Record Information Version
1.0 Update Date
1/22/2018 12:54:54 PM
Metabolite ID PAMDB110518
Identification Name:
UDP-α-D-galactose Description: Not Available
Structure
Synonyms:
UDP-α-D-galactopyranose
UDP-galactose
Chemical Formula:
C15 H22 N2 O17 P2
Average Molecular Weight:
566.0550203765 Monoisotopic Molecular
Weight:
566.0550203765 InChI Key:
HSCJRCZFDFQWRP-ABVWGUQPSA-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
Biological Properties Cellular Locations:
Not Available Reactions:
Pathways:
Spectra Spectra:
Not Available
References References:
Not Available Synthesis Reference:
Not Available Material Safety Data Sheet (MSDS)
Not Available
Links External Links:
This project is supported by
the University of Maryland ,
School of Pharmacy ,
Mass Spectrometry Center , a Waters Center of Excellence. The center is an NIH-investigator funded research and core facility that supports a wide range of cutting-edge metabolomic studies. The Center is supported through a center grant from the University of Maryland and NIH grants to its members. The PAMDB project is affiliated with
The Metabolomics Innovation Centre (TMIC) a leading metabolomics research and service center funded through Genome Alberta, Genome British Columbia and Genome Canada.
