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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:33:19 UTC

Update Date

2023-02-21 17:26:25 UTC

HMDB ID

HMDB0038270

Secondary Accession Numbers

HMDB38270

Metabolite Identification

Common Name

cis-3-Hexenyl cis-3-hexenoate

Description

cis-3-Hexenyl cis-3-hexenoate belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. Based on a literature review a small amount of articles have been published on cis-3-Hexenyl cis-3-hexenoate.

Structure

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

HMDB0038270
     RDKit          3D
cis-3-Hexenyl cis-3-hexenoate
 34 33  0  0  0  0  0  0  0  0999 V2000
   -5.1607   -1.0425   -0.5874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5355   -0.3927    0.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3126    1.0534    0.4340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1180    1.5660    0.4894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8969    0.8066    0.7477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0013    1.0124   -0.4846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2188    0.3048   -0.3217 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1606    0.3694   -1.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8938    1.0548   -2.3618 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773   -0.3601   -1.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4881   -1.0515    0.0703 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3489   -0.8687    1.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4747    0.0787    0.9746 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8070   -0.6728    1.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1944   -2.1380   -0.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6030   -0.7489   -1.4829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2119   -0.7162   -0.7243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7436   -0.9607    1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3893   -0.4336    1.4052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2053    1.7134    0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9711    2.6589    0.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3698    1.2303    1.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0035   -0.2567    0.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5123    0.6496   -1.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7394    2.0844   -0.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5752   -1.0664   -2.0837 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2377    0.4206   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6970   -1.8099    0.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2649   -1.4462    1.9703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3443    0.7734    1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5323    0.7203    0.1017 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6979   -1.7407    0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5937   -0.1751    0.5036 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1560   -0.6163    2.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END

HMDB0038270
     RDKit          3D
cis-3-Hexenyl cis-3-hexenoate
 34 33  0  0  0  0  0  0  0  0999 V2000
   -5.1607   -1.0425   -0.5874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5355   -0.3927    0.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3126    1.0534    0.4340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1180    1.5660    0.4894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8969    0.8066    0.7477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0013    1.0124   -0.4846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2188    0.3048   -0.3217 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1606    0.3694   -1.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8938    1.0548   -2.3618 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773   -0.3601   -1.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4881   -1.0515    0.0703 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3489   -0.8687    1.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4747    0.0787    0.9746 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8070   -0.6728    1.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1944   -2.1380   -0.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6030   -0.7489   -1.4829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2119   -0.7162   -0.7243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7436   -0.9607    1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3893   -0.4336    1.4052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2053    1.7134    0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9711    2.6589    0.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3698    1.2303    1.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0035   -0.2567    0.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5123    0.6496   -1.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7394    2.0844   -0.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5752   -1.0664   -2.0837 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2377    0.4206   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6970   -1.8099    0.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2649   -1.4462    1.9703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3443    0.7734    1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5323    0.7203    0.1017 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6979   -1.7407    0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5937   -0.1751    0.5036 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1560   -0.6163    2.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -2.310   5.954   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.026  -0.976   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.310   4.414   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.692  -0.206   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.644   3.644   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.692   1.334   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.644   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.358   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.310   1.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.025   1.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.976   2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.691   2.104   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.691   3.644   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       0.357   1.334   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   14                                                       
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   11   12                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

