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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:24:15 UTC

Update Date

2022-03-07 02:54:30 UTC

HMDB ID

HMDB0035425

Secondary Accession Numbers

HMDB35425

Metabolite Identification

Common Name

(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate

Description

(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. Based on a literature review a small amount of articles have been published on (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate.

Structure

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

HMDB0035425
     RDKit          3D
(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate
 35 34  0  0  0  0  0  0  0  0999 V2000
    8.2120    1.0644    0.0391 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6448   -0.3244   -0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6824   -1.2505   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3088   -0.8922   -0.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1590   -0.5711    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8071   -0.1751    0.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6663    0.1806    0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168    0.6264    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3506   -0.1595    1.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0447    0.3151    1.2901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9638   -0.4179    0.5010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -0.1114    0.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6608    0.8103    1.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3416   -0.8291   -0.2304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7058   -0.2560    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7536   -0.9796   -0.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7444    1.2411   -0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3103    1.3635   -0.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0223    1.7978   -0.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9298    1.1117    1.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6854   -0.5836   -0.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9916   -2.2599   -0.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120    1.6598    0.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5973   -1.1871    1.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2936    0.0929    2.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1447    1.3925    1.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1170   -0.8421   -1.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3095   -1.8863    0.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9528   -0.4333    1.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6314   -1.2721   -0.1307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1318   -0.2823   -1.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3032   -1.8987   -1.1747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8845    1.5946   -0.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7004    1.5524   -0.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7109    1.8090    0.8082 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  3  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 14 27  1  0
 14 28  1  0
 15 29  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
 17 33  1  0
 17 34  1  0
 17 35  1  0
M  END


  Mrv0541 05061308262D          

 17 16  0  0  0  0            999 V2000
   -3.9849    3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993    3.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993    2.5855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9849    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2704    1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270    0.5230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  4  2  0  0  0  0
  6  5  1  0  0  0  0
  7  6  3  0  0  0  0
  8  7  1  0  0  0  0
  9  8  3  0  0  0  0
 10  9  1  0  0  0  0
 11 10  2  0  0  0  0
 12 11  1  0  0  0  0
 14  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14 13  1  0  0  0  0
 15 13  1  0  0  0  0
 16 15  2  0  0  0  0
 17 12  1  0  0  0  0
 17 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035425

> <DATABASE_NAME>
hmdb

> <SMILES>
C\C=C/C#CC#C\C=C\COC(=O)CC(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O2/c1-4-5-6-7-8-9-10-11-12-17-15(16)13-14(2)3/h4-5,10-11,14H,12-13H2,1-3H3/b5-4-,11-10+

> <INCHI_KEY>
FPIBENZMUTVCEK-JWPKELMXSA-N

> <FORMULA>
C15H18O2

> <MOLECULAR_WEIGHT>
230.3022

> <EXACT_MASS>
230.13067982

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
27.800663809691976

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,8Z)-deca-2,8-dien-4,6-diyn-1-yl 3-methylbutanoate

> <ALOGPS_LOGP>
4.21

> <JCHEM_LOGP>
3.9474604306666663

> <ALOGPS_LOGS>
-4.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.046257748401184

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
73.4709

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.01e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,8Z)-deca-2,8-dien-4,6-diyn-1-yl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0035425
     RDKit          3D
(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate
 35 34  0  0  0  0  0  0  0  0999 V2000
    8.2120    1.0644    0.0391 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6448   -0.3244   -0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6824   -1.2505   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3088   -0.8922   -0.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1590   -0.5711    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8071   -0.1751    0.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6663    0.1806    0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168    0.6264    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3506   -0.1595    1.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0447    0.3151    1.2901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9638   -0.4179    0.5010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -0.1114    0.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6608    0.8103    1.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3416   -0.8291   -0.2304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7058   -0.2560    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7536   -0.9796   -0.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7444    1.2411   -0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3103    1.3635   -0.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0223    1.7978   -0.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9298    1.1117    1.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6854   -0.5836   -0.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9916   -2.2599   -0.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120    1.6598    0.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5973   -1.1871    1.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2936    0.0929    2.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1447    1.3925    1.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1170   -0.8421   -1.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3095   -1.8863    0.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9528   -0.4333    1.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6314   -1.2721   -0.1307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1318   -0.2823   -1.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3032   -1.8987   -1.1747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8845    1.5946   -0.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7004    1.5524   -0.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7109    1.8090    0.8082 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  3  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 14 27  1  0
 14 28  1  0
 15 29  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
 17 33  1  0
 17 34  1  0
 17 35  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      -7.438   7.136   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.898  -0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.772   6.366   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.772   4.826   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.438   4.056   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.105   3.286   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.771   2.516   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.437   1.746   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.104   0.976   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.231  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.565  -1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.897  -1.334   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.897  -2.874   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.564  -0.564   0.000  0.00  0.00           O+0
CONECT    1    4                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4    1    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   17                                                       
CONECT   13   14   15                                                       
CONECT   14    2    3   13                                                  
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   12   15                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

