Product Information
- 5-ß-D-Ribofuranosyl-2,4(1H,3H)-Pyrimidinedione
- 5-(ß-D-Ribofuranosyl)uracil
- 5-Ribosyluracil
- NSC 162405
- Pseudouridine C
- ß-D-Pseudouridine
- Pseudouridine
- ?-Uridine
- (1S)-1,4-anhydro-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-D-ribitol
- 1: PN: WO2017201317 SEQID: 1 claimed DNA
- See more synonyms
- 2,4(1H,3H)-Pyrimidinedione, 5-β-<span class="text-smallcaps">D</span>-ribofuranosyl-
- 5-(β-<span class="text-smallcaps">D</span>-Ribofuranosyl)uracil
- 5-b-D-ribofuranosyl-2,4(1H,3H)-Pyrimidinedione
- 5-β-<span class="text-smallcaps">D</span>-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione
- 5-β-D-ribofuranosyluracil
- B-Pseudouridine
- Uracil, 5-β-<span class="text-smallcaps">D</span>-ribofuranosyl-
- β-<span class="text-smallcaps">D</span>-Pseudouridine
- ψ-Uridine
- Uracil, 5-β-D-ribofuranosyl-
- 2,4(1H,3H)-Pyrimidinedione, 5-β-D-ribofuranosyl-
Applications An isomer of the nucleoside uridine found in all species and in many classes of RNA except mRNA. It is formed by enzymes called Ψ synthases, which post-transcriptionally isomerize specific uridine residues in RNA in a process termed pseudouridylation. Studies suggest that β-Pseudouridine reduces radiation-induced chromosome aberrations in human lymphocytes.
References Ferré-D'Amaré A.R. et al.: Curr. Opin. Struct. Biol., 13, 49 (2003); Hamma, T. et al.: Chem. Biol., 13, 1125 (2006); Liang, X.H. et al.: RNA, 8, 237 (2002); Monobe, M. et al.: Mut. Res. Gen. Toxicol. Env. Mutagen., 538, 93 (2003);
Chemical properties
Technical inquiry about: TR-P839605 β-Pseudouridine
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