Uridine(5')disodiodiphospho(1)-alpha-D-glucose

Base Information

• Chemical Name: Uridine(5')disodiodiphospho(1)-alpha-D-glucose
• CAS No.: 117756-22-6
• Molecular Formula: C15H24 N2 O17 P2 . x Na
• Molecular Weight: 610.27
• European Community (EC) Number: 248-801-6,683-053-8
• UNII: UYD77NZ2JQ
• DSSTox Substance ID: DTXSID60182331
• ChEMBL ID: CHEMBL5081317
• Mol file: 117756-22-6.mol

Synonyms:28053-08-9;UDPG sodium salt;Uridine(5')disodiodiphospho(1)-alpha-D-glucose;Uridine 5'-diphosphoglucose disodium;UYD77NZ2JQ;Uridine 5'-diphosphoglucose disodium salt;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;((2R,3S,4R,5R)-5-(2,4-Dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl ((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)diphosphate sodium;Uridine 5'-diphosphoglucose disodium salt hydrate;Toxepasi (TN);117756-22-6;DisodiumUDP-glucose;Bivitox (TN);UDP-Glucose sodium salt;UNII-UYD77NZ2JQ;Cogalactoisomerase sodium salt;UDP-a-D-Glucose sodium salt;COGALACTOISOMERASE SODIUM;CHEMBL5081317;DTXSID60182331;EINECS 248-801-6;Uridine 5'-diphosphoglucose disodium salt from Saccharomyces cerevisiae;AKOS025312542;Uridine 5'-diphosphoglucose disodium sal;COGALACTOISOMERASE SODIUM [WHO-DD];D07738;A855605;J-700267;Uridine 5'-diphosphoglucose disodium salt, >=98.0% (HPLC);URIDINE 5'-(TRIHYDROGEN DIPHOSPHATE), P'-.ALPHA.-D-GLUCOPYRANOSYL ESTER, SODIUM SALT (1:2)

Chemical Property of Uridine(5')disodiodiphospho(1)-alpha-D-glucose

Chemical Property:

• PSA: 322.27000
• LogP: -3.91730
• Storage Temp.: −20°C
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 17
• Rotatable Bond Count: 9
• Exact Mass: 610.01890980
• Heavy Atom Count: 38
• Complexity: 948

Purity/Quality:

99% ^*data from raw suppliers

UDP-D-glucose disodium salt ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OC3C(C(C(C(O3)CO)O)O)O)O)O.[Na+].[Na+]
• Isomeric SMILES: C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O.[Na+].[Na+]
• Use Description: Uridine 5'-diphosphoglucose disodium salt, often referred to as UDP-glucose, is a critical molecule with diverse applications in different fields. In the realm of biochemistry and cell biology, it serves as a key substrate for various enzymatic reactions involved in carbohydrate metabolism, glycogen synthesis, and the biosynthesis of glycoproteins and glycolipids. Its role is pivotal in energy storage and the regulation of cellular processes. In the pharmaceutical and biotechnology industries, UDP-glucose plays a crucial role in the development of glycosylation-based therapies and the production of therapeutic proteins. Additionally, in molecular biology and genetic engineering, it is used in the enzymatic synthesis of nucleotide sugars for glycosylation reactions, contributing to the study of gene function and the production of recombinant proteins. Its multifaceted utility underscores its significance in advancing biochemistry, pharmaceuticals, and genetic research, where it plays a crucial role in cellular processes, drug development, and biotechnology applications.