159496-17-0

Basic information

• Product Name: 5-METHYL-[1',2',3',4',5'-13C5]URIDINE
• Synonyms: 5-METHYL-[1',2',3',4',5'-13C5]URIDINE;[1',2',3',4',5'-13C5]RIBOTHYMIDINE;5-Methyluridine-1',2',3',4',5'-13C5;DWRXFEITVBNRMK-SJXXUHQYSA-N
• CAS NO: 159496-17-0
• Molecular Formula: C₁₀H₁₄N₂O₆
• Molecular Weight: 263.27
• Product Categories: Carbohydrates & Derivatives, Heterocycles, Isotope Labeled Compounds, Nucleotides, Bases & Related Reagents
• Mol File: 159496-17-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 5-METHYL-[1',2',3',4',5'-13C5]URIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHYL-[1',2',3',4',5'-13C5]URIDINE(159496-17-0)
• EPA Substance Registry System: 5-METHYL-[1',2',3',4',5'-13C5]URIDINE(159496-17-0)

Safety Data

• Hazardous Substances Data: 159496-17-0(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 159496-17-0 differently. You can refer to the following data:
1. Labeled 5-Methyluridine, a primary degradation product of tRNA,
2. Labeled 5-Methyluridine, a primary degradation product of tRNA, an urinary nucleoside as biological marker for patients with colorectal cancer.

Upstream product

• 159496-08-9 C₄⁽¹³⁾C₅H₁₆O₇S 
• 7288-28-0 2,4-bis(trimethylsiloxy)-5-methylpyrimidine 
• 503173-73-7 [glu-13C6]-1,2:5,6-di-O-isopropylidene-3-oxo-α-D-glucofuranose 
• 159496-09-0 [13C5]-1,2-di-O-acetyl-3,5-di-O-benzoyl-α,β-D-ribofuranose 
• 65-71-4 thymin 
• 126590-65-6 <1,2,3,4,5,6-13C6>-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 503173-75-9 ¹³C₅-1′, 2 ′-di-O-acetyl-3 ′ ,5 ′-di-O-benzoyl-β-D-ribofuranose 
• 503173-74-8 [ribose-13C5]-3,5-di-O-benzoyl-1,2-O-isopropylidene-α-D-ribofuranose 
• 238096-51-0 <1,2,3,4,5-13C5>-1,2-O-isopropylidene-α-D-ribofuranose 
• 503173-76-0 [ribose-13C5]-1-(2-O-acetyl-3,5-di-O-benzoyl-β-D-ribofuranosyl)-5-methyluracil 

Downstream Products

• 666824-09-5 C₂₆⁽¹³⁾C₅H₃₂N₂O₇ 
• 156968-81-9 D-thymidine-1'2'3'4'5'-13C₅ 

Relevant articles and documents

NMR Spectroscopic Determination of the Solution Structure of a Branched Nucleic Acid from Residual Dipolar Couplings by Using Isotopically Labeled Nucleotides

Only a small set of magnetic-field-induced residual dipolar couplings is required to determine the global structure of branched nucleic acids. This is demonstrated for the example of the Holliday junction (shown schematically) after 13C labelin

A multigram, stereoselective synthesis of D-[13C5]ribose from D-[13C6]glucose and its conversion into [13C5]nucleosides

The preparation of 13C-labeled ribonucleosides starting from D-[13D6]glucose in 45% overall yield is described. The key of this short synthetic way is the dehomologation of di-O-isopropylidene hexofuranose 2 with periodic acid and NaBH4 that afforded stereoselectively the labeled ribofuranose derivative 3 in high yield.