CHEBI:63519 - β-D-GalNAc4S-(1→4)-β-D-IdoA2S-(1→3)-β-D-GalNAc4S-(1→4)-β-D-GlcA-(1→3)-β-D-Gal-(1→3)-β-D-Gal-(1→4)-β-D-Xyl-yl group

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name β-D-GalNAc4S-(1→4)-β-D-IdoA2S-(1→3)-β-D-GalNAc4S-(1→4)-β-D-GlcA-(1→3)-β-D-Gal-(1→3)-β-D-Gal-(1→4)-β-D-Xyl-yl group
ChEBI ID CHEBI:63519
ChEBI ASCII Name beta-D-GalNAc4S-(1->4)-beta-D-IdoA2S-(1->3)-beta-D-GalNAc4S-(1->4)-beta-D-GlcA-(1->3)-beta-D-Gal-(1->3)-beta-D-Gal-(1->4)-beta-D-Xyl-yl group
Definition A linear heptasaccharide glycosyl group consisting of two N-acetylgalactosamine residues (both sulfated at the 4-position), one iduronic acid residue sulfated at the 2-position, one glucuronic acid residue and two galactosyl residues linked to a xylosyl residue at the reducing end.
Stars This entity has been manually annotated by the ChEBI Team.
Download Molfile XML SDF
Formula C45H71N2O45S3
Net Charge 0
Average Mass 1456.22700
Monoisotopic Mass 1455.24910
SMILES [C@@H]1([C@@H]([C@H]([C@H]([C@H](O1)CO)O)O[C@H]2[C@@H]([C@H]([C@H]([C@H](O2)CO)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)C(O)=O)O[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)OS(=O)(=O)O)O[C@H]5[C@H]([C@@H]([C@H]([C@H](O5)C(O)=O)O[C@H]6[C@@H]([C@H]([C@H]([C@H](O6)CO)OS(O)(=O)=O)O)NC(C)=O)O)OS(=O)(=O)O)NC(C)=O)O)O)O)O)O[C@H]7[C@@H]([C@H]([C@@H](OC7)*)O)O
ChEBI Ontology
Outgoing β-D-GalNAc4S-(1→4)-β-D-IdoA2S-(1→3)-β-D-GalNAc4S-(1→4)-β-D-GlcA-(1→3)-β-D-Gal-(1→3)-β-D-Gal-(1→4)-β-D-Xyl-yl group (CHEBI:63519) is a glycosyl group (CHEBI:24403)
IUPAC Names
2-acetamido-2-deoxy-4-O-sulfo-β-D-galactopyranosyl-(1→4)-(2-O-sulfo-β-D-idopyranosyluronic acid)-(1→3)-2-acetamido-2-deoxy-4-O-sulfo-β-D-galactopyranosyl-(1→4)-(β-D-glucopyranosyluronic acid)-(1→3)-β-D-galactopyranosyl-(1→3)-β-D-galactopyranosyl-(1→4)-β-D-xylopyranosyl
2-acetamido-2-deoxy-4-O-sulfo-β-D-galactopyranosyl-(1→4)-2-O-sulfo-β-D-idopyranuronosyl-(1→3)-2-acetamido-2-deoxy-4-O-sulfo-β-D-galactopyranosyl-(1→4)-β-D-glucopyranuronosyl-(1→3)-β-D-galactopyranosyl-(1→3)-β-D-galactopyranosyl-(1→4)-β-D-xylopyranosyl
Last Modified
05 January 2012