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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 21:37:52 UTC

Update Date

2021-09-26 22:52:14 UTC

HMDB ID

HMDB0244477

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Eicosa-5,8,11,14,17-pentaenoic acid

Description

Eicosa-5,8,11,14,17-pentaenoic acid belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. Based on a literature review very few articles have been published on Eicosa-5,8,11,14,17-pentaenoic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). Eicosa-5,8,11,14,17-pentaenoic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Eicosa-5,8,11,14,17-pentaenoic 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

HMDB0244477
     RDKit          3D
Eicosa-5,8,11,14,17-pentaenoic acid
 52 51  0  0  0  0  0  0  0  0999 V2000
    9.1753   -0.8709   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1976   -1.3572    0.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9190   -0.5508   -0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7418    0.4228   -0.8676 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6425    1.3055   -1.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4212    1.2605   -0.3591 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8981    0.5911    0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4784    0.9452    1.0487 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5762   -0.2000    0.8806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4912   -0.2282    0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0345    0.8789   -0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4001    1.2598   -0.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9529    0.5993    0.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3228    0.9807    1.2126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1794   -0.2196    1.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2396   -0.2365    0.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1160   -1.4238    0.0790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5146   -1.1220    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1122   -0.0060   -0.2962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1962   -0.2652   -1.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6231    0.6702   -2.4861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8565   -1.4361   -2.3806 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7116   -0.9818   -2.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4172    0.1941   -0.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1175   -1.4800   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6709   -1.2023    1.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9021   -2.3985   -0.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1623   -0.8326    0.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6425    0.6272   -1.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3614    1.2837   -2.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0543    2.4059   -1.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6866    2.0943   -0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3045   -0.2149    1.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.8681    0.5712 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6173    1.1694    2.1338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8584   -1.1099    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1052   -1.1578    0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0780    0.5122   -1.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5815    1.7786   -0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8913    2.0626   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4423   -0.2021    1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2626    1.2225    2.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7048    1.8444    0.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9247   -1.1144    1.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4922    0.6622   -0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6798   -2.2127    0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0694   -1.7493   -0.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4969   -0.8693    1.5780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1520   -2.0446    0.4325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4936    0.9125   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1274    0.2595    0.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3175   -2.3246   -2.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 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
 10 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 22 52  1  0
M  END


  Mrv1533004161514012D          

 22 21  0  0  0  0            999 V2000
    1.2375    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914    4.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6204    4.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6204    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  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
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0244477

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-19H2,1H3,(H,21,22)

> <INCHI_KEY>
JAZBEHYOTPTENJ-UHFFFAOYSA-N

> <FORMULA>
C20H30O2

> <MOLECULAR_WEIGHT>
302.458

> <EXACT_MASS>
302.224580206

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
36.74452754555985

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
icosa-5,8,11,14,17-pentaenoic acid

> <ALOGPS_LOGP>
6.53

> <JCHEM_LOGP>
6.225249154333334

> <ALOGPS_LOGS>
-6.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.819771840522258

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
101.0706

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.89e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
icosa-5,8,11,14,17-pentaenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0244477
     RDKit          3D
Eicosa-5,8,11,14,17-pentaenoic acid
 52 51  0  0  0  0  0  0  0  0999 V2000
    9.1753   -0.8709   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1976   -1.3572    0.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9190   -0.5508   -0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7418    0.4228   -0.8676 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6425    1.3055   -1.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4212    1.2605   -0.3591 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8981    0.5911    0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4784    0.9452    1.0487 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5762   -0.2000    0.8806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4912   -0.2282    0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0345    0.8789   -0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4001    1.2598   -0.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9529    0.5993    0.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3228    0.9807    1.2126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1794   -0.2196    1.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2396   -0.2365    0.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1160   -1.4238    0.0790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5146   -1.1220    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1122   -0.0060   -0.2962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1962   -0.2652   -1.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6231    0.6702   -2.4861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8565   -1.4361   -2.3806 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7116   -0.9818   -2.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4172    0.1941   -0.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1175   -1.4800   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6709   -1.2023    1.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9021   -2.3985   -0.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1623   -0.8326    0.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6425    0.6272   -1.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3614    1.2837   -2.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0543    2.4059   -1.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6866    2.0943   -0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3045   -0.2149    1.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.8681    0.5712 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6173    1.1694    2.1338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8584   -1.1099    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1052   -1.1578    0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0780    0.5122   -1.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5815    1.7786   -0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8913    2.0626   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4423   -0.2021    1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2626    1.2225    2.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7048    1.8444    0.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9247   -1.1144    1.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4922    0.6622   -0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6798   -2.2127    0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0694   -1.7493   -0.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4969   -0.8693    1.5780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1520   -2.0446    0.4325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4936    0.9125   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1274    0.2595    0.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3175   -2.3246   -2.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 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
 10 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 22 52  1  0
M  END

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       2.310   4.414   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.310   5.954   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.976   6.724   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.976   8.264   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.357   9.034   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.691   8.264   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.025   9.034   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.358   8.264   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.358   6.724   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.692   5.954   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.692   4.414   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.358   3.644   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.358   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.025   1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.691   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.357   1.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.976   2.104   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.977   1.334   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.311   2.104   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.977  -0.206   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                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   42    0
END

COMPND    HMDB0244477
HETATM    1  C1  UNL     1       9.175  -0.871  -1.001  1.00  0.00           C  
HETATM    2  C2  UNL     1       8.198  -1.357   0.028  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.919  -0.551  -0.025  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.742   0.423  -0.868  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.643   1.306  -1.097  1.00  0.00           C  
HETATM    6  C6  UNL     1       4.421   1.261  -0.359  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.898   0.591   0.583  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.478   0.945   1.049  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.576  -0.200   0.881  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.491  -0.228   0.138  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.035   0.879  -0.671  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.400   1.260  -0.235  1.00  0.00           C  
HETATM   13  C13 UNL     1      -1.953   0.599   0.775  1.00  0.00           C  
HETATM   14  C14 UNL     1      -3.323   0.981   1.213  1.00  0.00           C  
HETATM   15  C15 UNL     1      -4.179  -0.220   1.050  1.00  0.00           C  
HETATM   16  C16 UNL     1      -5.240  -0.237   0.262  1.00  0.00           C  
HETATM   17  C17 UNL     1      -6.116  -1.424   0.079  1.00  0.00           C  
HETATM   18  C18 UNL     1      -7.515  -1.122   0.493  1.00  0.00           C  
HETATM   19  C19 UNL     1      -8.112  -0.006  -0.296  1.00  0.00           C  
HETATM   20  C20 UNL     1      -8.196  -0.265  -1.738  1.00  0.00           C  
HETATM   21  O1  UNL     1      -8.623   0.670  -2.486  1.00  0.00           O  
HETATM   22  O2  UNL     1      -7.857  -1.436  -2.381  1.00  0.00           O  
HETATM   23  H1  UNL     1       8.712  -0.982  -2.014  1.00  0.00           H  
HETATM   24  H2  UNL     1       9.417   0.194  -0.820  1.00  0.00           H  
HETATM   25  H3  UNL     1      10.117  -1.480  -0.953  1.00  0.00           H  
HETATM   26  H4  UNL     1       8.671  -1.202   1.035  1.00  0.00           H  
HETATM   27  H5  UNL     1       7.902  -2.399  -0.124  1.00  0.00           H  
HETATM   28  H6  UNL     1       6.162  -0.833   0.681  1.00  0.00           H  
HETATM   29  H7  UNL     1       7.643   0.627  -1.580  1.00  0.00           H  
HETATM   30  H8  UNL     1       5.361   1.284  -2.242  1.00  0.00           H  
HETATM   31  H9  UNL     1       6.054   2.406  -1.097  1.00  0.00           H  
HETATM   32  H10 UNL     1       3.687   2.094  -0.741  1.00  0.00           H  
HETATM   33  H11 UNL     1       4.305  -0.215   1.127  1.00  0.00           H  
HETATM   34  H12 UNL     1       2.156   1.868   0.571  1.00  0.00           H  
HETATM   35  H13 UNL     1       2.617   1.169   2.134  1.00  0.00           H  
HETATM   36  H14 UNL     1       1.858  -1.110   1.442  1.00  0.00           H  
HETATM   37  H15 UNL     1      -0.105  -1.158   0.093  1.00  0.00           H  
HETATM   38  H16 UNL     1      -0.078   0.512  -1.738  1.00  0.00           H  
HETATM   39  H17 UNL     1       0.581   1.779  -0.704  1.00  0.00           H  
HETATM   40  H18 UNL     1      -1.891   2.063  -0.759  1.00  0.00           H  
HETATM   41  H19 UNL     1      -1.442  -0.202   1.286  1.00  0.00           H  
HETATM   42  H20 UNL     1      -3.263   1.222   2.294  1.00  0.00           H  
HETATM   43  H21 UNL     1      -3.705   1.844   0.641  1.00  0.00           H  
HETATM   44  H22 UNL     1      -3.925  -1.114   1.597  1.00  0.00           H  
HETATM   45  H23 UNL     1      -5.492   0.662  -0.287  1.00  0.00           H  
HETATM   46  H24 UNL     1      -5.680  -2.213   0.761  1.00  0.00           H  
HETATM   47  H25 UNL     1      -6.069  -1.749  -0.974  1.00  0.00           H  
HETATM   48  H26 UNL     1      -7.497  -0.869   1.578  1.00  0.00           H  
HETATM   49  H27 UNL     1      -8.152  -2.045   0.432  1.00  0.00           H  
HETATM   50  H28 UNL     1      -7.494   0.912  -0.084  1.00  0.00           H  
HETATM   51  H29 UNL     1      -9.127   0.260   0.119  1.00  0.00           H  
HETATM   52  H30 UNL     1      -8.318  -2.325  -2.212  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3   26   27
CONECT    3    4    4   28
CONECT    4    5   29
CONECT    5    6   30   31
CONECT    6    7    7   32
CONECT    7    8   33
CONECT    8    9   34   35
CONECT    9   10   10   36
CONECT   10   11   37
CONECT   11   12   38   39
CONECT   12   13   13   40
CONECT   13   14   41
CONECT   14   15   42   43
CONECT   15   16   16   44
CONECT   16   17   45
CONECT   17   18   46   47
CONECT   18   19   48   49
CONECT   19   20   50   51
CONECT   20   21   21   22
CONECT   22   52
END