COMPND    HMDB0035425
HETATM    1  C1  UNL     1       8.212   1.064   0.039  1.00  0.00           C  
HETATM    2  C2  UNL     1       8.645  -0.324  -0.285  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.682  -1.250  -0.361  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.309  -0.892  -0.135  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.159  -0.571   0.056  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.807  -0.175   0.264  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.666   0.181   0.436  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.317   0.626   0.635  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.351  -0.159   1.088  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.045   0.315   1.290  1.00  0.00           C  
HETATM   11  O1  UNL     1      -1.964  -0.418   0.501  1.00  0.00           O  
HETATM   12  C11 UNL     1      -3.302  -0.111   0.564  1.00  0.00           C  
HETATM   13  O2  UNL     1      -3.661   0.810   1.321  1.00  0.00           O  
HETATM   14  C12 UNL     1      -4.342  -0.829  -0.230  1.00  0.00           C  
HETATM   15  C13 UNL     1      -5.706  -0.256   0.063  1.00  0.00           C  
HETATM   16  C14 UNL     1      -6.754  -0.980  -0.738  1.00  0.00           C  
HETATM   17  C15 UNL     1      -5.744   1.241  -0.134  1.00  0.00           C  
HETATM   18  H1  UNL     1       7.310   1.363  -0.529  1.00  0.00           H  
HETATM   19  H2  UNL     1       9.022   1.798  -0.172  1.00  0.00           H  
HETATM   20  H3  UNL     1       7.930   1.112   1.122  1.00  0.00           H  
HETATM   21  H4  UNL     1       9.685  -0.584  -0.454  1.00  0.00           H  
HETATM   22  H5  UNL     1       7.992  -2.260  -0.596  1.00  0.00           H  
HETATM   23  H6  UNL     1       1.012   1.660   0.419  1.00  0.00           H  
HETATM   24  H7  UNL     1       0.597  -1.187   1.317  1.00  0.00           H  
HETATM   25  H8  UNL     1      -1.294   0.093   2.364  1.00  0.00           H  
HETATM   26  H9  UNL     1      -1.145   1.393   1.155  1.00  0.00           H  
HETATM   27  H10 UNL     1      -4.117  -0.842  -1.295  1.00  0.00           H  
HETATM   28  H11 UNL     1      -4.310  -1.886   0.122  1.00  0.00           H  
HETATM   29  H12 UNL     1      -5.953  -0.433   1.149  1.00  0.00           H  
HETATM   30  H13 UNL     1      -7.631  -1.272  -0.131  1.00  0.00           H  
HETATM   31  H14 UNL     1      -7.132  -0.282  -1.522  1.00  0.00           H  
HETATM   32  H15 UNL     1      -6.303  -1.899  -1.175  1.00  0.00           H  
HETATM   33  H16 UNL     1      -4.884   1.595  -0.763  1.00  0.00           H  
HETATM   34  H17 UNL     1      -6.700   1.552  -0.648  1.00  0.00           H  
HETATM   35  H18 UNL     1      -5.711   1.809   0.808  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3    3   21
CONECT    3    4   22
CONECT    4    5    5    5
CONECT    5    6
CONECT    6    7    7    7
CONECT    7    8
CONECT    8    9    9   23
CONECT    9   10   24
CONECT   10   11   25   26
CONECT   11   12
CONECT   12   13   13   14
CONECT   14   15   27   28
CONECT   15   16   17   29
CONECT   16   30   31   32
CONECT   17   33   34   35
END

HMDB0035425
     RDKit          3D
(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate
 35 34  0  0  0  0  0  0  0  0999 V2000
    8.2120    1.0644    0.0391 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6448   -0.3244   -0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6824   -1.2505   -0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3088   -0.8922   -0.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1590   -0.5711    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8071   -0.1751    0.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6663    0.1806    0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168    0.6264    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3506   -0.1595    1.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0447    0.3151    1.2901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9638   -0.4179    0.5010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3021   -0.1114    0.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6608    0.8103    1.3208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3416   -0.8291   -0.2304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7058   -0.2560    0.0631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7536   -0.9796   -0.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7444    1.2411   -0.1336 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3103    1.3635   -0.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0223    1.7978   -0.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9298    1.1117    1.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6854   -0.5836   -0.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9916   -2.2599   -0.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0120    1.6598    0.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5973   -1.1871    1.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2936    0.0929    2.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1447    1.3925    1.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1170   -0.8421   -1.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3095   -1.8863    0.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9528   -0.4333    1.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6314   -1.2721   -0.1307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1318   -0.2823   -1.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3032   -1.8987   -1.1747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8845    1.5946   -0.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7004    1.5524   -0.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7109    1.8090    0.8082 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  3  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  8 23  1  0
  9 24  1  0
 10 25  1  0
 10 26  1  0
 14 27  1  0
 14 28  1  0
 15 29  1  0
 16 30  1  0
 16 31  1  0
 16 32  1  0
 17 33  1  0
 17 34  1  0
 17 35  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoic acid	Generator

Chemical Formula

C₁₅H₁₈O₂

Average Molecular Weight

230.3022

Monoisotopic Molecular Weight

230.13067982

IUPAC Name

(2E,8Z)-deca-2,8-dien-4,6-diyn-1-yl 3-methylbutanoate

Traditional Name

(2E,8Z)-deca-2,8-dien-4,6-diyn-1-yl 3-methylbutanoate

CAS Registry Number

29444-87-9

SMILES

C\C=C/C#CC#C\C=C\COC(=O)CC(C)C

InChI Identifier

InChI=1S/C15H18O2/c1-4-5-6-7-8-9-10-11-12-17-15(16)13-14(2)3/h4-5,10-11,14H,12-13H2,1-3H3/b5-4-,11-10+

InChI Key

FPIBENZMUTVCEK-JWPKELMXSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohol esters

Direct Parent

Fatty alcohol esters

Alternative Parents

Substituents

Fatty alcohol ester
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

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0035425)
Cell membrane (HMDB: HMDB0035425)

Biofluid or Excreta

Urine (HMDB: HMDB0035425)

Cellular substructure

Extracellular (HMDB: HMDB0035425)
Membrane (HMDB: HMDB0035425)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035425)

Source

Endogenous

Endogenous (HMDB: HMDB0035425)

Plant

Plant (HMDB: HMDB0035425)

Animal

Animal (HMDB: HMDB0035425)

Exogenous

Food

Food (HMDB: HMDB0035425)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0035425)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0035425)

Cellular process

Cell signaling (HMDB: HMDB0035425)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0035425)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0035425)

Nutrient

Nutrient (HMDB: HMDB0035425)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035425)

Emulsifier (HMDB: HMDB0035425)

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	2.12 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.01 g/L	ALOGPS
logP	4.21	ALOGPS
logP	3.95	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Basic)	-7	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	73.47 m³·mol⁻¹	ChemAxon
Polarizability	27.8 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]+	161.603	31661259
DarkChem	[M-H]-	160.545	31661259
DeepCCS	[M+H]+	157.43	30932474
DeepCCS	[M-H]-	155.072	30932474
DeepCCS	[M-2H]-	188.03	30932474
DeepCCS	[M+Na]+	163.524	30932474
AllCCS	[M+H]+	156.3	32859911
AllCCS	[M+H-H2O]+	152.8	32859911
AllCCS	[M+NH4]+	159.6	32859911
AllCCS	[M+Na]+	160.6	32859911
AllCCS	[M-H]-	158.0	32859911
AllCCS	[M+Na-2H]-	158.6	32859911
AllCCS	[M+HCOO]-	159.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate	C\C=C/C#CC#C\C=C\COC(=O)CC(C)C	2714.9	Standard polar	33892256
(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate	C\C=C/C#CC#C\C=C\COC(=O)CC(C)C	1882.5	Standard non polar	33892256
(2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate	C\C=C/C#CC#C\C=C\COC(=O)CC(C)C	1852.4	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 - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a70-8900000000-6f4a67bdb1ab1e305d4e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 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 - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 10V, Positive-QTOF	splash10-003r-6890000000-42ebc799e038f2984382	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 20V, Positive-QTOF	splash10-004i-8900000000-4995e754149ba9603c92	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 40V, Positive-QTOF	splash10-0pdu-9100000000-7f2c74ebe05adcd98133	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 10V, Negative-QTOF	splash10-0059-8790000000-bc56d993737a7d767be9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 20V, Negative-QTOF	splash10-0ue9-7910000000-a5dbca922091fa4115df	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 40V, Negative-QTOF	splash10-053r-9300000000-f7bfcd8fea9b5db7fd35	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 10V, Positive-QTOF	splash10-004i-9700000000-b9d42bfb0b96155c6357	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 20V, Positive-QTOF	splash10-004r-9300000000-a731a728bedcc996f1c6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 40V, Positive-QTOF	splash10-004i-9100000000-054516868e4308ba6cb6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 10V, Negative-QTOF	splash10-004i-0940000000-a42d30f8096e7bcb8551	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 20V, Negative-QTOF	splash10-0ufr-4910000000-cf45478c80dc9984cc10	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate 40V, Negative-QTOF	splash10-001r-9300000000-0f532ce1fb8294974af9	2021-09-22	Wishart 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

FDB014103

KNApSAcK ID

Not Available

Chemspider ID

4509558

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5352701

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1849741

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 (2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate (HMDB0035425)

MOL for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

3D MOL for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

3D SDF for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

3D-SDF for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

PDB for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

3D PDB for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

SMILES for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

INCHI for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

Structure for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

3D Structure for HMDB0035425 ((2E,8Z)-Decadiene-4,6-diyn-1-yl 3-methylbutanoate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra