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Showing metabocard for (1E)-1-Phenyltriaz-1-ene (HMDB0242314)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-08-29 15:57:53 UTC
Update Date2021-09-26 22:48:55 UTC
HMDB IDHMDB0242314
Secondary Accession NumbersNone
Metabolite Identification
Common Name(1E)-1-Phenyltriaz-1-ene
Description(1E)-1-Phenyltriaz-1-ene belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. Based on a literature review very few articles have been published on (1E)-1-Phenyltriaz-1-ene. This compound has been identified in human blood as reported by (PMID: 31557052 ). (1e)-1-phenyltriaz-1-ene is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (1E)-1-Phenyltriaz-1-ene 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 HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)


  Mrv1652308292118072D          

  9  9  0  0  0  0            999 V2000
    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
    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    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 N   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
  4  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  4  0  0  0
M  END
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3D MOL for HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)

HMDB0242314
     RDKit          3D
(1E)-1-Phenyltriaz-1-ene
 16 16  0  0  0  0  0  0  0  0999 V2000
    3.6494   -0.1110   -0.5334 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3161    0.1649   -0.1946 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3874   -0.6145   -0.5528 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0656   -0.2835   -0.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802   -1.2727    0.2420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0912   -0.9567    0.6119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4974    0.3598    0.5373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6273    1.3486    0.1058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3374    1.0224   -0.2558 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9271   -1.0358   -0.8873 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3875    0.6180   -0.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4876   -2.3284    0.3124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7835   -1.7167    0.9511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5069    0.6217    0.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9782    2.3775    0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3565    1.8064   -0.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9  4  1  0
  1 10  1  0
  1 11  1  0
  5 12  1  0
  6 13  1  0
  7 14  1  0
  8 15  1  0
  9 16  1  0
M  END
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3D SDF for HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)


  Mrv1652308292118072D          

  9  9  0  0  0  0            999 V2000
    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
    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    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 N   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
  4  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  4  0  0  0
M  END
> <DATABASE_ID>
HMDB0242314

> <DATABASE_NAME>
hmdb

> <SMILES>
NN=NC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C6H7N3/c7-9-8-6-4-2-1-3-5-6/h1-5H,(H2,7,8)

> <INCHI_KEY>
FMTRXPVVZQQIKN-UHFFFAOYSA-N

> <FORMULA>
C6H7N3

> <MOLECULAR_WEIGHT>
121.143

> <EXACT_MASS>
121.063997237

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
16

> <JCHEM_AVERAGE_POLARIZABILITY>
12.624443074569841

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-phenyltriaz-1-ene

> <ALOGPS_LOGP>
1.74

> <JCHEM_LOGP>
2.0414473006666665

> <ALOGPS_LOGS>
-1.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.685488783678647

> <JCHEM_PKA_STRONGEST_BASIC>
0.6433054282919272

> <JCHEM_POLAR_SURFACE_AREA>
50.739999999999995

> <JCHEM_REFRACTIVITY>
40.1868

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.84e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-phenyltriaz-1-ene

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)

HMDB0242314
     RDKit          3D
(1E)-1-Phenyltriaz-1-ene
 16 16  0  0  0  0  0  0  0  0999 V2000
    3.6494   -0.1110   -0.5334 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3161    0.1649   -0.1946 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3874   -0.6145   -0.5528 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0656   -0.2835   -0.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802   -1.2727    0.2420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0912   -0.9567    0.6119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4974    0.3598    0.5373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6273    1.3486    0.1058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3374    1.0224   -0.2558 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9271   -1.0358   -0.8873 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3875    0.6180   -0.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4876   -2.3284    0.3124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7835   -1.7167    0.9511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5069    0.6217    0.8192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9782    2.3775    0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3565    1.8064   -0.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9  4  1  0
  1 10  1  0
  1 11  1  0
  5 12  1  0
  6 13  1  0
  7 14  1  0
  8 15  1  0
  9 16  1  0
M  END
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PDB for HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)

HEADER    PROTEIN                                 29-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-AUG-21         0                                  
HETATM    1  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -0.000   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  N   UNK     0       2.667   4.620   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0       2.667   6.160   0.000  0.00  0.00           N+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8                                                            
MASTER        0    0    0    0    0    0    0    0    9    0   18    0
END
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3D PDB for HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)

COMPND    HMDB0242314
HETATM    1  N1  UNL     1       3.649  -0.111  -0.533  1.00  0.00           N  
HETATM    2  N2  UNL     1       2.316   0.165  -0.195  1.00  0.00           N  
HETATM    3  N3  UNL     1       1.387  -0.615  -0.553  1.00  0.00           N  
HETATM    4  C1  UNL     1       0.066  -0.284  -0.182  1.00  0.00           C  
HETATM    5  C2  UNL     1      -0.780  -1.273   0.242  1.00  0.00           C  
HETATM    6  C3  UNL     1      -2.091  -0.957   0.612  1.00  0.00           C  
HETATM    7  C4  UNL     1      -2.497   0.360   0.537  1.00  0.00           C  
HETATM    8  C5  UNL     1      -1.627   1.349   0.106  1.00  0.00           C  
HETATM    9  C6  UNL     1      -0.337   1.022  -0.256  1.00  0.00           C  
HETATM   10  H1  UNL     1       3.927  -1.036  -0.887  1.00  0.00           H  
HETATM   11  H2  UNL     1       4.388   0.618  -0.433  1.00  0.00           H  
HETATM   12  H3  UNL     1      -0.488  -2.328   0.312  1.00  0.00           H  
HETATM   13  H4  UNL     1      -2.784  -1.717   0.951  1.00  0.00           H  
HETATM   14  H5  UNL     1      -3.507   0.622   0.819  1.00  0.00           H  
HETATM   15  H6  UNL     1      -1.978   2.378   0.058  1.00  0.00           H  
HETATM   16  H7  UNL     1       0.357   1.806  -0.599  1.00  0.00           H  
CONECT    1    2   10   11
CONECT    2    3    3
CONECT    3    4
CONECT    4    5    5    9
CONECT    5    6   12
CONECT    6    7    7   13
CONECT    7    8   14
CONECT    8    9    9   15
CONECT    9   16
END
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SMILES for HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)

NN=NC1=CC=CC=C1
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INCHI for HMDB0242314 ((1E)-1-Phenyltriaz-1-ene)

InChI=1S/C6H7N3/c7-9-8-6-4-2-1-3-5-6/h1-5H,(H2,7,8)
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View in JSmolView NMR AssignmentsView Stereo Labels
SynonymsNot Available
Chemical FormulaC6H7N3
Average Molecular Weight121.143
Monoisotopic Molecular Weight121.063997237
IUPAC Name1-phenyltriaz-1-ene
Traditional Name1-phenyltriaz-1-ene
CAS Registry NumberNot Available
SMILES
NN=NC1=CC=CC=C1
InChI Identifier
InChI=1S/C6H7N3/c7-9-8-6-4-2-1-3-5-6/h1-5H,(H2,7,8)
InChI KeyFMTRXPVVZQQIKN-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassNot Available
Direct ParentBenzene and substituted derivatives
Alternative Parents
Substituents
  • Monocyclic benzene moiety
  • Organic 1,3-dipolar compound
  • Propargyl-type 1,3-dipolar organic compound
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Organonitrogen compound
  • 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
logP1.74ALOGPS
logP2.04ChemAxon
logS-1.8ALOGPS
pKa (Strongest Acidic)19.69ChemAxon
pKa (Strongest Basic)0.64ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area50.74 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity40.19 m³·mol⁻¹ChemAxon
Polarizability12.62 ųChemAxon
Number of Rings1ChemAxon
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]+123.8830932474
DeepCCS[M-H]-121.06230932474
DeepCCS[M-2H]-157.69830932474
DeepCCS[M+Na]+132.51730932474
AllCCS[M+H]+125.332859911
AllCCS[M+H-H2O]+120.532859911
AllCCS[M+NH4]+129.832859911
AllCCS[M+Na]+131.132859911
AllCCS[M-H]-121.032859911
AllCCS[M+Na-2H]-123.032859911
AllCCS[M+HCOO]-125.332859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 202211.3628 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20222.78 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid1438.8 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid408.9 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid116.1 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid252.5 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid126.4 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid359.0 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 Acid438.1 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)114.1 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid877.7 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid307.1 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid1002.7 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid257.0 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid347.7 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate424.5 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA199.4 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water114.2 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(1E)-1-Phenyltriaz-1-eneNN=NC1=CC=CC=C11899.4Standard polar33892256
(1E)-1-Phenyltriaz-1-eneNN=NC1=CC=CC=C11197.6Standard non polar33892256
(1E)-1-Phenyltriaz-1-eneNN=NC1=CC=CC=C11364.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(1E)-1-Phenyltriaz-1-ene,1TMS,isomer #1C[Si](C)(C)NN=NC1=CC=CC=C11429.0Semi standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,1TMS,isomer #1C[Si](C)(C)NN=NC1=CC=CC=C11447.7Standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,1TMS,isomer #1C[Si](C)(C)NN=NC1=CC=CC=C12081.9Standard polar33892256
(1E)-1-Phenyltriaz-1-ene,2TMS,isomer #1C[Si](C)(C)N(N=NC1=CC=CC=C1)[Si](C)(C)C1474.4Semi standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,2TMS,isomer #1C[Si](C)(C)N(N=NC1=CC=CC=C1)[Si](C)(C)C1614.1Standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,2TMS,isomer #1C[Si](C)(C)N(N=NC1=CC=CC=C1)[Si](C)(C)C2057.1Standard polar33892256
(1E)-1-Phenyltriaz-1-ene,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NN=NC1=CC=CC=C11609.4Semi standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NN=NC1=CC=CC=C11590.0Standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NN=NC1=CC=CC=C12156.3Standard polar33892256
(1E)-1-Phenyltriaz-1-ene,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(N=NC1=CC=CC=C1)[Si](C)(C)C(C)(C)C1857.5Semi standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(N=NC1=CC=CC=C1)[Si](C)(C)C(C)(C)C1955.4Standard non polar33892256
(1E)-1-Phenyltriaz-1-ene,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)N(N=NC1=CC=CC=C1)[Si](C)(C)C(C)(C)C2164.7Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (1E)-1-Phenyltriaz-1-ene GC-MS (Non-derivatized) - 70eV, Positivesplash10-0096-9200000000-ad34710399235e3600642021-09-23Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1E)-1-Phenyltriaz-1-ene 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 - (1E)-1-Phenyltriaz-1-ene 10V, Positive-QTOFsplash10-05fr-0900000000-85dd120acdbfe0aba71e2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1E)-1-Phenyltriaz-1-ene 20V, Positive-QTOFsplash10-0a4i-1900000000-44b3bbe0aeddc42256d12021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1E)-1-Phenyltriaz-1-ene 40V, Positive-QTOFsplash10-00or-9000000000-0022baa0fa20cf4127bc2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1E)-1-Phenyltriaz-1-ene 10V, Negative-QTOFsplash10-00dl-5900000000-8c4b36de49d6cf8bdcb32021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1E)-1-Phenyltriaz-1-ene 20V, Negative-QTOFsplash10-006x-9500000000-be5613773bff58c00fea2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1E)-1-Phenyltriaz-1-ene 40V, Negative-QTOFsplash10-0006-9000000000-eef4c1f804c025cbb9782021-10-12Wishart 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 ID10302726
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound18388301
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 ]