HMDB0244477
     RDKit          3D
Eicosa-5,8,11,14,17-pentaenoic acid
 52 51  0  0  0  0  0  0  0  0999 V2000
    9.1753   -0.8709   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1976   -1.3572    0.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9190   -0.5508   -0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7418    0.4228   -0.8676 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6425    1.3055   -1.0965 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4212    1.2605   -0.3591 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8981    0.5911    0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4784    0.9452    1.0487 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5762   -0.2000    0.8806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4912   -0.2282    0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0345    0.8789   -0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4001    1.2598   -0.2347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9529    0.5993    0.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3228    0.9807    1.2126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1794   -0.2196    1.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2396   -0.2365    0.2623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1160   -1.4238    0.0790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5146   -1.1220    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1122   -0.0060   -0.2962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1962   -0.2652   -1.7375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6231    0.6702   -2.4861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8565   -1.4361   -2.3806 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7116   -0.9818   -2.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4172    0.1941   -0.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1175   -1.4800   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6709   -1.2023    1.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9021   -2.3985   -0.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1623   -0.8326    0.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6425    0.6272   -1.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3614    1.2837   -2.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0543    2.4059   -1.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6866    2.0943   -0.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3045   -0.2149    1.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.8681    0.5712 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6173    1.1694    2.1338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8584   -1.1099    1.4418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1052   -1.1578    0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0780    0.5122   -1.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5815    1.7786   -0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8913    2.0626   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4423   -0.2021    1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2626    1.2225    2.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7048    1.8444    0.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9247   -1.1144    1.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4922    0.6622   -0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6798   -2.2127    0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0694   -1.7493   -0.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4969   -0.8693    1.5780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1520   -2.0446    0.4325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4936    0.9125   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1274    0.2595    0.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3175   -2.3246   -2.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  2  3
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 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
 10 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  0
 19 51  1  0
 22 52  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Eicosa-5,8,11,14,17-pentaenoate	Generator
Icosa-5,8,11,14,17-pentaenoate	HMDB

Chemical Formula

C₂₀H₃₀O₂

Average Molecular Weight

302.458

Monoisotopic Molecular Weight

302.224580206

IUPAC Name

icosa-5,8,11,14,17-pentaenoic acid

Traditional Name

icosa-5,8,11,14,17-pentaenoic acid

CAS Registry Number

Not Available

SMILES

CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O

InChI Identifier

InChI=1S/C20H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-19H2,1H3,(H,21,22)

InChI Key

JAZBEHYOTPTENJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

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

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (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	6.53	ALOGPS
logP	6.23	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	4.82	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	13	ChemAxon
Refractivity	101.07 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]+	169.322	30932474
DeepCCS	[M-H]-	166.964	30932474
DeepCCS	[M-2H]-	201.268	30932474
DeepCCS	[M+Na]+	176.409	30932474
AllCCS	[M+H]+	181.2	32859911
AllCCS	[M+H-H2O]+	178.1	32859911
AllCCS	[M+NH4]+	184.0	32859911
AllCCS	[M+Na]+	184.9	32859911
AllCCS	[M-H]-	180.4	32859911
AllCCS	[M+Na-2H]-	182.0	32859911
AllCCS	[M+HCOO]-	183.9	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Eicosa-5,8,11,14,17-pentaenoic acid,1TMS,isomer #1	CCC=CCC=CCC=CCC=CCC=CCCCC(=O)O[Si](C)(C)C	2364.4	Semi standard non polar	33892256
Eicosa-5,8,11,14,17-pentaenoic acid,1TMS,isomer #1	CCC=CCC=CCC=CCC=CCC=CCCCC(=O)O[Si](C)(C)C	2334.3	Standard non polar	33892256
Eicosa-5,8,11,14,17-pentaenoic acid,1TMS,isomer #1	CCC=CCC=CCC=CCC=CCC=CCCCC(=O)O[Si](C)(C)C	2486.3	Standard polar	33892256
Eicosa-5,8,11,14,17-pentaenoic acid,1TBDMS,isomer #1	CCC=CCC=CCC=CCC=CCC=CCCCC(=O)O[Si](C)(C)C(C)(C)C	2613.9	Semi standard non polar	33892256
Eicosa-5,8,11,14,17-pentaenoic acid,1TBDMS,isomer #1	CCC=CCC=CCC=CCC=CCC=CCCCC(=O)O[Si](C)(C)C(C)(C)C	2547.9	Standard non polar	33892256
Eicosa-5,8,11,14,17-pentaenoic acid,1TBDMS,isomer #1	CCC=CCC=CCC=CCC=CCC=CCCCC(=O)O[Si](C)(C)C(C)(C)C	2511.0	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-004l-5490000000-ee15446245c5d0190ca2	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid 10V, Positive-QTOF	splash10-0f79-3985000000-f0a1f1db5a552a314689	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid 20V, Positive-QTOF	splash10-001l-5910000000-a82843e1aa65987b4a17	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid 40V, Positive-QTOF	splash10-00l6-9600000000-da4dd030385c445969bc	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid 10V, Negative-QTOF	splash10-0udi-0019000000-da419ae96bb8b07031de	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid 20V, Negative-QTOF	splash10-0ue9-1069000000-1175d959e564aa5bfc96	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Eicosa-5,8,11,14,17-pentaenoic acid 40V, Negative-QTOF	splash10-0596-9530000000-b5f6ca6a7368abde8826	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

3097

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3209

PDB ID

Not Available

ChEBI ID

92823

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 Eicosa-5,8,11,14,17-pentaenoic acid (HMDB0244477)

MOL for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

3D MOL for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

3D SDF for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

3D-SDF for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

PDB for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

3D PDB for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

SMILES for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

INCHI for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

Structure for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

3D Structure for HMDB0244477 (Eicosa-5,8,11,14,17-pentaenoic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra