Uridine Monophosphate Disodium

Description

Overview of Uridine Monophosphate Disodium

Uridine Monophosphate Disodium is also called UMP Disodium. It is the disodium salt of uridine 5'-monophosphate. This is a ribonucleotide composed of the nucleobase uracil. This means that it is a ribose sugar and a phosphate group. Being a nucleotide component, UMP Disodium is used in laboratory settings to investigate:

• nucleotide metabolism
• phosphorylation pathways
• ribonucleoprotein assembly
• and signal transduction mechanisms

All this is done in cell-free systems, biochemical assays, and controlled experimental models.

Chemical and Molecular Properties

Property	Description
Compound Name	Uridine 5'-monophosphate disodium salt
Synonyms	UMP Disodium; Uridine monophosphate sodium salt
Molecular Formula	C9H11N2Na2O9P
Molecular Weight	364.14 g/mol
CAS Number	17231-99-5
Structural Class	Ribonucleotide (nucleotide monophosphate)
Chemical Nature	Organic salt of nucleoside phosphate
Research Classification	Biochemical research nucleotide

Working Mechanism of Uridine Monophosphate Disodium

Nucleotide Structure and Role in Biochemical Pathways

UMP Disodium is a ribonucleotide consisting of:

• Uracil: a pyrimidine nucleobase
• Ribose: a pentose sugar
• Phosphate group: contributing to nucleotide charge and reactivity

In biochemical research, UMP Disodium is used to investigate:

1. enzymatic phosphorylation pathways
2. nucleotide interconversion processes
3. and the regulation of nucleotide pools in cell-free or in vitro systems.

Phosphorylation and Nucleotide Interconversion

In controlled mechanistic studies, UMP Disodium can be phosphorylated to generate diphosphate (UDP) or triphosphate (UTP) derivatives. This is done by using purified kinase systems. These transformations serve as substrates for kinase assays. They also include nucleotide metabolism analysis in experimental models.

Biochemical Signal Transduction Investigations

UMP and its derivatives are also used in research to probe signal transduction pathways associated with nucleotide-dependent enzymes. These include nucleoside diphosphate kinases and phosphotransferases. These studies help clarify mechanistic aspects of energy transfer and nucleotide regulation in biochemical contexts.

All mechanistic descriptions above are based on controlled laboratory investigations. They do not imply clinical or functional outcomes outside of research settings.

Uridine Monophosphate Disodium Research Applications (Laboratory Use Only)

• Enzymatic phosphorylation assays
• Nucleotide metabolism pathway analysis
• Phosphotransferase and kinase system studies
• In vitro biochemical signal transduction investigations

All research applications are strictly limited to laboratory and analytical settings.

Why Choose Purerawz for Uridine Monophosphate Disodium?

Buy Uridine Monophosphate Disodium for laboratory research use from our online shop. At Purerawz, we provide high-quality reference materials. Each research compound comes with a Certificate of Analysis for verification of purity and concentration.

Note: Uridine Monophosphate Disodium (UMP Disodium) is an investigational compound currently undergoing scientific evaluation and has not been established as safe or effective for any therapeutic use.

Disclaimer

This information is for educational purposes only and not medical advice. Products are for research use only. Research must follow IRB or IACUC guidelines. Verify information independently before purchasing. By ordering, you agree to our Terms and Conditions. If you are not 100% satisfied with the product you received, please contact us at support@staging.purerawz.co

ATTENTION: All our products are for LABORATORY AND RESEARCH PURPOSES ONLY, not for veterinary or human use.

Reference Links

Kornberg, A. (1955). The role of phosphate and phosphotransfer reactions in nucleotide metabolism. Journal of Biological Chemistry, 217(1), 1 - 14. https://doi.org/10.1016/S0021-9258(18)75361-8/

Hou, Y., et al. (2020). Uridine metabolism and its molecular pathways in nucleotide biosynthesis. Nature Communications, 11, 527. https://doi.org/10.1038/s41467-020-14374-2/