Hmdb loader

Showing metabocard for 2-Mercaptoacetamide (HMDB0245188)

Jump To Section:
IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesXML
Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-10 22:17:02 UTC
Update Date2021-09-26 22:53:31 UTC
HMDB IDHMDB0245188
Secondary Accession NumbersNone
Metabolite Identification
Common Name2-Mercaptoacetamide
Description2-Mercaptoacetamide belongs to the class of organic compounds known as primary carboxylic acid amides. Primary carboxylic acid amides are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2. Based on a literature review very few articles have been published on 2-Mercaptoacetamide. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2-mercaptoacetamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2-Mercaptoacetamide 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
Thumb
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0245188 (2-Mercaptoacetamide)


  Mrv1652309112100172D          

  5  4  0  0  0  0            999 V2000
    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
    2.0625   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  1  5  1  0  0  0  0
M  END
Download

3D MOL for HMDB0245188 (2-Mercaptoacetamide)

HMDB0245188
     RDKit          3D
2-Mercaptoacetamide
 10  9  0  0  0  0  0  0  0  0999 V2000
    1.3115    0.5927   -0.1848 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4629   -0.3097    0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7034   -0.6392    1.6998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7121   -0.8075   -0.2651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8992    0.5365   -0.3518 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0228    1.0646   -1.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2498    0.7804    0.2100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3500   -1.0094   -1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1094   -1.7536    0.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6796    1.5452    0.5949 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  1  6  1  0
  1  7  1  0
  4  8  1  0
  4  9  1  0
  5 10  1  0
M  END
Download

3D SDF for HMDB0245188 (2-Mercaptoacetamide)


  Mrv1652309112100172D          

  5  4  0  0  0  0            999 V2000
    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
    2.0625   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  1  5  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0245188

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(=O)CS

> <INCHI_IDENTIFIER>
InChI=1S/C2H5NOS/c3-2(4)1-5/h5H,1H2,(H2,3,4)

> <INCHI_KEY>
GYXHHICIFZSKKZ-UHFFFAOYSA-N

> <FORMULA>
C2H5NOS

> <MOLECULAR_WEIGHT>
91.13

> <EXACT_MASS>
91.009184959

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
8.57971765506452

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-sulfanylacetamide

> <ALOGPS_LOGP>
-0.26

> <JCHEM_LOGP>
-0.8037229066666667

> <ALOGPS_LOGS>
-0.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.0116504963763

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.452700195046745

> <JCHEM_PKA_STRONGEST_BASIC>
-4.065097454153811

> <JCHEM_POLAR_SURFACE_AREA>
43.09

> <JCHEM_REFRACTIVITY>
22.295099999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.23e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
sulfacetamide

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0245188 (2-Mercaptoacetamide)

HMDB0245188
     RDKit          3D
2-Mercaptoacetamide
 10  9  0  0  0  0  0  0  0  0999 V2000
    1.3115    0.5927   -0.1848 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4629   -0.3097    0.5174 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7034   -0.6392    1.6998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7121   -0.8075   -0.2651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8992    0.5365   -0.3518 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0228    1.0646   -1.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2498    0.7804    0.2100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3500   -1.0094   -1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1094   -1.7536    0.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6796    1.5452    0.5949 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  1  6  1  0
  1  7  1  0
  4  8  1  0
  4  9  1  0
  5 10  1  0
M  END
Download

PDB for HMDB0245188 (2-Mercaptoacetamide)

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       1.540   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.850  -1.334   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       1.540  -2.667   0.000  0.00  0.00           N+0
HETATM    5  S   UNK     0       0.000   0.000   0.000  0.00  0.00           S+0
CONECT    1    2    5                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    1                                                            
MASTER        0    0    0    0    0    0    0    0    5    0    8    0
END
Download

3D PDB for HMDB0245188 (2-Mercaptoacetamide)

