Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:48:43 UTC

Update Date

2023-02-21 17:21:47 UTC

HMDB ID

HMDB0032248

Secondary Accession Numbers

HMDB32248

Metabolite Identification

Common Name

11-Dodecenoic acid

Description

11-Dodecenoic acid, also known as 11-lauroleic acid or 11-lauroleate, belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. Based on a literature review a significant number of articles have been published on 11-Dodecenoic acid.

Structure

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

HMDB0032248
     RDKit          3D
11-Dodecenoic acid
 36 35  0  0  0  0  0  0  0  0999 V2000
   -4.7902    1.8657    0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5083    0.5500    0.8108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4177   -0.1686   -0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9989   -0.7388   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0422    0.4256   -0.5047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -0.0622   -0.5962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2374   -0.9883    0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1826   -1.4428    0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1901   -0.3049    0.4096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5589   -0.9202    0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6926    0.0393    0.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6034    0.9681   -0.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7132    0.8517   -1.7142 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5514    1.9854   -0.9345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8532    2.3778    1.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9493    2.3850   -0.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3434    0.0041    1.7351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1772   -0.9506   -0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931    0.5654   -1.3095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8825   -1.2285   -1.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8435   -1.4347    0.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2827    1.0649   -1.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1970    1.0638    0.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0265    0.8684   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4399   -0.5430   -1.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4851   -0.6040    1.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8839   -1.9080    0.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381   -2.0030   -0.5670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515   -2.1671    1.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9813    0.4563   -0.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1106    0.2280    1.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5469   -1.5756   -0.6293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7463   -1.6406    1.1213 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6681   -0.5193    0.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7614    0.5814    1.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3170    2.9191   -0.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 14 36  1  0
M  END

HMDB0032248
     RDKit          3D
11-Dodecenoic acid
 36 35  0  0  0  0  0  0  0  0999 V2000
   -4.7902    1.8657    0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5083    0.5500    0.8108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4177   -0.1686   -0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9989   -0.7388   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0422    0.4256   -0.5047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -0.0622   -0.5962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2374   -0.9883    0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1826   -1.4428    0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1901   -0.3049    0.4096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5589   -0.9202    0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6926    0.0393    0.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6034    0.9681   -0.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7132    0.8517   -1.7142 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5514    1.9854   -0.9345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8532    2.3778    1.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9493    2.3850   -0.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3434    0.0041    1.7351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1772   -0.9506   -0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931    0.5654   -1.3095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8825   -1.2285   -1.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8435   -1.4347    0.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2827    1.0649   -1.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1970    1.0638    0.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0265    0.8684   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4399   -0.5430   -1.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4851   -0.6040    1.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8839   -1.9080    0.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381   -2.0030   -0.5670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515   -2.1671    1.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9813    0.4563   -0.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1106    0.2280    1.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5469   -1.5756   -0.6293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7463   -1.6406    1.1213 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6681   -0.5193    0.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7614    0.5814    1.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3170    2.9191   -0.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 14 36  1  0
M  END

HEADER    PROTEIN                                 25-JUN-18   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-JUN-18         0                                  
HETATM    1  C   UNK     0      10.216   7.438   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.884   7.438   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.217   6.668   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.551   7.438   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.885   6.668   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      18.218   7.438   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.552   6.668   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.886   7.438   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      22.219   6.668   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      23.553   7.438   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      24.887   6.668   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      26.220   7.438   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      24.887   5.128   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

