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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 01:19:59 UTC

Update Date

2023-02-21 17:27:09 UTC

HMDB ID

HMDB0039795

Secondary Accession Numbers

HMDB39795

Metabolite Identification

Common Name

Ethyl 4Z-octenoate

Description

Ethyl 4Z-octenoate 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 Ethyl 4Z-octenoate.

Structure

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

HMDB0039795
     RDKit          3D
Ethyl 4Z-octenoate
 30 29  0  0  0  0  0  0  0  0999 V2000
    3.9255    1.1126    0.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1394   -0.2212    0.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4119   -1.2921    0.0772 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9623   -0.9528    0.0329 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3166   -0.7935   -1.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1015   -0.4585   -1.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8235   -0.2626    0.0961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2284    0.0468   -0.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8129   -0.6459   -1.0916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9561    1.0552    0.3776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3035    1.3650    0.0809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2529    0.2337    0.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8528    1.2313   -0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5161    1.1850   -0.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1777    1.9315    0.9063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8015   -0.1511    1.8989 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2384   -0.4848    0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7937   -1.1893   -0.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5764   -2.3057    0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3674   -0.8258    0.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8624   -0.9163   -2.0286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240   -1.2941   -1.7479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2089    0.5000   -1.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7200   -1.1832    0.7115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3059    0.5233    0.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5582    2.2845    0.6384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4482    1.5944   -0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2631   -0.5441   -0.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0552   -0.2471    1.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2796    0.7047    0.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  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  1  0
  1 13  1  0
  1 14  1  0
  1 15  1  0
  2 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 12 30  1  0
M  END

HMDB0039795
     RDKit          3D
Ethyl 4Z-octenoate
 30 29  0  0  0  0  0  0  0  0999 V2000
    3.9255    1.1126    0.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1394   -0.2212    0.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4119   -1.2921    0.0772 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9623   -0.9528    0.0329 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3166   -0.7935   -1.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1015   -0.4585   -1.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8235   -0.2626    0.0961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2284    0.0468   -0.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8129   -0.6459   -1.0916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9561    1.0552    0.3776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3035    1.3650    0.0809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2529    0.2337    0.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8528    1.2313   -0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5161    1.1850   -0.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1777    1.9315    0.9063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8015   -0.1511    1.8989 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2384   -0.4848    0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7937   -1.1893   -0.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5764   -2.3057    0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3674   -0.8258    0.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8624   -0.9163   -2.0286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240   -1.2941   -1.7479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2089    0.5000   -1.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7200   -1.1832    0.7115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3059    0.5233    0.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5582    2.2845    0.6384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4482    1.5944   -0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2631   -0.5441   -0.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0552   -0.2471    1.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2796    0.7047    0.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  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  1  0
  1 13  1  0
  1 14  1  0
  1 15  1  0
  2 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 12 30  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       8.566  -4.056   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.104   0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.232  -3.286   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.232  -1.746   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.898  -0.976   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.898   0.564   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.565   1.334   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.231   0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.897   1.334   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.897   2.874   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       0.564   0.564   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2   12                                                       
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12    4   10                                                       
MASTER        0    0    0    0    0    0    0    0   12    0   22    0
END

