Jump To Section:

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

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2017-03-16 03:42:39 UTC

Update Date

2022-03-07 03:17:52 UTC

HMDB ID

HMDB0062312

Secondary Accession Numbers

HMDB62312

Metabolite Identification

Common Name

1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate

Description

1-arachidonoyl-sn-glycerol 3-phosphate, also known as lpa(20:4(5Z,8Z,11Z,14Z)/0:0) or 1-arachidonoyl lpa, belongs to the class of organic compounds known as 1-acylglycerol-3-phosphates. These are lysophosphatidic acids where the glycerol is esterified with a fatty acid at O-1 position. 1-arachidonoyl-sn-glycerol 3-phosphate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

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

  Mrv1572008171514002D          

 40 39  0  0  1  0            999 V2000
   -2.4750    8.5736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    7.8591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    5.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    5.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    3.5723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8250    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    3.5723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625    0.7144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    1.5394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    0.7144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7144    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7125    5.0012    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    3.5723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    3.5723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7125    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    0.7144    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  2  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  2  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  2  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 19  1  0  0  0  0
 22 24  1  1  0  0  0
 25 23  2  0  0  0  0
 29 20  1  0  0  0  0
 29 23  1  0  0  0  0
 30 21  1  0  0  0  0
 31 26  1  0  0  0  0
 31 27  1  0  0  0  0
 31 28  2  0  0  0  0
 31 30  1  0  0  0  0
 32  6  1  0  0  0  0
 33  7  1  0  0  0  0
 34  9  1  0  0  0  0
 35 10  1  0  0  0  0
 36 12  1  0  0  0  0
 37 13  1  0  0  0  0
 38 15  1  0  0  0  0
 39 16  1  0  0  0  0
 22 40  1  1  0  0  0
M  END

HMDB0062312
     RDKit          3D
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate
 70 69  0  0  0  0  0  0  0  0999 V2000
   -6.8676    0.2362    2.9626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5571    0.9456    1.8095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7004    1.9895    1.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3794    1.6253    0.7100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2546    0.6517   -0.3788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6854   -0.7314   -0.1761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8499   -1.7519   -0.2581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4053   -1.6608   -0.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1481   -2.4556   -1.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331   -2.0150   -2.8866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2220   -0.6399   -3.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8113   -0.4096   -3.3407 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934   -1.2298   -3.3209 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3216   -2.6293   -3.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1413   -3.1036   -1.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7629   -2.4195   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8753   -0.9944   -0.8371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3291   -0.7478    0.6073 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4311    0.7303    0.8471 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8272    1.1871    0.7996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0722    2.4164    0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8728    0.3115    0.9178 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2103    0.7328    0.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5767    1.6914    1.9778 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3517    1.0494    3.2116 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0502    2.0383    1.8876 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2918    2.6754    0.6687 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9230    3.0776    0.5314 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.0329    4.4245   -0.1319 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6713    3.0940    2.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6805    1.9009   -0.4520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8267   -0.0146    2.7094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8296    0.8705    3.8720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3775   -0.7129    3.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0873    0.2858    1.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4273    1.5253    2.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2996    2.5438    0.4173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5952    2.8033    2.0024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6736    1.3146    1.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8359    2.5709    0.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2343    0.7366   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9246    1.0445   -1.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7582   -0.9564    0.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3089   -2.7588   -0.0795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9802   -0.6718   -0.5194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8655   -2.2116    0.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4143   -3.5409   -1.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5520   -2.7176   -3.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6085    0.0556   -2.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009   -0.2599   -4.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5328    0.6721   -3.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1834   -0.7139   -3.6304 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8372   -3.1179   -3.9842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6503   -3.2075   -3.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313   -4.2602   -1.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -3.0352   -0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3098   -0.3564   -1.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9589   -0.7108   -0.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2844   -1.0982    0.6351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0067   -1.2963    1.2794 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9780    0.9854    1.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8003    1.2757    0.1026 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    1.1408   -0.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8627   -0.1788    0.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9973    2.6078    1.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4421    1.3491    3.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6854    1.1332    1.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2808    2.7553    2.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3554    2.3733    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4848    1.0075   -0.0723 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  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 28 30  1  0
 28 31  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  1
 25 66  1  0
 26 67  1  0
 26 68  1  0
 30 69  1  0
 31 70  1  0
M  END

