5-Methyluridine

One of the five major nucleosides in nucleic acids From Wikipedia, the free encyclopedia

The chemical compound 5-methyluridine (symbol m5U), also called ribothymidine (rT)[footnote 1], 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.[4] It is a white solid.

Quick facts Names, Identifiers ...
5-Methyluridine
Skeletal formula of 5-methyluridine
Space-filling model of the 5-methyluridine molecule
Names
IUPAC name
5-Methyluridine
Systematic 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)
ChemSpider
ECHA InfoCard 100.014.522 Edit this at Wikidata
UNII
  • InChI=1S/C10H14N2O6/c1-4-2-12(10(17)11-8(4)16)9-7(15)6(14)5(3-13)18-9/h2,5-7,9,13-15H,3H2,1H3,(H,11,16,17)/t5-,6-,7-,9-/m1/s1 ☒N
    Key: DWRXFEITVBNRMK-JXOAFFINSA-N ☒N
  • InChI=1/C10H14N2O6/c1-4-2-12(10(17)11-8(4)16)9-7(15)6(14)5(3-13)18-9/h2,5-7,9,13-15H,3H2,1H3,(H,11,16,17)/t5-,6-,7-,9-/m1/s1
    Key: DWRXFEITVBNRMK-JXOAFFINBW
  • CC1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O
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).
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m5U is one of the most common modifications made to cellular RNA. It almost universally occurs in position 54 (part of the T arm) of eukaryotic and bacterial tRNA, serving to stabilize the molecule. The same "T-loop" motif occurs in many other forms of noncoding RNA such as tmRNA and rRNA. Loss of the tRNA modification does not usually produce a different, less fit, phenotype.[5]

See also

Footnotes

  1. The term ribothymidine is especially used to describe its unusual occurrence in RNA.[3]

References

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