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Showing metabocard for N-Propylurea (HMDB0255240)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-11 14:49:46 UTC
Update Date2021-09-26 23:09:52 UTC
HMDB IDHMDB0255240
Secondary Accession NumbersNone
Metabolite Identification
Common NameN-Propylurea
DescriptionN-propylcarbamimidic acid belongs to the class of organic compounds known as ureas. Ureas are compounds containing two amine groups joined by a carbonyl (C=O) functional group. Based on a literature review very few articles have been published on N-propylcarbamimidic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). N-propylurea is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N-Propylurea 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 HMDB0255240 (N-Propylurea)


  Mrv1652309112116502D          

  7  6  0  0  0  0            999 V2000
   -0.1914    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.1270    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
    1.9520    1.1270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.1105    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
M  END
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3D MOL for HMDB0255240 (N-Propylurea)

HMDB0255240
     RDKit          3D
N-Propylurea
 17 16  0  0  0  0  0  0  0  0999 V2000
   -2.5512    0.5146    0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0335    0.4763    0.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5068   -0.4024   -0.3862 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9303   -0.5358   -0.3677 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8171    0.5537   -0.4950 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2102    0.3266   -0.4655 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4006    1.7248   -0.6343 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0682    0.4549    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8544    1.3887   -0.0409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9067   -0.3822   -0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5918    1.4706    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8447   -0.0287    1.6917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9820   -1.3892   -0.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7891    0.0288   -1.3786 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3245   -1.4939   -0.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5998   -0.1785    0.3602 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8459    0.6441   -1.2318 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  1  8  1  0
  1  9  1  0
  1 10  1  0
  2 11  1  0
  2 12  1  0
  3 13  1  0
  3 14  1  0
  4 15  1  0
  6 16  1  0
  6 17  1  0
M  END
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3D SDF for HMDB0255240 (N-Propylurea)


  Mrv1652309112116502D          

  7  6  0  0  0  0            999 V2000
   -0.1914    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.1270    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
    1.9520    1.1270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.1105    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0255240

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCNC(N)=O

> <INCHI_IDENTIFIER>
InChI=1S/C4H10N2O/c1-2-3-6-4(5)7/h2-3H2,1H3,(H3,5,6,7)

> <INCHI_KEY>
ZQZJKHIIQFPZCS-UHFFFAOYSA-N

> <FORMULA>
C4H10N2O

> <MOLECULAR_WEIGHT>
102.137

> <EXACT_MASS>
102.07931295

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
17

> <JCHEM_AVERAGE_POLARIZABILITY>
11.096814863584463

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
propylurea

> <ALOGPS_LOGP>
-0.25

> <JCHEM_LOGP>
-0.26082744633333327

> <ALOGPS_LOGS>
0.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.84196157973886

> <JCHEM_PKA_STRONGEST_BASIC>
-1.7252600576105825

> <JCHEM_POLAR_SURFACE_AREA>
55.120000000000005

> <JCHEM_REFRACTIVITY>
27.3119

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.45e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
propylurea

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for HMDB0255240 (N-Propylurea)

HMDB0255240
     RDKit          3D
N-Propylurea
 17 16  0  0  0  0  0  0  0  0999 V2000
   -2.5512    0.5146    0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0335    0.4763    0.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5068   -0.4024   -0.3862 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9303   -0.5358   -0.3677 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8171    0.5537   -0.4950 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2102    0.3266   -0.4655 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4006    1.7248   -0.6343 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0682    0.4549    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8544    1.3887   -0.0409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9067   -0.3822   -0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5918    1.4706    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8447   -0.0287    1.6917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9820   -1.3892   -0.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7891    0.0288   -1.3786 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3245   -1.4939   -0.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5998   -0.1785    0.3602 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8459    0.6441   -1.2318 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  1  8  1  0
  1  9  1  0
  1 10  1  0
  2 11  1  0
  2 12  1  0
  3 13  1  0
  3 14  1  0
  4 15  1  0
  6 16  1  0
  6 17  1  0
M  END
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PDB for HMDB0255240 (N-Propylurea)

