 26247-1-18O |
IUPAC Name | (3S,4S,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol-2-18O |
Related CAS | 3458-28-4 (unlabelled) |
Purity | ≥95%; >90% atom 18O |
Solubility | Soluble in DMSO (Slightly), Methanol (Slightly), Water (Sparingly) |
Appearance | Off-white Solid |
Storage | Store at 2-8°C |
D-Mannose-[1-18O] is a labeled monosaccharide used in various scientific research applications. Here are some key applications of D-Mannose-[1-18O]:
Metabolic Pathway Tracing: D-Mannose-[1-18O] is utilized to trace metabolic pathways involving mannose, allowing researchers to track the biochemical transformations and fluxes of mannose in cellular systems. By following the labeled oxygen isotope, scientists can gain insights into the roles mannose plays in glycan synthesis and other metabolic processes. This is critical for understanding cellular metabolism and identifying any disruptions associated with diseases.
Diagnostic Imaging: In medical diagnostics, D-Mannose-[1-18O] can be used as a tracer in positron emission tomography (PET) imaging. When incorporated into metabolic pathways, it facilitates the visualization of specific biological processes in real-time. This is particularly useful in tumor imaging, where the uptake and utilization of mannose by cancer cells can be monitored, aiding in the assessment of tumor metabolism and the effectiveness of therapeutic interventions.
Glycosylation Studies: D-Mannose-[1-18O] is employed in glycosylation research to understand the synthesis and processing of glycoconjugates. By incorporating the labeled mannose into glycoproteins and glycolipids, researchers can analyze the kinetic processes and identify specific glycosylation sites. This application is fundamental to deciphering the roles of glycosylation in health and disease, including congenital disorders of glycosylation and cancer.
Enzyme Kinetics: In enzymology, D-Mannose-[1-18O] serves as a substrate to study the kinetics of mannose-utilizing enzymes. By measuring the incorporation of the labeled oxygen into enzyme products, researchers can determine catalytic rates, substrate affinities, and reaction mechanisms. This information is vital for characterizing enzyme functions and for the development of enzyme inhibitors as potential therapeutic agents.
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