Uridine 5′-diphosphoglucose disodium salt CAS#: 28053-08-9; ChemWhat Code: 95585
Identification
| Product Name | Uridine 5′-diphosphoglucose disodium salt |
| IUPAC Name | 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 |
| Molecular Structure |  |
| CAS Registry Number | 728053-08-9 |
| EINECS Number | 248-801-6 |
| MDL Number | MFCMFCD20441966 |
| Synonyms | 28053-08-9 Uridine 5′-diphosphoglucose disodium Uridine(5′)disodiodiphospho(1)-alpha-D-glucose Uridine 5′-diphosphoglucose disodium salt UYD77NZ2JQ 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 117756-22-6 Uridine 5′-diphosphoglucose disodium salt hydrate Toxepasi (TN) DisodiumUDP-glucose Bivitox (TN) UNII-UYD77NZ2JQ Cogalactoisomerase sodium salt Uridine 5′-diphosphoglucose? COGALACTOISOMERASE SODIUM CHEMBL5081317 DTXSID60182331 EINECS 248-801-6 Uridine 5′-diphosphoglucose disodium salt from Saccharomyces cerevisiae AKOS025312542 AT24909 DISODIUM UDP-?-D-GLUCOSE(2-) COGALACTOISOMERASE SODIUM [WHO-DD] D07738 J-700267 Uridine 5′-diphosphoglucose disodium salt, >=98.0% (HPLC) URIDINE 5′-(TRIHYDROGEN DIPHOSPHATE), P’-.ALPHA.-D-GLUCOPYRANOSYL ESTER, SODIUM SALT (1:2) |
| Molecular Formula | C15H22N2Na2O17P2 |
| Molecular Weight | 610.27 |
| InChI | InChI=1S/C15H24N2O17P2.2Na/c18-3-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)17-2-1-7(19)16-15(17)25;;/h1-2,5-6,8-14,18,20-24H,3-4H2,(H,26,27)(H,28,29)(H,16,19,25);;/q;2*+1/p-2/t5-,6-,8-,9-,10+,11-,12-,13-,14-;;/m1../s1 |
| InChI Key | PKJQEQVCYGYYMM-QBNUFUENSA-L |
| 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+] |
| Patent Information |
| No data available |
Physical Data
| Appearance | White powder or off- white powder |
Spectra
| No data available |
Route of Synthesis (ROS)
| No data available |
Safety and Hazards
| Pictogram(s) |  |
| Signal | Warning |
| GHS Hazard Statements | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation] |
| Precautionary Statement Codes | P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.) |
| Source: European Chemicals Agency (ECHA) License Note: Use of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is acknowledged as the source: “Source: European Chemicals Agency, http://echa.europa.eu/”. Such acknowledgement must be included in each copy of the material. ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions: Links can only be made to webpages that provide a link to the Legal Notice page. License URL: https://echa.europa.eu/web/guest/legal-notice Record Name: (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate URL: https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/213446 Description: The information provided here is aggregated from the “Notified classification and labelling” from ECHA’s C&L Inventory. Read more: https://echa.europa.eu/information-on-chemicals/cl-inventory-database |
Other Data
| Transportation | Store at -20°C for long time, in container tightly sealed; Protect from light. |
| HS Code | |
| Storage | Store at -20°C for long time, in container tightly sealed; Protect from light. |
| Shelf Life | 2 years |
| Market Price |
| Use Pattern |
| Intermediate in Carbohydrate Metabolism UDP-Glc (Uridine Diphosphate Glucose) is an essential intermediate in carbohydrate metabolism, playing a crucial role particularly in glycogen and glycoprotein synthesis. As an activated form of glucose, it participates in glycosyl transfer reactions by transferring glucose units to other molecules. Donor in Glycosylation Reactions UDP-Glc serves as the primary donor in glycosyltransferase reactions and is frequently used in the synthesis of polysaccharides, glycolipids, and glycoproteins. In these reactions, UDP-Glc provides glucose groups, transferring them to acceptor molecules to facilitate complex carbohydrate structures. Synthesis of Cell Wall and Extracellular Matrix In plants, bacteria, and other organisms, UDP-Glc is involved in the synthesis of cell wall components such as cellulose and hemicellulose. This function is crucial for maintaining structural integrity, enabling cells to sustain and reinforce their structure. Reagent in Metabolic Pathway Research In biochemical and pharmacological research, UDP-Glc is widely used to study carbohydrate metabolism pathways, including glycogen metabolism and glycosylation reactions in cellular signaling pathways. It helps researchers investigate key biochemical processes and metabolic functions. Precursor in Drug Metabolism UDP-Glc also participates in the metabolism of certain drugs, especially in the liver, where it facilitates glycosylation reactions that increase the water solubility of drugs, making them easier to excrete from the body. |
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