CHEBI:18056 - N-acetyl-α-D-galactosaminyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→3)-α-D-galactosyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramide

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ChEBI Name N-acetyl-α-D-galactosaminyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→3)-α-D-galactosyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramide ChEBI ID CHEBI:18056 ChEBI ASCII Name N-acetyl-alpha-D-galactosaminyl-(1->3)-N-acetyl-beta-D-galactosaminyl-(1->3)-alpha-D-galactosyl-(1->4)-beta-D-galactosyl-(1->4)-beta-D-glucosylceramide Definition A glycopentaosylceramide having α-D-GalNAc-(1→3)-β-D-GalNAc-(1→3)-α-D-Gal-(1→4)-β-D-Gal-(1→4)-β-D-Glc as the pentasaccharide portion; reported to be the Forssman hapten of horse spleen. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:12561, CHEBI:7119, CHEBI:21514 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C53H92N3O28R Net Charge 0 Average Mass (excl. R groups) 1219.303 Monoisotopic Mass (excl. R groups) 1218.58673 SMILES [C@@H]1([C@H](O[C@@H](O[C@@H]2[C@H]([C@H](O[C@H]3[C@H](O[C@@H](O[C@@H]4[C@H](O[C@@H](OC[C@@H]([C@@H](/C=C/CCCCCCCCCCCCC)O)NC(=O)*)[C@@H]([C@H]4O)O)CO)[C@@H]([C@H]3O)O)CO)O[C@@H]([C@@H]2O)CO)O)[C@@H]([C@H]1O[C@H]5[C@@H]([C@H]([C@@H](O)[C@H](O5)CO)O)NC(C)=O)NC(C)=O)CO)O Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Roles Classification Biological Role(s): mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). (via N-acetyl-alpha-D-galactosaminyl-(1->3)-N-acetyl-beta-D-galactosaminyl-(1->3)-alpha-D-galactosyl-(1->4)-beta-D-galactosyl-(1->4)-beta-D-glucosylceramide ) View more via ChEBI Ontology ChEBI Ontology Outgoing N-acetyl-α-D-galactosaminyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→3)-α-D-galactosyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramide (CHEBI:18056) has role mouse metabolite (CHEBI:75771) N-acetyl-α-D-galactosaminyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→3)-α-D-galactosyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramide (CHEBI:18056) is a α-D-GalNAc-(1→3)-β-D-GalNAc-(1→3)-α-D-Gal-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer (CHEBI:90400) N-acetyl-α-D-galactosaminyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→3)-α-D-galactosyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramide (CHEBI:18056) is a glycopentaosylceramide (CHEBI:23073) Incoming α-D-GalNAc-(1→3)-β-D-GalNAc-(1→3)-(β-D-Gal-(1→3)-β-D-GalNAc-(1→4))-α-D-Gal-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-ceramide(d18:1(4E)) (CHEBI:141190) has functional parent N-acetyl-α-D-galactosaminyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→3)-α-D-galactosyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramide (CHEBI:18056) IUPAC Name N-[(2S,3R,4E)-1-{[2-acetamido-2-deoxy-α-D-galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-D-galactopyranosyl-(1→3)-α-D-galactopyranosyl-(1→4)-β-D-galactopyranosyl-(1→4)-β-D-glucopyranosyl]oxy}-3-hydroxyoctadec-4-en-2-yl]alkanamide Synonyms Sources (Gal)2 (GalNAc)2 (Glc)1 (Cer)1 KEGG GLYCAN a globoside Forssman (d18:1(4E)) UniProt α-D-GalNAc-(1→3)-β-D-GalNAc-(1→3)-α-D-Gal-(1→4)-β-D-Gal-(1→4)-β-D-Glc(1↔1)Cer ChEBI Forssman hapten KEGG COMPOUND GalNAc-alpha1->3GalNAc-beta1->3Gal-alpha1->4Gal-beta1->4Glc-beta1->1'Cer KEGG COMPOUND GalNAc-alpha1->3GalNAc-beta1->3Gal-alpha1->4LacCer KEGG COMPOUND IV3GalNAcα-Gb4Cer ChEBI N-acetyl-α-D-galactosaminyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→3)-α-D-galactosyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramides ChEBI N-Acetyl-D-galactosaminyl-N-Acetyl-D-galactosaminyl-1,3-D-galactosyl-1,4-D-galactosyl-1,4-D-glucosylceramide KEGG COMPOUND Manual Xrefs Databases C04925 KEGG COMPOUND G00095 KEGG GLYCAN View more database links Citations Types Sources 10988247 PubMed citation Europe PMC 1193672 PubMed citation Europe PMC 13239189 PubMed citation Europe PMC 13239190 PubMed citation Europe PMC 1373469 PubMed citation Europe PMC 14210803 PubMed citation Europe PMC 1528196 PubMed citation Europe PMC 19351707 PubMed citation Europe PMC 4199759 PubMed citation Europe PMC 4358346 PubMed citation Europe PMC 4459265 PubMed citation Europe PMC 4474139 PubMed citation Europe PMC 4538505 PubMed citation Europe PMC 4605408 PubMed citation Europe PMC 469271 PubMed citation Europe PMC 5461254 PubMed citation Europe PMC 8623166 PubMed citation Europe PMC Last Modified 18 October 2023