CHEBI:62276 - α-L-Fucp-(1→3)-β-D-GlcpNAc

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name α-L-Fucp-(1→3)-β-D-GlcpNAc
ChEBI ID CHEBI:62276
ChEBI ASCII Name alpha-L-Fucp-(1->3)-beta-D-GlcpNAc
Definition An amino disaccharide consisting of an α-L-fucosyl residue attached to N-acetyl-β-D-glucosamine by a (1→3)-glycosidic linkage.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C14H25NO10
Net Charge 0
Average Mass 367.34900
Monoisotopic Mass 367.14785
InChI InChI=1S/C14H25NO10/c1-4-8(18)10(20)11(21)14(23-4)25-12-7(15-5(2)17)13(22)24-6(3-16)9(12)19/h4,6-14,16,18-22H,3H2,1-2H3,(H,15,17)/t4-,6+,7+,8+,9+,10+,11-,12+,13+,14-/m0/s1
InChIKey TUXVLTYUDHJDAL-QLAGSXOSSA-N
SMILES C[C@@H]1O[C@@H](O[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.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276) has role epitope (CHEBI:53000)
α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276) is a amino disaccharide (CHEBI:22480)
α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276) is a glucosamine oligosaccharide (CHEBI:22485)
Incoming α-L-Fucp-(1→3)-β-D-GlcpNAc-(1→2)-D-Galp (CHEBI:146731) has functional parent α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276)
α-L-Fucp-(1→3)-β-D-GlcpNAc-(1→2)-D-Manp (CHEBI:147017) has functional parent α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276)
α-L-Fucp-(1→3)-β-D-GlcpNAc-(1→6)-α-D-Manp (CHEBI:147655) has functional parent α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276)
α-L-Fucp-(1→3)-β-D-GlcpNAc-(1→6)-D-GalpNAc (CHEBI:148693) has functional parent α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276)
α-L-Fucp-(1→3)-[α-L-Fucp-(1→6)]-β-D-GlcpNAc (CHEBI:146752) has functional parent α-L-Fucp-(1→3)-β-D-GlcpNAc (CHEBI:62276)
IUPAC Name
α-L-fucopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D-glucopyranose
Synonyms Sources
2-(acetylamino)-2-deoxy-3-O-(6-deoxy-α-L-galactopyranosyl)-β-D-glucopyranose ChEBI
2-(acetylamino)-2-deoxy-3-O-(6-deoxy-α-L-galactopyranosyl)-β-D-glucopyranose IUPAC
2-(acetylamino)-2-deoxy-3-O-(α-L-fucopyranosyl)-β-D-glucopyranose ChEBI
2-acetamido-2-deoxy-3-O-(6-deoxy-α-L-galactopyranosyl)-β-D-glucopyranose IUPAC
2-acetamido-2-deoxy-3-O-(α-L-fucopyranosyl)-β-D-glucopyranose ChEBI
α-L-Fuc-(1-3)-β-D-GlcNAc ChEBI
α-L-Fuc-(1→3)-β-D-GlcNAc ChEBI
α-L-fucosyl-(1→3)-N-acetyl-β-D-glucosamine ChEBI
α-L-Fucp-(1→3)-β-D-GlcpNAc ChEBI
β-D-glucopyranose, 2-(acetylamino)-2-deoxy-3-O-(6-deoxy-α-L-galactopyranosyl)- ChEBI
Fuca1-3GlcNAcb ChEBI
WURCS=2.0/2,2,1/[a2122h-1b_1-5_2*NCC/3=O][a1221m-1a_1-5]/1-2/a3-b1 GlyTouCan
Manual Xrefs Databases
G80587NA GlyTouCan
G80587NA GlyGen
View more database links
Registry Number Type Source
285996-67-0 CAS Registry Number Reaxys
Citations Waiting for Citations Types Sources
15848768 PubMed citation Europe PMC
19443021 PubMed citation Europe PMC
25568069 PubMed citation Europe PMC
31537530 PubMed citation Europe PMC
32568414 PubMed citation Europe PMC
Last Modified
07 May 2024