Record Information Version
1.0 Update Date
1/22/2018 12:54:54 PM
Metabolite ID PAMDB110491
Identification Name:
GDP-β-L-fucose Description: Not Available
Structure
Synonyms:
a nucleic acid component →
a GDP-sugar →
GDP-L-fucose
all carbohydrates →
a carbohydrate →
a glycan →
a carbohydrate derivative →
a nucleotide sugar →
an NDP-sugar →
a GDP-sugar →
GDP-L-fucose
Chemical Formula:
C16 H23 N5 O15 P2
Average Molecular Weight:
589.08223818 Monoisotopic Molecular
Weight:
589.08223818 InChI Key:
LQEBEXMHBLQMDB-JGQUBWHWSA-L InChI:
InChI=1S/C16H25N5O15P2/c1-4-7(22)9(24)11(26)15(33-4)35-38(30,31)36-37(28,29)32-2-5-8(23)10(25)14(34-5)21-3-18-6-12(21)19-16(17)20-13(6)27/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H3,17,19,20,27)/p-2/t4-,5+,7+,8+,9+,10+,11-,14+,15+/m0/s1 CAS
number:
Not Available IUPAC Name: Not Available
Traditional IUPAC Name:
Not Available SMILES: CC4(OC(OP(OP(OCC3(C(C(C(N2(C1(=C(C(NC(=N1)N)=O)N=C2)))O3)O)O))([O-])=O)([O-])=O)C(C(C4O)O)O)
Chemical Taxonomy
Taxonomy Description This compound belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group.
Kingdom
Organic compounds Super Class Nucleosides, nucleotides, and analogues
Class
Purine nucleotides Sub Class Purine nucleotide sugars
Direct Parent
Purine nucleotide sugars Alternative Parents
Substituents
Purine nucleotide sugar Purine ribonucleoside diphosphate Purine ribonucleoside monophosphate Pentose phosphate Pentose-5-phosphate Glycosyl compound N-glycosyl compound 6-oxopurine Hypoxanthine Monosaccharide phosphate Organic pyrophosphate Imidazopyrimidine Purine Pyrimidone Aminopyrimidine Pyrimidine Alkyl phosphate Phosphoric acid ester Oxane Monosaccharide N-substituted imidazole Organic phosphoric acid derivative Vinylogous amide Azole Imidazole Oxolane Heteroaromatic compound Secondary alcohol 1,2-diol Polyol Organoheterocyclic compound Azacycle Oxacycle Hydrocarbon derivative Organic oxide Organic oxygen compound Organic nitrogen compound Primary amine Alcohol Organooxygen compound Organonitrogen compound Amine Organic anion Aromatic heteropolycyclic compound Molecular Framework
Aromatic heteropolycyclic compounds External Descriptors
a GDP-sugar (GUANOSINE_DIPHOSPHATE_FUCOSE)
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:
colanic acid building blocks biosynthesisCOLANSYN-PWY GDP-L-fucose biosynthesis I (from GDP-D-mannose)PWY-66
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.