  Mrv1572008171514002D          

 40 39  0  0  1  0            999 V2000
   -2.4750    8.5736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    7.8591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    5.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    5.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    3.5723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8250    2.8578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    3.5723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625    0.7144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    1.5394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    0.7144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7144    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7125    5.0012    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    3.5723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    3.5723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7125    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    0.7144    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  2  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  2  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  2  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 19  1  0  0  0  0
 22 24  1  1  0  0  0
 25 23  2  0  0  0  0
 29 20  1  0  0  0  0
 29 23  1  0  0  0  0
 30 21  1  0  0  0  0
 31 26  1  0  0  0  0
 31 27  1  0  0  0  0
 31 28  2  0  0  0  0
 31 30  1  0  0  0  0
 32  6  1  0  0  0  0
 33  7  1  0  0  0  0
 34  9  1  0  0  0  0
 35 10  1  0  0  0  0
 36 12  1  0  0  0  0
 37 13  1  0  0  0  0
 38 15  1  0  0  0  0
 39 16  1  0  0  0  0
 22 40  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0062312

> <DATABASE_NAME>
hmdb

> <SMILES>
[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H39O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-23(25)29-20-22(24)21-30-31(26,27)28/h6-7,9-10,12-13,15-16,22,24H,2-5,8,11,14,17-21H2,1H3,(H2,26,27,28)/b7-6-,10-9-,13-12-,16-15-/t22-/m1/s1

> <INCHI_KEY>
XBFQFMCUPHZKTI-NZRYSPDRSA-N

> <FORMULA>
C23H39O7P

> <MOLECULAR_WEIGHT>
458.532

> <EXACT_MASS>
458.243340594

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
49.473273911139316

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(2R)-2-hydroxy-3-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]propoxy]phosphonic acid

> <ALOGPS_LOGP>
5.01

> <JCHEM_LOGP>
5.289061881666667

> <ALOGPS_LOGS>
-5.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.531115837543949

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.5053177852360151

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4039997956636006

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
127.85079999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.17e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-hydroxy-3-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]propoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0062312
     RDKit          3D
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate
 70 69  0  0  0  0  0  0  0  0999 V2000
   -6.8676    0.2362    2.9626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5571    0.9456    1.8095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7004    1.9895    1.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3794    1.6253    0.7100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2546    0.6517   -0.3788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6854   -0.7314   -0.1761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8499   -1.7519   -0.2581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4053   -1.6608   -0.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1481   -2.4556   -1.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331   -2.0150   -2.8866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2220   -0.6399   -3.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8113   -0.4096   -3.3407 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934   -1.2298   -3.3209 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3216   -2.6293   -3.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1413   -3.1036   -1.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7629   -2.4195   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8753   -0.9944   -0.8371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3291   -0.7478    0.6073 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4311    0.7303    0.8471 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8272    1.1871    0.7996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0722    2.4164    0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8728    0.3115    0.9178 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2103    0.7328    0.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5767    1.6914    1.9778 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3517    1.0494    3.2116 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0502    2.0383    1.8876 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2918    2.6754    0.6687 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9230    3.0776    0.5314 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.0329    4.4245   -0.1319 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6713    3.0940    2.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6805    1.9009   -0.4520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8267   -0.0146    2.7094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8296    0.8705    3.8720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3775   -0.7129    3.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0873    0.2858    1.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4273    1.5253    2.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2996    2.5438    0.4173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5952    2.8033    2.0024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6736    1.3146    1.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8359    2.5709    0.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2343    0.7366   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9246    1.0445   -1.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7582   -0.9564    0.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3089   -2.7588   -0.0795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9802   -0.6718   -0.5194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8655   -2.2116    0.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4143   -3.5409   -1.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5520   -2.7176   -3.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6085    0.0556   -2.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009   -0.2599   -4.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5328    0.6721   -3.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1834   -0.7139   -3.6304 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8372   -3.1179   -3.9842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6503   -3.2075   -3.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313   -4.2602   -1.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -3.0352   -0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3098   -0.3564   -1.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9589   -0.7108   -0.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2844   -1.0982    0.6351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0067   -1.2963    1.2794 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9780    0.9854    1.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8003    1.2757    0.1026 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    1.1408   -0.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8627   -0.1788    0.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9973    2.6078    1.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4421    1.3491    3.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6854    1.1332    1.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2808    2.7553    2.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3554    2.3733    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4848    1.0075   -0.0723 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  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 28 30  1  0
 28 31  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  1
 25 66  1  0
 26 67  1  0
 26 68  1  0
 30 69  1  0
 31 70  1  0
M  END

