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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 23:38:15 UTC

Update Date

2021-09-26 22:55:49 UTC

HMDB ID

HMDB0246621

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4,7,10,13,16-Docosapentaenoic acid

Description

docosa-4,7,10,13,16-pentaenoic acid belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms. Based on a literature review very few articles have been published on docosa-4,7,10,13,16-pentaenoic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4,7,10,13,16-docosapentaenoic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4,7,10,13,16-Docosapentaenoic 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

HMDB0246621
     RDKit          3D
4,7,10,13,16-Docosapentaenoic acid
 58 57  0  0  0  0  0  0  0  0999 V2000
   -9.4189    0.4140   -1.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2358    0.1163   -0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7348    1.4495   -0.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5592    1.3038    0.7945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3728    0.6303    0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3039    0.5582    1.1569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8331   -0.6202    1.5157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616   -0.7988    2.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6196   -1.4815    1.8829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292   -1.8350    0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4505   -2.5332   -0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0239   -1.6418   -1.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1417   -1.1178   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2639   -1.2784   -0.2820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6248    0.0397    0.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7733    0.6189    0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9281    0.0153   -0.5877 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0170   -0.0971    0.4160 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1630    0.4671    0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6257    1.3124   -0.7830 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8707    0.6962   -1.4474 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9228    0.5912   -0.4158 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9395   -0.4197    0.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8606    1.6008   -0.2839 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1081    0.7063   -2.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0665    1.1974   -1.1027 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0761   -0.4974   -1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4373   -0.3974   -1.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5692   -0.4999    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5240    2.1587   -0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5593    1.8954    0.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8243    0.6973    1.6814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2326    2.3195    1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6352   -0.4000   -0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0432    1.1724   -0.7742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9059    1.4825    1.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2403   -1.5074    1.0536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4258    0.1686    2.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1819   -1.3775    3.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7495   -1.6819    2.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4795   -1.6449   -0.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7908   -3.5079   -0.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3436   -2.6508    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8043   -1.4225   -1.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3485   -0.4585   -2.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0743   -1.7755   -0.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0390   -2.0028    0.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8055    0.5569    0.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9458    1.6258    0.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7580   -0.9836   -0.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2433    0.7378   -1.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8188   -0.7121    1.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8986    0.3105    1.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0128    2.2874   -0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9381    1.5225   -1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1415    1.4063   -2.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6292   -0.2996   -1.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4690    1.6541    0.5394 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  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  2  3
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  0
 21 57  1  0
 24 58  1  0
M  END


  Mrv0541 02251203502D          

 24 23  0  0  0  0            999 V2000
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2388    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9533    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6677    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6677    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3822    4.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3822    5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6677    6.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6677    6.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9533    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2388    6.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5243    8.1395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    6.9020    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
  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
 18 17  1  4  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0246621

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h6-7,9-10,12-13,15-16,18-19H,2-5,8,11,14,17,20-21H2,1H3,(H,23,24)

> <INCHI_KEY>
AVKOENOBFIYBSA-UHFFFAOYSA-N

> <FORMULA>
C22H34O2

> <MOLECULAR_WEIGHT>
330.5042

> <EXACT_MASS>
330.255880332

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
40.56189258322923

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
docosa-4,7,10,13,16-pentaenoic acid

> <ALOGPS_LOGP>
7.18

> <JCHEM_LOGP>
7.114386484333333

> <ALOGPS_LOGS>
-6.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.8854984143453795

