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N-acetyl-D-mannosamine-[1-13C]

General Information
Catalog: BLP-013392
Molecular Formula: C7[13C]H15NO6
Molecular Weight: 222.20
Chemical Structure
N-acetyl-D-mannosamine-[1-13C]
Description N-acetyl-D-mannosamine-[1-13C] is a labelled compound of N-acetyl-D-mannosamine. N-acetyl-D-mannosamine is a derivative of D-Mannosamine.
Synonyms N-acetyl-D-[1-13C]mannosamine; 2-acetamido-2-deoxy-D-[1-13C]mannose
Related CAS 3615-17-6 (unlabelled)

N-acetyl-D-mannosamine-[1-13C], an isotopically labeled sugar derivative with wide utility in biomedical and biochemical research, offers unique applications:

Metabolic Flux Analysis: Delving into sialic acid biosynthesis pathways, N-acetyl-D-mannosamine-[1-13C] serves as a pivotal tool for tracing and scrutinizing metabolic fluxes. By monitoring the 13C label's integration, researchers gain insights into specific metabolic pathways, aiding in unraveling cellular metabolism intricacies, diagnosing metabolic disorders, and pinpointing potential therapeutic targets.

Glycoprotein and Glycolipid Labeling: Vital for dissecting glycoprotein and glycolipid dynamics, this labeled sugar derivative plays a critical role in studying glycan structures with precision. The incorporation of the 13C label enables exact identification and quantification of glycan structures using advanced techniques like NMR or mass spectrometry. This knowledge is fundamental for unraveling protein functions, cell-cell interactions, and disease mechanisms tied to glycosylation processes.

Imaging Studies: In the realm of imaging studies, N-acetyl-D-mannosamine-[1-13C] stands out as a valuable asset for visualizing in vivo metabolic activities through techniques like MRI or PET scanning. The stable isotope label provides a safe and non-radioactive approach to metabolic imaging, particularly crucial in cancer research. This application allows for real-time tracking of tumor metabolism and assessment of therapy responses, shedding light on intricate metabolic processes associated with tumorigenesis.

Enzyme Mechanism Investigation: Researchers leverage N-acetyl-D-mannosamine-[1-13C] to unravel the enzymatic intricacies within sialic acid metabolism. Through analysis of isotope effects and the fate of the labeled substrate, scientists gain profound insights into enzyme mechanisms and substrate specificities. This knowledge serves as a foundation for developing enzyme inhibitors as potential therapeutic agents, offering new avenues for combating enzyme-related disorders.

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