alpha-L-fucosyl-(1->2)-beta-D-galactosyl group (CHEBI:16124)

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ChEBI Name	α-L-fucosyl-(1→2)-β-D-galactosyl group

ChEBI ID	CHEBI:16124

ChEBI ASCII Name	alpha-L-fucosyl-(1->2)-beta-D-galactosyl group

Definition	A galactosyl group obtained by removing the hydroxy group from the hemiacetal function of α-L-fucosyl-(1→2)-β-D-galactose.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:12333, CHEBI:10292, CHEBI:5485, CHEBI:12334, CHEBI:22459, CHEBI:57648

Download	Molfile XML SDF

Formula

C12H21O9

Net Charge

Average Mass

309.28974

Monoisotopic Mass

309.11856

SMILES

[C@@H]1([C@@H](O[C@@H]([C@@H]([C@@H]1O)O)CO)*)O[C@H]2[C@H]([C@@H]([C@@H]([C@@H](O2)C)O)O)O

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.

ChEBI Ontology
Outgoing	α-L-fucosyl-(1→2)-β-D-galactosyl group (CHEBI:16124) has role epitope (CHEBI:53000) α-L-fucosyl-(1→2)-β-D-galactosyl group (CHEBI:16124) is a galactosyl group (CHEBI:24164) α-L-fucosyl-(1→2)-β-D-galactosyl group (CHEBI:16124) is substituent group from α-L-Fucp-(1→2)-β-D-Galp (CHEBI:61529)

IUPAC Name

α-L-fucopyranosyl-(1→2)-β-D-galactopyranosyl

Synonyms	Sources
2-O-(6-deoxy-α-L-galactopyranosyl)-β-D-galactopyranosyl	IUPAC
2-O-(6-deoxy-α-L-galactopyranosyl)-β-D-galactopyranosyl	ChEBI
2-O-(α-L-fucopyranosyl)-β-D-galactopyranosyl	ChEBI
6-deoxy-α-L-galactopyranosyl-(1→2)-β-D-galactopyranosyl	IUPAC
α-L-Fuc-(1→2)-β-D-Gal group	ChEBI
alpha-L-Fucosyl-(1->2)-D-galactosyl-R	KEGG COMPOUND
α-L-fucosyl-(1→2)-β-D-galactosyl	ChEBI
α-L-fucosyl-(1→2)-β-D-galactosyl group	UniProt
alpha-L-Fucosyl-1,2-beta-D-galactoside	KEGG COMPOUND
alpha-L-Fucosyl-1,2-beta-D-galactosyl-R	KEGG COMPOUND
Glycolipid alpha-L-fucosyl-1,2-beta-D-galactose	KEGG COMPOUND
Glycoprotein alpha-L-fucosyl-(1,2)-D-galactose	KEGG COMPOUND
Glycoprotein alpha-L-fucosyl-(1,2)-D-galactose	KEGG COMPOUND
H disaccharide	ChEBI

Citation	Type	Source
26014598	PubMed citation	Europe PMC

Last Modified

05 October 2018