Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	50355
Common Name:	N-acetylisatin
Systematic Name:	1-acetyl-1H-indole-2,3-dione
Synonyms:	1-Acetyl-indole-2,3-dione; 1-Acetylisatin; Acetylisatin; N-acetylisatin [PubChem Synonyms]
Exact Mass:	189.0426 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C10H7NO3
InChIKey:	LPGDEHBASRKTDG-UHFFFAOYSA-N
ClassyFire superclass:	Organoheterocyclic compounds [C0000002]
ClassyFire class:	Indoles and derivatives [C0000211]
ClassyFire subclass:	Indoles and derivatives [C0000211]
ClassyFire direct parent:	Aromatic heteropolycyclic compounds
SMILES:	CC(=O)N1c2ccccc2C(=O)C1=O
Studies:	Available studies(via PubChem CID)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	11321
CHEBI ID:	16050
MetaCyc ID:	N-ACETYLISATIN
Plant Metabolite Hub(Pmhub):	MS000008497

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