478506-63-7 Usage
Uses
Used in Pharmaceutical Research:
L-[2-13C]XYLOSE is used as a research compound for studying the metabolic pathways and interactions of L-Xylose in biological systems. The stable isotope labeling allows for the tracking and analysis of L-Xylose and its derivatives in complex biological matrices.
Used in Virology:
L-[2-13C]XYLOSE is used as an antiviral agent for studying the effects of L-Xylose on viruses such as herpes simplex virus 1 & 2 and influenza A virus. The stable isotope labeling enables researchers to differentiate between the labeled compound and endogenous L-Xylose, providing insights into the antiviral mechanisms and potential therapeutic applications.
Used in Analytical Chemistry:
L-[2-13C]XYLOSE is used as a labeled internal standard or reference compound in mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The stable isotope labeling provides a distinct mass or NMR signal, allowing for accurate quantification and identification of L-Xylose in complex samples.
Used in Metabolic Studies:
L-[2-13C]XYLOSE is used as a tracer compound in metabolic studies to investigate the metabolism of L-Xylose and its role in various biological processes. The stable isotope labeling allows for the tracking of L-Xylose metabolism in living organisms, providing valuable information on metabolic pathways and potential therapeutic targets.
Used in Drug Development:
L-[2-13C]XYLOSE is used as a starting material or intermediate in the synthesis of novel pharmaceutical compounds. The stable isotope labeling can be used to study the pharmacokinetics, pharmacodynamics, and metabolic fate of these compounds, aiding in the development of more effective and safer drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 478506-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,5,0 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 478506-63:
(8*4)+(7*7)+(6*8)+(5*5)+(4*0)+(3*6)+(2*6)+(1*3)=187
187 % 10 = 7
So 478506-63-7 is a valid CAS Registry Number.
478506-63-7Relevant academic research and scientific papers
SYNTHESIS OF L-(4-2H)ERYTHROSE, L-(1-13C, 5-2H)ARABINOSE AND L-(2-13C, 5-2H)ARABINOSE AND IDENTIFICATION OF THE INTERMEDIATES BY 2H AND 13C-N.M.R. SPECTROSCOPY
Han, Chung H.,Sillerud, Laurel O.
, p. 247 - 264 (2007/10/02)
L-(1-13C, 5-2H)Arabinose (6D) and L-(2-13C, 5-2H)arabinose (8D) have been synthesized by degradation of 2,3-O-isopropylidene-β-L-rhamnofuranose (2) to L-(4-2H)erythrose (5β, 5αD), with subsequent chain elongation to 6D plus L-(1-13C, 5-2H)ribose (7D), the latter being converted into 8D.Intermediates were identified by complete assignment of the 13C chemical shifts employing carbon-carbon and carbon-deuterium coupling constants, deuteration shifts, differential isotope-shifts, and deuterium spectra.The anomeric carbon atoms of 2 and 2,3-O-isopropylidene-L-(1-2H)erythrose (4D) gave only single 13C resonances, suggesting that these two compounds exists in only one major anomeric configuration, clarifying previously reported work.The synthesis of 2,3-O-isopropylidene-L-(1-2H)rhamnitol (3D) facilitated the assignment of the signals in the 13C spectra of the nondeuterated analog.Specific deuterium-enrichment and the observed carbon-deuterium coupling (1JC,D ca. 22 Hz) not only served to identify the deuterated carbon atom unambiguously in 3 but also permitted assignment of closely spaced resonances.The deuterium spectrum of 2,3-O-isopropylidene-L-(4-2H)erythrofuranose (4D) showed only a single resonance, indicating preponderance of one anomer, in accord with the observation of a single C-1 resonance in the 13C spectrum.
