CAS 957-77-7
:5-Hydroxyuridine
Description:
5-Hydroxyuridine is a nucleoside analog of uridine, characterized by the presence of a hydroxyl group at the 5-position of the uracil base. Its molecular formula is C₉H₁₁N₂O₅, and it has a molecular weight that reflects its composition of carbon, hydrogen, nitrogen, and oxygen. This compound is soluble in water, which facilitates its use in various biochemical applications. 5-Hydroxyuridine is known for its potential role in cellular processes, particularly in RNA metabolism and as a substrate for RNA polymerases. It may also exhibit biological activities that could be relevant in therapeutic contexts, such as antiviral or anticancer properties. The compound is typically studied in the context of nucleic acid research and may serve as a tool for understanding RNA modifications and their implications in cellular function. As with many nucleoside analogs, its structural modifications can influence its biological activity and interaction with nucleic acids.
Formula:C9H12N2O7
InChI:InChI=1S/C9H12N2O7/c12-2-4-5(14)6(15)8(18-4)11-1-3(13)7(16)10-9(11)17/h1,4-6,8,12-15H,2H2,(H,10,16,17)/t4-,5-,6-,8-/m1/s1
InChI key:InChIKey=QXDXBKZJFLRLCM-UAKXSSHOSA-N
SMILES:O[C@H]1[C@@H](O[C@H](CO)[C@H]1O)N2C(=O)NC(=O)C(O)=C2
Synonyms:- Uridine, 5-hydroxy-
- Isobarbituric acid, 1-β-D-ribofuranosyl-
- 5-Hydroxyuridine
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Found 7 products.
5-Hydroxyuridine
CAS:Formula:C9H12N2O7Purity:>95.0%(HPLC)(qNMR)Color and Shape:White to Light yellow powder to crystalMolecular weight:260.205-Hydroxyuridine
CAS:<p>5-Hydroxyuridine (OHUrd) is a purine nucleoside analogue with potential antitumour activity, showing cytotoxicity against human colon adenocarcinoma cell lines.</p>Formula:C9H12N2O7Purity:98.76%Color and Shape:SolidMolecular weight:260.25-Hydroxyuridine
CAS:<p>5-Hydroxyduridine is a nucleoside that is naturally found in the human body. It can be synthesized from uridine by oxidation of the 5-hydroxyl group to the corresponding aldehyde. It has been shown to have genotoxic effects in vitro and in prostate cancer cells. 5-Hydroxyduridine has also been shown to inhibit sugar transport, which may be due to its ability to form hydrogen bonds with glycosidic bonds. It has been reported that 5-hydroxyduridine causes acid formation and hydroxylation of cardiac lipids.</p>Formula:C9H12N2O7Purity:Min. 96 Area-%Color and Shape:White Off-White PowderMolecular weight:260.2 g/mol
