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-013248 |
Molecular Formula: C27[13C]H24O9 |
Molecular Weight: 505.49 |
Chemical Structure |
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Description | 1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[1-13C] is the labelled analogue of 1-O-Acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose, which is an inhibitor of neutrophil-keyhole limpet hemocyanin adhesion. It is an anti-inflammatory agent. |
Synonyms | 1-O-acetyl 2,3,5-tri-O-benzoyl-beta-D-[1-13C]ribofuranoside; 1-O-acetyl 2,3,5-tribenzoylribose (1-13C) |
Related CAS | 6974-32-9 (unlabelled) |
1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[1-13C] plays a pivotal role in bioscience research, particularly in metabolomic studies and drug metabolism. Here are the key applications of this labeled carbohydrate derivative:
Metabolomic Studies: Delving into metabolic pathways, researchers employ this labeled sugar derivative to trace and dissect biochemical processes within cells and organisms. By introducing the [1-13C] label, scientists can meticulously monitor the molecule's journey through various metabolic routes, unraveling intricate networks and shedding light on metabolic-related disease mechanisms.
NMR Spectroscopy: In the realm of nuclear magnetic resonance (NMR) spectroscopy, the [1-13C] label of this compound serves as a valuable tool, delivering a distinctive signal that simplifies the analysis of carbohydrate structures. Utilizing this compound, researchers explore conformational dynamics, carbohydrate-protein interactions, and other structural nuances, contributing to the advancement of carbohydrate-based pharmaceuticals and deepening our understanding of fundamental carbohydrate chemistry.
Synthetic Organic Chemistry: Serving as a crucial intermediate in the synthesis of complex labeled compounds, this compound empowers chemists to manipulate the benzoyl and acetyl groups, generating a diverse array of derivatives tailored for specific applications. This versatility proves invaluable in crafting isotopically labeled molecules for biochemical and pharmacological investigations, showcasing the intricate interplay between synthetic chemistry and cutting-edge research methodologies.
Drug Metabolism Studies: Leveraging 1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[1-13C], researchers delve into the realm of drug metabolism and pharmacokinetics, precisely tracking the metabolite within biological systems. The [1-13C] label offers a meticulous view of metabolic pathways and potential drug interactions, providing vital insights essential for optimizing and developing novel therapeutics, shaping the landscape of pharmacological research and innovation.
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