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1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[5-13C]

General Information
Catalog: BLP-013249
Molecular Formula: C27[13C]H24O9
Molecular Weight: 505.49
Chemical Structure
1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[5-13C]
Description 1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[5-13C] 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-[5-13C]ribofuranoside; 1-O-acetyl 2,3,5-tribenzoylribose (5-13C)
Related CAS 6974-32-9 (unlabelled)

1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[5-13C] is a chemically labeled nucleoside derivative with diverse research applications. Here are the key applications of 1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[5-13C]:

NMR Spectroscopy: This compound serves as a labeled standard in nuclear magnetic resonance (NMR) spectroscopy enabling in-depth analysis of molecular structures and dynamics. The incorporation of 13C provides a window into the carbon atoms within the molecule, offering profound insights into conformational changes and molecular interactions. This methodology is particularly valuable for unraveling the complexities of nucleosides and nucleotides, shedding light on their intricate structure-function relationships.

Biochemical Pathway Analysis: Scientists harness this labeled derivative to explore and dissect the metabolic pathways associated with ribonucleosides. By introducing the labeled sugar into cellular systems, researchers can track its journey through metabolic networks, gaining a holistic view of nucleotide metabolism. This approach aids in unraveling the intricacies of cellular processes and identifying potential targets for therapeutic modulation, contributing to advancements in precision medicine.

Synthetic Chemistry: Within the realm of synthetic chemistry, 1-O-acetyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside-[5-13C] acts as a pivotal building block for the synthesis of 13C-labeled nucleotides and nucleic acids. The presence of the 13C isotope enables precise tracking and characterization of synthetic products, facilitating the development of labeled biomolecules for diverse research and diagnostic applications. This synthetic strategy plays a critical role in advancing the field of chemical biology and molecular diagnostics.

Drug Metabolism Studies: This labeled nucleoside derivative plays a crucial role in pharmacokinetic investigations focused on understanding the metabolism and distribution of ribonucleoside-based drugs. By incorporating the 13C label, researchers can monitor the fate of the drug within biological systems using sophisticated techniques like mass spectrometry and NMR spectroscopy. This detailed insight into drug metabolism is indispensable for refining drug design, optimizing therapeutic efficacy, and advancing personalized medicine approaches.

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