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-007033 |
Molecular Formula: C6H10D2O6 |
Molecular Weight: 182.17 |
Chemical Structure |
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Description | D-Mannose-[6,6'-d2] is a labeled analog of D-Mannose. D-mannose is important in the glycosylation of molecules. It is involved in N and O glycosylation of bovine. It is also used for the O-glycosylation of the T helper cell-derived cytokine interlukin-17A. |
Synonyms | D-[6,6'-2H2]mannose; D-mannose-6,6-d2; D-[6,6'-D2]mannose |
IUPAC Name | (3S,4S,5S,6R)-6-(hydroxymethyl-d2)tetrahydro-2H-pyran-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-[6,6'-d2], a stable isotope-labeled variant of D-mannose, finds diverse applications in bioscience. Here are the key applications:
Metabolic Tracing: In the realm of metabolic research, D-mannose-[6,6'-d2] stands as an indispensable ally, empowering scientists to meticulously trace and quantify mannose pathways, both in vivo and in vitro. By leveraging this intricately labeled compound, researchers delve into the intricate realm of mannose, unveiling its pivotal role in glycosylation processes and its ultimate metabolic destiny. This deep dive sheds light on disorders intertwined with glycosylation and unravels the intricate metabolic interplay surrounding mannose.
Glycobiology Research: At the forefront of glycobiology, the stable isotope-labeled mannose emerges as a linchpin for scrutinizing glycoprotein synthesis and structural intricacies. Scientists ingeniously introduce D-mannose-[6,6'-d2] into cellular landscapes, unraveling the mysteries of how mannose weaves itself into the fabric of glycan structures on proteins. This voyage yields profound insights into cellular phenomena like signal transduction, cell-cell communication, and immune response dynamics, illuminating the intricate dance of cellular machinery.
Enzymology: Unveiling a realm where precision meets innovation, D-mannose-[6,6'-d2] serves as a beacon in enzymology studies, shedding light on the nuanced workings of enzymes entwined in mannose metabolism. Through its distinctive metabolic signature, the labeled mannose unfurls an intricate tapestry, enabling precise measurements of enzyme kinetics and substrate selectivity. This kaleidoscope of information serves as a cornerstone for crafting enzyme replacement therapies and unraveling the intricate dance of metabolic enzyme regulation, pushing the boundaries of scientific understanding.
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