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Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester

Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester structure

CAS No:
133-89-1
Formula:
C15H24N2O17P2
Chemical Name:
Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester
Synonyms:
Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester;Uridine 5'-pyrophosphate, D-glucosyl ester;Uridine diphosphoglucose;[(2R,3R,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-phosphoryl]oxy-phosphinic acid;Uridine-5''-diphospho-D-glucose;UDP-D-glucose;Uridine 5'-(trihydrogen diphosphate mono-β-D-glucopyranosyl;Uridine 5'-diphosphoric acid β-(α-D-glucopyranosyl) ester
Categories:
Biochemical Engineering > Saccharides

Description

Solid

UDP-alpha-D-glucose is the alpha-anomer of UDP-alpha-D-glucose. It is used in nucleotide sugars metabolism. It has a role as a fundamental metabolite. It is a conjugate acid of an UDP-alpha-D-glucose(2-).|A key intermediate in carbohydrate metabolism. Serves as a precursor of glycogen, can be metabolized into UDPgalactose and UDPglucuronic acid which can then be incorporated into polysaccharides as galactose and glucuronic acid. Also serves as a precursor of sucrose lipopolysaccharides, and glycosphingolipids.

An intermediate in the phase II reaction that results in the formation of glucose conjugates of xenobiotics which contain substituents such as hydroxyl, amino or sulfhydryl groups, the O-, N-, and S-glucosides, respectively. UDPG is formed from uridine triphosphate and glucose-1- phosphate in a reaction catalyzed by the enzyme UDPG pyro_x0002_phosphorylase. Glucoside formation is common in insects and plants, whereas animals other than insects utilize uridine diphosphate glucuronic acid to form glucuronides.

Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester Basic Attributes

Molecular Weight：

566.3

Exact Mass：

566.30

EC Number：

2051214

UNII：

V50K1D7P4Y

DSSTox ID：

DTXSID00157902

Color/Form：

White to off-white

Characteristics

Density：

1.97±0.1 g/cm3(Predicted)

Water Solubility：

Water : ≥ 50 mg/mL

Collision Cross Section：

209.2 Å² [M+Na]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|210.4 Å² [M+Na]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|210.5 Å² [M+Na]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|207.4 Å² [M-H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|207.5 Å² [M-H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|215.6 Å² [M+Na-2H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|215.7 Å² [M-2H+Na]-

Critical Temperature & Pressure：

Store at -20°C, protect from light, stored under nitrogen

Drug Information

MeSH Entry Terms：

Diphosphate Glucose, Uridine

Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester Use and Manufacturing

Uridine diphosphate glucose (Standard) is the analytical standard of Uridine diphosphate glucose. This product is intended for research and analytical applications. Uridine diphosphate glucose is the precursor of glucose-containing oligosaccharides, polysaccharides, glycoproteins, and glycolipids in animal tissues and in some microorganisms. Uridine diphosphate glucose is an agonist of the P2Y14 receptor, a neuroimmune system GPCR.

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CAS No.: 133-89-1

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Guide of Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester

Description
Basic Attributes
Characteristics
Drug Information
Use and Manufacturing
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Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester

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