CAS 21931-53-3|Uridine 5'-diphosphate sodium salt

Introduction:Basic information about CAS 21931-53-3|Uridine 5'-diphosphate sodium salt, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameUridine 5'-diphosphate sodium salt
CAS Number21931-53-3Molecular Weight448.125
Density/Boiling Point/
Molecular FormulaC9H14N2O12P2.xNaMelting Point/
MSDSUSAFlash Point/
Symbol
GHS07, GHS08
Signal WordWarning

Names

NameUridine 5,-Diphosphate Sodium Salt
SynonymMore Synonyms

Uridine 5'-diphosphate sodium salt BiologicalActivity

DescriptionUridine 5'-diphosphate sodium salt is a potent, selective P2Y6 receptor native agonist (EC50=300 nM; pEC50=6.52) and a potent P2Y14 antagonist (pEC50=7.28). Uridine 5'-diphosphate sodium salt, an endogenous metabolite, catalyzes the glucuronidation of a wide array of substrates and is used in nucleic acid (RNA) biosynthesis[1][2].
Related CatalogSignaling Pathways >>Cell Cycle/DNA Damage >>DNA/RNA SynthesisSignaling Pathways >>GPCR/G Protein >>P2Y ReceptorResearch Areas >>Inflammation/ImmunologyResearch Areas >>Metabolic Disease
Target

Human Endogenous Metabolite

In VitroUridine 5'-diphosphate sodium salt (100 μM; for 15 min) significantly induces microglial CCL2 and CCL3 mRNA expression[2]. Uridine 5'-diphosphate sodium salt (100 μM; 3 hours) induces chemokine expression in microglia[2]. Uridine 5'-diphosphate sodium salt (100 μM; 0.5, 1, 3, 6 12 hours) induces expression of mRNA encoding CCL2 and CCL3 within 30 min, and such expression reaches maximal levels at 1 h, returning to basal levels at 3-12 h[2]. UDP (10, 100, 1000 μM; 3 hours) induces a concentration-dependent increase in the expression of chemokines at both the mRNA and protein level[2]. Uridine 5'-diphosphate sodium salt (100 μM; for 15 min) induces activation of NFATc1 and NFATc2 in microglia[2]. RT-PCR[2] Cell Line: Primary microglia Concentration: 100 μM Incubation Time: For 15 min Result: Significantly induced microglial CCL2 and CCL3 mRNA expression.
References

[1]. Jacobson KA, et al. Development of selective agonists and antagonists of P2Y receptors. Purinergic Signal. 2009 Mar;5(1):75-89.

[2]. Kim B, et al. Uridine 5'-diphosphate induces chemokine expression in microglia and astrocytes through activation of the P2Y6 receptor. J Immunol. 2011 Mar 15;186(6):3701-9.

Chemical & Physical Properties

Molecular FormulaC9H14N2O12P2.xNa
Molecular Weight448.125
Exact Mass447.966095
PSA243.12000
Appearance of CharactersPowder | White
InChIKeyOCSYTSDILWGALR-IAIGYFSYSA-M
SMILESO=c1ccn(C2OC(COP(=O)(O)OP(=O)([O-])O)C(O)C2O)c(=O)[nH]1.[Na+]
Storage condition−20°C
Water SolubilityH2O: soluble100 mg/mL, clear, colorless to very faintly yellow | Soluble in water to 100mM

Safety Information

Symbol
GHS07, GHS08
Signal WordWarning
Hazard StatementsH302-H371
Precautionary StatementsP260
Hazard CodesXn
Risk PhrasesR22;R48/22
Safety Phrases36/37
RIDADRNONH for all modes of transport
WGK Germany3
HS Code29349990

Preparation


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Synonyms

Uridine, 5'-(trihydrogen diphosphate), sodium salt (1:2)
Disodium 5'-O-{[(hydroxyphosphinato)oxy]phosphinato}uridine
trisodium,[[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate
MFCD00006524
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