HEADER    PROTEIN                                 17-AUG-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-AUG-15         0                                  
HETATM    1  C   UNK     0      -4.620  16.004   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.390  14.670   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.620  13.337   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.390  12.003   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.620  10.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.390   9.336   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.620   8.002   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.080   8.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.310   6.668   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.080   5.335   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.620   5.335   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.390   4.001   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.620   2.667   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.080   2.667   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.310   1.334   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   2.667   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.770   4.001   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   5.335   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.850   4.001   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.540   5.335   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.850   1.334   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       2.310   6.668   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      10.010   1.334   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.470  -0.206   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       8.470   2.874   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.310   4.001   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.930   1.334   0.000  0.00  0.00           O+0
HETATM   31  P   UNK     0       8.470   1.334   0.000  0.00  0.00           P+0
HETATM   32  H   UNK     0      -6.930   9.336   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0      -5.390   6.668   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.770   6.668   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.310   4.001   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -6.930   4.001   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -5.390   1.334   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.080   0.000   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.390   4.001   0.000  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   32                                                  
CONECT    7    6    8   33                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   34                                                  
CONECT   10    9   11   35                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   36                                                  
CONECT   13   12   14   37                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   38                                                  
CONECT   16   15   17   39                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   23                                                       
CONECT   20   22   29                                                       
CONECT   21   22   30                                                       
CONECT   22   20   21   24   40                                             
CONECT   23   19   25   29                                                  
CONECT   24   22                                                            
CONECT   25   23                                                            
CONECT   26   31                                                            
CONECT   27   31                                                            
CONECT   28   31                                                            
CONECT   29   20   23                                                       
CONECT   30   21   31                                                       
CONECT   31   26   27   28   30                                             
CONECT   32    6                                                            
CONECT   33    7                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   12                                                            
CONECT   37   13                                                            
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   22                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   78    0
END

COMPND    HMDB0062312
HETATM    1  C1  UNL     1      -6.868   0.236   2.963  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.557   0.946   1.809  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.700   1.989   1.213  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.379   1.625   0.710  1.00  0.00           C  
HETATM    5  C5  UNL     1      -5.255   0.652  -0.379  1.00  0.00           C  
HETATM    6  C6  UNL     1      -5.685  -0.731  -0.176  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.850  -1.752  -0.258  1.00  0.00           C  
HETATM    8  C8  UNL     1      -3.405  -1.661  -0.557  1.00  0.00           C  
HETATM    9  C9  UNL     1      -3.148  -2.456  -1.775  1.00  0.00           C  
HETATM   10  C10 UNL     1      -2.633  -2.015  -2.887  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.222  -0.640  -3.100  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.811  -0.410  -3.341  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.193  -1.230  -3.321  1.00  0.00           C  
HETATM   14  C14 UNL     1       0.322  -2.629  -3.060  1.00  0.00           C  
HETATM   15  C15 UNL     1       1.141  -3.104  -1.938  1.00  0.00           C  
HETATM   16  C16 UNL     1       1.763  -2.419  -1.052  1.00  0.00           C  
HETATM   17  C17 UNL     1       1.875  -0.994  -0.837  1.00  0.00           C  
HETATM   18  C18 UNL     1       1.329  -0.748   0.607  1.00  0.00           C  
HETATM   19  C19 UNL     1       1.431   0.730   0.847  1.00  0.00           C  
HETATM   20  C20 UNL     1       2.827   1.187   0.800  1.00  0.00           C  
HETATM   21  O1  UNL     1       3.072   2.416   0.649  1.00  0.00           O  
HETATM   22  O2  UNL     1       3.873   0.311   0.918  1.00  0.00           O  
HETATM   23  C21 UNL     1       5.210   0.733   0.880  1.00  0.00           C  
HETATM   24  C22 UNL     1       5.577   1.691   1.978  1.00  0.00           C  
HETATM   25  O3  UNL     1       5.352   1.049   3.212  1.00  0.00           O  
HETATM   26  C23 UNL     1       7.050   2.038   1.888  1.00  0.00           C  
HETATM   27  O4  UNL     1       7.292   2.675   0.669  1.00  0.00           O  
HETATM   28  P1  UNL     1       8.923   3.078   0.531  1.00  0.00           P  
HETATM   29  O5  UNL     1       9.033   4.424  -0.132  1.00  0.00           O  
HETATM   30  O6  UNL     1       9.671   3.094   2.049  1.00  0.00           O  
HETATM   31  O7  UNL     1       9.680   1.901  -0.452  1.00  0.00           O  
HETATM   32  H1  UNL     1      -5.827  -0.015   2.709  1.00  0.00           H  
HETATM   33  H2  UNL     1      -6.830   0.871   3.872  1.00  0.00           H  
HETATM   34  H3  UNL     1      -7.377  -0.713   3.215  1.00  0.00           H  
HETATM   35  H4  UNL     1      -8.087   0.286   1.136  1.00  0.00           H  
HETATM   36  H5  UNL     1      -8.427   1.525   2.356  1.00  0.00           H  
HETATM   37  H6  UNL     1      -7.300   2.544   0.417  1.00  0.00           H  
HETATM   38  H7  UNL     1      -6.595   2.803   2.002  1.00  0.00           H  
HETATM   39  H8  UNL     1      -4.674   1.315   1.565  1.00  0.00           H  
HETATM   40  H9  UNL     1      -4.836   2.571   0.351  1.00  0.00           H  
HETATM   41  H10 UNL     1      -4.234   0.737  -0.826  1.00  0.00           H  
HETATM   42  H11 UNL     1      -5.925   1.044  -1.234  1.00  0.00           H  
HETATM   43  H12 UNL     1      -6.758  -0.956   0.031  1.00  0.00           H  
HETATM   44  H13 UNL     1      -5.309  -2.759  -0.079  1.00  0.00           H  
HETATM   45  H14 UNL     1      -2.980  -0.672  -0.519  1.00  0.00           H  
HETATM   46  H15 UNL     1      -2.865  -2.212   0.304  1.00  0.00           H  
HETATM   47  H16 UNL     1      -3.414  -3.541  -1.758  1.00  0.00           H  
HETATM   48  H17 UNL     1      -2.552  -2.718  -3.769  1.00  0.00           H  
HETATM   49  H18 UNL     1      -2.609   0.056  -2.298  1.00  0.00           H  
HETATM   50  H19 UNL     1      -2.801  -0.260  -4.023  1.00  0.00           H  
HETATM   51  H20 UNL     1      -0.533   0.672  -3.589  1.00  0.00           H  
HETATM   52  H21 UNL     1       1.183  -0.714  -3.630  1.00  0.00           H  
HETATM   53  H22 UNL     1       0.837  -3.118  -3.984  1.00  0.00           H  
HETATM   54  H23 UNL     1      -0.650  -3.208  -3.009  1.00  0.00           H  
HETATM   55  H24 UNL     1       1.231  -4.260  -1.854  1.00  0.00           H  
HETATM   56  H25 UNL     1       2.336  -3.035  -0.288  1.00  0.00           H  
HETATM   57  H26 UNL     1       1.310  -0.356  -1.480  1.00  0.00           H  
HETATM   58  H27 UNL     1       2.959  -0.711  -0.866  1.00  0.00           H  
HETATM   59  H28 UNL     1       0.284  -1.098   0.635  1.00  0.00           H  
HETATM   60  H29 UNL     1       2.007  -1.296   1.279  1.00  0.00           H  
HETATM   61  H30 UNL     1       0.978   0.985   1.841  1.00  0.00           H  
HETATM   62  H31 UNL     1       0.800   1.276   0.103  1.00  0.00           H  
HETATM   63  H32 UNL     1       5.448   1.141  -0.131  1.00  0.00           H  
HETATM   64  H33 UNL     1       5.863  -0.179   0.998  1.00  0.00           H  
HETATM   65  H34 UNL     1       4.997   2.608   1.887  1.00  0.00           H  
HETATM   66  H35 UNL     1       4.442   1.349   3.506  1.00  0.00           H  
HETATM   67  H36 UNL     1       7.685   1.133   1.948  1.00  0.00           H  
HETATM   68  H37 UNL     1       7.281   2.755   2.702  1.00  0.00           H  
HETATM   69  H38 UNL     1      10.355   2.373   2.094  1.00  0.00           H  
HETATM   70  H39 UNL     1       9.485   1.008  -0.072  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3   35   36
CONECT    3    4   37   38
CONECT    4    5   39   40
CONECT    5    6   41   42
CONECT    6    7    7   43
CONECT    7    8   44
CONECT    8    9   45   46
CONECT    9   10   10   47
CONECT   10   11   48
CONECT   11   12   49   50
CONECT   12   13   13   51
CONECT   13   14   52
CONECT   14   15   53   54
CONECT   15   16   16   55
CONECT   16   17   56
CONECT   17   18   57   58
CONECT   18   19   59   60
CONECT   19   20   61   62
CONECT   20   21   21   22
CONECT   22   23
CONECT   23   24   63   64
CONECT   24   25   26   65
CONECT   25   66
CONECT   26   27   67   68
CONECT   27   28
CONECT   28   29   29   30   31
CONECT   30   69
CONECT   31   70
END

HMDB0062312
     RDKit          3D
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate
 70 69  0  0  0  0  0  0  0  0999 V2000
   -6.8676    0.2362    2.9626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5571    0.9456    1.8095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7004    1.9895    1.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3794    1.6253    0.7100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2546    0.6517   -0.3788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6854   -0.7314   -0.1761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8499   -1.7519   -0.2581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4053   -1.6608   -0.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1481   -2.4556   -1.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331   -2.0150   -2.8866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2220   -0.6399   -3.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8113   -0.4096   -3.3407 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934   -1.2298   -3.3209 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3216   -2.6293   -3.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1413   -3.1036   -1.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7629   -2.4195   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8753   -0.9944   -0.8371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3291   -0.7478    0.6073 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4311    0.7303    0.8471 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8272    1.1871    0.7996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0722    2.4164    0.6488 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8728    0.3115    0.9178 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2103    0.7328    0.8796 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5767    1.6914    1.9778 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3517    1.0494    3.2116 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0502    2.0383    1.8876 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2918    2.6754    0.6687 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9230    3.0776    0.5314 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.0329    4.4245   -0.1319 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6713    3.0940    2.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6805    1.9009   -0.4520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8267   -0.0146    2.7094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8296    0.8705    3.8720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3775   -0.7129    3.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0873    0.2858    1.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4273    1.5253    2.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2996    2.5438    0.4173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5952    2.8033    2.0024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6736    1.3146    1.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8359    2.5709    0.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2343    0.7366   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9246    1.0445   -1.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7582   -0.9564    0.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3089   -2.7588   -0.0795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9802   -0.6718   -0.5194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8655   -2.2116    0.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4143   -3.5409   -1.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5520   -2.7176   -3.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6085    0.0556   -2.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8009   -0.2599   -4.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5328    0.6721   -3.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1834   -0.7139   -3.6304 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8372   -3.1179   -3.9842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6503   -3.2075   -3.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313   -4.2602   -1.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -3.0352   -0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3098   -0.3564   -1.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9589   -0.7108   -0.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2844   -1.0982    0.6351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0067   -1.2963    1.2794 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9780    0.9854    1.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8003    1.2757    0.1026 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    1.1408   -0.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8627   -0.1788    0.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9973    2.6078    1.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4421    1.3491    3.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6854    1.1332    1.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2808    2.7553    2.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3554    2.3733    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4848    1.0075   -0.0723 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  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 28 30  1  0
 28 31  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  1
 25 66  1  0
 26 67  1  0
 26 68  1  0
 30 69  1  0
 31 70  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-(5Z,8Z,11Z,14Z)-Eicosatetraenoyl-sn-glycero-3-phosphate	ChEBI
1-(5Z,8Z,11Z,14Z)-Icosatetraenoyl-sn-glycero-3-phosphate	ChEBI
1-(5Z,8Z,11Z,14Z-Eicosatetraenoyl)-sn-glycero-3-phosphate	ChEBI
1-Arachidonoyl lpa	ChEBI
1-Arachidonoyl lysophosphatidic acid	ChEBI
LPA(20:4(5Z,8Z,11Z,14Z)/0:0)	ChEBI
Lysophosphatidic acid (20:4(5Z,8Z,11Z,14Z)/0:0)	ChEBI
PA(20:4(5Z,8Z,11Z,14Z)/0:0)	ChEBI
PA(20:4/0:0)	ChEBI
1-(5Z,8Z,11Z,14Z)-Eicosatetraenoyl-sn-glycero-3-phosphoric acid	Generator
1-(5Z,8Z,11Z,14Z)-Icosatetraenoyl-sn-glycero-3-phosphoric acid	Generator
1-(5Z,8Z,11Z,14Z-Eicosatetraenoyl)-sn-glycero-3-phosphoric acid	Generator
1-Arachidonoyl lysophosphatidate	Generator
Lysophosphatidate (20:4(5Z,8Z,11Z,14Z)/0:0)	Generator
1-Arachidonoyl-sn-glycerol 3-phosphoric acid	Generator

