Metabolomics Structure Database

 
MW REGNO: 53184
Common Name:Gliotoxin
Systematic Name:(3R,5aS,6S,10aR)-6-hydroxy-3-(hydroxymethyl)-2-methyl-2,3,6,10-tetrahydro-5aH-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione
RefMet Name:Gliotoxin
Synonyms:Aspergillin [PubChem Synonyms]
Exact Mass:
326.0395 (neutral)    Calculate m/z:
Formula:C13H14N2O4S2
InChIKey:FIVPIPIDMRVLAY-RBJBARPLSA-N
ClassyFire superclass:Organoheterocyclic compounds
ClassyFire class:Diazinanes
ClassyFire subclass:Piperazines
ClassyFire direct parent:Gliotoxins
Massbank MS spectra:View MS spectra
SMILES:CN1C(=O)[C@]23CC4=CC=C[C@@H]([C@H]4N2C(=O)[C@@]1(CO)SS3)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:6223
CHEBI ID:5385
HMDB ID:HMDB0252746
KEGG ID:C10595
EPA CompTox DB:DTXCID701033031
Plant Metabolite Hub(Pmhub):MS000021760

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
NPClassifier classification: "NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products", Kim HW, Wang M, Leber CA, Nothias LF, Reher R, Kang KB, van der Hooft JJJ, Dorrestein PC, Gerwick WH and Cottrell GW. J Nat Prod. 2021 Nov 26;84(11):2795-2807.DOI: 10.1021/acs.jnatprod.1c00399.

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