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      -0.357   1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.976   2.104   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  N   UNK     0       3.644   2.104   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       4.977   1.334   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.311   2.104   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       4.977  -0.206   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
MASTER        0    0    0    0    0    0    0    0    7    0   12    0
END
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3D PDB for HMDB0255240 (N-Propylurea)

COMPND    HMDB0255240
HETATM    1  C1  UNL     1      -2.551   0.515   0.558  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.033   0.476   0.715  1.00  0.00           C  
HETATM    3  C3  UNL     1      -0.507  -0.402  -0.386  1.00  0.00           C  
HETATM    4  N1  UNL     1       0.930  -0.536  -0.368  1.00  0.00           N  
HETATM    5  C4  UNL     1       1.817   0.554  -0.495  1.00  0.00           C  
HETATM    6  N2  UNL     1       3.210   0.327  -0.466  1.00  0.00           N  
HETATM    7  O1  UNL     1       1.401   1.725  -0.634  1.00  0.00           O  
HETATM    8  H1  UNL     1      -3.068   0.455   1.536  1.00  0.00           H  
HETATM    9  H2  UNL     1      -2.854   1.389  -0.041  1.00  0.00           H  
HETATM   10  H3  UNL     1      -2.907  -0.382  -0.022  1.00  0.00           H  
HETATM   11  H4  UNL     1      -0.592   1.471   0.742  1.00  0.00           H  
HETATM   12  H5  UNL     1      -0.845  -0.029   1.692  1.00  0.00           H  
HETATM   13  H6  UNL     1      -0.982  -1.389  -0.328  1.00  0.00           H  
HETATM   14  H7  UNL     1      -0.789   0.029  -1.379  1.00  0.00           H  
HETATM   15  H8  UNL     1       1.325  -1.494  -0.253  1.00  0.00           H  
HETATM   16  H9  UNL     1       3.600  -0.179   0.360  1.00  0.00           H  
HETATM   17  H10 UNL     1       3.846   0.644  -1.232  1.00  0.00           H  
CONECT    1    2    8    9   10
CONECT    2    3   11   12
CONECT    3    4   13   14
CONECT    4    5   15
CONECT    5    6    7    7
CONECT    6   16   17
END
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SMILES for HMDB0255240 (N-Propylurea)

CCCNC(N)=O
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INCHI for HMDB0255240 (N-Propylurea)

