CHEBI:90465 - α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1)(1−)

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1)(1−) ChEBI ID CHEBI:90465 ChEBI ASCII Name alpha-Neu5Ac-(2->3)-beta-D-Gal-(1->4)-beta-D-Glc-(1<->1')-Cer(d16:1)(1-) Definition An anionic ganglioside that is the conjugate base of α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1) arising from deprotonation of the neuraminosyl carboxy group; major species at pH 7.3. Stars This entity has been manually annotated by the ChEBI Team. Submitter Nevila Nouspikel Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C40H68N2O21R Net Charge -1 Average Mass (excl. R groups) 912.970 Monoisotopic Mass (excl. R groups) 912.43146 SMILES O([C@@H]1[C@H]([C@H](O[C@@H]2[C@H](O[C@@H](OC[C@@H]([C@@H](/C=C/CCCCCCCCCCC)O)NC(=O)*)[C@@H]([C@H]2O)O)CO)O[C@@H]([C@@H]1O)CO)O)[C@]3(O[C@]([C@@H]([C@H](C3)O)NC(C)=O)([C@@H]([C@@H](CO)O)O)[H])C([O-])=O ChEBI Ontology Outgoing α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1)(1−) (CHEBI:90465) is a α-N-acetylneuraminyl-(2→3)-β-D-galactosyl-(1→4)-β-D-glucosyl-(1↔1)-ceramide(1−) (CHEBI:79210) α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1)(1−) (CHEBI:90465) is a organic molecular entity (CHEBI:50860) α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1)(1−) (CHEBI:90465) is conjugate base of α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1) (CHEBI:90592) Incoming α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1) (CHEBI:90592) is conjugate acid of α-Neu5Ac-(2→3)-β-D-Gal-(1→4)-β-D-Glc-(1↔1ʼ)-Cer(d16:1)(1−) (CHEBI:90465) Synonyms Sources α-N-acetylneuraminyl-(2→3)-β-D-galactosyl-(1→4)-β-D-glucosyl-(1↔1)-N-acylhexadecasphing-4-enine UniProt α-N-acetylneuraminyl-(2→3)-β-D-galactosyl-(1→4)-β-D-glucosyl-(1↔1)-N-acylhexadecasphingosine(1−) ChEBI α-Neup5Ac-(2→3)-β-D-Galp-(1→4)-β-D-Glcp-(1↔1ʼ)-Cer(d16:1)(1−) ChEBI ganglioside GM3(d16:1)(1−) SUBMITTER Citation Type Source 18703820 PubMed citation SUBMITTER Last Modified 30 November 2015