COMPND    HMDB0038270
HETATM    1  C1  UNL     1      -5.161  -1.043  -0.587  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.535  -0.393   0.637  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.313   1.053   0.434  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.118   1.566   0.489  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.897   0.807   0.748  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.001   1.012  -0.485  1.00  0.00           C  
HETATM    7  O1  UNL     1       0.219   0.305  -0.322  1.00  0.00           O  
HETATM    8  C7  UNL     1       1.161   0.369  -1.336  1.00  0.00           C  
HETATM    9  O2  UNL     1       0.894   1.055  -2.362  1.00  0.00           O  
HETATM   10  C8  UNL     1       2.477  -0.360  -1.224  1.00  0.00           C  
HETATM   11  C9  UNL     1       2.488  -1.052   0.070  1.00  0.00           C  
HETATM   12  C10 UNL     1       3.349  -0.869   1.029  1.00  0.00           C  
HETATM   13  C11 UNL     1       4.475   0.079   0.975  1.00  0.00           C  
HETATM   14  C12 UNL     1       5.807  -0.673   1.133  1.00  0.00           C  
HETATM   15  H1  UNL     1      -5.194  -2.138  -0.428  1.00  0.00           H  
HETATM   16  H2  UNL     1      -4.603  -0.749  -1.483  1.00  0.00           H  
HETATM   17  H3  UNL     1      -6.212  -0.716  -0.724  1.00  0.00           H  
HETATM   18  H4  UNL     1      -3.744  -0.961   1.095  1.00  0.00           H  
HETATM   19  H5  UNL     1      -5.389  -0.434   1.405  1.00  0.00           H  
HETATM   20  H6  UNL     1      -5.205   1.713   0.229  1.00  0.00           H  
HETATM   21  H7  UNL     1      -2.971   2.659   0.334  1.00  0.00           H  
HETATM   22  H8  UNL     1      -1.370   1.230   1.651  1.00  0.00           H  
HETATM   23  H9  UNL     1      -2.003  -0.257   0.962  1.00  0.00           H  
HETATM   24  H10 UNL     1      -1.512   0.650  -1.396  1.00  0.00           H  
HETATM   25  H11 UNL     1      -0.739   2.084  -0.588  1.00  0.00           H  
HETATM   26  H12 UNL     1       2.575  -1.066  -2.084  1.00  0.00           H  
HETATM   27  H13 UNL     1       3.238   0.421  -1.289  1.00  0.00           H  
HETATM   28  H14 UNL     1       1.697  -1.810   0.280  1.00  0.00           H  
HETATM   29  H15 UNL     1       3.265  -1.446   1.970  1.00  0.00           H  
HETATM   30  H16 UNL     1       4.344   0.773   1.859  1.00  0.00           H  
HETATM   31  H17 UNL     1       4.532   0.720   0.102  1.00  0.00           H  
HETATM   32  H18 UNL     1       5.698  -1.741   0.881  1.00  0.00           H  
HETATM   33  H19 UNL     1       6.594  -0.175   0.504  1.00  0.00           H  
HETATM   34  H20 UNL     1       6.156  -0.616   2.184  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3   18   19
CONECT    3    4    4   20
CONECT    4    5   21
CONECT    5    6   22   23
CONECT    6    7   24   25
CONECT    7    8
CONECT    8    9    9   10
CONECT   10   11   26   27
CONECT   11   12   12   28
CONECT   12   13   29
CONECT   13   14   30   31
CONECT   14   32   33   34
END

HMDB0038270
     RDKit          3D
cis-3-Hexenyl cis-3-hexenoate
 34 33  0  0  0  0  0  0  0  0999 V2000
   -5.1607   -1.0425   -0.5874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5355   -0.3927    0.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3126    1.0534    0.4340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1180    1.5660    0.4894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8969    0.8066    0.7477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0013    1.0124   -0.4846 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2188    0.3048   -0.3217 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1606    0.3694   -1.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8938    1.0548   -2.3618 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773   -0.3601   -1.2235 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4881   -1.0515    0.0703 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3489   -0.8687    1.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4747    0.0787    0.9746 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8070   -0.6728    1.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1944   -2.1380   -0.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6030   -0.7489   -1.4829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2119   -0.7162   -0.7243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7436   -0.9607    1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3893   -0.4336    1.4052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2053    1.7134    0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9711    2.6589    0.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3698    1.2303    1.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0035   -0.2567    0.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5123    0.6496   -1.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7394    2.0844   -0.5884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5752   -1.0664   -2.0837 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2377    0.4206   -1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6970   -1.8099    0.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2649   -1.4462    1.9703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3443    0.7734    1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5323    0.7203    0.1017 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6979   -1.7407    0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5937   -0.1751    0.5036 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1560   -0.6163    2.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
cis-3-Hexenyl cis-3-hexenoic acid	Generator
(3Z)-3-Hexen-1-yl ester(3Z)-3-hexenoic acid	HMDB
(3Z)-3-Hexenyl ester(3Z)-3-hexenoic acid	HMDB
(Z)-3-Hexenyl (Z)-3-hexenoate	HMDB
(Z)-Hex-3-enyl (Z)-hex-3-enoate	HMDB
3-Hexenyl ester(Z,Z)-3-hexenoic acid	HMDB
FEMA 3689	HMDB

Chemical Formula

C₁₂H₂₀O₂

Average Molecular Weight

196.286

Monoisotopic Molecular Weight

196.146329884

IUPAC Name

(3Z)-hex-3-en-1-yl (3Z)-hex-3-enoate

Traditional Name

(3Z)-hex-3-en-1-yl (3Z)-hex-3-enoate

CAS Registry Number

61444-38-0

SMILES

CC\C=C/CCOC(=O)C\C=C/CC

InChI Identifier

InChI=1S/C12H20O2/c1-3-5-7-9-11-14-12(13)10-8-6-4-2/h5-8H,3-4,9-11H2,1-2H3/b7-5-,8-6-

