CHEBI:63806 - α-D-GlcN-(1→4)-β-D-IdoA2S-(1→4)-α-D-GlcNS3S-(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 α-D-GlcN-(1→4)-β-D-IdoA2S-(1→4)-α-D-GlcNS3S-(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:63806
ChEBI ASCII Name alpha-D-GlcN-(1->4)-beta-D-IdoA2S-(1->4)-alpha-D-GlcNS3S-(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 consisisting of one iduronic acid residue sulfated on O-2, two glucosamine residues, one of which is sulfated on nitrogen and at O-3, one glucuronic acid residue, and two galactose residues linked to a xylosyl residue at the reducing end and which is commonly bonded to an amino acid residue.
Stars This entity has been manually annotated by the ChEBI Team.
Download Molfile XML SDF
Formula C41H67N2O43S3
Net Charge 0
Average Mass 1372.15300
Monoisotopic Mass 1371.22797
SMILES [C@@H]1([C@@H]([C@H]([C@H](O[C@@H]2O[C@@H]([C@@H]([C@@H]([C@H]2O)O[C@@H]3O[C@@H]([C@@H]([C@@H]([C@H]3O)O[C@@H]4O[C@@H]([C@H]([C@@H]([C@H]4O)O)O[C@H]5O[C@@H]([C@H]([C@@H]([C@H]5NS(=O)(O)=O)OS(O)(=O)=O)O[C@@H]6O[C@@H]([C@@H]([C@H]([C@@H]6OS(=O)(=O)O)O)O[C@H]7O[C@@H]([C@H]([C@@H]([C@H]7N)O)O)CO)C(O)=O)CO)C(O)=O)O)CO)O)CO)CO1)O)O)*
ChEBI Ontology
Outgoing α-D-GlcN-(1→4)-β-D-IdoA2S-(1→4)-α-D-GlcNS3S-(1→4)-β-D-GlcA-(1→3)-β-D-Gal-(1→3)-β-D-Gal-(1→4)-β-D-Xyl-yl group (CHEBI:63806) is a glycosyl group (CHEBI:24403)
IUPAC Names
2-deoxy-2-amino-α-D-glucopyranosyl-(1→4)-2-O-sulfo-β-D-(idopyranosyluronic acid)-(1→4)-2-deoxy-3-O-sulfo-2-(sulfoamino)-α-D-glucopyranosyl-(1→4)-β-D-(glucopyranosyluronic acid)-(1→3)-β-D-galactopyranosyl-(1→3)-β-D-galactopyranosyl-(1→4)-β-D-xylopyranosyl
2-deoxy-2-amino-α-D-glucopyranosyl-(1→4)-2-O-sulfo-β-D-idopyranuronosyl-(1→4)-2-deoxy-3-O-sulfo-2-(sulfoamino)-α-D-glucopyranosyl-(1→4)-β-D-glucopyranuronosyl-(1→3)-β-D-galactopyranosyl-(1→3)-β-D-galactopyranosyl-(1→4)-β-D-xylopyranosyl
Last Modified
03 February 2012