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Uridine Liquid

Uridine (CAS: 69-75-0) is a pyrimidine nucleoside consisting of uracil bound to a ribose sugar. The compound participates in nucleotide metabolism and serves as a precursor for uridine nucleotides involved in nucleic acid biosynthesis and phospholipid metabolism.

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Uridine Overview

Uridine (CAS: 69-75-0) is a pyrimidine nucleoside consisting of uracil bound to a ribose sugar. The compound participates in nucleotide metabolism and serves as a precursor for uridine nucleotides involved in nucleic acid biosynthesis and phospholipid metabolism.

Molecular and Biochemical Activity

Uridine participates in nucleoside salvage pathways where it undergoes phosphorylation to form uridine monophosphate (UMP), which may subsequently convert to UDP and UTP through enzymatic processes mediated by nucleoside kinases.

UTP functions as a substrate in multiple cellular pathways, including:

  • RNA synthesis through ribonucleotide incorporation
  • Glycosylation reactions mediated by UDP-activated sugar intermediates
  • Phospholipid biosynthesis pathways involving cytidine diphosphate-activated intermediates

Uridine nucleotides also participate in intracellular signaling mechanisms through purinergic receptor families such as P2Y receptors, which recognize extracellular nucleotides including UTP and UDP.

Membrane Phospholipid Pathway Involvement

Uridine-derived nucleotides contribute to phosphatidylcholine biosynthesis through cytidine-dependent phospholipid synthesis pathways. In these pathways, CTP functions as a cofactor in the generation of CDP-activated intermediates that participate in membrane phospholipid assembly.

Nucleic Acid Synthesis

Uridine serves as a fundamental nucleoside component of RNA. During transcriptional processes, uridine triphosphate (UTP) is incorporated into RNA polymers by RNA polymerases as part of ribonucleotide polymerization.

Cellular Transport

Uridine transport across cellular membranes occurs via nucleoside transporter proteins, including equilibrative nucleoside transporters (ENT) and concentrative nucleoside transporters (CNT). These transporter systems regulate intracellular nucleoside availability and nucleotide synthesis.

Reference Links

  • Ding, C., Zuo, R., Liao, Q., Guo, Z., He, J., Ye, Z., & Liu, G. (2025). Uridine alleviates the aging of alveolar epithelial cells in idiopathic pulmonary fibrosis through the Keap1-Nrf2 signaling pathway. Scientific Reports, 15(1), 22952. https://doi.org/10.1038/s41598-025-04053-w
  • Feagin, J. E., & Stuart, K. (1988). Developmental aspects of uridine addition within mitochondrial transcripts of Trypanosoma brucei. Molecular and Cellular Biology, 8(3), 1259-1265. https://doi.org/10.1128/mcb.8.3.1259
  • Lapointe, C. P., & Wickens, M. (2013). The nucleic acid-binding domain and translational repression activity of a xenopus terminal uridylyl transferase. Journal of Biological Chemistry, 288(28), 20723-20733. https://doi.org/10.1074/jbc.m113.455451

Proprietà

CAS Number69-75-0
Molecular FormulaC9H12N2O6
Molar Mass244.20 g/mol
IUPAC NameO3′-methyl-uridine

Uridine is classified as a ribonucleoside that contributes to intracellular pools of uridine triphosphate (UTP) and cytidine triphosphate (CTP) through nucleotide salvage and phosphorylation pathways.

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