Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 00:10:59 UTC
Update Date2023-02-21 17:26:44 UTC
HMDB IDHMDB0038835
Secondary Accession Numbers
  • HMDB38835
Metabolite Identification
Common Name(E)-1-Cinnamoylpyrrolidine
Description(E)-1-Cinnamoylpyrrolidine belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid (E)-1-Cinnamoylpyrrolidine has been detected, but not quantified in, beverages. This could make (e)-1-cinnamoylpyrrolidine a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on (E)-1-Cinnamoylpyrrolidine.
Structure
Data?1677000404
SynonymsNot Available
Chemical FormulaC13H15NO
Average Molecular Weight201.2643
Monoisotopic Molecular Weight201.115364107
IUPAC Name(2Z)-3-phenyl-1-(pyrrolidin-1-yl)prop-2-en-1-one
Traditional Name(2Z)-3-phenyl-1-(pyrrolidin-1-yl)prop-2-en-1-one
CAS Registry Number52438-21-8
SMILES
O=C(\C=C/C1=CC=CC=C1)N1CCCC1
InChI Identifier
InChI=1S/C13H15NO/c15-13(14-10-4-5-11-14)9-8-12-6-2-1-3-7-12/h1-3,6-9H,4-5,10-11H2/b9-8-
InChI KeyJSIGICUAXLIURX-HJWRWDBZSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassCinnamic acids and derivatives
Sub ClassNot Available
Direct ParentCinnamic acids and derivatives
Alternative Parents
Substituents
  • Cinnamic acid or derivatives
  • N-acylpyrrolidine
  • Styrene
  • Monocyclic benzene moiety
  • Benzenoid
  • Pyrrolidine
  • Tertiary carboxylic acid amide
  • Carboxamide group
  • Carboxylic acid derivative
  • Azacycle
  • Organoheterocyclic compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organopnictogen compound
  • Carbonyl group
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point101 - 103 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility408.9 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.92 g/LALOGPS
logP2.23ALOGPS
logP2.18ChemAxon
logS-2.3ALOGPS
pKa (Strongest Basic)1.64ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area20.31 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity62.22 m³·mol⁻¹ChemAxon
Polarizability22.63 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+147.58731661259
DarkChem[M-H]-145.28331661259
DeepCCS[M+H]+147.80430932474
DeepCCS[M-H]-145.40930932474
DeepCCS[M-2H]-179.41430932474
DeepCCS[M+Na]+153.94630932474
AllCCS[M+H]+146.032859911
AllCCS[M+H-H2O]+141.732859911
AllCCS[M+NH4]+149.932859911
AllCCS[M+Na]+151.132859911
AllCCS[M-H]-150.832859911
AllCCS[M+Na-2H]-151.132859911
AllCCS[M+HCOO]-151.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(E)-1-CinnamoylpyrrolidineO=C(\C=C/C1=CC=CC=C1)N1CCCC12744.5Standard polar33892256
(E)-1-CinnamoylpyrrolidineO=C(\C=C/C1=CC=CC=C1)N1CCCC11961.2Standard non polar33892256
(E)-1-CinnamoylpyrrolidineO=C(\C=C/C1=CC=CC=C1)N1CCCC12117.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (E)-1-Cinnamoylpyrrolidine GC-MS (Non-derivatized) - 70eV, Positivesplash10-0fn9-9810000000-20403e1237b3392ab9582017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (E)-1-Cinnamoylpyrrolidine GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 10V, Positive-QTOFsplash10-0udi-3290000000-604a6618bebc4169b5c92016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 20V, Positive-QTOFsplash10-0uk9-8940000000-3b6a8831cb01d50318f72016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 40V, Positive-QTOFsplash10-0fdo-9400000000-88807ea8fd42feb43cfe2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 10V, Negative-QTOFsplash10-0udi-0090000000-458bbd09492c18c019ed2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 20V, Negative-QTOFsplash10-0uk9-9560000000-ee86a2a723ded2306a432016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 40V, Negative-QTOFsplash10-0fk9-9200000000-d20bfc1be06a0b6245502016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 10V, Negative-QTOFsplash10-0udi-0970000000-0f0768acb459a70cf6f82021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 20V, Negative-QTOFsplash10-0udi-4940000000-14ac83aac3ded202bc1c2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 40V, Negative-QTOFsplash10-0fbc-9500000000-6b54cdf337dbd4c463f52021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 10V, Positive-QTOFsplash10-0ue9-0590000000-c12a29d59f58b9ce54682021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 20V, Positive-QTOFsplash10-0ue9-4940000000-68755330d0b12aece28c2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (E)-1-Cinnamoylpyrrolidine 40V, Positive-QTOFsplash10-0udi-3900000000-88b1198aad2babcd1c952021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB018270
KNApSAcK IDNot Available
Chemspider ID1549879
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound2056198
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1871861
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .