Metabolomics Structure Database

MW REGNO: 49863
Common Name:Glutathione oxidized
Systematic Name:(2S)-2-azanyl-5-[[(2R)-3-[[(2R)-2-[[(4S)-4-azanyl-5-oxidanyl-5-oxidanylidene-pentanoyl]amino]-3-(2-hydroxy-2-oxoethylamino)-3-oxidanylidene-propyl]disulfanyl]-1-(2-hydroxy-2-oxoethylamino)-1-oxidanylidene-propan-2-yl]amino]-5-oxidanylidene-pentanoic acid
RefMet Name:Oxidized glutathione
Synonyms:(2S)-2-amino-5-[[(1R)-1-[[[(2R)-2-[[(4S)-4-amino-4-carboxy-butanoyl]amino]-3-(carboxymethylamino)-3-keto-propyl]disulfanyl]methyl]-2-(carboxymethylamino)-2-keto-ethyl]amino]-5-keto-valeric acid [PubChem Synonyms]
Exact Mass:
612.1520 (neutral)    Calculate m/z:
ClassyFire superclass:Organic acids and derivatives [C0000264]
ClassyFire class:Carboxylic acids and derivatives [C0000265]
ClassyFire subclass:Amino acids, peptides, and analogues [C0000013]
ClassyFire direct parent:Oligopeptides [C0004831]
Massbank MS spectra:View MS spectra
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:65359
CHEBI ID:17858
KEGG ID:C00127
BMRB ID:bmse000906
Plant Metabolite Hub(Pmhub):MS000006322

Calculated physicochemical properties (?):

Heavy Atoms: 40  
Rings: 0  
Aromatic Rings: 0  
Rotatable Bonds: 21  
van der Waals Molecular volume: 541.94 Å3 molecule-1  
Toplogical Polar Sufrace Area: 317.64 Å2 molecule-1  
Hydrogen Bond Donors: 10  
Hydrogen Bond Acceptors: 12  
logP: -1.59  
Molar Refractivity: 143.77  
Fraction sp3 Carbons: 0.60  
sp3 Carbons: 12  


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