Compound

a ganglioside GT1c (d18:1(4E))

An anionic ganglioside obtained by deprotonation of the neuraminosyl carboxy groups of ganglioside GT1c; major species at pH 7.3.

CHEBI:87789ChEBI

Structure

2D depiction

Class: Organic compound, anion
Formula: C78H127N5O47R
Mass: 1886.851 g/mol
Charge: -3
SMILES: *C(=O)N[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@]3(C(=O)[O-])C[C@H](O)[C@@H](NC(C)=O)[C@]([H])([C@H](O)[C@@H](CO)O[C@]4(C(=O)[O-])C[C@H](O)[C@@H](NC(C)=O)[C@]([H])([C@H](O)[C@@H](CO)O[C@]5(C(=O)[O-])C[C@H](O)[C@@H](NC(C)=O)[C@]([H])([C@H](O)[C@H](O)CO)O5)O4)O3)[C@H]2O)[C@H](O)[C@H]1O)[C@H](O)/C=C/CCCCCCCCCCCCC
Look it up: ChEBI

Identity from ChEBI. Not evidence.

1 entity

1 entities reached.

0 reported hops1 assembled from the scaffold

1 statement

1 statement · 1 reference database · Subject: a ganglioside GT1c (d18:1(4E)) · Sources: Rhea

Order

a ganglioside GT1c (d18:1(4E)) is a substrate of ST3GAL4ProteinRhea RHEA:47588Inferred only

3 reactions

4 names

Resolves to: a ganglioside GT1c (d18:1(4E))

Structure

2D depiction

Class: Organic compound, anion
Formula: C78H127N5O47R
Mass: 1886.851 g/mol
Charge: -3
SMILES: *C(=O)N[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@]3(C(=O)[O-])C[C@H](O)[C@@H](NC(C)=O)[C@]([H])([C@H](O)[C@@H](CO)O[C@]4(C(=O)[O-])C[C@H](O)[C@@H](NC(C)=O)[C@]([H])([C@H](O)[C@@H](CO)O[C@]5(C(=O)[O-])C[C@H](O)[C@@H](NC(C)=O)[C@]([H])([C@H](O)[C@H](O)CO)O5)O4)O3)[C@H]2O)[C@H](O)[C@H]1O)[C@H](O)/C=C/CCCCCCCCCCCCC
Look it up: ChEBI

Identity from ChEBI. Not evidence.