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Uridine 5′-monophosphate disodium salt (CAS 3387-36-8)

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Alternate Names:
5′-UMP-Na2
Application:
Uridine 5′-monophosphate disodium salt is a nucleotide that is a major component of ribonucleic acid
CAS Number:
3387-36-8
Purity:
≥99%
Molecular Weight:
368.15
Molecular Formula:
C9H11N2Na2O9P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Uridine 5′-monophosphate disodium salt functions as a precursor in the biosynthesis of RNA. It plays a role in the synthesis of cellular RNA and is involved in the regulation of gene expression. At the molecular level, Uridine 5′-monophosphate disodium salt is incorporated into RNA molecules during transcription, contributing to the formation of the RNA strand. Its mechanism of action involves participating in the formation of phosphodiester linkages between nucleotides, thereby contributing to the structure and function of RNA. It is involved in the maintenance of cellular energy levels and the regulation of metabolic processes. Uridine 5′-monophosphate disodium salt also plays a role in the modulation of neurotransmitter receptors and synaptic plasticity in the central nervous system.


Uridine 5′-monophosphate disodium salt (CAS 3387-36-8) References

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  2. Dietary uridine-5'-monophosphate supplementation increases potassium-evoked dopamine release and promotes neurite outgrowth in aged rats.  |  Wang, L., et al. 2005. J Mol Neurosci. 27: 137-45. PMID: 16055952
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  6. Counter-current chromatographic separation of nucleic acid constituents with a hydrophilic solvent system.  |  Shibusawa, Y., et al. 2010. J Chromatogr A. 1217: 3457-60. PMID: 20362294
  7. A novel procedure for purification of uridine 5'-monophosphate based on adsorption methodology using a hyper-cross-linked resin.  |  Wu, J., et al. 2015. Bioprocess Biosyst Eng. 38: 967-79. PMID: 25575762
  8. Simple determination of erythrocyte pyrimidine 5'-nucleotidase activity in human blood by high-performance liquid chromatography.  |  Tomokuni, K. and Ichiba, M. 1986. Ind Health. 24: 227-33. PMID: 3028992
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  11. Physico-Chemical Properties and Biocompatibility of Thermosensitive Chitosan Lactate and Chitosan Chloride Hydrogels Developed for Tissue Engineering Application.  |  Pieklarz, K., et al. 2021. J Funct Biomater. 12: PMID: 34065271
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Uridine 5′-monophosphate disodium salt, 1 g

sc-222403
1 g
$52.00

Uridine 5′-monophosphate disodium salt, 5 g

sc-222403A
5 g
$124.00