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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 00:28:15 UTC

Update Date

2021-09-26 22:57:11 UTC

HMDB ID

HMDB0247466

Secondary Accession Numbers

None

Metabolite Identification

Common Name

8,12-Octadecadienoic acid

Description

8,12-Octadecadienoic acid belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. Based on a literature review a significant number of articles have been published on 8,12-Octadecadienoic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 8,12-octadecadienoic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 8,12-Octadecadienoic acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0247466
     RDKit          3D
8,12-Octadecadienoic acid
 52 51  0  0  0  0  0  0  0  0999 V2000
    8.0012   -1.0247   -1.6375 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3329    0.3091   -1.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4681    0.3456   -0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3497   -0.6797   -0.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5619   -0.5256    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4404   -1.4764    1.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1713   -1.2259    1.2260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227    0.1349    1.2985 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6612    0.4199    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1404    1.7823    0.2597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0891    2.1082    0.3912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2188    1.1736    0.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2130    1.3997   -0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3221    0.4172   -0.5544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1039    0.4802    0.7073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1975   -0.5583    0.6973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1833   -0.4050   -0.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2111   -1.4697   -0.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1340   -2.3060    0.6068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2151   -1.4911   -1.2782 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4523   -0.9842   -2.6714 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8455   -1.1678   -0.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3257   -1.8770   -1.6362 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7280    0.6211   -2.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1409    1.0535   -1.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0571    1.3727   -0.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0966    0.1920    0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7147   -1.6942   -0.4000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7058   -0.4242   -1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3278   -0.7339    1.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2513    0.5086    1.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7369   -2.5466    1.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4267   -2.0403    1.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0322    0.2825    2.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3498    0.9339    1.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0754   -0.3701    0.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2526    0.4011   -0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073    2.5873    0.2242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3647    3.1794    0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7554    1.2875    1.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8580    0.1395    0.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6840    1.2175   -1.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5213    2.4461   -0.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0194    0.5434   -1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8816   -0.6184   -0.6188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4794    0.3014    1.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5233    1.5128    0.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7339   -1.5634    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7648   -0.4266    1.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7451   -0.4926   -1.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6382    0.6061   -0.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1687   -1.6558   -0.9358 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  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 20 52  1  0
M  END

  Mrv1652309112102282D          

 20 19  0  0  0  0            999 V2000
   -0.5743    8.7434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    8.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    4.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0247466

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCC=CCCC=CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7,10-11H,2-5,8-9,12-17H2,1H3,(H,19,20)

> <INCHI_KEY>
FVIFMUSFIUXENC-UHFFFAOYSA-N

> <FORMULA>
C18H32O2

> <MOLECULAR_WEIGHT>
280.452

> <EXACT_MASS>
280.24023027

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
36.74361914405368

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
octadeca-8,12-dienoic acid

> <ALOGPS_LOGP>
7.04

> <JCHEM_LOGP>
6.421876794333333

> <ALOGPS_LOGS>
-6.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.885823686047827

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
88.51879999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.54e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
octadeca-8,12-dienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0247466
     RDKit          3D
8,12-Octadecadienoic acid
 52 51  0  0  0  0  0  0  0  0999 V2000
    8.0012   -1.0247   -1.6375 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3329    0.3091   -1.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4681    0.3456   -0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3497   -0.6797   -0.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5619   -0.5256    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4404   -1.4764    1.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1713   -1.2259    1.2260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227    0.1349    1.2985 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6612    0.4199    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1404    1.7823    0.2597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0891    2.1082    0.3912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2188    1.1736    0.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2130    1.3997   -0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3221    0.4172   -0.5544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1039    0.4802    0.7073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1975   -0.5583    0.6973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1833   -0.4050   -0.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2111   -1.4697   -0.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1340   -2.3060    0.6068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2151   -1.4911   -1.2782 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4523   -0.9842   -2.6714 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8455   -1.1678   -0.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3257   -1.8770   -1.6362 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7280    0.6211   -2.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1409    1.0535   -1.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0571    1.3727   -0.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0966    0.1920    0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7147   -1.6942   -0.4000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7058   -0.4242   -1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3278   -0.7339    1.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2513    0.5086    1.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7369   -2.5466    1.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4267   -2.0403    1.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0322    0.2825    2.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3498    0.9339    1.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0754   -0.3701    0.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2526    0.4011   -0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073    2.5873    0.2242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3647    3.1794    0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7554    1.2875    1.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8580    0.1395    0.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6840    1.2175   -1.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5213    2.4461   -0.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0194    0.5434   -1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8816   -0.6184   -0.6188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4794    0.3014    1.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5233    1.5128    0.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7339   -1.5634    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7648   -0.4266    1.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7451   -0.4926   -1.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6382    0.6061   -0.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1687   -1.6558   -0.9358 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  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 20 52  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -1.072  16.321   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.262  15.551   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.262  14.011   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.595  13.241   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.595  11.701   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.929  10.931   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.929   9.391   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.263   8.621   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.263   7.081   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.596   6.311   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      16.266   4.771   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      14.932   2.461   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                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   38    0
END

COMPND    HMDB0247466
HETATM    1  C1  UNL     1       8.001  -1.025  -1.638  1.00  0.00           C  
HETATM    2  C2  UNL     1       7.333   0.309  -1.423  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.468   0.346  -0.195  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.350  -0.680  -0.247  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.562  -0.526   1.056  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.440  -1.476   1.122  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.171  -1.226   1.226  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.623   0.135   1.299  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.661   0.420   0.147  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.140   1.782   0.260  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.089   2.108   0.391  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.219   1.174   0.456  1.00  0.00           C  
HETATM   13  C13 UNL     1      -3.213   1.400  -0.668  1.00  0.00           C  
HETATM   14  C14 UNL     1      -4.322   0.417  -0.554  1.00  0.00           C  
HETATM   15  C15 UNL     1      -5.104   0.480   0.707  1.00  0.00           C  
HETATM   16  C16 UNL     1      -6.197  -0.558   0.697  1.00  0.00           C  
HETATM   17  C17 UNL     1      -7.183  -0.405  -0.417  1.00  0.00           C  
HETATM   18  C18 UNL     1      -8.211  -1.470  -0.325  1.00  0.00           C  
HETATM   19  O1  UNL     1      -8.134  -2.306   0.607  1.00  0.00           O  
HETATM   20  O2  UNL     1      -9.215  -1.491  -1.278  1.00  0.00           O  
HETATM   21  H1  UNL     1       8.452  -0.984  -2.671  1.00  0.00           H  
HETATM   22  H2  UNL     1       8.845  -1.168  -0.954  1.00  0.00           H  
HETATM   23  H3  UNL     1       7.326  -1.877  -1.636  1.00  0.00           H  
HETATM   24  H4  UNL     1       6.728   0.621  -2.294  1.00  0.00           H  
HETATM   25  H5  UNL     1       8.141   1.053  -1.273  1.00  0.00           H  
HETATM   26  H6  UNL     1       6.057   1.373  -0.117  1.00  0.00           H  
HETATM   27  H7  UNL     1       7.097   0.192   0.712  1.00  0.00           H  
HETATM   28  H8  UNL     1       5.715  -1.694  -0.400  1.00  0.00           H  
HETATM   29  H9  UNL     1       4.706  -0.424  -1.118  1.00  0.00           H  
HETATM   30  H10 UNL     1       5.328  -0.734   1.860  1.00  0.00           H  
HETATM   31  H11 UNL     1       4.251   0.509   1.161  1.00  0.00           H  
HETATM   32  H12 UNL     1       3.737  -2.547   1.075  1.00  0.00           H  
HETATM   33  H13 UNL     1       1.427  -2.040   1.266  1.00  0.00           H  
HETATM   34  H14 UNL     1       1.032   0.283   2.253  1.00  0.00           H  
HETATM   35  H15 UNL     1       2.350   0.934   1.288  1.00  0.00           H  
HETATM   36  H16 UNL     1      -0.075  -0.370   0.030  1.00  0.00           H  
HETATM   37  H17 UNL     1       1.253   0.401  -0.830  1.00  0.00           H  
HETATM   38  H18 UNL     1       0.907   2.587   0.224  1.00  0.00           H  
HETATM   39  H19 UNL     1      -1.365   3.179   0.466  1.00  0.00           H  
HETATM   40  H20 UNL     1      -2.755   1.288   1.459  1.00  0.00           H  
HETATM   41  H21 UNL     1      -1.858   0.139   0.474  1.00  0.00           H  
HETATM   42  H22 UNL     1      -2.684   1.217  -1.623  1.00  0.00           H  
HETATM   43  H23 UNL     1      -3.521   2.446  -0.658  1.00  0.00           H  
HETATM   44  H24 UNL     1      -5.019   0.543  -1.409  1.00  0.00           H  
HETATM   45  H25 UNL     1      -3.882  -0.618  -0.619  1.00  0.00           H  
HETATM   46  H26 UNL     1      -4.479   0.301   1.618  1.00  0.00           H  
HETATM   47  H27 UNL     1      -5.523   1.513   0.830  1.00  0.00           H  
HETATM   48  H28 UNL     1      -5.734  -1.563   0.697  1.00  0.00           H  
HETATM   49  H29 UNL     1      -6.765  -0.427   1.647  1.00  0.00           H  
HETATM   50  H30 UNL     1      -6.745  -0.493  -1.436  1.00  0.00           H  
HETATM   51  H31 UNL     1      -7.638   0.606  -0.371  1.00  0.00           H  
HETATM   52  H32 UNL     1     -10.169  -1.656  -0.936  1.00  0.00           H  
CONECT    1    2   21   22   23
CONECT    2    3   24   25
CONECT    3    4   26   27
CONECT    4    5   28   29
CONECT    5    6   30   31
CONECT    6    7    7   32
CONECT    7    8   33
CONECT    8    9   34   35
CONECT    9   10   36   37
CONECT   10   11   11   38
CONECT   11   12   39
CONECT   12   13   40   41
CONECT   13   14   42   43
CONECT   14   15   44   45
CONECT   15   16   46   47
CONECT   16   17   48   49
CONECT   17   18   50   51
CONECT   18   19   19   20
CONECT   20   52
END

HMDB0247466
     RDKit          3D
8,12-Octadecadienoic acid
 52 51  0  0  0  0  0  0  0  0999 V2000
    8.0012   -1.0247   -1.6375 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3329    0.3091   -1.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4681    0.3456   -0.1948 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3497   -0.6797   -0.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5619   -0.5256    1.0564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4404   -1.4764    1.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1713   -1.2259    1.2260 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6227    0.1349    1.2985 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6612    0.4199    0.1473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1404    1.7823    0.2597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0891    2.1082    0.3912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2188    1.1736    0.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2130    1.3997   -0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3221    0.4172   -0.5544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1039    0.4802    0.7073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1975   -0.5583    0.6973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1833   -0.4050   -0.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2111   -1.4697   -0.3249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1340   -2.3060    0.6068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2151   -1.4911   -1.2782 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4523   -0.9842   -2.6714 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8455   -1.1678   -0.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3257   -1.8770   -1.6362 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7280    0.6211   -2.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1409    1.0535   -1.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0571    1.3727   -0.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0966    0.1920    0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7147   -1.6942   -0.4000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7058   -0.4242   -1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3278   -0.7339    1.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2513    0.5086    1.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7369   -2.5466    1.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4267   -2.0403    1.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0322    0.2825    2.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3498    0.9339    1.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0754   -0.3701    0.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2526    0.4011   -0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9073    2.5873    0.2242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3647    3.1794    0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7554    1.2875    1.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8580    0.1395    0.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6840    1.2175   -1.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5213    2.4461   -0.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0194    0.5434   -1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8816   -0.6184   -0.6188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4794    0.3014    1.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5233    1.5128    0.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7339   -1.5634    0.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7648   -0.4266    1.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7451   -0.4926   -1.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6382    0.6061   -0.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1687   -1.6558   -0.9358 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  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  3
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 20 52  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
8,12-Octadecadienoate	Generator

