Jump To Section:

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

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2017-08-02 20:48:26 UTC

Update Date

2023-02-21 17:31:19 UTC

HMDB ID

HMDB0094785

Secondary Accession Numbers

HMDB94785

Metabolite Identification

Common Name

1,7-octadienoylglycine

Description

2-[(1-oxoocta-1,7-dien-2-yl)amino]acetic acid belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 2-[(1-oxoocta-1,7-dien-2-yl)amino]acetic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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

HMDB0094785
     RDKit          3D
1,7-octadienoylglycine
 29 28  0  0  0  0  0  0  0  0999 V2000
   -4.6292   -0.3700    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4534   -0.6553   -0.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1353   -0.5469   -1.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1322   -0.0787   -0.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441    0.0694   -0.6153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359    0.5552    0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4954    0.7200    0.0386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0671    1.8832    0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    3.0564   -0.0622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1881   -0.3974   -0.4867 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6276   -0.2571   -0.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3343   -0.1480    0.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6570   -0.1892    1.6446 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6938   -0.0027    0.7159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7960   -0.0401    1.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5946   -0.4510    1.3685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018   -0.9797   -0.9585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1920    0.2301   -1.8528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8388   -1.4764   -1.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4416    0.9234    0.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0825   -0.8436    0.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3170   -0.8791   -0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7540    0.8368   -1.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0608   -0.1561    1.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2206    1.5281    0.9400 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7474   -1.2952   -0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7460    0.7483   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0324   -1.0114   -1.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3475   -0.7730    0.8010 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  2  0
  8  9  2  0
  7 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
 10 26  1  0
 11 27  1  0
 11 28  1  0
 14 29  1  0
M  END


  Mrv1652308021722482D          

 14 13  0  0  0  0            999 V2000
    1.7605    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9052    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  9  6  1  0  0  0  0
  9  8  2  0  0  0  0
 10  7  1  0  0  0  0
 11  7  1  0  0  0  0
 11  9  1  0  0  0  0
 12  8  2  0  0  0  0
 13 10  2  0  0  0  0
 14 10  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0094785

> <DATABASE_NAME>
hmdb

> <SMILES>
OC(=O)CNC(CCCCC=C)=C=O

> <INCHI_IDENTIFIER>
InChI=1S/C10H15NO3/c1-2-3-4-5-6-9(8-12)11-7-10(13)14/h2,11H,1,3-7H2,(H,13,14)

> <INCHI_KEY>
OEFQVBVKPTYRNN-UHFFFAOYSA-N

> <FORMULA>
C10H15NO3

> <MOLECULAR_WEIGHT>
197.234

> <EXACT_MASS>
197.105193347

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
29

> <JCHEM_AVERAGE_POLARIZABILITY>
21.02434092428439

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1-oxoocta-1,7-dien-2-yl)amino]acetic acid

> <ALOGPS_LOGP>
1.65

> <JCHEM_LOGP>
1.4038293559999997

> <ALOGPS_LOGS>
-2.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.58864637988465

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8148422189136477

> <JCHEM_PKA_STRONGEST_BASIC>
-9.40646887263307

> <JCHEM_POLAR_SURFACE_AREA>
66.4

> <JCHEM_REFRACTIVITY>
52.4164

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1-oxoocta-1,7-dien-2-yl)amino]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0094785
     RDKit          3D
1,7-octadienoylglycine
 29 28  0  0  0  0  0  0  0  0999 V2000
   -4.6292   -0.3700    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4534   -0.6553   -0.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1353   -0.5469   -1.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1322   -0.0787   -0.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441    0.0694   -0.6153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359    0.5552    0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4954    0.7200    0.0386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0671    1.8832    0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    3.0564   -0.0622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1881   -0.3974   -0.4867 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6276   -0.2571   -0.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3343   -0.1480    0.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6570   -0.1892    1.6446 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6938   -0.0027    0.7159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7960   -0.0401    1.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5946   -0.4510    1.3685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018   -0.9797   -0.9585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1920    0.2301   -1.8528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8388   -1.4764   -1.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4416    0.9234    0.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0825   -0.8436    0.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3170   -0.8791   -0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7540    0.8368   -1.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0608   -0.1561    1.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2206    1.5281    0.9400 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7474   -1.2952   -0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7460    0.7483   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0324   -1.0114   -1.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3475   -0.7730    0.8010 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  2  0
  8  9  2  0
  7 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
 10 26  1  0
 11 27  1  0
 11 28  1  0
 14 29  1  0
M  END

