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-012750 |
Molecular Formula: C6H12O5[18O] |
Molecular Weight: 182.16 |
Chemical Structure |
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Description | D-Mannose-[6-18O] 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-[6-18O]mannose; D-mannose-6-18O |
IUPAC Name | (3S,4S,5S,6R)-6-((hydroxy-18O)methyl)oxane-2,3,4,5-tetrol |
Related CAS | 3458-28-4 (unlabelled) |
Purity | ≥95%; >90% atom 18O |
Solubility | Soluble in DMSO (Slightly), Methanol (Slightly), Water (Sparingly) |
Appearance | White to Off-white Solid |
Storage | Store at 2-8°C |
D-Mannose-[6-18O], an isotopically labeled carbohydrate with diverse scientific uses, presents numerous applications for research endeavors. Here are the key applications of D-Mannose-[6-18O], articulated:
Metabolic Tracing: Delving into the intricate realm of carbohydrate metabolism, D-Mannose-[6-18O] serves as a valuable tracer for unraveling metabolic pathways within biological systems. By introducing this labeled mannose into metabolic cascades, researchers are able to trace the intricate flow and transformation of sugars through diverse biochemical reactions. This methodology aids in comprehending the complexities of metabolic networks and elucidating the pivotal role of mannose in various cellular processes.
Glycoprotein Research: In the exploration of glycoprotein biosynthesis and structure, scientists leverage D-Mannose-[6-18O] as a crucial tool. Through the incorporation of labeled mannose into glycan chains of glycoproteins, researchers gain insights into the formation and remodeling of these essential biomolecules. This application plays a pivotal role in unraveling the nuances of protein folding, stability, and deciphering intricate cellular signaling mechanisms.
Mass Spectrometry: A cornerstone in mass spectrometry-based analyses, D-Mannose-[6-18O] offers unparalleled utility. By utilizing this isotopically labeled compound, researchers can discern between various isotopes of mannose in mass spectrometric investigations. This capability enhances the precision and dependability of quantitative analyses in the realm of biomolecular research, facilitating the exploration of complex biological phenomena.
Drug Development: In the domain of pharmaceutical research, D-Mannose-[6-18O] emerges as a versatile asset for probing the pharmacokinetics and metabolism of mannose-containing drugs. Understanding the absorption, distribution, metabolism, and excretion dynamics of these drugs can provide valuable insights for designing more efficacious therapeutic agents. This application holds particular relevance in the development of drugs targeting metabolic disorders and infectious diseases, paving the way for enhanced treatment modalities.
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