U6375

Uridine 5′-monophosphate disodium salt

≥99%, (chemical), powder

• Synonym(s): 5′-UMP-Na₂, U 5′-P, UMP, Uridylic acid disodium salt
• Empirical Formula (Hill Notation): C₉H₁₁N₂Na₂O₉P
• CAS Number: 3387-36-8
• Molecular Weight: 368.15
• Beilstein/REAXYS Number: 3582885
• EC Number: 222-211-9
• MDL number: MFCD00006525
• UNSPSC Code: 12352204
• PubChem Substance ID: 24900433
• NACRES: NA.26

Properties

• Product Name: Uridine 5′-monophosphate disodium salt, ≥99%
• biological source: (chemical)
• assay: ≥99%
• form: powder
• storage temp.: −20°C
• SMILES string: [Na+].[Na+].O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP([O-])([O-])=O)N2C=CC(=O)NC2=O
• InChI: 1S/C9H13N2O9P.2Na/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);;/q;2*+1/p-2/t4-,6-,7-,8-;;/m1../s1
• InChI key: KURVIXMFFSNONZ-WFIJOQBCSA-L

Description

General description

Uridine 5′-monophosphate is a pyrimidine mononucleotide. It is formed by decarboxylation of orotidine 5′-monophosphate. UMP is further converted to UTP (uridine 5′-triphosphate) using kinases.[1]

Application

Uridine 5′-monophosphate disodium salt has been used to study the effect of pyrimidine synthesis inhibitor, 5-azacytidine, on cholesterol and lipid metabolism.[2] It has been used to study the effect of nucleotides on growth of specific intestinal bacteria.[3]

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)