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Showing metabocard for 4-Aminothiophenol (HMDB0246365)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-10 23:23:27 UTC
Update Date2021-09-26 22:55:24 UTC
HMDB IDHMDB0246365
Secondary Accession NumbersNone
Metabolite Identification
Common Name4-Aminothiophenol
Description4-Aminothiophenol, also known as 6976-04-1 (na salt) or p-mercaptoaniline, belongs to the class of organic compounds known as thiophenols. Thiophenols are compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom. Based on a literature review a significant number of articles have been published on 4-Aminothiophenol. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4-aminothiophenol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4-Aminothiophenol 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 HMDB0246365 (4-Aminothiophenol)


  Mrv1652309112101232D          

  8  8  0  0  0  0            999 V2000
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  3  8  1  0  0  0  0
M  END
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3D MOL for HMDB0246365 (4-Aminothiophenol)

HMDB0246365
     RDKit          3D
4-Aminothiophenol
 15 15  0  0  0  0  0  0  0  0999 V2000
   -2.6522   -0.1345    0.1076 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2381   -0.0604   -0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4874   -1.0414   -0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8932   -0.9240   -0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5737    0.1517   -0.1808 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3522    0.3175   -0.2771 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273    1.1328    0.4417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5536    1.0164    0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2050    0.7151   -0.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1804   -0.9778    0.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0018   -1.9034   -1.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4805   -1.6916   -1.1923 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9701   -0.3972    0.7928 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3461    1.9973    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1247    1.7996    1.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  8  2  1  0
  1  9  1  0
  1 10  1  0
  3 11  1  0
  4 12  1  0
  6 13  1  0
  7 14  1  0
  8 15  1  0
M  END
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3D SDF for HMDB0246365 (4-Aminothiophenol)


  Mrv1652309112101232D          

  8  8  0  0  0  0            999 V2000
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  3  8  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0246365

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=CC=C(S)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C6H7NS/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2

> <INCHI_KEY>
WCDSVWRUXWCYFN-UHFFFAOYSA-N

> <FORMULA>
C6H7NS

> <MOLECULAR_WEIGHT>
125.19

> <EXACT_MASS>
125.029920403

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
13.398611224427498

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-aminobenzene-1-thiol

> <ALOGPS_LOGP>
1.57

> <JCHEM_LOGP>
1.2375270416666666

> <ALOGPS_LOGS>
-1.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.8634940764075525

> <JCHEM_PKA_STRONGEST_BASIC>
4.817023705350993

> <JCHEM_POLAR_SURFACE_AREA>
26.02

> <JCHEM_REFRACTIVITY>
38.7682

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.81e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-aminobenzenethiol

> <JCHEM_VEBER_RULE>
1

$$$$
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3D-SDF for HMDB0246365 (4-Aminothiophenol)

HMDB0246365
     RDKit          3D
4-Aminothiophenol
 15 15  0  0  0  0  0  0  0  0999 V2000
   -2.6522   -0.1345    0.1076 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2381   -0.0604   -0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4874   -1.0414   -0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8932   -0.9240   -0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5737    0.1517   -0.1808 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3522    0.3175   -0.2771 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273    1.1328    0.4417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5536    1.0164    0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2050    0.7151   -0.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1804   -0.9778    0.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0018   -1.9034   -1.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4805   -1.6916   -1.1923 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9701   -0.3972    0.7928 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3461    1.9973    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1247    1.7996    1.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  8  2  1  0
  1  9  1  0
  1 10  1  0
  3 11  1  0
  4 12  1  0
  6 13  1  0
  7 14  1  0
  8 15  1  0
M  END
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PDB for HMDB0246365 (4-Aminothiophenol)

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       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       1.334   3.850   0.000  0.00  0.00           N+0
HETATM    8  S   UNK     0       1.334  -2.310   0.000  0.00  0.00           S+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    3                                                            
MASTER        0    0    0    0    0    0    0    0    8    0   16    0
END
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3D PDB for HMDB0246365 (4-Aminothiophenol)

COMPND    HMDB0246365
HETATM    1  N1  UNL     1      -2.652  -0.134   0.108  1.00  0.00           N  
HETATM    2  C1  UNL     1      -1.238  -0.060  -0.001  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.487  -1.041  -0.624  1.00  0.00           C  
HETATM    4  C3  UNL     1       0.893  -0.924  -0.705  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.574   0.152  -0.181  1.00  0.00           C  
HETATM    6  S1  UNL     1       3.352   0.317  -0.277  1.00  0.00           S  
HETATM    7  C5  UNL     1       0.827   1.133   0.442  1.00  0.00           C  
HETATM    8  C6  UNL     1      -0.554   1.016   0.523  1.00  0.00           C  
HETATM    9  H1  UNL     1      -3.205   0.715  -0.129  1.00  0.00           H  
HETATM   10  H2  UNL     1      -3.180  -0.978   0.407  1.00  0.00           H  
HETATM   11  H3  UNL     1      -1.002  -1.903  -1.047  1.00  0.00           H  
HETATM   12  H4  UNL     1       1.480  -1.692  -1.192  1.00  0.00           H  
HETATM   13  H5  UNL     1       3.970  -0.397   0.793  1.00  0.00           H  
HETATM   14  H6  UNL     1       1.346   1.997   0.866  1.00  0.00           H  
HETATM   15  H7  UNL     1      -1.125   1.800   1.018  1.00  0.00           H  
CONECT    1    2    9   10
CONECT    2    3    3    8
CONECT    3    4   11
CONECT    4    5    5   12
CONECT    5    6    7
CONECT    6   13
CONECT    7    8    8   14
CONECT    8   15
END
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SMILES for HMDB0246365 (4-Aminothiophenol)

NC1=CC=C(S)C=C1
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INCHI for HMDB0246365 (4-Aminothiophenol)

