P. aeruginosa Metabolome Database: UDP-α-D-glucose (PAMDB110506)

Identification Taxonomy Physical Properties Biological Properties Spectra Concentrations Links References Enzymes Transporters

Proteins (3280)

Record Information

Version

1.0

Update Date

1/22/2018 11:54:54 AM

Metabolite ID

PAMDB110506

Identification

Name:

UDP-α-D-glucose

Description:

Not Available

Structure

🔍MOL SDF PDB SMILES InChI View Structure

Synonyms:

UDPG
UDP-glucose
UDP-D-glucose

Chemical Formula:

C₁₅H₂₂N₂O₁₇P₂

Average Molecular Weight:

566.0550203765

Monoisotopic Molecular Weight:

566.0550203765

InChI Key:

HSCJRCZFDFQWRP-JZMIEXBBSA-L

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)/p-2/t5-,6-,8-,9-,10+,11-,12-,13-,14-/m1/s1

CAS number:

Not Available

IUPAC Name:

Not Available

Traditional IUPAC Name:

Not Available

SMILES:

C(O)C1(C(O)C(O)C(O)C(O1)OP(=O)([O-])OP(=O)([O-])OCC2(C(O)C(O)C(O2)N3(C=CC(=O)NC(=O)3)))

Chemical Taxonomy

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.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Sub Class

Pyrimidine nucleotide sugars

Direct Parent

Pyrimidine nucleotide sugars

Alternative Parents

Substituents

Pyrimidine nucleotide sugar
Pyrimidine ribonucleoside diphosphate
Pentose phosphate
Pentose-5-phosphate
Glycosyl compound
N-glycosyl compound
Monosaccharide phosphate
Organic pyrophosphate
Pyrimidone
Hydropyrimidine
Monosaccharide
Organic phosphoric acid derivative
Oxane
Phosphoric acid ester
Pyrimidine
Alkyl phosphate
Heteroaromatic compound
Vinylogous amide
Tetrahydrofuran
Lactam
Urea
Secondary alcohol
Polyol
Oxacycle
Organoheterocyclic compound
Azacycle
Organonitrogen compound
Organic nitrogen compound
Primary alcohol
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Organic anion
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

a UDP-sugar, a \u0026beta;-D-galactoside (UDP-GALACTOSE)

Physical Properties

State:

Not Available

Charge:

Not Available

Melting point:

Not Available

Experimental Properties:

Not Available

Predicted Properties

Property	Value	Source
Mass	564.2855	ChemAxon
logP	-3.9173	ChemAxon
H-bond acceptors	19	ChemAxon
H-bond donors	7	ChemAxon
Rotatable bonds	9	ChemAxon
PSA	322.2700	ChemAxon
RO5 violations	3	ChemAxon
RO3 violations	5	ChemAxon
Refractivity	105.4085	ChemAxon
Atoms	58	ChemAxon
Rings	3	ChemAxon
Heavy atoms	36	ChemAxon
Hydrogen atoms	22	ChemAxon
Heteroatoms	21	ChemAxon
N/O atoms	19	ChemAxon
Inorganic atoms	0	ChemAxon
Halogen atoms	0	ChemAxon
Chiral centers	9	ChemAxon
R/S chiral centers	0	ChemAxon
Unknown chiral centers	0	ChemAxon
Undefined chiral centers	9	ChemAxon
Stereo double bonds	0	ChemAxon
Cis/trans stereo double bonds	0	ChemAxon
Unknown stereo double bonds	0	ChemAxon
Undefined stereo double bonds	0	ChemAxon

Biological Properties

Cellular Locations:

Not Available

Reactions:

UDP-α-D-glucose + β-D-fructofuranose 6-phosphate → sucrose 6F-phosphate + UDP + Hydrogen ion
UDP-α-D-glucose + D-Fructose → Sucrose + UDP + Hydrogen ion
UDP-α-D-glucose + galactosyl-(glucosyl)2-(heptosyl)3-Kdo2-lipid A-bisphosphate → Hydrogen ion + galactosyl-(glucosyl)3-(heptosyl)3-Kdo2-lipid A-bisphosphate + UDP
UDP-α-D-glucose + galactosyl-glucosyl-(heptosyl)3-Kdo2-lipid A-bisphosphate → Hydrogen ion + galactosyl-(glucosyl)2-(heptosyl)3-Kdo2-lipid A-bisphosphate + UDP
UDP-α-D-glucose + Glucopyranose → Trehalose + UDP + Hydrogen ion
UDP-α-D-glucose + (heptosyl)2-Kdo2-lipid A → Hydrogen ion + glucosyl-(heptosyl)2-Kdo2-lipid A + UDP

Pathways:

colanic acid building blocks biosynthesisCOLANSYN-PWY
galactose metabolismGALACTMETAB-PWY
UDP-glucose conversionP61-PWY
UDP-D-galactose biosynthesisPWY-7344
UDP-glucose biosynthesisPWY-7343
trehalose biosynthesis VIIPWY-5985
sucrose biosynthesis I (from photosynthesis)SUCSYN-PWY
Lipid A-core biosynthesisLIPA-CORESYN-PWY
sucrose degradation II (sucrose synthase)PWY-3801
superpathway of lipopolysaccharide biosynthesisLPSSYN-PWY

Spectra

Spectra:

Not Available

References

References:

Not Available

Synthesis Reference:

Not Available

Material Safety Data Sheet (MSDS)

Not Available

Links

External Links:

Resource	Link
PseudoCyc	CPD-12575

UDP-α-D-glucose (PAMDB110506)

Structure for UDP-α-D-glucose (PAMDB110506)