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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 15:51:33 UTC

Update Date

2021-09-26 23:11:07 UTC

HMDB ID

HMDB0255895

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Octadecadienylcarnitine

Description

3-hydroxy-3-[(trimethylazaniumyl)methyl]henicosa-4,6-dienoate belongs to the class of organic compounds known as other hydroxyeicosapolyenoic acids. These are hydroxyeicosapolyenoic acids which do not belong to the Hydroxyeicosapentaenoic acids, the Hydroxyeicosatetraenoic acids, or the Hydroxyeicosatrienoic acids. Based on a literature review a significant number of articles have been published on 3-hydroxy-3-[(trimethylazaniumyl)methyl]henicosa-4,6-dienoate. This compound has been identified in human blood as reported by (PMID: 31557052 ). Octadecadienylcarnitine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Octadecadienylcarnitine 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


  Mrv1652309112117512D          

 29 28  0  0  0  0            999 V2000
    6.7105    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1395    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8539    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5684    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2829    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1408    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8552    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5697    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2842    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7131    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4276    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1421    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8565    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5710    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2855    5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9999    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7144    5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.9999    3.8743    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   19.9835    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5710    3.2704    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   18.8565    3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2855    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1585    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1585    5.4138    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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  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
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 19 29  1  0  0  0  0
M  CHG  2  23  -1  25   1
M  END

HMDB0255895
     RDKit          3D
Octadecadienylcarnitine
 76 75  0  0  0  0  0  0  0  0999 V2000
    6.1361   -1.1439   -3.3778 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0137   -2.1100   -2.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2010   -1.8115   -1.3034 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2355   -2.6844   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0090   -2.5084    0.7820 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8582   -1.0714    1.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6406   -0.8912    2.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5459    0.5432    2.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4474    1.5222    1.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2481    1.3140    0.5298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9877    1.4373    1.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337    1.2440    0.5201 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7012    2.2969   -0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5512    2.1620   -1.4202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6954    2.3110   -0.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182    1.4023   -0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6669    0.1162   -0.9888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5309   -0.8405   -0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7281   -0.6778    0.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1716   -0.1782    1.2129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2603   -2.0793    0.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3540   -2.3516    1.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6285   -1.6020    2.0359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1948   -3.4766    0.9643 O   0  0  0  0  0  1  0  0  0  0  0  0
   -5.6714    0.1909   -0.6796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8233    0.7667   -0.1467 N   0  0  0  0  0  4  0  0  0  0  0  0
   -6.6717    1.4542    1.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0524    0.0289   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0901    1.9356   -1.0798 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1234   -1.0595   -3.8189 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4247   -0.1697   -2.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8710   -1.5351   -4.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0657   -3.1599   -2.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0838   -1.8670   -1.6686 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1796   -0.7356   -1.0584 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1325   -1.9876   -1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1029   -2.3745    0.5463 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3385   -3.7434   -0.3518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0760   -2.8478    0.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228   -3.1101    1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7097   -0.4774    0.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472   -0.7667    1.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7162   -1.2375    1.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7584   -1.5046    3.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7057    0.6307    3.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4810    0.7608    3.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3538    1.4559    0.7882 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4524    2.5391    1.8755 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3268    2.0725   -0.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3443    0.3311    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031    2.4459    1.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0233    0.6448    2.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6831    0.2150    0.0928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.3427    1.2254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7447    3.2892   -0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5433    2.2058   -1.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5381    1.1875   -1.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5673    2.9969   -2.1711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7900    3.2610    0.0486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4212    1.7000    0.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8272   -0.0714   -1.6975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4597   -1.7452   -1.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5297   -0.5682    2.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4209   -2.8251    0.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6519   -2.3233   -0.8710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0042   -0.3490   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0331    1.0182   -1.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0732    2.5147    1.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2966    0.9966    1.9408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6126    1.5984    1.4207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5316   -0.1811    0.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7985    0.6232   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9194   -0.8994   -0.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8664    2.5267   -0.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4510    1.4433   -2.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1523    2.4408   -1.2982 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  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  2  3
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 19 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 12 53  1  0
 12 54  1  0
 13 55  1  0
 13 56  1  0
 14 57  1  0
 14 58  1  0
 15 59  1  0
 16 60  1  0
 17 61  1  0
 18 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 25 66  1  0
 25 67  1  0
 27 68  1  0
 27 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 28 73  1  0
 29 74  1  0
 29 75  1  0
 29 76  1  0
M  CHG  2  24  -1  26   1
M  END


  Mrv1652309112117512D          

 29 28  0  0  0  0            999 V2000
    6.7105    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1395    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8539    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5684    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2829    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1408    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8552    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5697    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2842    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7131    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4276    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1421    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8565    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5710    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2855    5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9999    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7144    5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.9999    3.8743    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   19.9835    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5710    3.2704    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   18.8565    3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2855    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1585    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1585    5.4138    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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  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
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 19 29  1  0  0  0  0
M  CHG  2  23  -1  25   1
M  END
> <DATABASE_ID>
HMDB0255895

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCCCCCCCC=CC=CC(O)(CC([O-])=O)C[N+](C)(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H47NO3/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25(29,22-24(27)28)23-26(2,3)4/h18-21,29H,5-17,22-23H2,1-4H3

> <INCHI_KEY>
RHIDLCOXTYRESP-UHFFFAOYSA-N

> <FORMULA>
C25H47NO3

> <MOLECULAR_WEIGHT>
409.655

> <EXACT_MASS>
409.355594377

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
53.17860371008434

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-hydroxy-3-[(trimethylazaniumyl)methyl]henicosa-4,6-dienoate

> <ALOGPS_LOGP>
1.87

> <JCHEM_LOGP>
2.4607558018615885

> <ALOGPS_LOGS>
-7.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.768322509429666

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.426739165745814

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9000896800333367

> <JCHEM_POLAR_SURFACE_AREA>
60.36

> <JCHEM_REFRACTIVITY>
148.34269999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.23e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-3-[(trimethylammonio)methyl]henicosa-4,6-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0255895
     RDKit          3D
Octadecadienylcarnitine
 76 75  0  0  0  0  0  0  0  0999 V2000
    6.1361   -1.1439   -3.3778 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0137   -2.1100   -2.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2010   -1.8115   -1.3034 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2355   -2.6844   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0090   -2.5084    0.7820 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8582   -1.0714    1.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6406   -0.8912    2.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5459    0.5432    2.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4474    1.5222    1.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2481    1.3140    0.5298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9877    1.4373    1.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337    1.2440    0.5201 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7012    2.2969   -0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5512    2.1620   -1.4202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6954    2.3110   -0.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182    1.4023   -0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6669    0.1162   -0.9888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5309   -0.8405   -0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7281   -0.6778    0.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1716   -0.1782    1.2129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2603   -2.0793    0.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3540   -2.3516    1.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6285   -1.6020    2.0359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1948   -3.4766    0.9643 O   0  0  0  0  0  1  0  0  0  0  0  0
   -5.6714    0.1909   -0.6796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8233    0.7667   -0.1467 N   0  0  0  0  0  4  0  0  0  0  0  0
   -6.6717    1.4542    1.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0524    0.0289   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0901    1.9356   -1.0798 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1234   -1.0595   -3.8189 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4247   -0.1697   -2.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8710   -1.5351   -4.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0657   -3.1599   -2.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0838   -1.8670   -1.6686 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1796   -0.7356   -1.0584 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1325   -1.9876   -1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1029   -2.3745    0.5463 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3385   -3.7434   -0.3518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0760   -2.8478    0.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228   -3.1101    1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7097   -0.4774    0.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472   -0.7667    1.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7162   -1.2375    1.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7584   -1.5046    3.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7057    0.6307    3.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4810    0.7608    3.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3538    1.4559    0.7882 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4524    2.5391    1.8755 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3268    2.0725   -0.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3443    0.3311    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031    2.4459    1.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0233    0.6448    2.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6831    0.2150    0.0928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.3427    1.2254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7447    3.2892   -0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5433    2.2058   -1.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5381    1.1875   -1.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5673    2.9969   -2.1711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7900    3.2610    0.0486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4212    1.7000    0.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8272   -0.0714   -1.6975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4597   -1.7452   -1.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5297   -0.5682    2.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4209   -2.8251    0.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6519   -2.3233   -0.8710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0042   -0.3490   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0331    1.0182   -1.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0732    2.5147    1.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2966    0.9966    1.9408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6126    1.5984    1.4207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5316   -0.1811    0.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7985    0.6232   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9194   -0.8994   -0.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8664    2.5267   -0.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4510    1.4433   -2.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1523    2.4408   -1.2982 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  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  2  3
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 19 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 12 53  1  0
 12 54  1  0
 13 55  1  0
 13 56  1  0
 14 57  1  0
 14 58  1  0
 15 59  1  0
 16 60  1  0
 17 61  1  0
 18 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 25 66  1  0
 25 67  1  0
 27 68  1  0
 27 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 28 73  1  0
 29 74  1  0
 29 75  1  0
 29 76  1  0
M  CHG  2  24  -1  26   1
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      12.526   8.772   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.860   8.002   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.194   8.772   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.527   8.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.861   8.772   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.195   8.002   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.528   8.772   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.862   8.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.196   8.772   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.529   8.002   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      25.863   8.772   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      27.197   8.002   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      28.530   8.772   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      29.864   8.002   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      31.198   8.772   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      32.532   8.002   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      33.865   8.772   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      35.199   8.002   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      36.533   8.772   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      37.866   9.542   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      39.200   8.772   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      40.534   9.542   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      39.200   7.232   0.000  0.00  0.00           O-1
HETATM   24  C   UNK     0      37.303   7.438   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      36.533   6.105   0.000  0.00  0.00           N+1
HETATM   26  C   UNK     0      35.199   6.875   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      37.866   5.335   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      35.763   4.771   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      35.763  10.106   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   24   29                                             
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25                                                            
CONECT   29   19                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   56    0
END

COMPND    HMDB0255895
HETATM    1  C1  UNL     1       6.136  -1.144  -3.378  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.014  -2.110  -2.191  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.201  -1.812  -1.303  1.00  0.00           C  
HETATM    4  C4  UNL     1       7.236  -2.684  -0.068  1.00  0.00           C  
HETATM    5  C5  UNL     1       6.009  -2.508   0.782  1.00  0.00           C  
HETATM    6  C6  UNL     1       5.858  -1.071   1.251  1.00  0.00           C  
HETATM    7  C7  UNL     1       4.641  -0.891   2.099  1.00  0.00           C  
HETATM    8  C8  UNL     1       4.546   0.543   2.539  1.00  0.00           C  
HETATM    9  C9  UNL     1       4.447   1.522   1.420  1.00  0.00           C  
HETATM   10  C10 UNL     1       3.248   1.314   0.530  1.00  0.00           C  
HETATM   11  C11 UNL     1       1.988   1.437   1.342  1.00  0.00           C  
HETATM   12  C12 UNL     1       0.734   1.244   0.520  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.701   2.297  -0.550  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.551   2.162  -1.420  1.00  0.00           C  
HETATM   15  C15 UNL     1      -1.695   2.311  -0.522  1.00  0.00           C  
HETATM   16  C16 UNL     1      -2.618   1.402  -0.342  1.00  0.00           C  
HETATM   17  C17 UNL     1      -2.667   0.116  -0.989  1.00  0.00           C  
HETATM   18  C18 UNL     1      -3.531  -0.841  -0.872  1.00  0.00           C  
HETATM   19  C19 UNL     1      -4.728  -0.678   0.081  1.00  0.00           C  
HETATM   20  O1  UNL     1      -4.172  -0.178   1.213  1.00  0.00           O  
HETATM   21  C20 UNL     1      -5.260  -2.079   0.175  1.00  0.00           C  
HETATM   22  C21 UNL     1      -6.354  -2.352   1.082  1.00  0.00           C  
HETATM   23  O2  UNL     1      -6.628  -1.602   2.036  1.00  0.00           O  
HETATM   24  O3  UNL     1      -7.195  -3.477   0.964  1.00  0.00           O1-
HETATM   25  C22 UNL     1      -5.671   0.191  -0.680  1.00  0.00           C  
HETATM   26  N1  UNL     1      -6.823   0.767  -0.147  1.00  0.00           N1+
HETATM   27  C23 UNL     1      -6.672   1.454   1.133  1.00  0.00           C  
HETATM   28  C24 UNL     1      -8.052   0.029  -0.232  1.00  0.00           C  
HETATM   29  C25 UNL     1      -7.090   1.936  -1.080  1.00  0.00           C  
HETATM   30  H1  UNL     1       5.123  -1.060  -3.819  1.00  0.00           H  
HETATM   31  H2  UNL     1       6.425  -0.170  -2.953  1.00  0.00           H  
HETATM   32  H3  UNL     1       6.871  -1.535  -4.117  1.00  0.00           H  
HETATM   33  H4  UNL     1       6.066  -3.160  -2.549  1.00  0.00           H  
HETATM   34  H5  UNL     1       5.084  -1.867  -1.669  1.00  0.00           H  
HETATM   35  H6  UNL     1       7.180  -0.736  -1.058  1.00  0.00           H  
HETATM   36  H7  UNL     1       8.133  -1.988  -1.905  1.00  0.00           H  
HETATM   37  H8  UNL     1       8.103  -2.374   0.546  1.00  0.00           H  
HETATM   38  H9  UNL     1       7.338  -3.743  -0.352  1.00  0.00           H  
HETATM   39  H10 UNL     1       5.076  -2.848   0.297  1.00  0.00           H  
HETATM   40  H11 UNL     1       6.123  -3.110   1.710  1.00  0.00           H  
HETATM   41  H12 UNL     1       5.710  -0.477   0.324  1.00  0.00           H  
HETATM   42  H13 UNL     1       6.747  -0.767   1.833  1.00  0.00           H  
HETATM   43  H14 UNL     1       3.716  -1.238   1.595  1.00  0.00           H  
HETATM   44  H15 UNL     1       4.758  -1.505   3.034  1.00  0.00           H  
HETATM   45  H16 UNL     1       3.706   0.631   3.258  1.00  0.00           H  
HETATM   46  H17 UNL     1       5.481   0.761   3.105  1.00  0.00           H  
HETATM   47  H18 UNL     1       5.354   1.456   0.788  1.00  0.00           H  
HETATM   48  H19 UNL     1       4.452   2.539   1.875  1.00  0.00           H  
HETATM   49  H20 UNL     1       3.327   2.072  -0.284  1.00  0.00           H  
HETATM   50  H21 UNL     1       3.344   0.331   0.040  1.00  0.00           H  
HETATM   51  H22 UNL     1       1.903   2.446   1.802  1.00  0.00           H  
HETATM   52  H23 UNL     1       2.023   0.645   2.116  1.00  0.00           H  
HETATM   53  H24 UNL     1       0.683   0.215   0.093  1.00  0.00           H  
HETATM   54  H25 UNL     1      -0.119   1.343   1.225  1.00  0.00           H  
HETATM   55  H26 UNL     1       0.745   3.289  -0.069  1.00  0.00           H  
HETATM   56  H27 UNL     1       1.543   2.206  -1.238  1.00  0.00           H  
HETATM   57  H28 UNL     1      -0.538   1.188  -1.901  1.00  0.00           H  
HETATM   58  H29 UNL     1      -0.567   2.997  -2.171  1.00  0.00           H  
HETATM   59  H30 UNL     1      -1.790   3.261   0.049  1.00  0.00           H  
HETATM   60  H31 UNL     1      -3.421   1.700   0.385  1.00  0.00           H  
HETATM   61  H32 UNL     1      -1.827  -0.071  -1.698  1.00  0.00           H  
HETATM   62  H33 UNL     1      -3.460  -1.745  -1.410  1.00  0.00           H  
HETATM   63  H34 UNL     1      -4.530  -0.568   2.049  1.00  0.00           H  
HETATM   64  H35 UNL     1      -4.421  -2.825   0.277  1.00  0.00           H  
HETATM   65  H36 UNL     1      -5.652  -2.323  -0.871  1.00  0.00           H  
HETATM   66  H37 UNL     1      -6.004  -0.349  -1.635  1.00  0.00           H  
HETATM   67  H38 UNL     1      -5.033   1.018  -1.136  1.00  0.00           H  
HETATM   68  H39 UNL     1      -7.073   2.515   1.091  1.00  0.00           H  
HETATM   69  H40 UNL     1      -7.297   0.997   1.941  1.00  0.00           H  
HETATM   70  H41 UNL     1      -5.613   1.598   1.421  1.00  0.00           H  
HETATM   71  H42 UNL     1      -8.532  -0.181   0.746  1.00  0.00           H  
HETATM   72  H43 UNL     1      -8.798   0.623  -0.789  1.00  0.00           H  
HETATM   73  H44 UNL     1      -7.919  -0.899  -0.853  1.00  0.00           H  
HETATM   74  H45 UNL     1      -7.866   2.527  -0.594  1.00  0.00           H  
HETATM   75  H46 UNL     1      -7.451   1.443  -2.004  1.00  0.00           H  
HETATM   76  H47 UNL     1      -6.152   2.441  -1.298  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3   33   34
CONECT    3    4   35   36
CONECT    4    5   37   38
CONECT    5    6   39   40
CONECT    6    7   41   42
CONECT    7    8   43   44
CONECT    8    9   45   46
CONECT    9   10   47   48
CONECT   10   11   49   50
CONECT   11   12   51   52
CONECT   12   13   53   54
CONECT   13   14   55   56
CONECT   14   15   57   58
CONECT   15   16   16   59
CONECT   16   17   60
CONECT   17   18   18   61
CONECT   18   19   62
CONECT   19   20   21   25
CONECT   20   63
CONECT   21   22   64   65
CONECT   22   23   23   24
CONECT   25   26   66   67
CONECT   26   27   28   29
CONECT   27   68   69   70
CONECT   28   71   72   73
CONECT   29   74   75   76
END

HMDB0255895
     RDKit          3D
Octadecadienylcarnitine
 76 75  0  0  0  0  0  0  0  0999 V2000
    6.1361   -1.1439   -3.3778 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0137   -2.1100   -2.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2010   -1.8115   -1.3034 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2355   -2.6844   -0.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0090   -2.5084    0.7820 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8582   -1.0714    1.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6406   -0.8912    2.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5459    0.5432    2.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4474    1.5222    1.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2481    1.3140    0.5298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9877    1.4373    1.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337    1.2440    0.5201 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7012    2.2969   -0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5512    2.1620   -1.4202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6954    2.3110   -0.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182    1.4023   -0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6669    0.1162   -0.9888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5309   -0.8405   -0.8719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7281   -0.6778    0.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1716   -0.1782    1.2129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2603   -2.0793    0.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3540   -2.3516    1.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6285   -1.6020    2.0359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1948   -3.4766    0.9643 O   0  0  0  0  0  1  0  0  0  0  0  0
   -5.6714    0.1909   -0.6796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8233    0.7667   -0.1467 N   0  0  0  0  0  4  0  0  0  0  0  0
   -6.6717    1.4542    1.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0524    0.0289   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0901    1.9356   -1.0798 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1234   -1.0595   -3.8189 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4247   -0.1697   -2.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8710   -1.5351   -4.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0657   -3.1599   -2.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0838   -1.8670   -1.6686 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1796   -0.7356   -1.0584 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1325   -1.9876   -1.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1029   -2.3745    0.5463 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3385   -3.7434   -0.3518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0760   -2.8478    0.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228   -3.1101    1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7097   -0.4774    0.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472   -0.7667    1.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7162   -1.2375    1.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7584   -1.5046    3.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7057    0.6307    3.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4810    0.7608    3.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3538    1.4559    0.7882 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4524    2.5391    1.8755 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3268    2.0725   -0.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3443    0.3311    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9031    2.4459    1.8020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0233    0.6448    2.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6831    0.2150    0.0928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.3427    1.2254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7447    3.2892   -0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5433    2.2058   -1.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5381    1.1875   -1.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5673    2.9969   -2.1711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7900    3.2610    0.0486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4212    1.7000    0.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8272   -0.0714   -1.6975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4597   -1.7452   -1.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5297   -0.5682    2.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4209   -2.8251    0.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6519   -2.3233   -0.8710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0042   -0.3490   -1.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0331    1.0182   -1.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0732    2.5147    1.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2966    0.9966    1.9408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6126    1.5984    1.4207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5316   -0.1811    0.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7985    0.6232   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9194   -0.8994   -0.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8664    2.5267   -0.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4510    1.4433   -2.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1523    2.4408   -1.2982 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  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 17 18  2  3
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 19 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 12 53  1  0
 12 54  1  0
 13 55  1  0
 13 56  1  0
 14 57  1  0
 14 58  1  0
 15 59  1  0
 16 60  1  0
 17 61  1  0
 18 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 25 66  1  0
 25 67  1  0
 27 68  1  0
 27 69  1  0
 27 70  1  0
 28 71  1  0
 28 72  1  0
 28 73  1  0
 29 74  1  0
 29 75  1  0
 29 76  1  0
M  CHG  2  24  -1  26   1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3-Hydroxy-3-[(trimethylazaniumyl)methyl]henicosa-4,6-dienoic acid	Generator

Chemical Formula

C₂₅H₄₇NO₃

Average Molecular Weight

409.655

Monoisotopic Molecular Weight

409.355594377

IUPAC Name

3-hydroxy-3-[(trimethylazaniumyl)methyl]henicosa-4,6-dienoate

Traditional Name

3-hydroxy-3-[(trimethylammonio)methyl]henicosa-4,6-dienoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCC=CC=CC(O)(CC([O-])=O)C[N+](C)(C)C

InChI Identifier

InChI=1S/C25H47NO3/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25(29,22-24(27)28)23-26(2,3)4/h18-21,29H,5-17,22-23H2,1-4H3

InChI Key

RHIDLCOXTYRESP-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as other hydroxyeicosapolyenoic acids. These are hydroxyeicosapolyenoic acids which do not belong to the Hydroxyeicosapentaenoic acids, the Hydroxyeicosatetraenoic acids, or the Hydroxyeicosatrienoic acids.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Other hydroxyeicosapolyenoic acids

Alternative Parents

Substituents

Hydroxyeicosapolyenoic acid
Long-chain fatty acid
Amino fatty acid
Branched fatty acid
Hydroxy fatty acid
Methyl-branched fatty acid
Unsaturated fatty acid
Fatty acid
Tertiary alcohol
Quaternary ammonium salt
Tetraalkylammonium salt
Carboxylic acid salt
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic salt
Organonitrogen compound
Organooxygen compound
Organic oxide
Organopnictogen compound
Alcohol
Hydrocarbon derivative
Organic zwitterion
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Amine
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	1.87	ALOGPS
logP	2.46	ChemAxon
logS	-7.8	ALOGPS
pKa (Strongest Acidic)	4.43	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	60.36 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	148.34 m³·mol⁻¹	ChemAxon
Polarizability	53.18 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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]+	217.023	30932474
DeepCCS	[M-H]-	213.003	30932474
DeepCCS	[M-2H]-	249.547	30932474
DeepCCS	[M+Na]+	225.838	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Octadecadienylcarnitine	CCCCCCCCCCCCCCC=CC=CC(O)(CC([O-])=O)C[N+](C)(C)C	3638.2	Standard polar	33892256
Octadecadienylcarnitine	CCCCCCCCCCCCCCC=CC=CC(O)(CC([O-])=O)C[N+](C)(C)C	2551.1	Standard non polar	33892256
Octadecadienylcarnitine	CCCCCCCCCCCCCCC=CC=CC(O)(CC([O-])=O)C[N+](C)(C)C	2868.1	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 - Octadecadienylcarnitine GC-MS (Non-derivatized) - 70eV, Positive	splash10-00di-9112000000-aba37470c5b8e9f15d3f	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Octadecadienylcarnitine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Octadecadienylcarnitine GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Octadecadienylcarnitine GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-04	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

132277610

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 Octadecadienylcarnitine (HMDB0255895)

MOL for HMDB0255895 (Octadecadienylcarnitine)

3D MOL for HMDB0255895 (Octadecadienylcarnitine)

3D SDF for HMDB0255895 (Octadecadienylcarnitine)

3D-SDF for HMDB0255895 (Octadecadienylcarnitine)

PDB for HMDB0255895 (Octadecadienylcarnitine)

3D PDB for HMDB0255895 (Octadecadienylcarnitine)

SMILES for HMDB0255895 (Octadecadienylcarnitine)

INCHI for HMDB0255895 (Octadecadienylcarnitine)

Structure for HMDB0255895 (Octadecadienylcarnitine)

3D Structure for HMDB0255895 (Octadecadienylcarnitine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra