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D-arabinose-[2,3,4,5,5'-d5]

General Information
Catalog: BLP-007003
Molecular Formula: C5H5D5O5
Molecular Weight: 155.16
Chemical Structure
D-arabinose-[2,3,4,5,5'-d5]
Synonyms D-arabinose-2,3,4,5,5-d5; D-[2,3,4,5,5'-D5]arabinose
IUPAC Name (3S,4S,5S)-tetrahydro-2H-pyran-3,4,5,6,6-d5-2,3,4,5-tetraol
Related CAS 10323-20-3 (unlabelled)
Solubility Soluble in Water
Appearance White Solid
Storage Store at -20°C

D-arabinose-[2,3,4,5,5'-d5], a deuterated variant of the sugar D-arabinose, stands at the forefront of scientific research, offering a multitude of versatile applications. Here are the key applications of D-arabinose-[2,3,4,5,5'-d5]:

Tracer Studies in Metabolism: Serving as a metabolic tracer, D-arabinose-[2,3,4,5,5'-d5] plays a pivotal role in biochemical investigations by tracing the intricate pathways of sugars within organisms or cellular systems. Its deuterium labeling feature allows researchers to distinguish its metabolic byproducts from those of non-labeled sugars, employing cutting-edge techniques like mass spectrometry or nuclear magnetic resonance (NMR) spectroscopy. This application is fundamental for delving deep into metabolic pathways and energy dynamics within cells, providing invaluable insights into the complex realm of cellular metabolism.

Glycosylation Research: In the realm of glycosylation research, D-arabinose-[2,3,4,5,5'-d5] emerges as a crucial tool for exploring the significance of sugar moieties attached to proteins and lipids. By integrating this labeled sugar into glycoproteins or glycolipids, scientists embark on a journey to unravel the synthesis and modification of glycan structures. This knowledge is pivotal for deciphering the functional implications of proteins, comprehending intercellular signaling mechanisms, and advancing the development of therapeutic glycoproteins with precision and clarity, propelling the field of glycosylation research into new realms of discovery.

Structural Biology: By incorporating D-arabinose-[2,3,4,5,5'-d5] into structural biology studies, researchers unlock doors to investigate carbohydrate-protein interactions with heightened accuracy and intricate detail. The deuterated form enhances contrast in NMR or neutron scattering experiments, facilitating the elucidation of complex binding mechanisms and structural configurations of carbohydrate-binding proteins. These profound insights play a pivotal role in designing novel drugs and identifying potential therapeutic targets, driving the field of structural biology forward with groundbreaking discoveries that revolutionize the understanding of biological structures and interactions.

Isotope-Labeled Standards: Serving as a cornerstone in quantitative mass spectrometry analysis, D-arabinose-[2,3,4,5,5'-d5] acts as a reliable internal standard for precise measurement of sugars in complex biological samples. Its stable isotope labeling feature ensures the accurate quantification of D-arabinose, serving as a reference point in clinical diagnostics, pharmacokinetics, and various analytical settings where meticulous measurement of sugars is imperative. This application underpins the accuracy and reliability of analytical processes, highlighting the crucial role of D-arabinose-[2,3,4,5,5'-d5] in high-precision quantitative analyses that drive forward advancements in scientific research and diagnostics.

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