Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	39032
Common Name:	Indole-5,6-quinone
Systematic Name:	5,6-dihydro-1H-indole-5,6-dione
RefMet Name:	Indole-5,6-quinone
Synonyms:	[PubChem Synonyms]
Exact Mass:	147.0320 (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:	C8H5NO2
InChIKey:	IGGVVGHJSQSLFO-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:	c1c[nH]c2=CC(=O)C(=O)C=c12
Studies:	Available studies (via RefMet name)

Select appropriate tab below to view additional details:

All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	440728
CHEBI ID:	27406
HMDB ID:	HMDB0006779
KEGG ID:	C05579
Chemspider ID:	389600
MetaCyc ID:	CPD-12373
EPA CompTox DB:	DTXCID101304509
Plant Metabolite Hub(Pmhub):	MS000018780

Calculated physicochemical properties (?):

Heavy Atoms:	11
Rings:	2
Aromatic Rings:	0
Rotatable Bonds:	0
van der Waals Molecular volume:	137.62 Å3 molecule-1
Toplogical Polar Sufrace Area:	46.17 Å2 molecule-1
Hydrogen Bond Donors:	1
Hydrogen Bond Acceptors:	2
logP:	0.07
Molar Refractivity:	38.46
Fraction sp3 Carbons:	0.00
sp3 Carbons:	0

Human Pathway links:

HMDB and KEGG 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