Record Information |
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Version |
1.0 |
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Update Date |
1/22/2018 11:54:54 AM |
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Metabolite ID | PAMDB000127 |
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Identification |
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Name: |
Uridine diphosphategalactose |
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Description: | Uridine diphosphategalactose (UDPgal) is a nucleoside diphosphate sugar which can be epimerized into UDPglucose for entry into the mainstream of carbohydrate metabolism. UDPgal is a pivotal compound in the metabolism of galactose. UDPgal is a product of the galactose-L-phosphate uridyl transferase (EC 2.7.7.10) reaction but may also be made from Glucose-L-P, involving uridine diphosphate galactose-4-epimerase (EC 5.1.3.2). UDPgal is the necessary galactosyl donor of galactose in the metabolism to incorporate it into complex oligosaccharides, glycoproteins and glycolipids (galactosides). (PMID: 2122114, 7671968) |
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Structure |
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Synonyms: | - GDU
- UDP Galactose
- UDP-a-D-Galactose
- UDP-a-delta-Galactose
- UDP-a-δ-Galactose
- UDP-alpha-D-Galactose
- UDP-alpha-delta-Galactose
- UDP-D-Galactopyranose
- UDP-D-Galactose
- UDP-delta-Galactopyranose
- UDP-delta-Galactose
- UDP-Gal
- UDP-Galactopyranose
- UDP-Galactose
- UDP-α-D-Galactose
- UDP-α-δ-Galactose
- UDP-δ-Galactopyranose
- UDP-δ-Galactose
- Udpgal
- UDPgalactose
- UPG
- Uridine 5'-(a-D-galactopyranosyl pyrophosphate)
- Uridine 5'-(a-D-galactopyranosyl pyrophosphoric acid)
- Uridine 5'-(a-delta-galactopyranosyl pyrophosphate)
- Uridine 5'-(a-delta-galactopyranosyl pyrophosphoric acid)
- Uridine 5'-(a-δ-galactopyranosyl pyrophosphate)
- Uridine 5'-(a-δ-galactopyranosyl pyrophosphoric acid)
- Uridine 5'-(alpha-D-galactopyranosyl pyrophosphate)
- Uridine 5'-(alpha-D-galactopyranosyl pyrophosphoric acid)
- Uridine 5'-(alpha-delta-galactopyranosyl pyrophosphate)
- Uridine 5'-(alpha-delta-galactopyranosyl pyrophosphoric acid)
- Uridine 5'-(α-D-galactopyranosyl pyrophosphate)
- Uridine 5'-(α-D-galactopyranosyl pyrophosphoric acid)
- Uridine 5'-(α-δ-galactopyranosyl pyrophosphate)
- Uridine 5'-(α-δ-galactopyranosyl pyrophosphoric acid)
- Uridine 5'-diphosphate galactose
- Uridine 5'-diphosphogalactose
- Uridine 5'-diphosphoric acid galactose
- Uridine 5'-pyrophosphate a-D-galactopyranosyl ester
- Uridine 5'-pyrophosphate a-D-galactosyl ester
- Uridine 5'-pyrophosphate a-delta-galactopyranosyl ester
- Uridine 5'-pyrophosphate a-delta-galactosyl ester
- Uridine 5'-pyrophosphate a-δ-galactopyranosyl ester
- Uridine 5'-pyrophosphate a-δ-galactosyl ester
- Uridine 5'-pyrophosphate alpha-D-galactosyl ester
- Uridine 5'-pyrophosphate alpha-delta-galactosyl ester
- Uridine 5'-pyrophosphate D-galactosyl ester
- Uridine 5'-pyrophosphate α-D-galactosyl ester
- Uridine 5'-pyrophosphate α-δ-galactosyl ester
- Uridine 5'-pyrophosphoric acid a-D-galactopyranosyl ester
- Uridine 5'-pyrophosphoric acid a-D-galactosyl ester
- Uridine 5'-pyrophosphoric acid a-delta-galactopyranosyl ester
- Uridine 5'-pyrophosphoric acid a-delta-galactosyl ester
- Uridine 5'-pyrophosphoric acid a-δ-galactopyranosyl ester
- Uridine 5'-pyrophosphoric acid a-δ-galactosyl ester
- Uridine 5'-pyrophosphoric acid alpha-D-galactosyl ester
- Uridine 5'-pyrophosphoric acid alpha-delta-galactosyl ester
- Uridine 5'-pyrophosphoric acid D-galactosyl ester
- Uridine 5'-pyrophosphoric acid α-D-galactosyl ester
- Uridine 5'-pyrophosphoric acid α-δ-galactosyl ester
- Uridine 5'-[3-(D-galactopyranosyl) dihydrogen diphosphate]
- Uridine 5'-[3-(D-galactopyranosyl) dihydrogen diphosphoric acid]
- Uridine diphosphate galactose
- Uridine diphosphate-D-galactose
- Uridine diphosphate-delta-galactose
- Uridine diphosphate-galactose
- Uridine diphosphate-δ-galactose
- Uridine diphosphogalactose
- Uridine diphosphoric acid galactose
- Uridine diphosphoric acid-D-galactose
- Uridine diphosphoric acid-delta-galactose
- Uridine diphosphoric acid-galactose
- Uridine diphosphoric acid-δ-galactose
- Uridine pyrophosphate a-D-galactopyranosyl ester
- Uridine pyrophosphate a-delta-galactopyranosyl ester
- Uridine pyrophosphate a-δ-galactopyranosyl ester
- Uridine pyrophosphate alpha-D-galactopyranosyl ester
- Uridine pyrophosphate alpha-delta-galactopyranosyl ester
- Uridine pyrophosphate α-D-galactopyranosyl ester
- Uridine pyrophosphate α-δ-galactopyranosyl ester
- Uridine pyrophosphogalactose
- Uridine pyrophosphoric acid a-D-galactopyranosyl ester
- Uridine pyrophosphoric acid a-delta-galactopyranosyl ester
- Uridine pyrophosphoric acid a-δ-galactopyranosyl ester
- Uridine pyrophosphoric acid alpha-D-galactopyranosyl ester
- Uridine pyrophosphoric acid alpha-delta-galactopyranosyl ester
- Uridine pyrophosphoric acid α-D-galactopyranosyl ester
- Uridine pyrophosphoric acid α-δ-galactopyranosyl ester
- Uridinediphosphate galactose
- Uridinediphosphogalactose
- Uridinediphosphoric acid galactose
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Chemical Formula: |
C15H24N2O17P2 |
