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Showing metabocard for Propanal, 2-amino- (HMDB0245023)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-10 22:08:10 UTC
Update Date2021-09-26 22:53:11 UTC
HMDB IDHMDB0245023
Secondary Accession NumbersNone
Metabolite Identification
Common NamePropanal, 2-amino-
DescriptionPropanal, 2-amino-, also known as alanine aldehyde, belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group. Based on a literature review a significant number of articles have been published on Propanal, 2-amino-. This compound has been identified in human blood as reported by (PMID: 31557052 ). Propanal, 2-amino- is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Propanal, 2-amino- is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.
Structure
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0245023 (Propanal, 2-amino-)


  Mrv1652309112100082D          

  5  4  0  0  0  0            999 V2000
    1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  2  5  1  0  0  0  0
M  END
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3D MOL for HMDB0245023 (Propanal, 2-amino-)

HMDB0245023
     RDKit          3D
Propanal, 2-amino-
 12 11  0  0  0  0  0  0  0  0999 V2000
   -0.9518   -0.7583    0.1078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2308    0.0157   -0.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0745    1.4279   -0.2989 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4670   -0.2649    0.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0264    0.6235    0.8862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7873   -1.1217    1.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8580   -0.1224    0.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1719   -1.5774   -0.6172 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3350   -0.1749   -1.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0418    1.5545   -0.6988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0360    1.6590    0.7024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8621   -1.2609    0.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  1  6  1  0
  1  7  1  0
  1  8  1  0
  2  9  1  0
  3 10  1  0
  3 11  1  0
  4 12  1  0
M  END
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3D SDF for HMDB0245023 (Propanal, 2-amino-)


  Mrv1652309112100082D          

  5  4  0  0  0  0            999 V2000
    1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  2  5  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0245023

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(N)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C3H7NO/c1-3(4)2-5/h2-3H,4H2,1H3

> <INCHI_KEY>
QPMCUNAXNMSGTK-UHFFFAOYSA-N

> <FORMULA>
C3H7NO

> <MOLECULAR_WEIGHT>
73.095

> <EXACT_MASS>
73.052763849

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
7.662269553664992

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-aminopropanal

> <ALOGPS_LOGP>
-0.95

> <JCHEM_LOGP>
-0.7373275669999999

> <ALOGPS_LOGS>
0.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.24512346974374

> <JCHEM_PKA_STRONGEST_BASIC>
8.049721885326548

> <JCHEM_POLAR_SURFACE_AREA>
43.09

> <JCHEM_REFRACTIVITY>
19.571900000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.72e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
propanal, 2-amino-

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for HMDB0245023 (Propanal, 2-amino-)

HMDB0245023
     RDKit          3D
Propanal, 2-amino-
 12 11  0  0  0  0  0  0  0  0999 V2000
   -0.9518   -0.7583    0.1078 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2308    0.0157   -0.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0745    1.4279   -0.2989 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4670   -0.2649    0.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0264    0.6235    0.8862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7873   -1.1217    1.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8580   -0.1224    0.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1719   -1.5774   -0.6172 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3350   -0.1749   -1.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0418    1.5545   -0.6988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0360    1.6590    0.7024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8621   -1.2609    0.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  1  6  1  0
  1  7  1  0
  1  8  1  0
  2  9  1  0
  3 10  1  0
  3 11  1  0
  4 12  1  0
M  END
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PDB for HMDB0245023 (Propanal, 2-amino-)

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.540   2.667   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    5                                                  
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2                                                            
MASTER        0    0    0    0    0    0    0    0    5    0    8    0
END
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3D PDB for HMDB0245023 (Propanal, 2-amino-)

COMPND    HMDB0245023
HETATM    1  C1  UNL     1      -0.952  -0.758   0.108  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.231   0.016  -0.440  1.00  0.00           C  
HETATM    3  N1  UNL     1      -0.074   1.428  -0.299  1.00  0.00           N  
HETATM    4  C3  UNL     1       1.467  -0.265   0.304  1.00  0.00           C  
HETATM    5  O1  UNL     1       2.026   0.624   0.886  1.00  0.00           O  
HETATM    6  H1  UNL     1      -0.787  -1.122   1.133  1.00  0.00           H  
HETATM    7  H2  UNL     1      -1.858  -0.122   0.136  1.00  0.00           H  
HETATM    8  H3  UNL     1      -1.172  -1.577  -0.617  1.00  0.00           H  
HETATM    9  H4  UNL     1       0.335  -0.175  -1.536  1.00  0.00           H  
HETATM   10  H5  UNL     1      -1.042   1.555  -0.699  1.00  0.00           H  
HETATM   11  H6  UNL     1      -0.036   1.659   0.702  1.00  0.00           H  
HETATM   12  H7  UNL     1       1.862  -1.261   0.322  1.00  0.00           H  
CONECT    1    2    6    7    8
CONECT    2    3    4    9
CONECT    3   10   11
CONECT    4    5    5   12
END
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SMILES for HMDB0245023 (Propanal, 2-amino-)

CC(N)C=O
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INCHI for HMDB0245023 (Propanal, 2-amino-)

InChI=1S/C3H7NO/c1-3(4)2-5/h2-3H,4H2,1H3
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
Alanine aldehydeHMDB
Chemical FormulaC3H7NO
Average Molecular Weight73.095
Monoisotopic Molecular Weight73.052763849
IUPAC Name2-aminopropanal
Traditional Namepropanal, 2-amino-
CAS Registry NumberNot Available
SMILES
CC(N)C=O
InChI Identifier
InChI=1S/C3H7NO/c1-3(4)2-5/h2-3H,4H2,1H3
InChI KeyQPMCUNAXNMSGTK-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group.
KingdomOrganic compounds
Super ClassOrganic nitrogen compounds
ClassOrganonitrogen compounds
Sub ClassAmines
Direct ParentMonoalkylamines
Alternative Parents
Substituents
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Primary aliphatic amine
  • Carbonyl group
  • Aldehyde
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
logP-0.95ALOGPS
logP-0.74ChemAxon
logS0.81ALOGPS
pKa (Strongest Acidic)19.25ChemAxon
pKa (Strongest Basic)8.05ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area43.09 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity19.57 m³·mol⁻¹ChemAxon
Polarizability7.66 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+121.56930932474
DeepCCS[M-H]-119.67430932474
DeepCCS[M-2H]-155.01830932474
DeepCCS[M+Na]+129.48530932474
AllCCS[M+H]+122.432859911
AllCCS[M+H-H2O]+117.932859911
AllCCS[M+NH4]+126.632859911
AllCCS[M+Na]+127.832859911
AllCCS[M-H]-129.432859911
AllCCS[M+Na-2H]-135.032859911
AllCCS[M+HCOO]-141.132859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 20227.8286 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20224.54 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid459.3 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid317.3 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid80.0 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid226.8 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid66.3 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid256.9 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid242.4 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)609.0 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid528.8 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid39.2 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid559.6 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid204.0 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid274.0 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate619.1 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA482.7 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water295.6 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Propanal, 2-amino-CC(N)C=O1280.0Standard polar33892256
Propanal, 2-amino-CC(N)C=O614.3Standard non polar33892256
Propanal, 2-amino-CC(N)C=O669.9Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Propanal, 2-amino-,1TMS,isomer #1CC(N)=CO[Si](C)(C)C975.6Semi standard non polar33892256
Propanal, 2-amino-,1TMS,isomer #1CC(N)=CO[Si](C)(C)C954.2Standard non polar33892256
Propanal, 2-amino-,1TMS,isomer #1CC(N)=CO[Si](C)(C)C1420.0Standard polar33892256
Propanal, 2-amino-,1TMS,isomer #2CC(C=O)N[Si](C)(C)C917.2Semi standard non polar33892256
Propanal, 2-amino-,1TMS,isomer #2CC(C=O)N[Si](C)(C)C888.3Standard non polar33892256
Propanal, 2-amino-,1TMS,isomer #2CC(C=O)N[Si](C)(C)C1173.3Standard polar33892256
Propanal, 2-amino-,2TMS,isomer #1CC(=CO[Si](C)(C)C)N[Si](C)(C)C1184.3Semi standard non polar33892256
Propanal, 2-amino-,2TMS,isomer #1CC(=CO[Si](C)(C)C)N[Si](C)(C)C1111.4Standard non polar33892256
Propanal, 2-amino-,2TMS,isomer #1CC(=CO[Si](C)(C)C)N[Si](C)(C)C1250.2Standard polar33892256
Propanal, 2-amino-,2TMS,isomer #2CC(C=O)N([Si](C)(C)C)[Si](C)(C)C1140.2Semi standard non polar33892256
Propanal, 2-amino-,2TMS,isomer #2CC(C=O)N([Si](C)(C)C)[Si](C)(C)C1080.8Standard non polar33892256
Propanal, 2-amino-,2TMS,isomer #2CC(C=O)N([Si](C)(C)C)[Si](C)(C)C1199.2Standard polar33892256
Propanal, 2-amino-,3TMS,isomer #1CC(=CO[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1334.9Semi standard non polar33892256
Propanal, 2-amino-,3TMS,isomer #1CC(=CO[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1255.9Standard non polar33892256
Propanal, 2-amino-,3TMS,isomer #1CC(=CO[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1239.4Standard polar33892256
Propanal, 2-amino-,1TBDMS,isomer #1CC(N)=CO[Si](C)(C)C(C)(C)C1210.7Semi standard non polar33892256
Propanal, 2-amino-,1TBDMS,isomer #1CC(N)=CO[Si](C)(C)C(C)(C)C1174.3Standard non polar33892256
Propanal, 2-amino-,1TBDMS,isomer #1CC(N)=CO[Si](C)(C)C(C)(C)C1666.0Standard polar33892256
Propanal, 2-amino-,1TBDMS,isomer #2CC(C=O)N[Si](C)(C)C(C)(C)C1163.8Semi standard non polar33892256
Propanal, 2-amino-,1TBDMS,isomer #2CC(C=O)N[Si](C)(C)C(C)(C)C1104.1Standard non polar33892256
Propanal, 2-amino-,1TBDMS,isomer #2CC(C=O)N[Si](C)(C)C(C)(C)C1304.4Standard polar33892256
Propanal, 2-amino-,2TBDMS,isomer #1CC(=CO[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C1642.3Semi standard non polar33892256
Propanal, 2-amino-,2TBDMS,isomer #1CC(=CO[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C1527.2Standard non polar33892256
Propanal, 2-amino-,2TBDMS,isomer #1CC(=CO[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C1496.1Standard polar33892256
Propanal, 2-amino-,2TBDMS,isomer #2CC(C=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1550.3Semi standard non polar33892256
Propanal, 2-amino-,2TBDMS,isomer #2CC(C=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1519.1Standard non polar33892256
Propanal, 2-amino-,2TBDMS,isomer #2CC(C=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1418.8Standard polar33892256
Propanal, 2-amino-,3TBDMS,isomer #1CC(=CO[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1953.0Semi standard non polar33892256
Propanal, 2-amino-,3TBDMS,isomer #1CC(=CO[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1886.9Standard non polar33892256
Propanal, 2-amino-,3TBDMS,isomer #1CC(=CO[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1615.2Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Propanal, 2-amino- GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-9000000000-f038c807552f20e6ecd62021-09-24Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Propanal, 2-amino- 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 - Propanal, 2-amino- 10V, Positive-QTOFsplash10-05fu-9000000000-9d356621c35b398afe782021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Propanal, 2-amino- 20V, Positive-QTOFsplash10-0a4i-9000000000-7a085b6ab189c109d40f2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Propanal, 2-amino- 40V, Positive-QTOFsplash10-0006-9000000000-b12d2e5c36cf1f23280f2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Propanal, 2-amino- 10V, Negative-QTOFsplash10-00di-9000000000-bc974757d0839ce6b57c2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Propanal, 2-amino- 20V, Negative-QTOFsplash10-05fr-9000000000-fe13f8ff82b26c0577622021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Propanal, 2-amino- 40V, Negative-QTOFsplash10-0a4i-9000000000-9f13c491e60aee1d73382021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-12Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID164210
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound188982
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]