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

storage temp. 

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

Density 

1.97±0.1 g/cm3(Predicted)

pka

1.10±0.50(Predicted)

Water Solubility 

Water : ≥ 50 mg/mL

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

Description

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.

Definition

ChEBI: 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-).

Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester (133-89-1)Related Product Information

• 1,2-O-Isopropylidene-D-glucofuranose
• D-Glucuronic acid
• α-L-Rhamnopyranose monohydrate
• L-Arabinose
• L-Arabinopyranose
• D-Glucaric acid
• L(+)-Rhamnose monohydrate
• D-Galactose
• (2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic
• N-Acetyl-D-Glucosamine
• LIQUID GLUCOSE
• Uridine 5'-diphospho-galuronic acid trisodium
• Deoxyglucose
• DIACETONE-D-GLUCOSE
• Uridine 5'-(trihydrogen diphosphate) P'-(6-azido-6-deoxy-alpha-D-glucopyranosyl) ester
• Pentabenzologlucose
• D-deoxyglucose
• Condensed glucose