Uridine 5′-monophosphate
SIGMA/U1752 - ≥98%
Synonym: U 5′-P; UMP; Uridylic acid
CAS Number: 58-97-9
Empirical Formula (Hill Notation): C9H13N2O9P
Molecular Weight: 324.18
EC Number: 200-408-0
MDL Number: MFCD00067346
Linear Formula: C9H13N2O9P
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: U1752-1G
| assay | ≥98% |
| biological source | natural (organic) |
| form | powder |
| InChI | 1S/C9H13N2O9P/c12-5-1-2-1 |
| InChI key | DJJCXFVJDGTHFX-UHFFFAOYSA |
| Quality Level | 200  |
| SMILES string | OC1C(O)C(OC1COP(O)(O)=O)N |
| solubility | H2O: soluble 50 mg/mL, clear, colorless |
| storage temp. | −20°C |
| 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. |
| General description: | Uridine 5′-monophosphate acts as a precursor for all pyrimidine nucleotides. |
| Packaging: | 1 g in poly bottle |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | ≥98% |
| Storage Temp. | −20°C |
| UNSPSC | 41106305 |