HEADER    PROTEIN                                 02-AUG-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-AUG-17         0                                  
HETATM    1  C   UNK     0       3.286   3.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.287   2.667   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.621   3.437   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.955   2.667   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.956   3.437   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.288   4.977   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.288   3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.289   2.667   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      12.622   2.667   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0      11.288   6.517   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      16.623   3.437   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      15.289   1.127   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    9                                                       
CONECT    7   10   11                                                       
CONECT    8    9   12                                                       
CONECT    9    6    8   11                                                  
CONECT   10    7   13   14                                                  
CONECT   11    7    9                                                       
CONECT   12    8                                                            
CONECT   13   10                                                            
CONECT   14   10                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

COMPND    HMDB0094785
HETATM    1  C1  UNL     1      -4.629  -0.370   0.889  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.453  -0.655  -0.380  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.135  -0.547  -1.043  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.132  -0.079  -0.035  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.744   0.069  -0.615  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.136   0.555   0.546  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.495   0.720   0.039  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.067   1.883   0.067  1.00  0.00           C  
HETATM    9  O1  UNL     1       2.500   3.056  -0.062  1.00  0.00           O  
HETATM   10  N1  UNL     1       2.188  -0.397  -0.487  1.00  0.00           N  
HETATM   11  C9  UNL     1       3.628  -0.257  -0.701  1.00  0.00           C  
HETATM   12  C10 UNL     1       4.334  -0.148   0.589  1.00  0.00           C  
HETATM   13  O2  UNL     1       3.657  -0.189   1.645  1.00  0.00           O  
HETATM   14  O3  UNL     1       5.694  -0.003   0.716  1.00  0.00           O  
HETATM   15  H1  UNL     1      -3.796  -0.040   1.501  1.00  0.00           H  
HETATM   16  H2  UNL     1      -5.595  -0.451   1.369  1.00  0.00           H  
HETATM   17  H3  UNL     1      -5.302  -0.980  -0.958  1.00  0.00           H  
HETATM   18  H4  UNL     1      -3.192   0.230  -1.853  1.00  0.00           H  
HETATM   19  H5  UNL     1      -2.839  -1.476  -1.561  1.00  0.00           H  
HETATM   20  H6  UNL     1      -2.442   0.923   0.326  1.00  0.00           H  
HETATM   21  H7  UNL     1      -2.082  -0.844   0.755  1.00  0.00           H  
HETATM   22  H8  UNL     1      -0.317  -0.879  -0.972  1.00  0.00           H  
HETATM   23  H9  UNL     1      -0.754   0.837  -1.411  1.00  0.00           H  
HETATM   24  H10 UNL     1       0.061  -0.156   1.397  1.00  0.00           H  
HETATM   25  H11 UNL     1      -0.221   1.528   0.940  1.00  0.00           H  
HETATM   26  H12 UNL     1       1.747  -1.295  -0.726  1.00  0.00           H  
HETATM   27  H13 UNL     1       3.746   0.748  -1.204  1.00  0.00           H  
HETATM   28  H14 UNL     1       4.032  -1.011  -1.388  1.00  0.00           H  
HETATM   29  H15 UNL     1       6.348  -0.773   0.801  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    8   10
CONECT    8    9    9
CONECT   10   11   26
CONECT   11   12   27   28
CONECT   12   13   13   14
CONECT   14   29
END

HMDB0094785
     RDKit          3D
1,7-octadienoylglycine
 29 28  0  0  0  0  0  0  0  0999 V2000
   -4.6292   -0.3700    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4534   -0.6553   -0.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1353   -0.5469   -1.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1322   -0.0787   -0.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441    0.0694   -0.6153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1359    0.5552    0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4954    0.7200    0.0386 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0671    1.8832    0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    3.0564   -0.0622 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1881   -0.3974   -0.4867 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6276   -0.2571   -0.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3343   -0.1480    0.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6570   -0.1892    1.6446 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6938   -0.0027    0.7159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7960   -0.0401    1.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5946   -0.4510    1.3685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018   -0.9797   -0.9585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1920    0.2301   -1.8528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8388   -1.4764   -1.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4416    0.9234    0.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0825   -0.8436    0.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3170   -0.8791   -0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7540    0.8368   -1.4108 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0608   -0.1561    1.3968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2206    1.5281    0.9400 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7474   -1.2952   -0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7460    0.7483   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0324   -1.0114   -1.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3475   -0.7730    0.8010 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  2  0
  8  9  2  0
  7 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
 10 26  1  0
 11 27  1  0
 11 28  1  0
 14 29  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-[(1-Oxoocta-1,7-dien-2-yl)amino]acetate	Generator

Chemical Formula

C₁₀H₁₅NO₃

Average Molecular Weight

197.234

Monoisotopic Molecular Weight

197.105193347

IUPAC Name

2-[(1-oxoocta-1,7-dien-2-yl)amino]acetic acid

Traditional Name

[(1-oxoocta-1,7-dien-2-yl)amino]acetic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CNC(CCCCC=C)=C=O

InChI Identifier

InChI=1S/C10H15NO3/c1-2-3-4-5-6-9(8-12)11-7-10(13)14/h2,11H,1,3-7H2,(H,13,14)