InChI=1S/C4H10N2O/c1-2-3-6-4(5)7/h2-3H2,1H3,(H3,5,6,7)
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
N-PropylcarbamimidateGenerator
PropylureaMeSH
Chemical FormulaC4H10N2O
Average Molecular Weight102.137
Monoisotopic Molecular Weight102.07931295
IUPAC Namepropylurea
Traditional Namepropylurea
CAS Registry NumberNot Available
SMILES
CCCNC(N)=O
InChI Identifier
InChI=1S/C4H10N2O/c1-2-3-6-4(5)7/h2-3H2,1H3,(H3,5,6,7)
InChI KeyZQZJKHIIQFPZCS-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as ureas. Ureas are compounds containing two amine groups joined by a carbonyl (C=O) functional group.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassOrganic carbonic acids and derivatives
Sub ClassUreas
Direct ParentUreas
Alternative Parents
Substituents
  • Urea
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organonitrogen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological location
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-0.25ALOGPS
logP-0.26ChemAxon
logS0.53ALOGPS
pKa (Strongest Acidic)15.84ChemAxon
pKa (Strongest Basic)-1.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area55.12 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity27.31 m³·mol⁻¹ChemAxon
Polarizability11.1 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]+128.24130932474
DeepCCS[M-H]-126.36330932474
DeepCCS[M-2H]-161.79630932474
DeepCCS[M+Na]+135.96530932474
AllCCS[M+H]+125.932859911
AllCCS[M+H-H2O]+121.632859911
AllCCS[M+NH4]+129.932859911
AllCCS[M+Na]+131.132859911
AllCCS[M-H]-126.532859911
AllCCS[M+Na-2H]-130.432859911
AllCCS[M+HCOO]-134.832859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
N-PropylureaCCCNC(N)=O2094.2Standard polar33892256
N-PropylureaCCCNC(N)=O987.8Standard non polar33892256
N-PropylureaCCCNC(N)=O1230.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
N-Propylurea,1TMS,isomer #1CCCNC(=O)N[Si](C)(C)C1338.6Semi standard non polar33892256
N-Propylurea,1TMS,isomer #1CCCNC(=O)N[Si](C)(C)C1139.1Standard non polar33892256
N-Propylurea,1TMS,isomer #1CCCNC(=O)N[Si](C)(C)C1720.5Standard polar33892256
N-Propylurea,1TMS,isomer #2CCCN(C(N)=O)[Si](C)(C)C1242.2Semi standard non polar33892256
N-Propylurea,1TMS,isomer #2CCCN(C(N)=O)[Si](C)(C)C1156.1Standard non polar33892256
N-Propylurea,1TMS,isomer #2CCCN(C(N)=O)[Si](C)(C)C1772.0Standard polar33892256
N-Propylurea,2TMS,isomer #1CCCN(C(=O)N[Si](C)(C)C)[Si](C)(C)C1311.0Semi standard non polar33892256
N-Propylurea,2TMS,isomer #1CCCN(C(=O)N[Si](C)(C)C)[Si](C)(C)C1260.6Standard non polar33892256
N-Propylurea,2TMS,isomer #1CCCN(C(=O)N[Si](C)(C)C)[Si](C)(C)C1485.8Standard polar33892256
N-Propylurea,2TMS,isomer #2CCCNC(=O)N([Si](C)(C)C)[Si](C)(C)C1345.0Semi standard non polar33892256
N-Propylurea,2TMS,isomer #2CCCNC(=O)N([Si](C)(C)C)[Si](C)(C)C1255.0Standard non polar33892256
N-Propylurea,2TMS,isomer #2CCCNC(=O)N([Si](C)(C)C)[Si](C)(C)C1566.1Standard polar33892256
N-Propylurea,3TMS,isomer #1CCCN(C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C1392.5Semi standard non polar33892256
N-Propylurea,3TMS,isomer #1CCCN(C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C1378.1Standard non polar33892256
N-Propylurea,3TMS,isomer #1CCCN(C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C1372.8Standard polar33892256
N-Propylurea,1TBDMS,isomer #1CCCNC(=O)N[Si](C)(C)C(C)(C)C1509.5Semi standard non polar33892256
N-Propylurea,1TBDMS,isomer #1CCCNC(=O)N[Si](C)(C)C(C)(C)C1309.4Standard non polar33892256
N-Propylurea,1TBDMS,isomer #1CCCNC(=O)N[Si](C)(C)C(C)(C)C1782.5Standard polar33892256
N-Propylurea,1TBDMS,isomer #2CCCN(C(N)=O)[Si](C)(C)C(C)(C)C1443.1Semi standard non polar33892256
N-Propylurea,1TBDMS,isomer #2CCCN(C(N)=O)[Si](C)(C)C(C)(C)C1354.6Standard non polar33892256
N-Propylurea,1TBDMS,isomer #2CCCN(C(N)=O)[Si](C)(C)C(C)(C)C1895.0Standard polar33892256
N-Propylurea,2TBDMS,isomer #1CCCN(C(=O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1732.2Semi standard non polar33892256
N-Propylurea,2TBDMS,isomer #1CCCN(C(=O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1656.4Standard non polar33892256
N-Propylurea,2TBDMS,isomer #1CCCN(C(=O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1724.4Standard polar33892256
N-Propylurea,2TBDMS,isomer #2CCCNC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1743.7Semi standard non polar33892256
N-Propylurea,2TBDMS,isomer #2CCCNC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1641.6Standard non polar33892256
N-Propylurea,2TBDMS,isomer #2CCCNC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1725.8Standard polar33892256
N-Propylurea,3TBDMS,isomer #1CCCN(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2049.8Semi standard non polar33892256
N-Propylurea,3TBDMS,isomer #1CCCN(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2001.0Standard non polar33892256
N-Propylurea,3TBDMS,isomer #1CCCN(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1787.0Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - N-Propylurea GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-9000000000-87838b207b6927875de82021-09-24Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - N-Propylurea GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-25Wishart 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 ID11800
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
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 ]