Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	42819
Common Name:	Fluoxetine
Systematic Name:	methyl({3-phenyl-3-[4-(trifluoromethyl)phenoxy]propyl})amine
RefMet Name:	Fluoxetine
Synonyms:	[PubChem Synonyms]
Exact Mass:	309.1340 (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:	C17H18F3NO
InChIKey:	RTHCYVBBDHJXIQ-UHFFFAOYSA-N
ClassyFire superclass:	Benzenoids [C0002448]
ClassyFire class:	Benzene and substituted derivatives [C0002279]
ClassyFire subclass:	Trifluoromethylbenzenes [C0004551]
ClassyFire direct parent:	Trifluoromethylbenzenes [C0004551]
Massbank MS spectra:	View MS spectra
SMILES:	CNCCC(c1ccccc1)Oc1ccc(cc1)C(F)(F)F
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	3386
CHEBI ID:	86990
HMDB ID:	HMDB0014615
Chemspider ID:	3269
EPA CompTox DB:	DTXCID903067
Plant Metabolite Hub(Pmhub):	MS000003472

Calculated physicochemical properties (?):

Heavy Atoms:	22
Rings:	2
Aromatic Rings:	2
Rotatable Bonds:	7
van der Waals Molecular volume:	278.30 Å3 molecule-1
Toplogical Polar Sufrace Area:	21.26 Å2 molecule-1
Hydrogen Bond Donors:	1
Hydrogen Bond Acceptors:	1
logP:	4.72
Molar Refractivity:	80.29
Fraction sp3 Carbons:	0.29
sp3 Carbons:	5

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