Metabolomics Structure Database

 
MW REGNO: 63020
Common Name:3)-beta-D-GalpNAc4S-(1->4)-beta-D-GlcpA-(1->3)-beta-D-Galp-(1->3)-beta-D-Galp-(1->4)-beta-D-Xylp>beta-D-IdopA-(1->3)-beta-D-GalpNAc4S-(1->4)-beta-D-GlcpA-(1->3)-beta-D-Galp-(1->3)-beta-D-Galp-(1->4)-beta-D-Xylp
Systematic Name:(beta-D-idopyranosyluronic acid)-(1->3)-2-acetamido-2-deoxy-4-O-sulfo-beta-D-galactopyranosyl-(1->4)-(beta-D-glucopyranosyluronic acid)-(1->3)-beta-D-galactopyranosyl-(1->3)-beta-D-galactopyranosyl-(1->4)-beta-D-xylopyranose;beta-D-idopyranuronosyl-(1->3)-2-acetamido-2-deoxy-4-O-sulfo-beta-D-galactopyranosyl-(1->4)-beta-D-glucopyranuronosyl-(1->3)-beta-D-galactopyranosyl-(1->3)-beta-D-galactopyranosyl-(1->4)-beta-D-xylopyranose
Synonyms:IdoA-GalNAc(4S)-GlcA-Gal-Gal-Xyl; beta-D-IdoA-(1->3)-beta-D-GalNAc4S-(1->4)-beta-D-GlcA-(1->3)-beta-D-Gal-(1->3)-beta-D-Gal-(1->4)-beta-D-Xyl [PubChem Synonyms]
Exact Mass:
1109.2588 (neutral)    Calculate m/z:
Formula:C37H59NO35S
InChIKey:JQNKZLWLZZKAFE-NUBKIDDFSA-N
ClassyFire superclass:Organic oxygen compounds [C0004603]
ClassyFire class:Organooxygen compounds [C0000323]
ClassyFire subclass:Carbohydrates and carbohydrate conjugates [C0000011]
ClassyFire direct parent:Oligosaccharide sulfates [C0003308]
SMILES:CC(=O)N[C@@H]1[C@H]([C@H]([C@@H](CO)O[C@H]1O[C@H]1[C@@H]([C@H]([C@H](O[C@H]2[C@H]([C@@H](CO)O[C@H]([C@@H]2O)O[C@H]2[C@H]([C@@H](CO)O[C@H]([C@@H]2O)O[C@@H]2CO[C@H]([C@@H]([C@H]2O)O)O)O)O)O[C@@H]1C(=O)O)O)O)OS(=O)(=O)O)O[C@H]1[C@H]([C@@H]([C@H]([C@@H](C(=O)O)O1)O)O)O
Studies:-

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Human Pathway links:

REACTOME pathways containing this metabolite

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y

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