Chemical Formula

C₁₈H₃₂O₂

Average Molecular Weight

280.452

Monoisotopic Molecular Weight

280.24023027

IUPAC Name

octadeca-8,12-dienoic acid

Traditional Name

octadeca-8,12-dienoic acid

CAS Registry Number

Not Available

SMILES

CCCCCC=CCCC=CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7,10-11H,2-5,8-9,12-17H2,1H3,(H,19,20)

InChI Key

FVIFMUSFIUXENC-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Long-chain fatty acid
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

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

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	7.04	ALOGPS
logP	6.42	ChemAxon
logS	-6.3	ALOGPS
pKa (Strongest Acidic)	4.89	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	14	ChemAxon
Refractivity	88.52 m³·mol⁻¹	ChemAxon
Polarizability	36.74 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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
DeepCCS	[M+H]+	174.808	30932474
DeepCCS	[M-H]-	170.788	30932474
DeepCCS	[M-2H]-	207.946	30932474
DeepCCS	[M+Na]+	183.857	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
8,12-Octadecadienoic acid	CCCCCC=CCCC=CCCCCCCC(O)=O	3183.5	Standard polar	33892256
8,12-Octadecadienoic acid	CCCCCC=CCCC=CCCCCCCC(O)=O	2092.4	Standard non polar	33892256
8,12-Octadecadienoic acid	CCCCCC=CCCC=CCCCCCCC(O)=O	2141.4	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 - 8,12-Octadecadienoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-07bf-8930000000-e9443a5f1e2ebd49eda1	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8,12-Octadecadienoic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8,12-Octadecadienoic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8,12-Octadecadienoic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	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 - 8,12-Octadecadienoic acid 10V, Positive-QTOF	splash10-01q9-4490000000-473d549ae397b88b7330	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8,12-Octadecadienoic acid 20V, Positive-QTOF	splash10-05nb-9510000000-fbef270b5137453d95ee	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8,12-Octadecadienoic acid 40V, Positive-QTOF	splash10-0apl-9000000000-ec939f5c1e9a32bd780f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8,12-Octadecadienoic acid 10V, Negative-QTOF	splash10-004i-0090000000-03fd7d53d39127d02766	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8,12-Octadecadienoic acid 20V, Negative-QTOF	splash10-01t9-1090000000-049ebf7bae228dd70d7b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8,12-Octadecadienoic acid 40V, Negative-QTOF	splash10-0006-9220000000-43ecd74174cdf6fa5e97	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	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

21231940

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122193

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 8,12-Octadecadienoic acid (HMDB0247466)

MOL for HMDB0247466 (8,12-Octadecadienoic acid)

3D MOL for HMDB0247466 (8,12-Octadecadienoic acid)

3D SDF for HMDB0247466 (8,12-Octadecadienoic acid)

3D-SDF for HMDB0247466 (8,12-Octadecadienoic acid)

PDB for HMDB0247466 (8,12-Octadecadienoic acid)

3D PDB for HMDB0247466 (8,12-Octadecadienoic acid)

SMILES for HMDB0247466 (8,12-Octadecadienoic acid)

INCHI for HMDB0247466 (8,12-Octadecadienoic acid)

Structure for HMDB0247466 (8,12-Octadecadienoic acid)

3D Structure for HMDB0247466 (8,12-Octadecadienoic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra