4-Thiouridine

Chemical compound From Wikipedia, the free encyclopedia

4-Thiouridine is an atypical nucleoside formed with the 4-thiouracil base found in transfer RNA (tRNA).[1] Its biosynthesis has been determined.[2]

Quick facts Names, Identifiers ...
4-Thiouridine
Names
IUPAC name
4-Thiouridine
Systematic IUPAC name
1-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidene-3,4-dihydropyrimidin-2(1H)-one
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.034.291 Edit this at Wikidata
EC Number
  • 237-735-3
MeSH Thiouridine
UNII
  • InChI=1S/C9H12N2O5S/c12-3-4-6(13)7(14)8(16-4)11-2-1-5(17)10-9(11)15/h1-2,4,6-8,12-14H,3H2,(H,10,15,17)/t4-,6-,7-,8-/m1/s1
    Key: ZLOIGESWDJYCTF-XVFCMESISA-N
  • C1=CN(C(=O)NC1=S)C2C(C(C(O2)CO)O)O
Properties
C9H12N2O5S
Molar mass 260.26 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The IUPAC reserved the single-letter nucleobase code "S" for thiouridine in 1970, but the convention does not appear very common.[3] "S" was repurposed to mean "C or G" in 1984.[4]

References

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