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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 19:03:17 UTC
Update Date2022-03-07 02:54:02 UTC
HMDB IDHMDB0034251
Secondary Accession Numbers
  • HMDB34251
Metabolite Identification
Common NameN-Benzoylaspartic acid
DescriptionN-Benzoylaspartic acid, also known as N-benzoylaspartate, belongs to the class of organic compounds known as aspartic acid and derivatives. Aspartic acid and derivatives are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. N-Benzoylaspartic acid has been detected, but not quantified in, common peas (Pisum sativum) and pulses. This could make N-benzoylaspartic acid a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on N-Benzoylaspartic acid.
Structure
Data?1563862534
Synonyms
ValueSource
N-BenzoylaspartateGenerator
2-{[hydroxy(phenyl)methylidene]amino}butanedioateGenerator
Chemical FormulaC11H11NO5
Average Molecular Weight237.2087
Monoisotopic Molecular Weight237.063722467
IUPAC Name2-(phenylformamido)butanedioic acid
Traditional Name2-(phenylformamido)butanedioic acid
CAS Registry Number4631-12-3
SMILES
OC(=O)CC(NC(=O)C1=CC=CC=C1)C(O)=O
InChI Identifier
InChI=1S/C11H11NO5/c13-9(14)6-8(11(16)17)12-10(15)7-4-2-1-3-5-7/h1-5,8H,6H2,(H,12,15)(H,13,14)(H,16,17)
InChI KeyDJLTZJGULPLVOA-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as aspartic acid and derivatives. Aspartic acid and derivatives are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentAspartic acid and derivatives
Alternative Parents
Substituents
  • Aspartic acid or derivatives
  • Hippuric acid or derivatives
  • Hippuric acid
  • N-acyl-alpha-amino acid
  • N-acyl-alpha amino acid or derivatives
  • Benzamide
  • Benzoic acid or derivatives
  • Benzoyl
  • Monocyclic benzene moiety
  • Dicarboxylic acid or derivatives
  • Benzenoid
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Carboxylic acid
  • Hydrocarbon derivative
  • Organic oxide
  • Organic nitrogen compound
  • Carbonyl group
  • Organopnictogen compound
  • Organic oxygen compound
  • Organonitrogen compound
  • Organooxygen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point171 - 173 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility68220 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility2.33 g/LALOGPS
logP0.5ALOGPS
logP0.45ChemAxon
logS-2ALOGPS
pKa (Strongest Acidic)3.37ChemAxon
pKa (Strongest Basic)-1.4ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area103.7 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity56.65 m³·mol⁻¹ChemAxon
Polarizability22.41 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+155.91531661259
DarkChem[M-H]-149.61531661259
DeepCCS[M+H]+148.25930932474
DeepCCS[M-H]-145.90130932474
DeepCCS[M-2H]-179.80930932474
DeepCCS[M+Na]+154.7330932474
AllCCS[M+H]+152.032859911
AllCCS[M+H-H2O]+148.432859911
AllCCS[M+NH4]+155.432859911
AllCCS[M+Na]+156.432859911
AllCCS[M-H]-150.832859911
AllCCS[M+Na-2H]-151.032859911
AllCCS[M+HCOO]-151.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
N-Benzoylaspartic acidOC(=O)CC(NC(=O)C1=CC=CC=C1)C(O)=O3428.3Standard polar33892256
N-Benzoylaspartic acidOC(=O)CC(NC(=O)C1=CC=CC=C1)C(O)=O1909.2Standard non polar33892256
N-Benzoylaspartic acidOC(=O)CC(NC(=O)C1=CC=CC=C1)C(O)=O2239.1Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
N-Benzoylaspartic acid,1TMS,isomer #1C[Si](C)(C)OC(=O)CC(NC(=O)C1=CC=CC=C1)C(=O)O2248.5Semi standard non polar33892256
N-Benzoylaspartic acid,1TMS,isomer #2C[Si](C)(C)OC(=O)C(CC(=O)O)NC(=O)C1=CC=CC=C12244.6Semi standard non polar33892256
N-Benzoylaspartic acid,1TMS,isomer #3C[Si](C)(C)N(C(=O)C1=CC=CC=C1)C(CC(=O)O)C(=O)O2191.0Semi standard non polar33892256
N-Benzoylaspartic acid,2TMS,isomer #1C[Si](C)(C)OC(=O)CC(NC(=O)C1=CC=CC=C1)C(=O)O[Si](C)(C)C2227.8Semi standard non polar33892256
N-Benzoylaspartic acid,2TMS,isomer #2C[Si](C)(C)OC(=O)CC(C(=O)O)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C2187.4Semi standard non polar33892256