COMPND    HMDB0039795
HETATM    1  C1  UNL     1       3.926   1.113   0.169  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.139  -0.221   0.848  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.412  -1.292   0.077  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.962  -0.953   0.033  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.317  -0.793  -1.094  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.102  -0.458  -1.212  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.824  -0.263   0.096  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.228   0.047  -0.219  1.00  0.00           C  
HETATM    9  O1  UNL     1      -2.813  -0.646  -1.092  1.00  0.00           O  
HETATM   10  O2  UNL     1      -2.956   1.055   0.378  1.00  0.00           O  
HETATM   11  C9  UNL     1      -4.304   1.365   0.081  1.00  0.00           C  
HETATM   12  C10 UNL     1      -5.253   0.234   0.395  1.00  0.00           C  
HETATM   13  H1  UNL     1       2.853   1.231  -0.029  1.00  0.00           H  
HETATM   14  H2  UNL     1       4.516   1.185  -0.744  1.00  0.00           H  
HETATM   15  H3  UNL     1       4.178   1.932   0.906  1.00  0.00           H  
HETATM   16  H4  UNL     1       3.802  -0.151   1.899  1.00  0.00           H  
HETATM   17  H5  UNL     1       5.238  -0.485   0.864  1.00  0.00           H  
HETATM   18  H6  UNL     1       3.794  -1.189  -0.979  1.00  0.00           H  
HETATM   19  H7  UNL     1       3.576  -2.306   0.447  1.00  0.00           H  
HETATM   20  H8  UNL     1       1.367  -0.826   0.951  1.00  0.00           H  
HETATM   21  H9  UNL     1       1.862  -0.916  -2.029  1.00  0.00           H  
HETATM   22  H10 UNL     1      -0.624  -1.294  -1.748  1.00  0.00           H  
HETATM   23  H11 UNL     1      -0.209   0.500  -1.776  1.00  0.00           H  
HETATM   24  H12 UNL     1      -0.720  -1.183   0.711  1.00  0.00           H  
HETATM   25  H13 UNL     1      -0.306   0.523   0.659  1.00  0.00           H  
HETATM   26  H14 UNL     1      -4.558   2.285   0.638  1.00  0.00           H  
HETATM   27  H15 UNL     1      -4.448   1.594  -0.996  1.00  0.00           H  
HETATM   28  H16 UNL     1      -5.263  -0.544  -0.390  1.00  0.00           H  
HETATM   29  H17 UNL     1      -5.055  -0.247   1.387  1.00  0.00           H  
HETATM   30  H18 UNL     1      -6.280   0.705   0.482  1.00  0.00           H  
CONECT    1    2   13   14   15
CONECT    2    3   16   17
CONECT    3    4   18   19
CONECT    4    5    5   20
CONECT    5    6   21
CONECT    6    7   22   23
CONECT    7    8   24   25
CONECT    8    9    9   10
CONECT   10   11
CONECT   11   12   26   27
CONECT   12   28   29   30
END

HMDB0039795
     RDKit          3D
Ethyl 4Z-octenoate
 30 29  0  0  0  0  0  0  0  0999 V2000
    3.9255    1.1126    0.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1394   -0.2212    0.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4119   -1.2921    0.0772 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9623   -0.9528    0.0329 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3166   -0.7935   -1.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1015   -0.4585   -1.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8235   -0.2626    0.0961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2284    0.0468   -0.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8129   -0.6459   -1.0916 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9561    1.0552    0.3776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3035    1.3650    0.0809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2529    0.2337    0.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8528    1.2313   -0.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5161    1.1850   -0.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1777    1.9315    0.9063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8015   -0.1511    1.8989 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2384   -0.4848    0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7937   -1.1893   -0.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5764   -2.3057    0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3674   -0.8258    0.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8624   -0.9163   -2.0286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240   -1.2941   -1.7479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2089    0.5000   -1.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7200   -1.1832    0.7115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3059    0.5233    0.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5582    2.2845    0.6384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4482    1.5944   -0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2631   -0.5441   -0.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0552   -0.2471    1.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2796    0.7047    0.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  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  1  0
  1 13  1  0
  1 14  1  0
  1 15  1  0
  2 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  5 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 12 30  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Ethyl 4Z-octenoic acid	Generator
( Z)-Ethyl 4-octenoate	HMDB
(Z)-Ethyl 4-octenoate	HMDB
4-Octenoic acid, ethyl ether	HMDB
Ethyl (4Z)-4-octenoate	HMDB
Ethyl (Z)-4-octenoate	HMDB
Ethyl (Z)-oct-4-enoate	HMDB
Ethyl cis-4-octenoate	HMDB
Ethyl ester(4Z)-4-octenoic acid	HMDB
Ethyl ester(Z)-4-octenoic acid	HMDB
FEMA 3344	HMDB

Chemical Formula

C₁₀H₁₈O₂

Average Molecular Weight

170.2487

Monoisotopic Molecular Weight

170.13067982

IUPAC Name

ethyl (4E)-oct-4-enoate

Traditional Name

ethyl (4E)-oct-4-enoate

CAS Registry Number

34495-71-1

SMILES

CCC\C=C\CCC(=O)OCC

InChI Identifier

InChI=1S/C10H18O2/c1-3-5-6-7-8-9-10(11)12-4-2/h6-7H,3-5,8-9H2,1-2H3/b7-6+

InChI Key

WRUZCQAJIHSQPL-VOTSOKGWSA-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: HMDB0039795)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0039795)

Source

Endogenous

Endogenous (HMDB: HMDB0039795)

Plant

Plant (HMDB: HMDB0039795)

Animal

Animal (HMDB: HMDB0039795)

Exogenous

Food

Food (HMDB: HMDB0039795)

Fruit

Pome

Asian pear (FooDB: FOOD00291)

Fruits (FooDB: FOOD00871)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0039795)

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0039795)

Cellular process

Cell signaling (HMDB: HMDB0039795)

Biochemical process

Lipid transport (HMDB: HMDB0039795)

Role

Biological role

Energy storage (HMDB: HMDB0039795)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0039795)

Food and nutrition

Food additive

Flavoring agent

Flavoring Agent (HMDB: HMDB0039795)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	105.00 °C. @ 11.00 mm Hg	The Good Scents Company Information System
Water Solubility	52.1 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	3.406 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.21 g/L	ALOGPS
logP	3.27	ALOGPS
logP	2.84	ChemAxon
logS	-2.9	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	7	ChemAxon
Refractivity	50.91 m³·mol⁻¹	ChemAxon
Polarizability	20.68 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]+	143.134	31661259
DarkChem	[M-H]-	138.845	31661259
DeepCCS	[M+H]+	139.034	30932474
DeepCCS	[M-H]-	136.583	30932474
DeepCCS	[M-2H]-	173.003	30932474
DeepCCS	[M+Na]+	148.157	30932474
AllCCS	[M+H]+	143.0	32859911
AllCCS	[M+H-H2O]+	139.1	32859911
AllCCS	[M+NH4]+	146.6	32859911
AllCCS	[M+Na]+	147.6	32859911
AllCCS	[M-H]-	144.5	32859911
AllCCS	[M+Na-2H]-	146.3	32859911
AllCCS	[M+HCOO]-	148.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ethyl 4Z-octenoate	CCC\C=C\CCC(=O)OCC	1475.0	Standard polar	33892256
Ethyl 4Z-octenoate	CCC\C=C\CCC(=O)OCC	1157.4	Standard non polar	33892256
Ethyl 4Z-octenoate	CCC\C=C\CCC(=O)OCC	1217.7	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 - Ethyl 4Z-octenoate GC-MS (Non-derivatized) - 70eV, Positive	splash10-00or-9200000000-d4144d3c533f16b44d83	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Ethyl 4Z-octenoate 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 - Ethyl 4Z-octenoate 10V, Positive-QTOF	splash10-00di-1900000000-068674c61b6ce36d3e70	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 20V, Positive-QTOF	splash10-0092-9600000000-8156076dd07f538c0e51	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 40V, Positive-QTOF	splash10-0006-9000000000-76077f7aed9fbcd6bcff	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 10V, Negative-QTOF	splash10-01b9-1900000000-d2262a94d2e36ad7debf	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 20V, Negative-QTOF	splash10-00xs-4900000000-02fd81a9f7e577b95aa4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 40V, Negative-QTOF	splash10-0005-9200000000-ba0f6dd4a528b15e63fe	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 10V, Positive-QTOF	splash10-00kb-9200000000-ddd08818f1c734e30037	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 20V, Positive-QTOF	splash10-05mn-9000000000-2c80f344c24eed8bce20	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 40V, Positive-QTOF	splash10-0a4i-9000000000-33f8c38592cd3d25b05a	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 10V, Negative-QTOF	splash10-00di-0900000000-af12a5356b7df3e44545	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 20V, Negative-QTOF	splash10-0a4i-0900000000-353ee3a5f125d8435ef9	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Ethyl 4Z-octenoate 40V, Negative-QTOF	splash10-0006-9100000000-d067d9e2900d7c90d244	2021-09-24	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

FDB019445

KNApSAcK ID

Not Available

Chemspider ID

4509630

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5352799

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1022991

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 Ethyl 4Z-octenoate (HMDB0039795)

MOL for HMDB0039795 (Ethyl 4Z-octenoate)

3D MOL for HMDB0039795 (Ethyl 4Z-octenoate)

3D SDF for HMDB0039795 (Ethyl 4Z-octenoate)

3D-SDF for HMDB0039795 (Ethyl 4Z-octenoate)

PDB for HMDB0039795 (Ethyl 4Z-octenoate)

3D PDB for HMDB0039795 (Ethyl 4Z-octenoate)

SMILES for HMDB0039795 (Ethyl 4Z-octenoate)

INCHI for HMDB0039795 (Ethyl 4Z-octenoate)

Structure for HMDB0039795 (Ethyl 4Z-octenoate)

3D Structure for HMDB0039795 (Ethyl 4Z-octenoate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra