Weight | 244.203 g/mol |
---|---|
Formula | C9H12N2O6 |
Hydrogen Acceptors | 7 |
Hydrogen Donors | 4 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
uridine (58-96-8)
Allo Uridine · Allo-Uridine · Allouridine

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Suppliers
- Sigma-Aldrich - uridine43.70 - 382.20 USD
- Fisher Scientific - Search for uridine
- TCI - uridine27.00 - 66.00 USD
Most-cited Publications
- U6 promoter-driven siRNAs with four uridine 3' overhangs efficiently suppress targeted gene expression in mammalian cells. (Nature Biotechnology, 2002)
- Genetic predisposition to the metabolism of irinotecan (CPT-11): Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes (Journal of Clinical Investigation, 1998)
- Studies on uridine-diphosphate-glucose. (Biochemical Journal, 1952)
- Incorporation of 3H-uridine and 3H-uracil into RNA: A simple technique for the detection of mycoplasma contamination of cultured cells (Experimental Cell Research, 1974)
- Uridine nucleotide selectivity of three phospholipase C-activating P2 receptors: identification of a UDP-selective, a UTP-selective, and an ATP- and UTP-specific receptor. (Molecular Pharmacology, 1996)
- Mitogen-Activated Protein Kinase-Activated Protein Kinase 2 Regulates Tumor Necrosis Factor mRNA Stability and Translation Mainly by Altering Tristetraprolin Expression, Stability, and Binding to Adenine/Uridine-Rich Element (Molecular and Cellular Biology, 2006)
Areas of Application
Safety
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more.
Trends
Alternate Names
- Allo Uridine
- Allo-Uridine
- Allouridine
-
SMILESC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O
-
InChIKeyDRTQHJPVMGBUCF-UHFFFAOYSA-N
External Links
- Pubchem - uridine
- Wikipedia - uridine
Uridine is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, a ribofuranose) via a -N1-glycosidic bond. It is one of the five standard nucleosides which make up nucleic acids, the others being adenosine, thymidine, cytidine and guanosine. The five nucleosides are commonly abbreviated to their one-letter codes U, A, T, C and G respectively.
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