5-Methyluridine
The chemical compound 5-methyluridine (symbol m⁵U or m5U), also called ribothymidine, is a pyrimidine nucleoside. 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.[3] It is a white solid.
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| Names | |
|---|---|
| IUPAC name
 5-Methyluridine  | |
| Preferred IUPAC name
 1-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4(1H,3H)-dione  | |
| Other names
 Ribothymidine, Ribosylthymine; Thymine riboside, m5U  | |
| Identifiers | |
3D model (JSmol)  | 
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| ChemSpider | |
| ECHA InfoCard | 100.014.522 | 
PubChem CID  | 
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| UNII | |
CompTox Dashboard (EPA)  | 
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| Properties | |
| C10H14N2O6 | |
| Molar mass | 258.23 g/mol | 
| Density | 1,6 g/cm3[1] | 
| Melting point | 184[2] °C (363 °F; 457 K) | 
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |
See also
    
    
References
    
- "5-Methyluridine". ChemSpider. Retrieved December 6, 2018.
 - William M. Haynes (2016). CRC Handbook of Chemistry and Physics (97th ed.). Boca Raton: CRC Press. p. 3-400. ISBN 978-1-4987-5429-3.
 - Shobbir Hussain (2019). "Catalytic crosslinking-based methods for enzyme-specified profiling of RNAribonucleotide modifications". Methods. 156: 60-65. doi:10.1016/j.ymeth.2018.10.003.
 
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