Uridine 5′-diphosphoglucose disodium salt

Modify Date: 2025-08-22 21:59:18

Uridine 5′-diphosphoglucose disodium salt Structure
Uridine 5′-diphosphoglucose disodium salt structure
Common Name Uridine 5′-diphosphoglucose disodium salt
CAS Number 28053-08-9 Molecular Weight 456.231
Density 1.9±0.1 g/cm3 Boiling Point 780.3±70.0 °C at 760 mmHg
Molecular Formula C15H22N2Na2O17P2 Melting Point N/A
MSDS USA Flash Point 425.7±35.7 °C

 Use of Uridine 5′-diphosphoglucose disodium salt


Uridine 5′-diphosphoglucose disodium salt (UDP-D-Glucose disodium salt) is the precursor of glucose-containing oligosaccharides, polysaccharides, glycoproteins, and glycolipids in animal tissues and in some microorganisms. Uridine-5′-diphosphoglucose is an agonist of the P2Y14 receptor, a neuroimmune system GPCR[1].

 Names

Name Uridine 5'-Diphosphoglucose Disodium Salt
Synonym More Synonyms

  Biological Activity

Description Uridine 5′-diphosphoglucose disodium salt (UDP-D-Glucose disodium salt) is the precursor of glucose-containing oligosaccharides, polysaccharides, glycoproteins, and glycolipids in animal tissues and in some microorganisms. Uridine-5′-diphosphoglucose is an agonist of the P2Y14 receptor, a neuroimmune system GPCR[1].
Related Catalog
References

[1]. DietrichKeppler, et al. Uridine-5′-diphosphoglucose. Methods of Enzymatic Analysis (Second English Edition). 1974;4:2225-2228.

[2]. Das A, et al. Human P2Y(14) receptor agonists: truncation of the hexose moiety of uridine-5'-diphosphoglucose and its replacement with alkyl and aryl groups. J Med Chem. 2010 Jan 14;53(1):471-80.

 Chemical & Physical Properties

Density 1.9±0.1 g/cm3
Boiling Point 780.3±70.0 °C at 760 mmHg
Molecular Formula C15H22N2Na2O17P2
Molecular Weight 456.231
Flash Point 425.7±35.7 °C
Exact Mass 456.043396
PSA 330.11000
LogP -4.05
Vapour Pressure 0.0±6.1 mmHg at 25°C
Index of Refraction 1.612
Storage condition −20°C
Water Solubility H2O: soluble50mg/mL, clear

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Risk Phrases R36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
HS Code 29400090

 Articles15

More Articles
Hysteresis in human UDP-glucose dehydrogenase is due to a restrained hexameric structure that favors feedback inhibition.

Biochemistry 53(51) , 8043-51, (2014)

Human UDP-α-d-glucose-6-dehydrogenase (hUGDH) displays hysteresis because of a slow isomerization from an inactive state (E*) to an active state (E). Here we show that the structure of E* constrains h...

Transporter-mediated uptake of UDP-glucuronic acid by human liver microsomes: assay conditions, kinetics, and inhibition.

Drug Metab. Dispos. 43(1) , 147-53, (2014)

This study characterized the kinetics, variability, and factors that affect UDP-glucuronic acid (UDP-GlcUA) uptake by human liver microsomes (HLM). Biphasic kinetics were observed for UDP-GlcUA uptake...

UDP-glucose pyrophosphorylase influences polysaccharide synthesis, cell wall components, and hyphal branching in Ganoderma lucidum via regulation of the balance between glucose-1-phosphate and UDP-glucose.

Fungal Genet. Biol. 82 , 251-63, (2015)

UDP-glucose pyrophosphorylase (UGP) is a key enzyme involved in carbohydrate metabolism, but there are few studies on the functions of this enzyme in fungi. The ugp gene of Ganoderma lucidum was clone...

 Synonyms

disodium,[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate
UDP-Glc UDP-glucose UDPG
UDP-glc
(3,4-Dihydroxytetrahydro-2-furanyl)methyl 3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl dihydrogen diphosphate
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