5-Methyluridine

5-Methyluridine
  • CAS No.:1463-10-1
Other grades of this product :
5-Methyluridine Basic information
Product Name:5-Methyluridine
Synonyms:5-methyl-uridin;5-methyuridine;5-Methyluridine (Patent );THYMINERIBOSIDE;URIDINE, 5-METHYL-;5-METHYLURIDINE(5-Methyl-1-ˉ-ribofuranosyl uracil;1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione;5-methyluridine/ribothymidine
CAS:1463-10-1
MF:C10H14N2O6
MW:258.23
EINECS:215-973-9
Product Categories:Carbohydrates & Derivatives;Heterocycles;Biochemistry;Nucleosides and their analogs;Nucleosides, Nucleotides & Related Reagents;Bases & Related Reagents;Pyridines, Pyrimidines, Purines and Pteredines;Miscellaneous Biochemicals;Nucleotides and Nucleosides;Nucleotides;bc0001
Mol File:1463-10-1.mol
5-Methyluridine Chemical Properties
Melting point 183-184 °C(lit.)
density 1.576±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Methanol (Slightly, Heated, Sonicated), Water (Sparingly, Sonicated)
pka9.55±0.10(Predicted)
form powder
color white
InChIKeyDWRXFEITVBNRMK-JXOAFFINSA-N
CAS DataBase Reference1463-10-1(CAS DataBase Reference)
Safety Information
Hazard Codes T+
Risk Statements 26/27/28
Safety Statements 24/25
WGK Germany 3
HS Code 29349990
MSDS Information
ProviderLanguage
SigmaAldrich English
5-Methyluridine Usage And Synthesis
Description5-Methyluridine is a pyrimidine nucleoside and methylated form of uridine. It is the ribonucleoside counterpart to the deoxyribonucleoside thymidine, which lacks a hydroxyl group at the 2' position. 5-Methyluridine contains a thymine base joined to a ribose pentose sugar. It is an endogenous methylated nucleoside found in human fluids. In cells, 5-methyluridine is present in tRNA, formed during its post-transcriptional modification by the methylation of uridine.
Chemical PropertiesWhite Powder
UsesA primary degradation product of tRNA, an urinary nucleoside as biological marker for patients with colorectal cancer.It enhances the antitumor activity of 5-fluorouracil in a mouse Erlich solid carcinoma model and a P388 murine leukemia model. It has been used to characterize the activity of a variety of enzymes, including uridine nucleosidase.

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