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Average Molecular Weight: |
566.3018 |
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Monoisotopic Molecular
Weight: |
566.055020376 |
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InChI Key: |
HSCJRCZFDFQWRP-ABVWGUQPSA-N |
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InChI: | InChI=1S/C15H24N2O17P2/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)/t5-,6-,8+,9-,10+,11-,12-,13-,14-/m1/s1 |
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CAS
number: |
2956-16-3 |
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IUPAC Name: | [({[(2S,3R,4R,5R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})phosphinic acid |
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Traditional IUPAC Name: |
udp galactose |
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SMILES: | OC[C@H]1O[C@H](O[P@@](O)(=O)O[P@@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)[C@H](O)[C@@H](O)[C@H]1O |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group. |
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Kingdom |
Organic compounds |
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Super Class | Nucleosides, nucleotides, and analogues |
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Class |
Pyrimidine nucleotides |
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Sub Class | Pyrimidine nucleotide sugars |
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Direct Parent |
Pyrimidine nucleotide sugars |
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Alternative Parents |
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Substituents |
- Pyrimidine nucleotide sugar
- Pyrimidine ribonucleoside diphosphate
- N-glycosyl compound
- Glycosyl compound
- Organic pyrophosphate
- Monosaccharide phosphate
- Monoalkyl phosphate
- Pyrimidone
- Alkyl phosphate
- Pyrimidine
- Phosphoric acid ester
- Oxane
- Organic phosphoric acid derivative
- Organic phosphate
- Monosaccharide
- Hydropyrimidine
- Heteroaromatic compound
- Vinylogous amide
- Oxolane
- Urea
- Secondary alcohol
- Polyol
- Lactam
- 1,2-diol
- Oxacycle
- Azacycle
- Organoheterocyclic compound
- Hydrocarbon derivative
- Primary alcohol
- Organooxygen compound
- Organonitrogen compound
- Alcohol
- Aromatic heteromonocyclic compound
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Molecular Framework |
Aromatic heteromonocyclic compounds |
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External Descriptors |
Not Available |
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Physical Properties |
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State: |
Solid |
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Charge: | -2 |
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Melting point: |
Not Available |
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Experimental Properties: |
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Predicted Properties |
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Biological Properties |
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Cellular Locations: |
Cytoplasm |
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Reactions: | |
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Pathways: |
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Spectra |
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Spectra: |
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References |
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References: |
- Holton, J. B. (1990). "Galactose disorders: an overview." J Inherit Metab Dis 13:476-486. Pubmed: 2122114
- Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., Tanabe, M. (2012). "KEGG for integration and interpretation of large-scale molecular data sets." Nucleic Acids Res 40:D109-D114. Pubmed: 22080510
- Keseler, I. M., Collado-Vides, J., Santos-Zavaleta, A., Peralta-Gil, M., Gama-Castro, S., Muniz-Rascado, L., Bonavides-Martinez, C., Paley, S., Krummenacker, M., Altman, T., Kaipa, P., Spaulding, A., Pacheco, J., Latendresse, M., Fulcher, C., Sarker, M., Shearer, A. G., Mackie, A., Paulsen, I., Gunsalus, R. P., Karp, P. D. (2011). "EcoCyc: a comprehensive database of Escherichia coli biology." Nucleic Acids Res 39:D583-D590. Pubmed: 21097882
- van der Werf, M. J., Overkamp, K. M., Muilwijk, B., Coulier, L., Hankemeier, T. (2007). "Microbial metabolomics: toward a platform with full metabolome coverage." Anal Biochem 370:17-25. Pubmed: 17765195
- Winder, C. L., Dunn, W. B., Schuler, S., Broadhurst, D., Jarvis, R., Stephens, G. M., Goodacre, R. (2008). "Global metabolic profiling of Escherichia coli cultures: an evaluation of methods for quenching and extraction of intracellular metabolites." Anal Chem 80:2939-2948. Pubmed: 18331064
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Synthesis Reference: |
Takeda, Satoshi; Noguchi, Toshitada. Enzymic manufacture of 5'-uridine diphosphate galactose (UDP-Gal) from UMP. Jpn. Kokai Tokkyo Koho (2001), 9 pp. |
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Material Safety Data Sheet (MSDS) |
Download (PDF) |
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Links |
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External Links: |
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