COMPND    HMDB0032248
HETATM    1  C1  UNL     1      -4.790   1.866   0.864  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.508   0.550   0.811  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.418  -0.169  -0.465  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.999  -0.739  -0.557  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.042   0.426  -0.505  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.614  -0.062  -0.596  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.237  -0.988   0.514  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.183  -1.443   0.378  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.190  -0.305   0.410  1.00  0.00           C  
HETATM   10  C10 UNL     1       3.559  -0.920   0.270  1.00  0.00           C  
HETATM   11  C11 UNL     1       4.693   0.039   0.281  1.00  0.00           C  
HETATM   12  C12 UNL     1       4.603   0.968  -0.854  1.00  0.00           C  
HETATM   13  O1  UNL     1       3.713   0.852  -1.714  1.00  0.00           O  
HETATM   14  O2  UNL     1       5.551   1.985  -0.935  1.00  0.00           O  
HETATM   15  H1  UNL     1      -4.853   2.378   1.805  1.00  0.00           H  
HETATM   16  H2  UNL     1      -4.949   2.385  -0.057  1.00  0.00           H  
HETATM   17  H3  UNL     1      -4.343   0.004   1.735  1.00  0.00           H  
HETATM   18  H4  UNL     1      -5.177  -0.951  -0.610  1.00  0.00           H  
HETATM   19  H5  UNL     1      -4.493   0.565  -1.310  1.00  0.00           H  
HETATM   20  H6  UNL     1      -2.883  -1.228  -1.534  1.00  0.00           H  
HETATM   21  H7  UNL     1      -2.844  -1.435   0.302  1.00  0.00           H  
HETATM   22  H8  UNL     1      -2.283   1.065  -1.386  1.00  0.00           H  
HETATM   23  H9  UNL     1      -2.197   1.064   0.381  1.00  0.00           H  
HETATM   24  H10 UNL     1       0.027   0.868  -0.572  1.00  0.00           H  
HETATM   25  H11 UNL     1      -0.440  -0.543  -1.580  1.00  0.00           H  
HETATM   26  H12 UNL     1      -0.485  -0.604   1.515  1.00  0.00           H  
HETATM   27  H13 UNL     1      -0.884  -1.908   0.397  1.00  0.00           H  
HETATM   28  H14 UNL     1       1.338  -2.003  -0.567  1.00  0.00           H  
HETATM   29  H15 UNL     1       1.451  -2.167   1.191  1.00  0.00           H  
HETATM   30  H16 UNL     1       1.981   0.456  -0.341  1.00  0.00           H  
HETATM   31  H17 UNL     1       2.111   0.228   1.401  1.00  0.00           H  
HETATM   32  H18 UNL     1       3.547  -1.576  -0.629  1.00  0.00           H  
HETATM   33  H19 UNL     1       3.746  -1.641   1.121  1.00  0.00           H  
HETATM   34  H20 UNL     1       5.668  -0.519   0.173  1.00  0.00           H  
HETATM   35  H21 UNL     1       4.761   0.581   1.263  1.00  0.00           H  
HETATM   36  H22 UNL     1       5.317   2.919  -0.601  1.00  0.00           H  
CONECT    1    2    2   15   16
CONECT    2    3   17
CONECT    3    4   18   19
CONECT    4    5   20   21
CONECT    5    6   22   23
CONECT    6    7   24   25
CONECT    7    8   26   27
CONECT    8    9   28   29
CONECT    9   10   30   31
CONECT   10   11   32   33
CONECT   11   12   34   35
CONECT   12   13   13   14
CONECT   14   36
END

HMDB0032248
     RDKit          3D
11-Dodecenoic acid
 36 35  0  0  0  0  0  0  0  0999 V2000
   -4.7902    1.8657    0.8644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5083    0.5500    0.8108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4177   -0.1686   -0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9989   -0.7388   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0422    0.4256   -0.5047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141   -0.0622   -0.5962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2374   -0.9883    0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1826   -1.4428    0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1901   -0.3049    0.4096 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5589   -0.9202    0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6926    0.0393    0.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6034    0.9681   -0.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7132    0.8517   -1.7142 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5514    1.9854   -0.9345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8532    2.3778    1.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9493    2.3850   -0.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3434    0.0041    1.7351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1772   -0.9506   -0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931    0.5654   -1.3095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8825   -1.2285   -1.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8435   -1.4347    0.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2827    1.0649   -1.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1970    1.0638    0.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0265    0.8684   -0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4399   -0.5430   -1.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4851   -0.6040    1.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8839   -1.9080    0.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381   -2.0030   -0.5670 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515   -2.1671    1.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9813    0.4563   -0.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1106    0.2280    1.4012 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5469   -1.5756   -0.6293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7463   -1.6406    1.1213 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6681   -0.5193    0.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7614    0.5814    1.2626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3170    2.9191   -0.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 14 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
11-Lauroleic acid	ChEBI
11-Lauroleate	Generator
11-Dodecenoate	Generator
Dodecenoic acid	HMDB
11-Dodecenoic acid	ChEBI

Chemical Formula

C₁₂H₂₂O₂

Average Molecular Weight

198.3019

Monoisotopic Molecular Weight

198.161979948

IUPAC Name

dodec-11-enoic acid

Traditional Name

11-dodecenoic acid

CAS Registry Number

65423-25-8

SMILES

OC(=O)CCCCCCCCCC=C

InChI Identifier

InChI=1S/C12H22O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2H,1,3-11H2,(H,13,14)

InChI Key

GZZPOFFXKUVNSW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Unsaturated fatty acid
Straight chain fatty acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

dodecenoic acid (CHEBI:38381 )
Unsaturated fatty acids (LMFA01030043 )

Ontology

Cellular substructure

Organelle

Adiposome (HMDB: HMDB0032248)

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0032248)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0032248)

Source

Endogenous

Endogenous (HMDB: HMDB0032248)

Animal

Animal (HMDB: HMDB0032248)