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
110.2726

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.04e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
docosa-4,7,10,13,16-pentaenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0246621
     RDKit          3D
4,7,10,13,16-Docosapentaenoic acid
 58 57  0  0  0  0  0  0  0  0999 V2000
   -9.4189    0.4140   -1.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2358    0.1163   -0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7348    1.4495   -0.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5592    1.3038    0.7945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3728    0.6303    0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3039    0.5582    1.1569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8331   -0.6202    1.5157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616   -0.7988    2.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6196   -1.4815    1.8829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292   -1.8350    0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4505   -2.5332   -0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0239   -1.6418   -1.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1417   -1.1178   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2639   -1.2784   -0.2820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6248    0.0397    0.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7733    0.6189    0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9281    0.0153   -0.5877 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0170   -0.0971    0.4160 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1630    0.4671    0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6257    1.3124   -0.7830 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8707    0.6962   -1.4474 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9228    0.5912   -0.4158 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9395   -0.4197    0.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8606    1.6008   -0.2839 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1081    0.7063   -2.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0665    1.1974   -1.1027 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0761   -0.4974   -1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4373   -0.3974   -1.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5692   -0.4999    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5240    2.1587   -0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5593    1.8954    0.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8243    0.6973    1.6814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2326    2.3195    1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6352   -0.4000   -0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0432    1.1724   -0.7742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9059    1.4825    1.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2403   -1.5074    1.0536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4258    0.1686    2.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1819   -1.3775    3.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7495   -1.6819    2.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4795   -1.6449   -0.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7908   -3.5079   -0.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3436   -2.6508    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8043   -1.4225   -1.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3485   -0.4585   -2.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0743   -1.7755   -0.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0390   -2.0028    0.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8055    0.5569    0.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9458    1.6258    0.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7580   -0.9836   -0.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2433    0.7378   -1.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8188   -0.7121    1.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8986    0.3105    1.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0128    2.2874   -0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9381    1.5225   -1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1415    1.4063   -2.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6292   -0.2996   -1.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4690    1.6541    0.5394 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  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  2  3
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  0
 21 57  1  0
 24 58  1  0
M  END

HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
HETATM    1  C   UNK     0      -0.357   1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.976   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.977   1.334   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.311   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.645   1.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.978   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.978   3.644   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.312   4.414   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.312   5.954   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.646   6.724   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.979   5.954   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.313   6.724   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.313   8.264   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.647   9.034   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.647  10.574   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.313  11.344   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.313  12.884   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.979  13.654   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.646  12.884   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.312  13.654   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.312  15.194   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       8.978  12.884   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                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

COMPND    HMDB0246621
HETATM    1  C1  UNL     1      -9.419   0.414  -1.549  1.00  0.00           C  
HETATM    2  C2  UNL     1      -8.236   0.116  -0.635  1.00  0.00           C  
HETATM    3  C3  UNL     1      -7.735   1.450  -0.127  1.00  0.00           C  
HETATM    4  C4  UNL     1      -6.559   1.304   0.794  1.00  0.00           C  
HETATM    5  C5  UNL     1      -5.373   0.630   0.136  1.00  0.00           C  
HETATM    6  C6  UNL     1      -4.304   0.558   1.157  1.00  0.00           C  
HETATM    7  C7  UNL     1      -3.833  -0.620   1.516  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.762  -0.799   2.531  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.620  -1.481   1.883  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.629  -1.835   0.624  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.450  -2.533  -0.022  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.024  -1.642  -1.115  1.00  0.00           C  
HETATM   13  C13 UNL     1       1.142  -1.118  -1.204  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.264  -1.278  -0.282  1.00  0.00           C  
HETATM   15  C15 UNL     1       2.625   0.040   0.249  1.00  0.00           C  
HETATM   16  C16 UNL     1       3.773   0.619   0.128  1.00  0.00           C  
HETATM   17  C17 UNL     1       4.928   0.015  -0.588  1.00  0.00           C  
HETATM   18  C18 UNL     1       6.017  -0.097   0.416  1.00  0.00           C  
HETATM   19  C19 UNL     1       7.163   0.467   0.311  1.00  0.00           C  
HETATM   20  C20 UNL     1       7.626   1.312  -0.783  1.00  0.00           C  
HETATM   21  C21 UNL     1       8.871   0.696  -1.447  1.00  0.00           C  
HETATM   22  C22 UNL     1       9.923   0.591  -0.416  1.00  0.00           C  
HETATM   23  O1  UNL     1       9.940  -0.420   0.321  1.00  0.00           O  
HETATM   24  O2  UNL     1      10.861   1.601  -0.284  1.00  0.00           O  
HETATM   25  H1  UNL     1      -9.108   0.706  -2.554  1.00  0.00           H  
HETATM   26  H2  UNL     1     -10.066   1.197  -1.103  1.00  0.00           H  
HETATM   27  H3  UNL     1     -10.076  -0.497  -1.650  1.00  0.00           H  
HETATM   28  H4  UNL     1      -7.437  -0.397  -1.211  1.00  0.00           H  
HETATM   29  H5  UNL     1      -8.569  -0.500   0.208  1.00  0.00           H  
HETATM   30  H6  UNL     1      -7.524   2.159  -0.933  1.00  0.00           H  
HETATM   31  H7  UNL     1      -8.559   1.895   0.482  1.00  0.00           H  
HETATM   32  H8  UNL     1      -6.824   0.697   1.681  1.00  0.00           H  
HETATM   33  H9  UNL     1      -6.233   2.320   1.086  1.00  0.00           H  
HETATM   34  H10 UNL     1      -5.635  -0.400  -0.165  1.00  0.00           H  
HETATM   35  H11 UNL     1      -5.043   1.172  -0.774  1.00  0.00           H  
HETATM   36  H12 UNL     1      -3.906   1.483   1.613  1.00  0.00           H  
HETATM   37  H13 UNL     1      -4.240  -1.507   1.054  1.00  0.00           H  
HETATM   38  H14 UNL     1      -2.426   0.169   2.953  1.00  0.00           H  
HETATM   39  H15 UNL     1      -3.182  -1.378   3.381  1.00  0.00           H  
HETATM   40  H16 UNL     1      -0.749  -1.682   2.515  1.00  0.00           H  
HETATM   41  H17 UNL     1      -2.479  -1.645  -0.013  1.00  0.00           H  
HETATM   42  H18 UNL     1      -0.791  -3.508  -0.450  1.00  0.00           H  
HETATM   43  H19 UNL     1       0.344  -2.651   0.713  1.00  0.00           H  
HETATM   44  H20 UNL     1      -0.804  -1.423  -1.920  1.00  0.00           H  
HETATM   45  H21 UNL     1       1.348  -0.458  -2.077  1.00  0.00           H  
HETATM   46  H22 UNL     1       3.074  -1.775  -0.880  1.00  0.00           H  
HETATM   47  H23 UNL     1       2.039  -2.003   0.536  1.00  0.00           H  
HETATM   48  H24 UNL     1       1.806   0.557   0.802  1.00  0.00           H  
HETATM   49  H25 UNL     1       3.946   1.626   0.570  1.00  0.00           H  
HETATM   50  H26 UNL     1       4.758  -0.984  -0.994  1.00  0.00           H  
HETATM   51  H27 UNL     1       5.243   0.738  -1.376  1.00  0.00           H  
HETATM   52  H28 UNL     1       5.819  -0.712   1.315  1.00  0.00           H  
HETATM   53  H29 UNL     1       7.899   0.311   1.136  1.00  0.00           H  
HETATM   54  H30 UNL     1       8.013   2.287  -0.377  1.00  0.00           H  
HETATM   55  H31 UNL     1       6.938   1.522  -1.587  1.00  0.00           H  
HETATM   56  H32 UNL     1       9.142   1.406  -2.267  1.00  0.00           H  
HETATM   57  H33 UNL     1       8.629  -0.300  -1.867  1.00  0.00           H  
HETATM   58  H34 UNL     1      11.469   1.654   0.539  1.00  0.00           H  
CONECT    1    2   25   26   27
CONECT    2    3   28   29
CONECT    3    4   30   31
CONECT    4    5   32   33
CONECT    5    6   34   35
CONECT    6    7    7   36
CONECT    7    8   37
CONECT    8    9   38   39
CONECT    9   10   10   40
CONECT   10   11   41
CONECT   11   12   42   43
CONECT   12   13   13   44
CONECT   13   14   45
CONECT   14   15   46   47
CONECT   15   16   16   48
CONECT   16   17   49
CONECT   17   18   50   51
CONECT   18   19   19   52
CONECT   19   20   53
CONECT   20   21   54   55
CONECT   21   22   56   57
CONECT   22   23   23   24
CONECT   24   58
END

HMDB0246621
     RDKit          3D
4,7,10,13,16-Docosapentaenoic acid
 58 57  0  0  0  0  0  0  0  0999 V2000
   -9.4189    0.4140   -1.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2358    0.1163   -0.6348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7348    1.4495   -0.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5592    1.3038    0.7945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3728    0.6303    0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3039    0.5582    1.1569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8331   -0.6202    1.5157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616   -0.7988    2.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6196   -1.4815    1.8829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6292   -1.8350    0.6239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4505   -2.5332   -0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0239   -1.6418   -1.1152 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1417   -1.1178   -1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2639   -1.2784   -0.2820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6248    0.0397    0.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7733    0.6189    0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9281    0.0153   -0.5877 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0170   -0.0971    0.4160 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1630    0.4671    0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6257    1.3124   -0.7830 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8707    0.6962   -1.4474 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9228    0.5912   -0.4158 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9395   -0.4197    0.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8606    1.6008   -0.2839 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1081    0.7063   -2.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0665    1.1974   -1.1027 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0761   -0.4974   -1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4373   -0.3974   -1.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5692   -0.4999    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5240    2.1587   -0.9329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5593    1.8954    0.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8243    0.6973    1.6814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2326    2.3195    1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6352   -0.4000   -0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0432    1.1724   -0.7742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9059    1.4825    1.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2403   -1.5074    1.0536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4258    0.1686    2.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1819   -1.3775    3.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7495   -1.6819    2.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4795   -1.6449   -0.0129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7908   -3.5079   -0.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3436   -2.6508    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8043   -1.4225   -1.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3485   -0.4585   -2.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0743   -1.7755   -0.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0390   -2.0028    0.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8055    0.5569    0.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9458    1.6258    0.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7580   -0.9836   -0.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2433    0.7378   -1.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8188   -0.7121    1.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8986    0.3105    1.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0128    2.2874   -0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9381    1.5225   -1.5868 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1415    1.4063   -2.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6292   -0.2996   -1.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4690    1.6541    0.5394 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  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  2  3
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 21 56  1  0
 21 57  1  0
 24 58  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Docosa-4,7,10,13,16-pentaenoate	Generator
4,7,10,13,16-Docosapentaenoate	Generator
(all-Z)-7, 10, 13, 16, 19-Docosapentaenoic acid	MeSH
7,10,13,16,19-Docosapentaenoic acid	MeSH
7,10,13,16,19-Docosapentaenoic acid, (Z,Z,Z,Z,e)-isomer	MeSH
7,10,13,16,19-Docosapentaenoic acid, lithium salt	MeSH
Docosapentaenoic acid, (all Z)-isomer	MeSH
Clupanodonic acid	MeSH
Docosapentaenoic acid	MeSH
7,10,13,16,19-Docosapentaenoic acid, (all-Z)-isomer	MeSH
7,10,13,16,19-Docosapentaenoic acid, lithium salt, (all-Z)-isomer	MeSH
Docosa-4,7,10,13,16-pentaenoic acid, (all-Z)-isomer	MeSH
Docosapentaenoic acid (C22:5 N3)	MeSH
Osbond acid	MeSH
cis-7,10,13,16,19-Docosapentaenoic acid	MeSH
Docosa-4,7,10,13,16-pentaenoic acid 5-(14)C-labeled CPD, (all-Z)-isomer	MeSH
Docosapentaenoic acid (C22:5 N6)	MeSH

