U6375
Uridine 5′-monophosphate disodium salt
≥99%, (chemical), powder
Synonym(s):
5′-UMP-Na2, U 5′-P, UMP, Uridylic acid disodium salt
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About This Item
Empirical Formula (Hill Notation):
C9H11N2Na2O9P
CAS Number:
Molecular Weight:
368.15
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
222-211-9
MDL number:
Beilstein/REAXYS Number:
3582885
Assay:
≥99%
Biological source:
(chemical)
Form:
powder
Solubility:
water: 50 mg/mL, clear, colorless
Storage temp.:
−20°C
Product Name
Uridine 5′-monophosphate disodium salt, ≥99%
biological source
(chemical)
Quality Segment
assay
≥99%
form
powder
solubility
water: 50 mg/mL, clear, colorless
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
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.
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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