RefMet Compound Details

Created with Raphaƫl 2.1.0OOOONHNH
RefMet ID, RefMet name, exact mass and formula
RefMet IDRM0050245
RefMet nameAcetyl-N-formyl-5-methoxykynurenamine
Systematic nameN-[3-(2-formamido-5-methoxyphenyl)-3-oxopropyl]acetamide
SynonymsPubChem Synonyms
Exact mass264.111008 (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
FormulaC13H16N2O4View other entries in RefMet with this formula
Molecular descriptors
Molfile38505 (Download molfile/View MW Metabolite Database details)
InChIInChI=1S/C13H16N2O4/c1-9(17)14-6-5-13(18)11-7-10(19-2)3-4-12(11)15-8-16/h3-4,7-8H,5-6H2,1-2H3,(H,14,17)(H,15,16)
InChIKeyJYWNYMJKURVPFH-UHFFFAOYSA-NView other enantiomers/diastereomers of this metabolite in RefMet
SMILESCC(=O)NCCC(=O)c1cc(ccc1NC=O)OC
Run Tanimoto similarity search (with similarity coefficient >=0.6)
Chemical/Biochemical Classification
Super ClassBenzenoids
Main ClassPhenylpropylamines
Sub ClassPhenylpropylamines
Distribution of Acetyl-N-formyl-5-methoxykynurenamine 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 Acetyl-N-formyl-5-methoxykynurenamine
External Links
Pubchem CID171161
ChEBI ID194285
KEGG IDC05642
HMDB IDHMDB0004259
Chemspider ID149637
MetaCyc IDCPD-12022
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 Acetyl-N-formyl-5-methoxykynurenamine

Rxn IDKEGG ReactionEnzyme
R03628 Melatonin + Oxygen <=> Formyl-N-acetyl-5-methoxykynurenaminemelatonin:oxygen 2,3-dioxygenase (indole-decyclizing)

Table of KEGG human pathways containing Acetyl-N-formyl-5-methoxykynurenamine

Pathway IDHuman Pathway# of reactions
hsa00380 Tryptophan metabolism 1
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