InChI Key

OEFQVBVKPTYRNN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids

Alternative Parents

Substituents

Alpha-amino acid
Amino acid
Carboxylic acid
Secondary aliphatic amine
Monocarboxylic acid or derivatives
Secondary amine
Ynolate
Carbonyl group
Organooxygen compound
Organonitrogen compound
Amine
Organic nitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organopnictogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Urine (PMID: 20971021)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.65	ALOGPS
logP	1.4	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	3.81	ChemAxon
pKa (Strongest Basic)	-9.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.4 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	52.42 m³·mol⁻¹	ChemAxon
Polarizability	21.02 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	149.968	31661259
DarkChem	[M-H]-	146.266	31661259
DeepCCS	[M+H]+	144.174	30932474
DeepCCS	[M-H]-	141.04	30932474
DeepCCS	[M-2H]-	177.776	30932474
DeepCCS	[M+Na]+	153.313	30932474
AllCCS	[M+H]+	146.7	32859911
AllCCS	[M+H-H2O]+	143.0	32859911
AllCCS	[M+NH4]+	150.2	32859911
AllCCS	[M+Na]+	151.2	32859911
AllCCS	[M-H]-	146.1	32859911
AllCCS	[M+Na-2H]-	147.3	32859911
AllCCS	[M+HCOO]-	148.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1,7-octadienoylglycine	OC(=O)CNC(CCCCC=C)=C=O	2591.7	Standard polar	33892256
1,7-octadienoylglycine	OC(=O)CNC(CCCCC=C)=C=O	1501.0	Standard non polar	33892256
1,7-octadienoylglycine	OC(=O)CNC(CCCCC=C)=C=O	1724.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1,7-octadienoylglycine,1TMS,isomer #1	C=CCCCCC(=C=O)NCC(=O)O[Si](C)(C)C	1752.3	Semi standard non polar	33892256
1,7-octadienoylglycine,1TMS,isomer #2	C=CCCCCC(=C=O)N(CC(=O)O)[Si](C)(C)C	1846.1	Semi standard non polar	33892256
1,7-octadienoylglycine,2TMS,isomer #1	C=CCCCCC(=C=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C	1854.4	Semi standard non polar	33892256
1,7-octadienoylglycine,2TMS,isomer #1	C=CCCCCC(=C=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C	1785.4	Standard non polar	33892256
1,7-octadienoylglycine,2TMS,isomer #1	C=CCCCCC(=C=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C	2051.4	Standard polar	33892256
1,7-octadienoylglycine,1TBDMS,isomer #1	C=CCCCCC(=C=O)NCC(=O)O[Si](C)(C)C(C)(C)C	1987.2	Semi standard non polar	33892256
1,7-octadienoylglycine,1TBDMS,isomer #2	C=CCCCCC(=C=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C	2084.9	Semi standard non polar	33892256
1,7-octadienoylglycine,2TBDMS,isomer #1	C=CCCCCC(=C=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2337.0	Semi standard non polar	33892256
1,7-octadienoylglycine,2TBDMS,isomer #1	C=CCCCCC(=C=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2160.1	Standard non polar	33892256
1,7-octadienoylglycine,2TBDMS,isomer #1	C=CCCCCC(=C=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2289.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1,7-octadienoylglycine GC-MS (Non-derivatized) - 70eV, Positive	splash10-00ou-9500000000-3b9b77896d8f006eead6	2017-09-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1,7-octadienoylglycine GC-MS (1 TMS) - 70eV, Positive	splash10-0fmr-9120000000-b5ad3c6f79aa66c5dc4e	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1,7-octadienoylglycine 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 - 1,7-octadienoylglycine 10V, Negative-QTOF	splash10-0002-0900000000-989a239286b1cdfb89ac	2017-09-14	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 20V, Negative-QTOF	splash10-0f6t-1900000000-73c34e9cb30669aa372e	2017-09-14	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 40V, Negative-QTOF	splash10-074l-9200000000-26bca6d21ca4e5edb2dd	2017-09-14	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 10V, Positive-QTOF	splash10-0002-0900000000-fd6b3d03087090cffa8c	2017-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 20V, Positive-QTOF	splash10-0pc0-5900000000-87a4f094eb8e492592ce	2017-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 40V, Positive-QTOF	splash10-0a6r-9000000000-39fe7c84439a8711cb5a	2017-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 10V, Positive-QTOF	splash10-0032-2900000000-b60457027797e6596fba	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 20V, Positive-QTOF	splash10-00ai-9500000000-fb43ed9713a35b5b9b5a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 40V, Positive-QTOF	splash10-0ar0-9000000000-127e53eea3033c2f1287	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 10V, Negative-QTOF	splash10-014i-0900000000-8fad3fa29aa0c94ea92f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 20V, Negative-QTOF	splash10-01b9-1900000000-03fadd1a74f6befbcbca	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1,7-octadienoylglycine 40V, Negative-QTOF	splash10-00yi-9300000000-e643af631661d14e0f57	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+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

Not Available

Biospecimen Locations

Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Urine	Detected but not Quantified	Not Quantified	Adult (24-38years old)	Not Specified	Normal	20971021	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131802965

PDB ID

Not Available

ChEBI ID

Not Available

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

Not Available

Showing metabocard for 1,7-octadienoylglycine (HMDB0094785)

MOL for HMDB0094785 (1,7-octadienoylglycine)

3D MOL for HMDB0094785 (1,7-octadienoylglycine)

3D SDF for HMDB0094785 (1,7-octadienoylglycine)

3D-SDF for HMDB0094785 (1,7-octadienoylglycine)

PDB for HMDB0094785 (1,7-octadienoylglycine)

3D PDB for HMDB0094785 (1,7-octadienoylglycine)

SMILES for HMDB0094785 (1,7-octadienoylglycine)

INCHI for HMDB0094785 (1,7-octadienoylglycine)

Structure for HMDB0094785 (1,7-octadienoylglycine)

3D Structure for HMDB0094785 (1,7-octadienoylglycine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

IR Spectra