Exogenous

Food

Food (HMDB: HMDB0032248)

Animal origin

Poultry

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Milk and milk product

Unfermented milk

Milk (Cow) (FooDB: FOOD00618)

Exogenous (HMDB: HMDB0032248)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0032248)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0032248)

Lipid metabolism pathway (HMDB: HMDB0032248)

Cellular process

Cell signaling (HMDB: HMDB0032248)

Biochemical process

Lipid transport (HMDB: HMDB0032248)

Role

Biological role

Energy source (HMDB: HMDB0032248)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0032248)

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
Water Solubility	0.0082 g/L	ALOGPS
logP	4.37	ALOGPS
logP	4.17	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	4.95	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	58.72 m³·mol⁻¹	ChemAxon
Polarizability	24.88 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]+	149.613	31661259
DarkChem	[M-H]-	148.494	31661259
DeepCCS	[M+H]+	153.592	30932474
DeepCCS	[M-H]-	150.957	30932474
DeepCCS	[M-2H]-	186.588	30932474
DeepCCS	[M+Na]+	161.771	30932474
AllCCS	[M+H]+	151.9	32859911
AllCCS	[M+H-H2O]+	148.2	32859911
AllCCS	[M+NH4]+	155.3	32859911
AllCCS	[M+Na]+	156.3	32859911
AllCCS	[M-H]-	153.4	32859911
AllCCS	[M+Na-2H]-	154.8	32859911
AllCCS	[M+HCOO]-	156.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
11-Dodecenoic acid	OC(=O)CCCCCCCCCC=C	2450.8	Standard polar	33892256
11-Dodecenoic acid	OC(=O)CCCCCCCCCC=C	1498.0	Standard non polar	33892256
11-Dodecenoic acid	OC(=O)CCCCCCCCCC=C	1576.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
11-Dodecenoic acid,1TMS,isomer #1	C=CCCCCCCCCCC(=O)O[Si](C)(C)C	1643.9	Semi standard non polar	33892256
11-Dodecenoic acid,1TBDMS,isomer #1	C=CCCCCCCCCCC(=O)O[Si](C)(C)C(C)(C)C	1888.7	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 - 11-Dodecenoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a6u-9600000000-e6e6fff2e72e432d342e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 11-Dodecenoic acid GC-MS (1 TMS) - 70eV, Positive	splash10-0079-9320000000-210dbe39869194640305	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 11-Dodecenoic acid 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 - 11-Dodecenoic acid 10V, Positive-QTOF	splash10-001i-0900000000-bb1e6c584d1cd364c3d5	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 20V, Positive-QTOF	splash10-0f8a-4900000000-57d8e6ace01184864dec	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 40V, Positive-QTOF	splash10-05mo-9200000000-1308c8a11881469d1061	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 10V, Negative-QTOF	splash10-0002-0900000000-62f845deea8b99b8fe1c	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 20V, Negative-QTOF	splash10-0f92-1900000000-f2b01b3c67367b5b65c3	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 40V, Negative-QTOF	splash10-0a4l-9300000000-f1e1eed19d3b80f32bc4	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 10V, Negative-QTOF	splash10-0002-0900000000-0e919ff6564c9c0b165a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 20V, Negative-QTOF	splash10-004j-0900000000-819fe69fda172a277b22	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 40V, Negative-QTOF	splash10-05vo-9500000000-eee1dbcf10eaa65faeb8	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 10V, Positive-QTOF	splash10-001j-9600000000-693b26a6afd0312ee8bc	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 20V, Positive-QTOF	splash10-067i-9000000000-16d7bae75d816820f380	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 11-Dodecenoic acid 40V, Positive-QTOF	splash10-0aou-9000000000-fb7f5c0779451d74df10	2021-09-23	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

FDB009340

KNApSAcK ID

Not Available

Chemspider ID

111443

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

125207

PDB ID

Not Available

ChEBI ID

38381

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

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 ]
(). EAFUS: Everything Added to Food in the United States.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 11-Dodecenoic acid (HMDB0032248)

MOL for HMDB0032248 (11-Dodecenoic acid)

3D MOL for HMDB0032248 (11-Dodecenoic acid)

3D SDF for HMDB0032248 (11-Dodecenoic acid)

3D-SDF for HMDB0032248 (11-Dodecenoic acid)

PDB for HMDB0032248 (11-Dodecenoic acid)

3D PDB for HMDB0032248 (11-Dodecenoic acid)

SMILES for HMDB0032248 (11-Dodecenoic acid)

INCHI for HMDB0032248 (11-Dodecenoic acid)

Structure for HMDB0032248 (11-Dodecenoic acid)

3D Structure for HMDB0032248 (11-Dodecenoic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra