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D-erythrose-[4,4'-d2]

General Information
Catalog: BLP-007018
Molecular Formula: C42H6D2O4
Molecular Weight: 122.12
Chemical Structure
D-erythrose-[4,4'-d2]
Synonyms D-[4,4'-2H2]erythrose; D-erythrose-4,4-d2; D-[4,4'-D2]erythrose
Related CAS 583-50-6 (unlabelled)
Solubility Soluble in water
Appearance White to Off-white Solid
Storage Store at -20°C

D-erythrose-[4,4'-d2], a deuterium-labeled derivative of D-erythrose, finds extensive applications in diverse biochemical and metabolic investigations. Here are the key applications of D-erythrose-[4,4'-d2]:

Metabolic Pathway Tracing: Delving into the intricate metabolic pathways of carbohydrates within cellular systems, researchers employ D-erythrose-[4,4'-d2] as a valuable tool. By integrating this labeled sugar into metabolic explorations, scientists can meticulously track its conversion processes and pinpoint the specific enzymes and intermediates involved. This application aids in unraveling the dynamic landscape of cellular metabolism, shedding light on metabolic flux and intricate cellular processes.

Stable Isotope Labeling Studies: In the realm of mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy, D-erythrose-[4,4'-d2] plays a pivotal role in conducting stable isotope labeling experiments. This non-radioactive labeling strategy enables researchers to trace and monitor molecules within complex biological systems in real time. Such techniques are instrumental in probing the synthesis and turnover dynamics of biomolecules, providing crucial insights into cellular processes with exceptional detail and precision.

Glycoprotein Research: Within the domain of glycoprotein biosynthesis investigations, D-erythrose-[4,4'-d2] emerges as a cornerstone for labeling the sugar constituents of glycoproteins. Researchers leverage this labeled compound to delve into the intricate formation and modification pathways of glycoproteins, unraveling the roles of these molecules in cellular functionalities. This research is fundamental for understanding cellular mechanisms and holds promise for the development of innovative therapeutic interventions, enhancing our comprehension of cellular processes and disease mechanisms.

Enzyme Mechanism Studies: Employed in studies aiming to elucidate the mechanisms of enzymes acting on erythrose and related sugars, D-erythrose-[4,4'-d2] stands as a potent investigative tool. By scrutinizing the isotopic distribution of products through advanced analytical methodologies, scientists gain valuable insights into enzyme specificity and catalytic mechanisms. This information plays a pivotal role in designing targeted enzyme inhibitors and refining industrial biocatalysis processes, propelling advancements in the field of enzymology and bioprocess engineering.

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