Uridine diphosphate glucuronic acid
Chemical compound
From Wikipedia, the free encyclopedia
UDP-glucuronic acid is a sugar used in the creation of polysaccharides and is an intermediate in the biosynthesis of ascorbic acid (except in primates and guinea pigs). It is central to the glucuronidation reaction, in which waste molecules in the body, such as heme, are made more hydrophilic to facilitate their excretion.
| Names | |
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| IUPAC name
3-[(5′-Deoxyuridin-5′-yl)oxy]-1,3-dihydroxy-1,3-dioxo-1λ5,3λ5-diphosphoxan-1-yl α-D-glucopyranosiduronic acid | |
| Systematic IUPAC name
(2S,3S,4S,5R,6R)-6-[(3-{[(2R,3S,4R,5R)-5-(2,4-Dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}-1,3-dihydroxy-1,3-dioxo-1λ5,3λ5-diphosphoxan-1-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid | |
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3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| MeSH | UDP+glucuronic+acid |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C15H22N2O18P2 | |
| Molar mass | 580.285 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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It is made from UDP-glucose by UDP-glucose 6-dehydrogenase (EC 1.1.1.22) using NAD+ as a cofactor. It is the source of the glucuronosyl group in glucuronosyltransferase reactions.[1][2]
