RefMet Compound Details

RefMet ID, RefMet name, exact mass and formula
RefMet IDRM0188051
RefMet nameCitalopram N-oxide
Systematic name3-[5-cyano-1-(4-fluorophenyl)-3H-isobenzofuran-1-yl]-N,N-dimethyl-propan-1-amine oxide
SynonymsPubChem Synonyms
Exact mass340.158706 (neutral)
Calculate m/z:   
View other RefMet entries with this exact (neutral) mass:   +/- 0.05 amu   +/- 0.1 amu   +/- 0.2 amu   +/- 0.5 amu
FormulaC20H21FN2O2View other entries in RefMet with this formula
Molecular descriptors
Molfile206759 (Download molfile/View MW Metabolite Database details)
InChI
InChIKeyDIOGFDCEWUUSBQ-UHFFFAOYSA-NView other enantiomers/diastereomers of this metabolite in RefMet
SMILESC[N+](C)(CCCC1(c2ccc(cc2)F)c2ccc(cc2CO1)C#N)[O-]
Run Tanimoto similarity search (with similarity coefficient >=0.6)
Chemical/Biochemical Classification
Super ClassOrganoheterocyclic compounds
Main ClassIsocoumarans
Sub ClassIsocoumarans
Distribution of Citalopram N-oxide in NMDR studies
SpeciesPlot Species distribution
Sample sourcePlot Sample source(tissue) distribution
PlatformPlatform (MS/NMR) used for detection
ChromatographyChromatography methods used for detection
StudiesNMDR Studies reporting Citalopram N-oxide
External Links
Pubchem CID10068142
ChEBI ID80602
KEGG IDC16607
HMDB IDHMDB0060654
Chemspider ID8243682
Spectral data for Citalopram N-oxide standards
MassBank(EU)View MS spectra
Structural annotation level
Annotation level1   (1:Known structure; 2:Known regiochemistry; 3:Partial structure; 4:Sum-composition)

Table of KEGG reactions in human pathways involving Citalopram N-oxide

Rxn IDKEGG ReactionEnzyme
R08344 Citalopram <=> Citalopram N-oxideCitalopram <=> Citalopram N-oxide

Table of KEGG human pathways containing Citalopram N-oxide

Pathway IDHuman Pathway# of reactions
hsa00982 Drug metabolism - cytochrome P450 1
  logo