Chemical Formula

C₂₃H₃₉O₇P

Average Molecular Weight

458.532

Monoisotopic Molecular Weight

458.243340594

IUPAC Name

[(2R)-2-hydroxy-3-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]propoxy]phosphonic acid

Traditional Name

(2R)-2-hydroxy-3-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]propoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O

InChI Identifier

InChI=1S/C23H39O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-23(25)29-20-22(24)21-30-31(26,27)28/h6-7,9-10,12-13,15-16,22,24H,2-5,8,11,14,17-21H2,1H3,(H2,26,27,28)/b7-6-,10-9-,13-12-,16-15-/t22-/m1/s1

InChI Key

XBFQFMCUPHZKTI-NZRYSPDRSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-acylglycerol-3-phosphates. These are lysophosphatidic acids where the glycerol is esterified with a fatty acid at O-1 position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphates

Direct Parent

1-acylglycerol-3-phosphates

Alternative Parents

Substituents

1-acylglycerol-3-phosphate
Fatty acid ester
Monoalkyl phosphate
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

1-acyl-sn-glycerol 3-phosphate (CHEBI:73792 )
Monoacylglycerophosphates (LMGP10050013 )

Ontology

Not Available

Exogenous (HMDB: HMDB0062312)

Process

Naturally occurring process

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	0.0032 g/l	ALOGPS
LogP	5.01	ALOGPS

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	5.01	ALOGPS
logP	5.29	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	1.51	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	127.85 m³·mol⁻¹	ChemAxon
Polarizability	49.47 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	220.277	31661259
DarkChem	[M-H]-	216.401	31661259
DeepCCS	[M+H]+	216.761	30932474
DeepCCS	[M-H]-	214.936	30932474
DeepCCS	[M-2H]-	248.177	30932474
DeepCCS	[M+Na]+	222.367	30932474
AllCCS	[M+H]+	215.4	32859911
AllCCS	[M+H-H2O]+	213.5	32859911
AllCCS	[M+NH4]+	217.2	32859911
AllCCS	[M+Na]+	217.7	32859911
AllCCS	[M-H]-	211.3	32859911
AllCCS	[M+Na-2H]-	214.5	32859911
AllCCS	[M+HCOO]-	218.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O	4461.9	Standard polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O	2892.1	Standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate	[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])C\C([H])=C(\[H])C\C([H])=C(\[H])CCCC(=O)OC[C@@]([H])(O)COP(O)(O)=O	3475.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,1TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O)O[Si](C)(C)C	3485.7	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,1TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O)O[Si](C)(C)C	3444.1	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3468.0	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3177.8	Standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3922.8	Standard polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3431.9	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3182.5	Standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3691.0	Standard polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,3TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3460.0	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,3TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3204.5	Standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,3TMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3360.5	Standard polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,1TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	3717.2	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,1TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C	3652.4	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3913.0	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3502.2	Standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3941.5	Standard polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3870.8	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3476.3	Standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,2TBDMS,isomer #2	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3781.6	Standard polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,3TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4097.3	Semi standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,3TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3606.2	Standard non polar	33892256
1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate,3TBDMS,isomer #1	CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3501.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate GC-MS (1 TMS) - 70eV, Positive	splash10-01p2-9250100000-2b98f1bf6a134876725c	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate 10V, Negative-QTOF	splash10-0a4i-0000900000-28f76f19f9c7cd489319	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate 20V, Negative-QTOF	splash10-0a4i-0000900000-28f76f19f9c7cd489319	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate 40V, Negative-QTOF	splash10-0udi-2905600000-4a1ee19d8767776f2014	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate 10V, Positive-QTOF	splash10-0a4i-0000900000-4e238532d685199e7218	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate 20V, Positive-QTOF	splash10-0a4i-0000900000-4e238532d685199e7218	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate 40V, Positive-QTOF	splash10-00du-0950700000-bb2c6d0f2992e42414b1	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

42607498

PDB ID

Not Available

ChEBI ID

73792

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

Moritz A, De Graan PN, Gispen WH, Wirtz KW: Phosphatidic acid is a specific activator of phosphatidylinositol-4-phosphate kinase. J Biol Chem. 1992 Apr 15;267(11):7207-10. [PubMed:1313792 ]
Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Divecha N, Irvine RF: Phospholipid signaling. Cell. 1995 Jan 27;80(2):269-78. [PubMed:7834746 ]
Moolenaar WH, Kruijer W, Tilly BC, Verlaan I, Bierman AJ, de Laat SW: Growth factor-like action of phosphatidic acid. Nature. 1986 Sep 11-17;323(6084):171-3. [PubMed:3748188 ]
Yang CY, Frohman MA: Mitochondria: signaling with phosphatidic acid. Int J Biochem Cell Biol. 2012 Aug;44(8):1346-50. doi: 10.1016/j.biocel.2012.05.006. Epub 2012 May 15. [PubMed:22609101 ]
Cevc, Gregor (1993). Phospholipids Handbook. Marcel Dekker.
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate (HMDB0062312)

MOL for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

3D MOL for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

3D SDF for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

3D-SDF for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

PDB for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

3D PDB for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

SMILES for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

INCHI for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

Structure for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

3D Structure for HMDB0062312 (1-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphate)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra