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U6375 Sigma-Aldrich

Uridine 5′-monophosphate disodium salt

≥99%

Synonym: 5′-UMP-Na2, U 5′-P, UMP, Uridylic acid disodium salt

  • CAS Number 3387-36-8

  • Empirical Formula (Hill Notation) C9H11N2Na2O9P

  • Molecular Weight 368.15

  •  Beilstein/REAXYS Number 3582885

  •  EC Number 222-211-9

  •  MDL number MFCD00006525

  •  PubChem Substance ID 24900433

  •  NACRES NA.26

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Properties

Related Categories Cell Biology, Metabolic Pathways, Metabolites and Cofactors on the Metabolic Pathways Chart, Metabolomics, Nucleotide More...
Quality Level   100
assay   ≥99%
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.

Application

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

Packaging

1 g in poly tube

5, 10 g in poly bottle

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 2
RTECS 
YU7975000
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Protocols & Articles
Peer-Reviewed Papers
15

References

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