CHEBI:42548 - α-L-fucose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name α-L-fucose
ChEBI ID CHEBI:42548
ChEBI ASCII Name alpha-L-fucose
Definition An L-fucopyranose having α-configuration at the anomeric centre.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C6H12O5
Net Charge 0
Average Mass 164.15650
Monoisotopic Mass 164.06847
InChI InChI=1S/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3+,4+,5-,6+/m0/s1
InChIKey SHZGCJCMOBCMKK-SXUWKVJYSA-N
SMILES C[C@@H]1O[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O
Roles Classification
Biological Role(s): epitope
The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via L-fucopyranose )
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-fucopyranose )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via L-fucose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing α-L-fucose (CHEBI:42548) has role epitope (CHEBI:53000)
α-L-fucose (CHEBI:42548) is a L-fucopyranose (CHEBI:2181)
α-L-fucose (CHEBI:42548) is enantiomer of α-D-fucose (CHEBI:42564)
Incoming α-L-fucose 1-phosphate (CHEBI:6220) has functional parent α-L-fucose (CHEBI:42548)
2,4-di-O-methyl-α-L-fucopyranose (CHEBI:59364) has functional parent α-L-fucose (CHEBI:42548)
4-O-acetyl-2,3-di-O-methyl-α-L-fucopyranose (CHEBI:59372) has functional parent α-L-fucose (CHEBI:42548)
4-aminobutyl α-L-fucopyranoside (CHEBI:140447) has functional parent α-L-fucose (CHEBI:42548)
quercetin 3-O-α-L-fucopyranoside (CHEBI:75863) has functional parent α-L-fucose (CHEBI:42548)
α-D-fucose (CHEBI:42564) is enantiomer of α-L-fucose (CHEBI:42548)
IUPAC Names
6-deoxy-α-L-galactopyranose
α-L-fucopyranose
Synonyms Sources
α-L-Fuc JCBN
α-L-fucose UniProt
ALPHA-L-FUCOSE PDBeChem
α-L-Fucp ChEBI
Manual Xrefs Databases
DB04473 DrugBank
FUC PDBeChem
View more database links
Registry Numbers Types Sources
1422661 Reaxys Registry Number Reaxys
1422661 Beilstein Registry Number Beilstein
1998814 Gmelin Registry Number Gmelin
6696-41-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
19443021 PubMed citation Europe PMC
25568069 PubMed citation Europe PMC
Last Modified
19 March 2018