InChI=1S/C6H7NS/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
6976-04-1 (Na salt)HMDB
p-AminothiophenolHMDB
p-MercaptoanilineHMDB
Chemical FormulaC6H7NS
Average Molecular Weight125.19
Monoisotopic Molecular Weight125.029920403
IUPAC Name4-aminobenzene-1-thiol
Traditional Name4-aminobenzenethiol
CAS Registry NumberNot Available
SMILES
NC1=CC=C(S)C=C1
InChI Identifier
InChI=1S/C6H7NS/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2
InChI KeyWCDSVWRUXWCYFN-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as thiophenols. Thiophenols are compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom.
KingdomOrganic compounds
Super ClassBenzenoids
ClassThiophenols
Sub ClassNot Available
Direct ParentThiophenols
Alternative Parents
Substituents
  • Aniline or substituted anilines
  • Thiophenol
  • Monocyclic benzene moiety
  • Arylthiol
  • Organic nitrogen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Primary amine
  • Organosulfur compound
  • Organonitrogen compound
  • Amine
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic 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
logP1.57ALOGPS
logP1.24ChemAxon
logS-1.6ALOGPS
pKa (Strongest Acidic)6.86ChemAxon
pKa (Strongest Basic)4.82ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area26.02 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity38.77 m³·mol⁻¹ChemAxon
Polarizability13.4 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+126.21330932474
DeepCCS[M-H]-122.77330932474
DeepCCS[M-2H]-159.63130932474
DeepCCS[M+Na]+134.8130932474
AllCCS[M+H]+125.532859911
AllCCS[M+H-H2O]+120.632859911
AllCCS[M+NH4]+129.932859911
AllCCS[M+Na]+131.232859911
AllCCS[M-H]-122.932859911
AllCCS[M+Na-2H]-125.532859911
AllCCS[M+HCOO]-128.432859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 20229.9153 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20222.0 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid1017.6 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid350.7 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid91.4 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid223.8 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid64.9 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid254.6 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 Acid301.1 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)122.4 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid742.4 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid190.9 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid826.7 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid227.2 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid268.0 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate441.2 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA254.1 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water170.4 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
4-AminothiophenolNC1=CC=C(S)C=C12472.2Standard polar33892256
4-AminothiophenolNC1=CC=C(S)C=C11297.6Standard non polar33892256
4-AminothiophenolNC1=CC=C(S)C=C11321.6Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
4-Aminothiophenol,1TMS,isomer #1C[Si](C)(C)SC1=CC=C(N)C=C11547.8Semi standard non polar33892256
4-Aminothiophenol,1TMS,isomer #1C[Si](C)(C)SC1=CC=C(N)C=C11537.8Standard non polar33892256
4-Aminothiophenol,1TMS,isomer #1C[Si](C)(C)SC1=CC=C(N)C=C12026.1Standard polar33892256
4-Aminothiophenol,1TMS,isomer #2C[Si](C)(C)NC1=CC=C(S)C=C11643.9Semi standard non polar33892256
4-Aminothiophenol,1TMS,isomer #2C[Si](C)(C)NC1=CC=C(S)C=C11553.0Standard non polar33892256
4-Aminothiophenol,1TMS,isomer #2C[Si](C)(C)NC1=CC=C(S)C=C11640.8Standard polar33892256
4-Aminothiophenol,2TMS,isomer #1C[Si](C)(C)NC1=CC=C(S[Si](C)(C)C)C=C11743.7Semi standard non polar33892256
4-Aminothiophenol,2TMS,isomer #1C[Si](C)(C)NC1=CC=C(S[Si](C)(C)C)C=C11645.6Standard non polar33892256
4-Aminothiophenol,2TMS,isomer #1C[Si](C)(C)NC1=CC=C(S[Si](C)(C)C)C=C11657.7Standard polar33892256
4-Aminothiophenol,2TMS,isomer #2C[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C1674.9Semi standard non polar33892256
4-Aminothiophenol,2TMS,isomer #2C[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C1698.4Standard non polar33892256
4-Aminothiophenol,2TMS,isomer #2C[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C1651.5Standard polar33892256
4-Aminothiophenol,3TMS,isomer #1C[Si](C)(C)SC1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C11763.9Semi standard non polar33892256
4-Aminothiophenol,3TMS,isomer #1C[Si](C)(C)SC1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C11755.8Standard non polar33892256
4-Aminothiophenol,3TMS,isomer #1C[Si](C)(C)SC1=CC=C(N([Si](C)(C)C)[Si](C)(C)C)C=C11611.4Standard polar33892256
4-Aminothiophenol,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)SC1=CC=C(N)C=C11782.4Semi standard non polar33892256
4-Aminothiophenol,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)SC1=CC=C(N)C=C11763.7Standard non polar33892256
4-Aminothiophenol,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)SC1=CC=C(N)C=C12156.0Standard polar33892256
4-Aminothiophenol,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(S)C=C11837.5Semi standard non polar33892256
4-Aminothiophenol,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(S)C=C11754.8Standard non polar33892256
4-Aminothiophenol,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC1=CC=C(S)C=C11799.1Standard polar33892256
4-Aminothiophenol,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=CC=C(S[Si](C)(C)C(C)(C)C)C=C12255.5Semi standard non polar33892256
4-Aminothiophenol,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=CC=C(S[Si](C)(C)C(C)(C)C)C=C12076.3Standard non polar33892256
4-Aminothiophenol,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC1=CC=C(S[Si](C)(C)C(C)(C)C)C=C11951.0Standard polar33892256
4-Aminothiophenol,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C(C)(C)C2082.1Semi standard non polar33892256
4-Aminothiophenol,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C(C)(C)C2121.7Standard non polar33892256
4-Aminothiophenol,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N(C1=CC=C(S)C=C1)[Si](C)(C)C(C)(C)C1880.2Standard polar33892256
4-Aminothiophenol,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)SC1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12468.7Semi standard non polar33892256
4-Aminothiophenol,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)SC1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12342.0Standard non polar33892256
4-Aminothiophenol,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)SC1=CC=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C12017.8Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 4-Aminothiophenol GC-MS (Non-derivatized) - 70eV, Positivesplash10-004i-8900000000-adbcfaebcaf51234928a2021-09-24Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 4-Aminothiophenol 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 - 4-Aminothiophenol 10V, Positive-QTOFsplash10-004i-0900000000-982c1029cfb7ba6c6d732021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminothiophenol 20V, Positive-QTOFsplash10-004i-1900000000-e7d08716dbe5d10580112021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminothiophenol 40V, Positive-QTOFsplash10-0159-9000000000-e1c2e07562715e7c08042021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminothiophenol 10V, Negative-QTOFsplash10-00di-0900000000-0b3c38cc956ef5ade3792021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminothiophenol 20V, Negative-QTOFsplash10-00di-0900000000-0b3c38cc956ef5ade3792021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 4-Aminothiophenol 40V, Negative-QTOFsplash10-0ab9-9300000000-e2420bc4834274553d5e2021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart 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 ID13854
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkAminothiophenol
METLIN IDNot Available
PubChem Compound14510
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 ]