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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 21:46:12 UTC

Update Date

2022-11-23 22:29:21 UTC

HMDB ID

HMDB0259263

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Triphenylethylene

Description

(1,2-diphenylethenyl)benzene belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. Based on a literature review very few articles have been published on (1,2-diphenylethenyl)benzene. This compound has been identified in human blood as reported by (PMID: 31557052 ). Triphenylethylene is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Triphenylethylene 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

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0259263
     RDKit          3D
TRIPHENYLETHYLENE
 36 38  0  0  0  0  0  0  0  0999 V2000
    0.9955    0.8862    0.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.6109    0.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7163   -0.7426   -0.1814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8640   -0.9955   -0.9240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3527   -2.2668   -1.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7234   -3.3528   -0.5022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6059   -3.1494    0.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1215   -1.8455    0.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2496    1.6825    0.1345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    3.0233   -0.0523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    4.0346    0.0918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1810    3.7428    0.4380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5123    2.4344    0.6266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5583    1.4283    0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1548    0.0101    0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1400    0.0087    1.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2656   -0.7765    1.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4531   -1.5882   -0.0897 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5092   -1.6096   -1.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3726   -0.8134   -0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2368    1.9614    0.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3683   -0.1636   -1.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2537   -2.4943   -1.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1226   -4.3667   -0.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0884   -3.9738    0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7581   -1.7074    1.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    3.2791   -0.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6102    5.0728   -0.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8746    4.5731    0.5371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5170    2.1711    0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8651    0.4080    0.6827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664    0.6478    1.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0320   -0.7860    1.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3352   -2.2250   -0.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6835   -2.2582   -1.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6509   -0.8597   -1.7621 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  2  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  1 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
  8  3  1  0
 14  9  1  0
 20 15  1  0
  1 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END

  Mrv1572004221603122D          

 20 22  0  0  0  0            999 V2000
    1.4289    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  2  0  0  0  0
  5  1  1  0  0  0  0
  6  2  2  0  0  0  0
  7  2  1  0  0  0  0
  8  3  2  0  0  0  0
  9  3  1  0  0  0  0
 10  4  1  0  0  0  0
 11  5  2  0  0  0  0
 12  6  1  0  0  0  0
 13  7  2  0  0  0  0
 14  8  1  0  0  0  0
 15  9  2  0  0  0  0
 17 10  2  0  0  0  0
 17 11  1  0  0  0  0
 17 16  1  0  0  0  0
 18 12  2  0  0  0  0
 18 13  1  0  0  0  0
 19 14  2  0  0  0  0
 19 15  1  0  0  0  0
 20 16  2  0  0  0  0
 20 18  1  0  0  0  0
 20 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0259263

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C20H16/c1-4-10-17(11-5-1)16-20(18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-16H

> <INCHI_KEY>
MKYQPGPNVYRMHI-UHFFFAOYSA-N

> <FORMULA>
C20H16

> <MOLECULAR_WEIGHT>
256.348

> <EXACT_MASS>
256.125200515

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
30.983868809112813

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1,2-diphenylethenyl)benzene

> <ALOGPS_LOGP>
5.50

> <JCHEM_LOGP>
5.746285428999999

> <ALOGPS_LOGS>
-5.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
95.06550000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.88e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
triphenylethylene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0259263
     RDKit          3D
TRIPHENYLETHYLENE
 36 38  0  0  0  0  0  0  0  0999 V2000
    0.9955    0.8862    0.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.6109    0.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7163   -0.7426   -0.1814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8640   -0.9955   -0.9240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3527   -2.2668   -1.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7234   -3.3528   -0.5022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6059   -3.1494    0.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1215   -1.8455    0.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2496    1.6825    0.1345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    3.0233   -0.0523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    4.0346    0.0918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1810    3.7428    0.4380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5123    2.4344    0.6266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5583    1.4283    0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1548    0.0101    0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1400    0.0087    1.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2656   -0.7765    1.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4531   -1.5882   -0.0897 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5092   -1.6096   -1.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3726   -0.8134   -0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2368    1.9614    0.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3683   -0.1636   -1.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2537   -2.4943   -1.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1226   -4.3667   -0.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0884   -3.9738    0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7581   -1.7074    1.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    3.2791   -0.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6102    5.0728   -0.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8746    4.5731    0.5371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5170    2.1711    0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8651    0.4080    0.6827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664    0.6478    1.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0320   -0.7860    1.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3352   -2.2250   -0.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6835   -2.2582   -1.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6509   -0.8597   -1.7621 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  2  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  1 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
  8  3  1  0
 14  9  1  0
 20 15  1  0
  1 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END

HEADER    PROTEIN                                 22-APR-16   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-APR-16         0                                  
HETATM    1  C   UNK     0       2.667  13.860   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002  10.780   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  13.090   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  13.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  11.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  11.550   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  10.780   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  10.780   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001   8.470   0.000  0.00  0.00           C+0
CONECT    1    4    5                                                       
CONECT    2    6    7                                                       
CONECT    3    8    9                                                       
CONECT    4    1   10                                                       
CONECT    5    1   11                                                       
CONECT    6    2   12                                                       
CONECT    7    2   13                                                       
CONECT    8    3   14                                                       
CONECT    9    3   15                                                       
CONECT   10    4   17                                                       
CONECT   11    5   17                                                       
CONECT   12    6   18                                                       
CONECT   13    7   18                                                       
CONECT   14    8   19                                                       
CONECT   15    9   19                                                       
CONECT   16   17   20                                                       
CONECT   17   10   11   16                                                  
CONECT   18   12   13   20                                                  
CONECT   19   14   15   20                                                  
CONECT   20   16   18   19                                                  
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

COMPND    HMDB0259263
HETATM    1  C1  UNL     1       0.996   0.886   0.204  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.262   0.611   0.071  1.00  0.00           C  
HETATM    3  C3  UNL     1      -0.716  -0.743  -0.181  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.864  -0.996  -0.924  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.353  -2.267  -1.078  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.723  -3.353  -0.502  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.606  -3.149   0.227  1.00  0.00           C  
HETATM    8  C8  UNL     1      -0.122  -1.845   0.376  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.250   1.683   0.134  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.935   3.023  -0.052  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.860   4.035   0.092  1.00  0.00           C  
HETATM   12  C12 UNL     1      -3.181   3.743   0.438  1.00  0.00           C  
HETATM   13  C13 UNL     1      -3.512   2.434   0.627  1.00  0.00           C  
HETATM   14  C14 UNL     1      -2.558   1.428   0.477  1.00  0.00           C  
HETATM   15  C15 UNL     1       2.155   0.010   0.128  1.00  0.00           C  
HETATM   16  C16 UNL     1       3.140   0.009   1.123  1.00  0.00           C  
HETATM   17  C17 UNL     1       4.266  -0.777   1.014  1.00  0.00           C  
HETATM   18  C18 UNL     1       4.453  -1.588  -0.090  1.00  0.00           C  
HETATM   19  C19 UNL     1       3.509  -1.610  -1.081  1.00  0.00           C  
HETATM   20  C20 UNL     1       2.373  -0.813  -0.963  1.00  0.00           C  
HETATM   21  H1  UNL     1       1.237   1.961   0.426  1.00  0.00           H  
HETATM   22  H2  UNL     1      -2.368  -0.164  -1.421  1.00  0.00           H  
HETATM   23  H3  UNL     1      -3.254  -2.494  -1.656  1.00  0.00           H  
HETATM   24  H4  UNL     1      -2.123  -4.367  -0.632  1.00  0.00           H  
HETATM   25  H5  UNL     1      -0.088  -3.974   0.689  1.00  0.00           H  
HETATM   26  H6  UNL     1       0.758  -1.707   1.013  1.00  0.00           H  
HETATM   27  H7  UNL     1       0.088   3.279  -0.338  1.00  0.00           H  
HETATM   28  H8  UNL     1      -1.610   5.073  -0.055  1.00  0.00           H  
HETATM   29  H9  UNL     1      -3.875   4.573   0.537  1.00  0.00           H  
HETATM   30  H10 UNL     1      -4.517   2.171   0.893  1.00  0.00           H  
HETATM   31  H11 UNL     1      -2.865   0.408   0.683  1.00  0.00           H  
HETATM   32  H12 UNL     1       2.966   0.648   1.969  1.00  0.00           H  
HETATM   33  H13 UNL     1       5.032  -0.786   1.770  1.00  0.00           H  
HETATM   34  H14 UNL     1       5.335  -2.225  -0.211  1.00  0.00           H  
HETATM   35  H15 UNL     1       3.683  -2.258  -1.942  1.00  0.00           H  
HETATM   36  H16 UNL     1       1.651  -0.860  -1.762  1.00  0.00           H  
CONECT    1    2    2   15   21
CONECT    2    3    9
CONECT    3    4    4    8
CONECT    4    5   22
CONECT    5    6    6   23
CONECT    6    7   24
CONECT    7    8    8   25
CONECT    8   26
CONECT    9   10   10   14
CONECT   10   11   27
CONECT   11   12   12   28
CONECT   12   13   29
CONECT   13   14   14   30
CONECT   14   31
CONECT   15   16   16   20
CONECT   16   17   32
CONECT   17   18   18   33
CONECT   18   19   34
CONECT   19   20   20   35
CONECT   20   36
END

HMDB0259263
     RDKit          3D
TRIPHENYLETHYLENE
 36 38  0  0  0  0  0  0  0  0999 V2000
    0.9955    0.8862    0.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.6109    0.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7163   -0.7426   -0.1814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8640   -0.9955   -0.9240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3527   -2.2668   -1.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7234   -3.3528   -0.5022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6059   -3.1494    0.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1215   -1.8455    0.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2496    1.6825    0.1345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    3.0233   -0.0523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    4.0346    0.0918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1810    3.7428    0.4380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5123    2.4344    0.6266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5583    1.4283    0.4771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1548    0.0101    0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1400    0.0087    1.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2656   -0.7765    1.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4531   -1.5882   -0.0897 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5092   -1.6096   -1.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3726   -0.8134   -0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2368    1.9614    0.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3683   -0.1636   -1.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2537   -2.4943   -1.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1226   -4.3667   -0.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0884   -3.9738    0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7581   -1.7074    1.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    3.2791   -0.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6102    5.0728   -0.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8746    4.5731    0.5371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5170    2.1711    0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8651    0.4080    0.6827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664    0.6478    1.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0320   -0.7860    1.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3352   -2.2250   -0.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6835   -2.2582   -1.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6509   -0.8597   -1.7621 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  2  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  1 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
  8  3  1  0
 14  9  1  0
 20 15  1  0
  1 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  7 25  1  0
  8 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 16 32  1  0
 17 33  1  0
 18 34  1  0
 19 35  1  0
 20 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆

Average Molecular Weight

256.348

Monoisotopic Molecular Weight

256.125200515

IUPAC Name

(1,2-diphenylethenyl)benzene

Traditional Name

triphenylethylene

CAS Registry Number

Not Available

SMILES

C(=C(C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C20H16/c1-4-10-17(11-5-1)16-20(18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-16H

InChI Key

MKYQPGPNVYRMHI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Diphenylmethane
Styrene
Benzenoid
Monocyclic benzene moiety
Aromatic hydrocarbon
Branched unsaturated hydrocarbon
Cyclic olefin
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

stilbenoid (CHEBI:35034 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	5.5	ALOGPS
logP	5.75	ChemAxon
logS	-6	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.07 m³·mol⁻¹	ChemAxon
Polarizability	30.98 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	159.195	30932474
DeepCCS	[M-H]-	156.837	30932474
DeepCCS	[M-2H]-	189.723	30932474
DeepCCS	[M+Na]+	165.288	30932474
AllCCS	[M+H]+	160.2	32859911
AllCCS	[M+H-H2O]+	156.2	32859911
AllCCS	[M+NH4]+	163.9	32859911
AllCCS	[M+Na]+	165.0	32859911
AllCCS	[M-H]-	163.0	32859911
AllCCS	[M+Na-2H]-	161.8	32859911
AllCCS	[M+HCOO]-	160.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
TRIPHENYLETHYLENE	C(=C(C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1	3129.1	Standard polar	33892256
TRIPHENYLETHYLENE	C(=C(C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1	2083.9	Standard non polar	33892256
TRIPHENYLETHYLENE	C(=C(C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1	2199.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Triphenylethylene GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-0190000000-716fc8cdae3c1a34a360	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Triphenylethylene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Triphenylethylene 10V, Positive-QTOF	splash10-0a4i-1190000000-b4b8d3fb15a0c39f79c2	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Triphenylethylene 20V, Positive-QTOF	splash10-0a4i-2690000000-a4e3ed49f892a2cf3c8d	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Triphenylethylene 40V, Positive-QTOF	splash10-014i-3910000000-f0d39107cead0e580266	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Triphenylethylene 10V, Negative-QTOF	splash10-0a4i-0090000000-b0fda579f41844220f60	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Triphenylethylene 20V, Negative-QTOF	splash10-0a4i-0090000000-6cc20f81dbb35f3ce43f	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Triphenylethylene 40V, Negative-QTOF	splash10-0570-7690000000-31e51707481c4f544171	2016-08-03	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

5803

KEGG Compound ID

C14134

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1540141

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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 ]

Showing metabocard for Triphenylethylene (HMDB0259263)

MOL for HMDB0259263 (Triphenylethylene)

3D MOL for HMDB0259263 (Triphenylethylene)

3D SDF for HMDB0259263 (Triphenylethylene)

3D-SDF for HMDB0259263 (Triphenylethylene)

PDB for HMDB0259263 (Triphenylethylene)

3D PDB for HMDB0259263 (Triphenylethylene)

SMILES for HMDB0259263 (Triphenylethylene)

INCHI for HMDB0259263 (Triphenylethylene)

Structure for HMDB0259263 (Triphenylethylene)

3D Structure for HMDB0259263 (Triphenylethylene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra