5-Methyluridine triphosphate

5-Methyluridine triphosphate
Identifiers
	IUPAC name [(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl (hydroxy-phosphonooxyphosphoryl) hydrogen phosphate;
CAS Number	23198-01-8 ;
PubChem CID	451388;
ChemSpider	397621 ;
UNII	26L4U23SYM;
ChEMBL	ChEMBL607677 ;
CompTox Dashboard (EPA)	DTXSID001303289 ;
Chemical and physical data
Formula	C10H17N2O15P3
Molar mass	498.166 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES 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 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 ; Key:RZCIEJXAILMSQK-JXOAFFINSA-N ;
	(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

^ Kaneko K (2016). "5.24: Nucleosides". Molecular mechanisms in the pathogenesis of idiopathic nephrotic syndrome. Tokyo: Springer. ISBN 978-4-431-55270-3.
^ 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.

This biochemistry article is a stub. You can help Wikipedia by expanding it.