Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	38725
Common Name:	Enterodiol
Systematic Name:	(2R,3R)-2,3-bis[(3-hydroxyphenyl)methyl]butane-1,4-diol
RefMet Name:	Enterodiol
Synonyms:	[PubChem Synonyms]
Exact Mass:	302.1518 (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:	C18H22O4
InChIKey:	DWONJCNDULPHLV-HOTGVXAUSA-N
ClassyFire superclass:	Lignans, neolignans and related compounds [C0001392]
ClassyFire class:	Dibenzylbutane lignans [C0001969]
ClassyFire subclass:	Dibenzylbutanediol lignans [C0001624]
ClassyFire direct parent:	Dibenzylbutanediol lignans [C0001624]
Massbank MS spectra:	View MS spectra
SMILES:	c1cc(C[C@@H](CO)[C@@H](Cc2cccc(c2)O)CO)cc(c1)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:	115089
CHEBI ID:	81556
HMDB ID:	HMDB0005056
KEGG ID:	C18166
Chemspider ID:	102992
Plant Metabolite Hub(Pmhub):	MS000014121
PhytoHub ID:	PHUB001386

Calculated physicochemical properties (?):

Heavy Atoms:	22
Rings:	2
Aromatic Rings:	2
Rotatable Bonds:	7
van der Waals Molecular volume:	292.76 Å3 molecule-1
Toplogical Polar Sufrace Area:	80.92 Å2 molecule-1
Hydrogen Bond Donors:	4
Hydrogen Bond Acceptors:	4
logP:	2.67
Molar Refractivity:	85.75
Fraction sp3 Carbons:	0.33
sp3 Carbons:	6

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