CHEBI:59296 - α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc
ChEBI ID CHEBI:59296
ChEBI ASCII Name alpha-L-Fucp-(1->2)-beta-D-Galp-(1->3)-beta-D-GlcpNAc
Definition An amino trisaccharide consisting of α-L-fucose, β-D-galactose and N-acetyl-β-D-glucosamine residues joined by sequential (1→2)- and (1→3)-linkages.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C20H35NO15
Net Charge 0
Average Mass 529.48960
Monoisotopic Mass 529.20067
InChI InChI=1S/C20H35NO15/c1-5-10(25)13(28)15(30)19(32-5)36-17-14(29)11(26)7(3-22)34-20(17)35-16-9(21-6(2)24)18(31)33-8(4-23)12(16)27/h5,7-20,22-23,25-31H,3-4H2,1-2H3,(H,21,24)/t5-,7+,8+,9+,10+,11-,12+,13+,14-,15-,16+,17+,18+,19-,20-/m0/s1
InChIKey MGSDFCKWGHNUSM-QVPNGJTFSA-N
SMILES C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]2O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](O)[C@@H]2NC(C)=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.
(via alpha-L-Fucp-(1->2)-beta-D-Galp-(1->3)-D-GlcpNAc )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc (CHEBI:59296) has role epitope (CHEBI:53000)
α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc (CHEBI:59296) is a α-L-Fucp-(1→2)-β-D-Galp-(1→3)-D-GlcpNAc (CHEBI:62259)
Incoming α-L-Fucp-(1→2)-β-D-Galp-(1→3)-[β-D-GalpNAc-(1→6)]-β-D-GlcpNAc (CHEBI:147734) has functional parent α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc (CHEBI:59296)
α-L-fucosyl-(1→2)-β-D-galactosyl-(1→3)-N-acetyl-β-D-glucosaminide (CHEBI:133509) has functional parent α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc (CHEBI:59296)
α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc-yl group (CHEBI:88085) is substituent group from α-L-Fucp-(1→2)-β-D-Galp-(1→3)-β-D-GlcpNAc (CHEBI:59296)
IUPAC Name
α-L-fucopyranosyl-(1→2)-β-D-galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D-glucopyranose
Synonyms Sources
6-deoxy-α-L-galactopyranosyl-(1→2)-β-D-galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D-glucopyranose IUPAC
α-L-Fuc-(1→2)-β-D-Gal-(1→3)-β-D-GlcNAc ChEBI
β-D-glucopyranose, O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-2-(acetylamino)-2-deoxy- ChEBI
Fuca1-2Galb1-3GlcNAcb ChEBI
Fucα1-2Galβ1-3GlcNAcβ ChEBI
globo-H ChEBI
H type I ChEBI
H type I epitope ChEBI
human blood group H type 1 trisaccharide ChEBI
O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-2-(acetylamino)-2-deoxy-β-D-glucopyranose ChEBI
WURCS=2.0/3,3,2/[a2122h-1b_1-5_2*NCC/3=O][a2112h-1b_1-5][a1221m-1a_1-5]/1-2-3/a3-b1_b2-c1 GlyTouCan
Manual Xrefs Databases
DB04679 DrugBank
G40696TO GlyGen
G40696TO GlyTouCan
View more database links
Registry Numbers Types Sources
5784996 Beilstein Registry Number Beilstein
5784996 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
10992504 PubMed citation Europe PMC
17386027 PubMed citation Europe PMC
19443021 PubMed citation Europe PMC
19874068 PubMed citation Europe PMC
2093727 PubMed citation Europe PMC
25568069 PubMed citation Europe PMC
31537530 PubMed citation Europe PMC
7510273 PubMed citation Europe PMC
8737251 PubMed citation Europe PMC
Last Modified
27 April 2024