| Weight | 244.203 g/mol |
|---|---|
| Formula | C9H12N2O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
PSEUDOURIDINE (1445-07-4)
Score:
#1885 in Biochemistry
,
#4043 in Biology
,
#5094 in Chemistry
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- Site-Specific Pseudouridine Formation in Preribosomal RNA Is Guided by Small Nucleolar RNAs (Cell, 1997)
- Small nucleolar RNAs direct site-specific synthesis of pseudouridine in ribosomal RNA. (Cell, 1997)
- The box H+ACA snoRNAs carry Cbf5p, the putative rRNA pseudouridine synthase (Genes & Development, 1998)
- Pseudouridine in RNA: what, where, how, and why. (Iubmb Life, 2000)
- Incorporation of Pseudouridine Into mRNA Yields Superior Nonimmunogenic Vector With Increased Translational Capacity and Biological Stability (Molecular Therapy, 2008)
- Pseudouridine profiling reveals regulated mRNA pseudouridylation in yeast and human cells (Nature, 2014)
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SMILESC1=C(C(=O)NC(=O)N1)C2C(C(C(O2)CO)O)O
-
InChIKeyPTJWIQPHWPFNBW-UHFFFAOYSA-N
- Pubchem - PSEUDOURIDINE
- Wikipedia - pseudouridine
Pseudouridine (abbreviated by the Greek letter psi- or the letter Q) is an isomer of the nucleoside uridine in which the uracil is attached via a carbon-carbon instead of a nitrogen-carbon glycosidic bond. (In this configuration uracil is sometimes referred to as 'pseudouracil'.) It is the most prevalent of the over one hundred different modified nucleosides found in RNA. is found in all species and in many classes of RNA.
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