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D-talose-[1-13C,1-d]

General Information
Catalog: BLP-006995
Molecular Formula: C5[13C]H11DO6
Molecular Weight: 182.16
Chemical Structure
D-talose-[1-13C,1-d]
Synonyms D-[1-13C,1-2H]talose; D-talose-1-13C,1-d; D-[1-13C,1-D]talose
IUPAC Name (3S,4S,5R,6R)-6-(hydroxymethyl)tetrahydro-2H-pyran-2-13C-2-d-2,3,4,5-tetraol
Related CAS 2595-98-4 (unlabelled)
Solubility Soluble in DMSO, Water
Appearance White to Off-white Solid
Storage Store at -20°C

D-talose-[1-13C,1-d], a specially labeled sugar molecule, finds application in diverse scientific inquiries. Here are the key uses of D-talose-[1-13C,1-d]:

Metabolic Flux Analysis: In the realm of metabolic flux analysis, D-talose-[1-13C,1-d] is a pivotal tool for mapping the intricate pathways of carbohydrate metabolism. By integrating this labeled sugar into metabolic experiments, researchers illuminate the cellular processing dynamics, offering deep insights into the fluidity of metabolic pathways. This technique is instrumental in unraveling the complexities of cellular metabolism and pinpointing crucial junctures for metabolic engineering endeavors.

NMR Spectroscopy Studies: Within the domain of nuclear magnetic resonance (NMR) spectroscopy, D-talose-[1-13C,1-d] takes center stage as a probing agent for delving into sugar dynamics and conformations. The incorporation of carbon-13 isotopes elevates the precision and sensitivity of NMR analyses, empowering researchers to glean intricate details regarding carbohydrate structures, interactions, and behaviors across diverse settings. This application opens a window into the nuanced world of sugar dynamics.

Glycosylation Pathway Research: For those delving into glycosylation pathways, D-talose-[1-13C,1-d] emerges as a key player in unraveling the intricate mechanisms within cells. By tracing the journey of the labeled sugar as it integrates into glycoproteins and glycolipids, scientists shed light on the inner workings and regulatory mechanisms governing glycosylation processes. This knowledge forms the bedrock for understanding the profound impact of glycosylation on health, disease, and the formulation of cutting-edge glycoengineering strategies.

Isotope-Labeled Compound Synthesis: Serving as a cornerstone for the synthesis of isotope-labeled compounds, D-talose-[1-13C,1-d] stands as a precursor with immense utility. Through chemical modifications of this labeled sugar, researchers can introduce isotopic labels into complex molecules, facilitating the production of labeled standards vital for analytical chemistry and mass spectrometry applications. This capability transforms the landscape of isotope-labeled compound synthesis, underpinning advancements in analytical methodologies and scientific exploration.

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