Metabolomics Structure Database

 
MW REGNO: 50402
Common Name:O-succinyl-L-homoserine
Systematic Name:(2S)-2-amino-4-(3-carboxypropanoyloxy)butanoic acid
RefMet Name:o-Succinylhomoserine
Synonyms: [PubChem Synonyms]
Exact Mass:
219.0743 (neutral)    Calculate m/z:
Formula:C8H13NO6
InChIKey:GNISQJGXJIDKDJ-YFKPBYRVSA-N
ClassyFire superclass:Organic acids and derivatives
ClassyFire class:Carboxylic acids and derivatives
ClassyFire subclass:Amino acids, peptides, and analogues
ClassyFire direct parent:Alpha amino acids
Massbank MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:C(CC(=O)OCC[C@@H](C(=O)O)N)C(=O)O
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:439406
CHEBI ID:16160
HMDB ID:HMDB0255868
KEGG ID:C01118
BMRB ID:bmse000058
NP-MRD ID(NMR):NP0002606
Plant Metabolite Hub(Pmhub):MS000008317

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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