Uridine 5′-diphosphoglucose-13C6 disodium MedChemExpress (MCE)

Product Name	URIDINE DIPHOSPHATE-ALPHA-D-GLUCOSE, DISODIUM SALT (GLUCOSE-13C6, 99%)
Synonyms	URIDINE DIPHOSPHATE-ALPHA-D-GLUCOSE, DISODIUM SALT (GLUCOSE-13C6, 99%)
CAS	2483735-04-0
EINECS
Chemical Formula	C6C9H22N2Na2O17P2
Molecular Weight
inchi
Package	1 mg
Price	Email to quote
Descriptions	Uridine 5′-diphosphoglucose-13C6 disodium Uridine 5′-diphosphoglucose-13C6 disodium MedChemExpress (MCE) HY-N7032S1 2483735-04-0 UDP-D-Glucose-13C6 disodium 98.35% 4°C, sealed storage, away from moisture In solvent : -80°C, 6 months Descriptions Uridine 5′-diphosphoglucose-13C6 disodium Uridine 5′-diphosphoglucose-13C6 disodium MedChemExpress (MCE) HY-N7032S1 2483735-04-0 UDP-D-Glucose-13C6 disodium 98.35% 4°C, sealed storage, away from moisture In solvent : -80°C, 6 months -20°C, 1 month (sealed storage, away from moisture) Room temperature in continental US may vary elsewhere. Uridine 5′-diphosphoglucose-13C6 (disodium) is the 13C labeled Uridine 5′-diphosphoglucose disodium salt[1]. 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[2]. Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1]. \| \| \| \| \| \| \| \| \| \| [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb 53(2):211-216. [Content Brief] [2]. DietrichKeppler, et al. Uridine-5′-diphosphoglucose. Methods of Enzymatic Analysis (Second English Edition). 1974 4:2225-2228. [3]. 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 1453(1):471-80. [Content Brief]
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Last Update	2025-05-21 16:50:25

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