Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	42931
Common Name:	Linezolid
Systematic Name:	N-{[(5S)-3-[3-fluoro-4-(morpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide
RefMet Name:	Linezolid
Synonyms:	[PubChem Synonyms]
Exact Mass:	337.1438 (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:	C16H20FN3O4
InChIKey:	TYZROVQLWOKYKF-ZDUSSCGKSA-N
ClassyFire superclass:	Organoheterocyclic compounds [C0000002]
ClassyFire class:	Oxazinanes [C0000107]
ClassyFire subclass:	Morpholines [C0000392]
ClassyFire direct parent:	Phenylmorpholines [C0000370]
Massbank MS spectra:	View MS spectra
SMILES:	CC(=O)NC[C@H]1CN(c2ccc(c(c2)F)N2CCOCC2)C(=O)O1
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	441401
CHEBI ID:	63607
HMDB ID:	HMDB0014739
KEGG ID:	C08146
Chemspider ID:	390139
EPA CompTox DB:	DTXCID40210106
Plant Metabolite Hub(Pmhub):	MS000001671

Calculated physicochemical properties (?):

Heavy Atoms:	24
Rings:	3
Aromatic Rings:	1
Rotatable Bonds:	4
van der Waals Molecular volume:	298.41 Å3 molecule-1
Toplogical Polar Sufrace Area:	75.25 Å2 molecule-1
Hydrogen Bond Donors:	1
Hydrogen Bond Acceptors:	6
logP:	3.12
Molar Refractivity:	89.18
Fraction sp3 Carbons:	0.50
sp3 Carbons:	8

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