COMPND    HMDB0245188
HETATM    1  N1  UNL     1       1.311   0.593  -0.185  1.00  0.00           N  
HETATM    2  C1  UNL     1       0.463  -0.310   0.517  1.00  0.00           C  
HETATM    3  O1  UNL     1       0.703  -0.639   1.700  1.00  0.00           O  
HETATM    4  C2  UNL     1      -0.712  -0.807  -0.265  1.00  0.00           C  
HETATM    5  S1  UNL     1      -1.899   0.536  -0.352  1.00  0.00           S  
HETATM    6  H1  UNL     1       1.023   1.065  -1.081  1.00  0.00           H  
HETATM    7  H2  UNL     1       2.250   0.780   0.210  1.00  0.00           H  
HETATM    8  H3  UNL     1      -0.350  -1.009  -1.293  1.00  0.00           H  
HETATM    9  H4  UNL     1      -1.109  -1.754   0.154  1.00  0.00           H  
HETATM   10  H5  UNL     1      -1.680   1.545   0.595  1.00  0.00           H  
CONECT    1    2    6    7
CONECT    2    3    3    4
CONECT    4    5    8    9
CONECT    5   10
END
Download

SMILES for HMDB0245188 (2-Mercaptoacetamide)

NC(=O)CS
Download

INCHI for HMDB0245188 (2-Mercaptoacetamide)