InChI Key

UZJQQWFHPLYECS-SFECMWDFSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Fatty acid ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Cellular substructure

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0038270)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038270)

Source

Endogenous

Endogenous (HMDB: HMDB0038270)

Animal

Animal (HMDB: HMDB0038270)

Exogenous

Food

Food (HMDB: HMDB0038270)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0038270)

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0038270)

Cellular process

Cell signaling (HMDB: HMDB0038270)

Biochemical process

Lipid transport (HMDB: HMDB0038270)

Role

Biological role

Energy storage (HMDB: HMDB0038270)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038270)

Food and nutrition

Food additive

Flavoring agent

Flavoring Agent (HMDB: HMDB0038270)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	60.00 °C. @ 0.50 mm Hg	The Good Scents Company Information System
Water Solubility	8.59 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	4.298 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.037 g/L	ALOGPS
logP	4.08	ALOGPS
logP	3.45	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	61.15 m³·mol⁻¹	ChemAxon
Polarizability	23.26 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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
DarkChem	[M+H]+	149.363	31661259
DarkChem	[M-H]-	144.451	31661259
DeepCCS	[M+H]+	150.85	30932474
DeepCCS	[M-H]-	148.492	30932474
DeepCCS	[M-2H]-	183.749	30932474
DeepCCS	[M+Na]+	159.036	30932474
AllCCS	[M+H]+	151.1	32859911
AllCCS	[M+H-H2O]+	147.6	32859911
AllCCS	[M+NH4]+	154.5	32859911
AllCCS	[M+Na]+	155.4	32859911
AllCCS	[M-H]-	151.4	32859911
AllCCS	[M+Na-2H]-	152.8	32859911
AllCCS	[M+HCOO]-	154.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
cis-3-Hexenyl cis-3-hexenoate	CC\C=C/CCOC(=O)C\C=C/CC	1740.0	Standard polar	33892256
cis-3-Hexenyl cis-3-hexenoate	CC\C=C/CCOC(=O)C\C=C/CC	1344.1	Standard non polar	33892256
cis-3-Hexenyl cis-3-hexenoate	CC\C=C/CCOC(=O)C\C=C/CC	1433.9	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 - cis-3-Hexenyl cis-3-hexenoate GC-MS (Non-derivatized) - 70eV, Positive	splash10-00l2-9200000000-83aeba98af4a9c3a2011	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-3-Hexenyl cis-3-hexenoate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 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 - cis-3-Hexenyl cis-3-hexenoate 10V, Positive-QTOF	splash10-0002-6900000000-90ea7ff9684ba7c6b48c	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 20V, Positive-QTOF	splash10-001j-9200000000-0e477495fa1f1d51dc1c	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 40V, Positive-QTOF	splash10-0k9x-9000000000-72413531f580e6bf1f4f	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 10V, Negative-QTOF	splash10-0002-7900000000-2087171e128f43273dae	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 20V, Negative-QTOF	splash10-01ot-9800000000-5945866e7cb4e7d38563	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 40V, Negative-QTOF	splash10-07be-9100000000-110766e505480ac38b55	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 10V, Negative-QTOF	splash10-0002-3900000000-7d64926751fdc15aed14	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 20V, Negative-QTOF	splash10-01ot-9700000000-7ccc384ea16a88be2e49	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 40V, Negative-QTOF	splash10-014j-9000000000-3a49063170a65f0f9b51	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 10V, Positive-QTOF	splash10-001j-9000000000-98fbfe56199f09b991cb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 20V, Positive-QTOF	splash10-067j-9000000000-9bd0b7dbc781b52bf9ff	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - cis-3-Hexenyl cis-3-hexenoate 40V, Positive-QTOF	splash10-05q9-9000000000-b923d3f31c215bf3eeef	2021-09-22	Wishart Lab	View Spectrum

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-04	FELIX lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB017568

KNApSAcK ID

Not Available

Chemspider ID

4940571

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6435882

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1026771

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for cis-3-Hexenyl cis-3-hexenoate (HMDB0038270)

MOL for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

3D MOL for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

3D SDF for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

3D-SDF for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

PDB for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

3D PDB for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

SMILES for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

INCHI for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

Structure for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

3D Structure for HMDB0038270 (cis-3-Hexenyl cis-3-hexenoate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra