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About This Item
Empirical Formula (Hill Notation):
C9H13N2O9P
CAS Number:
Molecular Weight:
324.18
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
200-408-0
MDL number:
Assay:
≥98%
Biological source:
natural (organic)
Form:
powder
Solubility:
H2O: soluble 50 mg/mL, clear, colorless
Storage temp.:
−20°C
Product Name
Uridine 5′-monophosphate, ≥98%
biological source
natural (organic)
Quality Level
assay
≥98%
form
powder
solubility
H2O: soluble 50 mg/mL, clear, colorless
storage temp.
−20°C
SMILES string
OC1C(O)C(OC1COP(O)(O)=O)N2C=CC(=O)NC2=O
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)
InChI key
DJJCXFVJDGTHFX-UHFFFAOYSA-N
General description
Uridine 5′-monophosphate acts as a precursor for all pyrimidine nucleotides.
Application
Uridine 5′-monophosphate has been used as a component in isotonic E3 medium for isotonic reconstitution experiments to study its effects on the basal cell response or epithelial cell migration to the wound in the isotonic medium.
Biochem/physiol Actions
Uridine 5′-monophosphate (UMP) is a nucleotide monomer in RNA. It contains the nucleobase uracil along with the ribose sugar and a phosphate group. UMP dietary supplementation enhances neurotransmitter release and neurite outgrowth and also promotes membrane phosphatide production in adult rats. Oral supplementation of DHA, co-administered with UMP, in adult gerbils shows an increase in dendritic spines and neuronal membrane synthesis. It suggests a strategy for the treatment of cognitive disorders resulting from synapse loss.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Masahiro Fujihashi et al.
The Journal of biological chemistry, 288(13), 9011-9016 (2013-02-12)
Orotidine 5'-monophosphate decarboxylase (ODCase) accelerates the decarboxylation of its substrate by 17 orders of magnitude. One argument brought forward against steric/electrostatic repulsion causing substrate distortion at the carboxylate substituent as part of the catalysis has been the weak binding affinity
Edward J Gane et al.
The New England journal of medicine, 368(1), 34-44 (2013-01-04)
The standard treatment for hepatitis C virus (HCV) infection is interferon, which is administered subcutaneously and can have troublesome side effects. We evaluated sofosbuvir, an oral nucleotide inhibitor of HCV polymerase, in interferon-sparing and interferon-free regimens for the treatment of
Regulation of uridylic acid biosynthesis in the cyanobacterium Anabaena variabilis.
Currier TC and Wolk CP
Journal of Bacteriology, 136(2), 682-687 (1978)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| U1752-1G | 04061837409363 |