Uridine 5’-Monophosphate

• CAT Number: R032104
• CAS Number: 58-97-9
• Molecular Formula: C9H13N2O9P
• Molecular Weight: 324.18
• Purity: ≥95%
• Synonyms: 5’-Uridylic Acid; Uridylic Acid; 5’-UMP; UMP; Uridine 5’-(Dihydrogen Phosphate); Uridine 5’-Phosphate; Uridine 5’-Phosphoric Acid; Uridine Monophosphate; Uridine Phosphate
• Target: Endogenous Metabolite
• Storage: Store at -20C
• IUPAC Name: [(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
• InChI: InChI=1S/C9H13N2O9P/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
• InChIKey: DJJCXFVJDGTHFX-XVFCMESISA-N
• SMILES: C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O

Uridine 5’-Monophosphate (Cat No.:R032104), a nucleotide derivative, holds pivotal roles in cellular processes. Functioning as a building block of RNA, it participates in genetic information transfer and protein synthesis. Beyond its structural role, uridine 5’-monophosphate is involved in energy metabolism as a precursor to Coenzyme Q10. Pharmacologically, it engages purinergic receptors, influencing neurotransmission and synaptic plasticity. This compound finds applications in nutritional supplements and pharmaceuticals, potentially supporting cognitive function, mitochondrial health, and neurological modulation.