N-Benzoylaspartic acid,2TMS,isomer #3C[Si](C)(C)OC(=O)C(CC(=O)O)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C2193.3Semi standard non polar33892256
N-Benzoylaspartic acid,3TMS,isomer #1C[Si](C)(C)OC(=O)CC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C2203.3Semi standard non polar33892256
N-Benzoylaspartic acid,3TMS,isomer #1C[Si](C)(C)OC(=O)CC(C(=O)O[Si](C)(C)C)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C2166.9Standard non polar33892256
N-Benzoylaspartic acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC(NC(=O)C1=CC=CC=C1)C(=O)O2498.5Semi standard non polar33892256
N-Benzoylaspartic acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)C(CC(=O)O)NC(=O)C1=CC=CC=C12487.5Semi standard non polar33892256
N-Benzoylaspartic acid,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)N(C(=O)C1=CC=CC=C1)C(CC(=O)O)C(=O)O2432.7Semi standard non polar33892256
N-Benzoylaspartic acid,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC(NC(=O)C1=CC=CC=C1)C(=O)O[Si](C)(C)C(C)(C)C2678.4Semi standard non polar33892256
N-Benzoylaspartic acid,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CC(C(=O)O)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C(C)(C)C2682.2Semi standard non polar33892256
N-Benzoylaspartic acid,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)C(CC(=O)O)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C(C)(C)C2664.4Semi standard non polar33892256
N-Benzoylaspartic acid,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C(C)(C)C2851.4Semi standard non polar33892256
N-Benzoylaspartic acid,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C(C)(C)C2737.2Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - N-Benzoylaspartic acid GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4i-1900000000-68e992d21116c33d23df2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - N-Benzoylaspartic acid GC-MS (2 TMS) - 70eV, Positivesplash10-0a4i-7952000000-37a8c69a3a58dc15f1b32017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - N-Benzoylaspartic acid GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - N-Benzoylaspartic acid 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 - N-Benzoylaspartic acid 10V, Positive-QTOFsplash10-00di-0290000000-1bd906635fb735518b9b2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 20V, Positive-QTOFsplash10-00fu-1920000000-770657f75843042da2bb2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 40V, Positive-QTOFsplash10-00fs-9800000000-5e9c32233536616920392015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 10V, Negative-QTOFsplash10-00ku-0690000000-5832b19f9beea8a19e502015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 20V, Negative-QTOFsplash10-00rf-2940000000-9db382c3d66e6874fafd2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 40V, Negative-QTOFsplash10-0096-9400000000-35c64ed92335c72f7e6c2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 10V, Positive-QTOFsplash10-0a4i-0920000000-7c1bbd60ab5ddc3821ee2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 20V, Positive-QTOFsplash10-0a4i-0900000000-a22730d137932e04d9842021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 40V, Positive-QTOFsplash10-0a6r-7900000000-002a1ca355e69c87e0572021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 10V, Negative-QTOFsplash10-00dl-2920000000-37522f325cffc51567072021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 20V, Negative-QTOFsplash10-00dl-9500000000-f7c8ec8085b8cdb20c2b2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Benzoylaspartic acid 40V, Negative-QTOFsplash10-006x-9000000000-f3929bb6fa5f619a4bd02021-09-25Wishart 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 IDFDB012566
KNApSAcK IDNot Available
Chemspider ID86355
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound95664
PDB IDNot Available
ChEBI ID169334
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1841431
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.. .