Pseudouridine 5'-triphosphate

Modify Date: 2024-01-09 19:32:47

Pseudouridine 5'-triphosphate Structure
Pseudouridine 5'-triphosphate structure
Common Name Pseudouridine 5'-triphosphate
CAS Number 1175-34-4 Molecular Weight 484.14100
Density N/A Boiling Point N/A
Molecular Formula C9H15N2O15P3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Pseudouridine 5'-triphosphate


pseudouridine-5’-triphosphate (Pseudo-UTP) is one of the most commonly used modified nucleoside for the polymerase-mediated synthesis of RNA molecules. Compared with uridine-containing unmodified mRNAs, the application of pseudouridine-containing modified mRNAs exhibits better nuclease stability, immunogenicity, and translational properties.

 Names

Name (1S)-1,4-Anhydro-1-(2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)-5 -O-(hydroxy{[hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl)-D-ri bitol
Synonym More Synonyms

 Pseudouridine 5'-triphosphate Biological Activity

Description pseudouridine-5’-triphosphate (Pseudo-UTP) is one of the most commonly used modified nucleoside for the polymerase-mediated synthesis of RNA molecules. Compared with uridine-containing unmodified mRNAs, the application of pseudouridine-containing modified mRNAs exhibits better nuclease stability, immunogenicity, and translational properties.
Related Catalog
References

[1]. Shanmugasundaram M, Senthilvelan A, Kore AR. Gram-Scale Chemical Synthesis of Base-Modified Ribonucleoside-5'-O-Triphosphates. Curr Protoc Nucleic Acid Chem. 2016;67:13.15.1-13.15.10.

[2]. Borchardt EK, Martinez NM, Gilbert WV. Regulation and Function of RNA Pseudouridylation in Human Cells. Annu Rev Genet. 2020;54:309-336.

[3]. Anderson BR, Muramatsu H, Nallagatla SR, et al. Incorporation of pseudouridine into mRNA enhances translation by diminishing PKR activation. Nucleic Acids Res. 2010;38(17):5884-5892.

 Chemical & Physical Properties

Molecular Formula C9H15N2O15P3
Molecular Weight 484.14100
Exact Mass 483.96900
PSA 305.18000
Storage condition -20°C

 Synonyms

Pseudouridine 5`-Triphosphate