Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	21372
Common Name:	Sterigmatocystin
Systematic Name:	(3S,7R)-15-hydroxy-11-methoxy-6,8,20-trioxapentacyclo[10.8.0.02,9.03,7.014,19]icosa-1,4,9,11,14,16,18-heptaen-13-one
RefMet Name:	Sterigmatocystin
Synonyms:	[PubChem Synonyms]
Exact Mass:	324.0634 (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:	C18H12O6
InChIKey:	UTSVPXMQSFGQTM-DCXZOGHSSA-N
LIPID MAPS Category:	Polyketides [PK]
LIPID MAPS mainclass:	Aflatoxins and related substances [PK10]
Massbank MS spectra:	View MS spectra
NP-MRD NMR spectra:	View NMR spectra
SMILES:	COc1cc2c([C@@H]3C=CO[C@@H]3O2)c2c1c(=O)c1c(cccc1o2)O
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:	5280389
LIPID MAPS ID:	LMPK10000001
CHEBI ID:	18227
HMDB ID:	HMDB0030588
KEGG ID:	C00961
Natural Products Atlas ID:	NP005925
NP-MRD ID(NMR):	NP0034325
EPA CompTox DB:	DTXCID901280
Plant Metabolite Hub(Pmhub):	MS000004150

Calculated physicochemical properties (?):

Heavy Atoms:	24
Rings:	5
Aromatic Rings:	3
Rotatable Bonds:	1
van der Waals Molecular volume:	257.08 Å3 molecule-1
Toplogical Polar Sufrace Area:	82.27 Å2 molecule-1
Hydrogen Bond Donors:	1
Hydrogen Bond Acceptors:	6
logP:	4.19
Molar Refractivity:	86.21
Fraction sp3 Carbons:	0.17
sp3 Carbons:	3

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