5-Methyluridine triphosphate
Skeletal formula of 5-methyluridine triphosphate
Space-filling model of the 5-methyluridine triphosphate molecule as an anion
Identifiers
  • [(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl (hydroxy-phosphonooxyphosphoryl) hydrogen phosphate
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC10H17N2O15P3
Molar mass498.166 g·mol−1
3D model (JSmol)
  • CC1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O
  • InChI=1S/C10H17N2O15P3/c1-4-2-12(10(16)11-8(4)15)9-7(14)6(13)5(25-9)3-24-29(20,21)27-30(22,23)26-28(17,18)19/h2,5-7,9,13-14H,3H2,1H3,(H,20,21)(H,22,23)(H,11,15,16)(H2,17,18,19)/t5-,6-,7-,9-/m1/s1 ☒N
  • Key:RZCIEJXAILMSQK-JXOAFFINSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

5-Methyluridine triphosphate or m5UTP is one of five nucleoside triphosphates.[1] It is the ribonucleoside triphosphate of thymidine, but the nomenclature with "5-methyluridine" is used because the term thymidine triphosphate is used for the deoxyribonucleoside by convention.[2]

References

  1. ^ Kaneko K (2016). "5.24: Nucleosides". Molecular mechanisms in the pathogenesis of idiopathic nephrotic syndrome. Tokyo: Springer. ISBN 978-4-431-55270-3.
  2. ^ Coghill AM, Garson LR, eds. (2006). The ACS style guide: effective communication of scientific information (3rd ed.). Washington, D.C.: American Chemical Society. p. 244. ISBN 978-0-8412-3999-9.


Categories