Pseudouridine
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Pseudouridine
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CAS No:
1445-07-4
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Formula:
C9H12N2O6
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Chemical Name:
Pseudouridine
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Synonyms:
2,4(1H,3H)-Pyrimidinedione,5-β-D-ribofuranosyl-;Uracil,5-β-D-ribofuranosyl-;5-β-D-Ribofuranosyl-2,4(1H,3H)-pyrimidinedione;Pseudouridine C;5-Ribosyluracil;β-Pseudouridine;Pseudouridine;β-D-Pseudouridine;ψ-Uridine;5-(β-D-Ribofuranosyl)uracil;NSC 162405;1: PN: WO2017201317 SEQID: 1 claimed DNA
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CAS No:
Description
ChEBI: A C-glycosyl pyrimidine that consists of uracil having a beta-D-ribofuranosyl residue attached at position 5. The C-glycosyl isomer of the nucleoside uridine.
Solid
Pseudouridine is a C-glycosyl pyrimidine that consists of uracil having a beta-D-ribofuranosyl residue attached at position 5. The C-glycosyl isomer of the nucleoside uridine. It has a role as a fundamental metabolite.|A naturally-occurring isomer of URIDINE found in RNA, in which ribosyl is attached to a carbon instead of a nitrogen atom.
Characteristics
135.64000
-3.77
Solid
1.641±0.06 g/cm3(Predicted)
222 °C
598.4±60.0 °C at 760 mmHg
315.7±32.9 °C
1.697
159 Ų [M+Na]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|145.23 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|150.3 Ų [M-H]-
Pseudouridine Use and Manufacturing
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.
Computed Properties
Molecular Weight:244.20
XLogP3:-2.8
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:244.06953611
Monoisotopic Mass:244.06953611
Topological Polar Surface Area:128
Heavy Atom Count:17
Complexity:382
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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