InChI=1S/C2H5NOS/c3-2(4)1-5/h5H,1H2,(H2,3,4)
Download
View in JSmolView NMR AssignmentsView Stereo Labels
SynonymsNot Available
Chemical FormulaC2H5NOS
Average Molecular Weight91.13
Monoisotopic Molecular Weight91.009184959
IUPAC Name2-sulfanylacetamide
Traditional Namesulfacetamide
CAS Registry NumberNot Available
SMILES
NC(=O)CS
InChI Identifier
InChI=1S/C2H5NOS/c3-2(4)1-5/h5H,1H2,(H2,3,4)
InChI KeyGYXHHICIFZSKKZ-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as primary carboxylic acid amides. Primary carboxylic acid amides are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassCarboxylic acid derivatives
Direct ParentPrimary carboxylic acid amides
Alternative Parents
Substituents
  • Primary carboxylic acid amide
  • Alkylthiol
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organosulfur compound
  • 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-0.26ALOGPS
logP-0.8ChemAxon
logS-0.61ALOGPS
pKa (Strongest Acidic)9.45ChemAxon
pKa (Strongest Basic)-4.1ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area43.09 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity22.3 m³·mol⁻¹ChemAxon
Polarizability8.58 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]+120.92830932474
DeepCCS[M-H]-119.03230932474
DeepCCS[M-2H]-154.38730932474
DeepCCS[M+Na]+128.75330932474
AllCCS[M+H]+125.032859911
AllCCS[M+H-H2O]+120.632859911
AllCCS[M+NH4]+129.032859911
AllCCS[M+Na]+130.232859911
AllCCS[M-H]-136.232859911
AllCCS[M+Na-2H]-141.932859911
AllCCS[M+HCOO]-148.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
2-MercaptoacetamideNC(=O)CS2084.6Standard polar33892256
2-MercaptoacetamideNC(=O)CS833.8Standard non polar33892256
2-MercaptoacetamideNC(=O)CS1123.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
2-Mercaptoacetamide,1TMS,isomer #1C[Si](C)(C)SCC(N)=O1236.0Semi standard non polar33892256
2-Mercaptoacetamide,1TMS,isomer #1C[Si](C)(C)SCC(N)=O1207.2Standard non polar33892256
2-Mercaptoacetamide,1TMS,isomer #1C[Si](C)(C)SCC(N)=O1826.3Standard polar33892256
2-Mercaptoacetamide,1TMS,isomer #2C[Si](C)(C)NC(=O)CS1128.0Semi standard non polar33892256
2-Mercaptoacetamide,1TMS,isomer #2C[Si](C)(C)NC(=O)CS1109.4Standard non polar33892256
2-Mercaptoacetamide,1TMS,isomer #2C[Si](C)(C)NC(=O)CS1504.1Standard polar33892256
2-Mercaptoacetamide,2TMS,isomer #1C[Si](C)(C)NC(=O)CS[Si](C)(C)C1334.4Semi standard non polar33892256
2-Mercaptoacetamide,2TMS,isomer #1C[Si](C)(C)NC(=O)CS[Si](C)(C)C1320.8Standard non polar33892256
2-Mercaptoacetamide,2TMS,isomer #1C[Si](C)(C)NC(=O)CS[Si](C)(C)C1505.3Standard polar33892256
2-Mercaptoacetamide,2TMS,isomer #2C[Si](C)(C)N(C(=O)CS)[Si](C)(C)C1293.5Semi standard non polar33892256
2-Mercaptoacetamide,2TMS,isomer #2C[Si](C)(C)N(C(=O)CS)[Si](C)(C)C1276.2Standard non polar33892256
2-Mercaptoacetamide,2TMS,isomer #2C[Si](C)(C)N(C(=O)CS)[Si](C)(C)C1427.9Standard polar33892256
2-Mercaptoacetamide,3TMS,isomer #1C[Si](C)(C)SCC(=O)N([Si](C)(C)C)[Si](C)(C)C1486.3Semi standard non polar33892256
2-Mercaptoacetamide,3TMS,isomer #1C[Si](C)(C)SCC(=O)N([Si](C)(C)C)[Si](C)(C)C1435.5Standard non polar33892256
2-Mercaptoacetamide,3TMS,isomer #1C[Si](C)(C)SCC(=O)N([Si](C)(C)C)[Si](C)(C)C1423.8Standard polar33892256
2-Mercaptoacetamide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)SCC(N)=O1449.1Semi standard non polar33892256
2-Mercaptoacetamide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)SCC(N)=O1450.3Standard non polar33892256
2-Mercaptoacetamide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)SCC(N)=O1987.1Standard polar33892256
2-Mercaptoacetamide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)CS1372.1Semi standard non polar33892256
2-Mercaptoacetamide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)CS1322.1Standard non polar33892256
2-Mercaptoacetamide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)CS1655.7Standard polar33892256
2-Mercaptoacetamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)CS[Si](C)(C)C(C)(C)C1774.1Semi standard non polar33892256
2-Mercaptoacetamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)CS[Si](C)(C)C(C)(C)C1730.7Standard non polar33892256
2-Mercaptoacetamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)CS[Si](C)(C)C(C)(C)C1706.8Standard polar33892256
2-Mercaptoacetamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(C(=O)CS)[Si](C)(C)C(C)(C)C1749.1Semi standard non polar33892256
2-Mercaptoacetamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(C(=O)CS)[Si](C)(C)C(C)(C)C1715.2Standard non polar33892256
2-Mercaptoacetamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(C(=O)CS)[Si](C)(C)C(C)(C)C1618.4Standard polar33892256
2-Mercaptoacetamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)SCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2119.6Semi standard non polar33892256
2-Mercaptoacetamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)SCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2052.5Standard non polar33892256
2-Mercaptoacetamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)SCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1805.9Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 2-Mercaptoacetamide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-9000000000-858e6c89f1d47e241dbd2021-09-23Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Mercaptoacetamide 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 - 2-Mercaptoacetamide 10V, Positive-QTOFsplash10-00dl-9000000000-911e1dd52d4c75ce02072021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Mercaptoacetamide 20V, Positive-QTOFsplash10-00di-9000000000-4857af2b0c7e195f383f2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Mercaptoacetamide 40V, Positive-QTOFsplash10-0002-9000000000-c729dcdea9c1486802ca2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Mercaptoacetamide 10V, Negative-QTOFsplash10-0006-9000000000-1685c59701a4dd7cc70b2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Mercaptoacetamide 20V, Negative-QTOFsplash10-0006-9000000000-2f1917d0d32a87f478502021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Mercaptoacetamide 40V, Negative-QTOFsplash10-0006-9000000000-90726b17dc36e29c52992021-10-12Wishart 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 ID12421
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound12961
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 ]