Chemical Formula

C₂₂H₃₄O₂

Average Molecular Weight

330.5042

Monoisotopic Molecular Weight

330.255880332

IUPAC Name

docosa-4,7,10,13,16-pentaenoic acid

Traditional Name

docosa-4,7,10,13,16-pentaenoic acid

CAS Registry Number

Not Available

SMILES

CCCCCC=CCC=CCC=CCC=CCC=CCCC(O)=O

InChI Identifier

InChI=1S/C22H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h6-7,9-10,12-13,15-16,18-19H,2-5,8,11,14,17,20-21H2,1H3,(H,23,24)

InChI Key

AVKOENOBFIYBSA-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Very long-chain fatty acids

Alternative Parents

Substituents

Very 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	7.18	ALOGPS
logP	7.11	ChemAxon
logS	-6.5	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	15	ChemAxon
Refractivity	110.27 m³·mol⁻¹	ChemAxon
Polarizability	40.56 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]+	180.299	30932474
DeepCCS	[M-H]-	177.941	30932474
DeepCCS	[M-2H]-	210.826	30932474
DeepCCS	[M+Na]+	186.407	30932474
AllCCS	[M+H]+	190.1	32859911
AllCCS	[M+H-H2O]+	187.2	32859911
AllCCS	[M+NH4]+	192.7	32859911
AllCCS	[M+Na]+	193.4	32859911
AllCCS	[M-H]-	189.0	32859911
AllCCS	[M+Na-2H]-	191.0	32859911
AllCCS	[M+HCOO]-	193.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4,7,10,13,16-Docosapentaenoic acid	CCCCCC=CCC=CCC=CCC=CCC=CCCC(O)=O	3962.9	Standard polar	33892256
4,7,10,13,16-Docosapentaenoic acid	CCCCCC=CCC=CCC=CCC=CCC=CCCC(O)=O	2272.3	Standard non polar	33892256
4,7,10,13,16-Docosapentaenoic acid	CCCCCC=CCC=CCC=CCC=CCC=CCCC(O)=O	2510.3	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 - 4,7,10,13,16-Docosapentaenoic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-00fu-7490000000-97ad3e356a5f908f9003	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4,7,10,13,16-Docosapentaenoic 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 - 4,7,10,13,16-Docosapentaenoic acid 10V, Positive-QTOF	splash10-03di-0039000000-92ed61a36adfd10a5233	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 20V, Positive-QTOF	splash10-03l9-3492000000-f8a5d9f173a783000a56	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 40V, Positive-QTOF	splash10-00kf-7960000000-9bdeec2dbacd50f957c0	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 10V, Negative-QTOF	splash10-004i-0019000000-4d8832b1fd953fd8ec08	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 20V, Negative-QTOF	splash10-01ti-1039000000-f6df0e4a8ec7c01d9955	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 40V, Negative-QTOF	splash10-0a4l-9140000000-8192a4ad85e4df29c777	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 10V, Positive-QTOF	splash10-01q9-1239000000-b1d4cd921a69d9f8653f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 20V, Positive-QTOF	splash10-01q9-6933000000-1d63fd3f377179dddb82	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 40V, Positive-QTOF	splash10-053u-9800000000-eeb640c3008512e3c40a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 10V, Negative-QTOF	splash10-004i-0009000000-f4bd181f937819513660	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 20V, Negative-QTOF	splash10-01t9-1009000000-9f6e2aedf2759dd3c7b5	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4,7,10,13,16-Docosapentaenoic acid 40V, Negative-QTOF	splash10-052f-9041000000-f6b90f282a7eccd547fd	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

FDB029296

KNApSAcK ID

Not Available

Chemspider ID

21237899

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

159656

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 4,7,10,13,16-Docosapentaenoic acid (HMDB0246621)

MOL for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

3D MOL for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

3D SDF for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

3D-SDF for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

PDB for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

3D PDB for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

SMILES for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

INCHI for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

Structure for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

3D Structure for HMDB0246621 (4,7,10,13,16-Docosapentaenoic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra