CHEBI:27938 - β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer

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ChEBI Name β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer ChEBI ID CHEBI:27938 ChEBI ASCII Name beta-D-Gal-(1->3)-beta-D-GalNAc-(1->4)-beta-D-Gal-(1->4)-beta-D-Glc-(1<->1')-Cer Definition A D-galactosyl-N-acetyl-D-glucosaminyl-D-galactosyl-D-glucosylceramide containing β-linkages exclusively. Stars This entity has been manually annotated by the ChEBI Team. Submitter Nevila Nouspikel Secondary ChEBI IDs CHEBI:78564, CHEBI:5207, CHEBI:21148 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C45H79N2O23R Net Charge 0 Average Mass (excl. R groups) 1016.10840 Monoisotopic Mass (excl. R groups) 1015.50736 SMILES CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[C@@H]3O[C@H](CO)[C@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O)[C@H]3NC(C)=O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)NC([*])=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). View more via ChEBI Ontology ChEBI Ontology Outgoing β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer (CHEBI:27938) has part β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-yl group (CHEBI:142508) β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer (CHEBI:27938) has role mouse metabolite (CHEBI:75771) β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer (CHEBI:27938) is a β-D-galactosyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosyl-(1↔1ʼ)-Cer (CHEBI:88069) β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer (CHEBI:27938) is a D-galactosyl-N-acetyl-D-glucosaminyl-D-galactosyl-D-glucosylceramide (CHEBI:36507) Incoming β-D-galactosyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosyl-(1↔1ʼ)-N-stearoylsphingosine (CHEBI:78484) is a β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1')-Cer (CHEBI:27938) IUPAC Name N-[(2S,3R,4E)-1-{[β-D-galactopyranosyl-(1→3)-2-acetamido-2-deoxy-β-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)1 (Glc)1 (Cer)1 KEGG GLYCAN a ganglioside GA1 (d18:1(4E)) UniProt asialo GM1 ChEBI asialo GM1 glycolipid ChEBI asialo-GM1 ganglioside ChEBI β-D-Gal-(1→3)-β-D-GalNAc-(1→4)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer SUBMITTER β-D-galactosyl-(1→3)-N-acetyl-β-D-galactosaminyl-(1→4)-β-D-galactosyl-(1→4)-β-D-glucosylceramides ChEBI β-D-Galp-(1→3)-β-D-GalpNAc-(1→4)-β-D-Galp-(1→4)-β-D-Glcp-(1↔1')-Cer ChEBI GA1 KEGG COMPOUND Gal-beta1->3GalNAc-beta1->4Gal-beta1->4Glc-beta1->1'Cer KEGG COMPOUND Gal-beta1->3GalNAc-beta1->4LacCer KEGG COMPOUND Galβ1-3GalNAcβ1-4Galβ1-4Glcβ1-1'Cer ChEBI Ganglio-N-tetraosylceramide ChEBI Ganglioside GA1 ChEBI Gg4Cer JCBN GgOse4Cer ChEBI Manual Xrefs Databases C06136 KEGG COMPOUND G00124 KEGG GLYCAN LMSP0503AB00 LIPID MAPS View more database links Citations Types Sources 10695716 PubMed citation Europe PMC 11854201 PubMed citation Europe PMC 16341241 PubMed citation Europe PMC 1724444 PubMed citation Europe PMC 17855742 PubMed citation Europe PMC 19221437 PubMed citation Europe PMC 21174147 PubMed citation Europe PMC 22638862 PubMed citation Europe PMC 2430018 PubMed citation Europe PMC 2448252 PubMed citation Europe PMC 2457654 PubMed citation Europe PMC 25748038 PubMed citation Europe PMC 28188832 PubMed citation Europe PMC 2917140 PubMed citation Europe PMC 6171919 PubMed citation Europe PMC 7186222 PubMed citation Europe PMC 7334007 PubMed citation Europe PMC 7494493 PubMed citation Europe PMC 7691279 PubMed citation Europe PMC 7693874 PubMed citation Europe PMC 7806377 PubMed citation Europe PMC 7927723 PubMed citation Europe PMC 8410057 PubMed citation Europe PMC 8799726 PubMed citation Europe PMC 9209156 PubMed citation Europe PMC 9582303 PubMed citation SUBMITTER Last Modified 22 September 2023