Uridine diphosphate glucose: Difference between revisions

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	\| PubChem = 8629		\| PubChem = 8629
	\| IUPHAR_ligand = 1783		\| IUPHAR_ligand = 1783
	\| ChEBI_Ref = {{ebicite\|~~changed~~\|EBI}}		\| ChEBI_Ref = {{ebicite\|correct\|EBI}}
	\| ChEBI = 52249		\| ChEBI = 52249
	\| SMILES = O=P(O1O((O)(O)1O)CO)(O)OP(=O)(O)OC3O(N2/C=C\C(=O)NC2=O)(O)3O		\| SMILES = O=P(O1O((O)(O)1O)CO)(O)OP(=O)(O)OC3O(N2/C=C\C(=O)NC2=O)(O)3O

Revision as of 21:12, 12 January 2012

Uridine diphosphate glucose
Names

IUPAC name methoxy-hydroxyphosphoryl] hydrogen phosphate
Other names UDP-glucose
Identifiers
CAS Number	133-89-1
3D model (JSmol)	Interactive image
ChEBI	CHEBI:52249
ChEMBL	ChEMBL375951
ChemSpider	8308
ECHA InfoCard	100.004.657
IUPHAR/BPS	1783
MeSH	Uridine+Diphosphate+Glucose
PubChem CID	8629
CompTox Dashboard (EPA)	DTXSID00157902
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/s1Key: HSCJRCZFDFQWRP-JZMIEXBBSA-N InChI=1/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/s1Key: HSCJRCZFDFQWRP-JZMIEXBBBU
SMILES O=P(O1O((O)(O)1O)CO)(O)OP(=O)(O)OC3O(N2/C=C\C(=O)NC2=O)(O)3O
Properties
Chemical formula	C₁₅H₂₄N₂O₁₇P₂
Molar mass	566.302 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references

Chemical compound

Uridine diphosphate glucose (uracil-diphosphate glucose, UDP-glucose) is a nucleotide sugar. It is involved in glycosyltransferase reactions in metabolism.

It is used in nucleotide sugars metabolism as an activated form of glucose as a substrate for enzymes called glucosyltransferases.

It is a precursor of glycogen and can be converted into UDP-galactose and UDP-glucuronic acid, which can then be used as substrates by the enzymes that make polysaccharides containing galactose and glucuronic acid.

UDP-glucose can also be used as a precursor of sucrose lipopolysaccharides, and glycosphingolipids.

Rademacher T, Parekh R, Dwek R (1988). "Glycobiology". Annu Rev Biochem. 57: 785–838. doi:10.1146/annurev.bi.57.070188.004033. PMID 3052290.{{cite journal}}: CS1 maint: multiple names: authors list (link)