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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1) Show 1 protein XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2009-01-08 17:23:05 UTC

Update Date

2022-11-30 19:03:59 UTC

HMDB ID

HMDB0011479

Secondary Accession Numbers

HMDB11479

Metabolite Identification

Common Name

LysoPE(0:0/18:3(9Z,12Z,15Z))

Description

LysoPE(0:0/18:3(9Z,12Z,15Z)) is a lysophosphatidylethanolamine or a lysophospholipid. The term 'lysophospholipid' (LPL) refers to any phospholipid that is missing one of its two O-acyl chains. Thus, LPLs have a free alcohol in either the sn-1 or sn-2 position. The prefix 'lyso-' comes from the fact that lysophospholipids were originally found to be hemolytic however it is now used to refer generally to phospholipids missing an acyl chain. LPLs are usually the result of phospholipase A-type enzymatic activity on regular phospholipids such as phosphatidylcholine or phosphatidic acid, although they can also be generated by the acylation of glycerophospholipids or the phosphorylation of monoacylglycerols. Some LPLs serve important signaling functions such as lysophosphatidic acid. Lysophosphatidylethanolamines (LPEs) can function as plant growth regulators with several diverse uses. (LPEs) are approved for outdoor agricultural use to accelerate ripening and improve the quality of fresh produce. They are also approved for indoor use to preserve stored crops and commercial cut flowers. As a breakdown product of phosphatidylethanolamine (PE), LPE is present in cells of all organisms.

Structure

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


  Mrv0541 02241201412D          

 33 32  0  0  1  0            999 V2000
   25.9644   -8.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.2893   -9.1155    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   24.6142   -8.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.6396   -9.1155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9390   -9.1155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.7625   -9.8951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.3146   -8.7257    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   26.9249   -8.0505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.7044   -9.4008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.9898   -8.3359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.6649   -8.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.3400   -8.3359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0151   -8.7257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.8771   -9.9248    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9019  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6164   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3309  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0453  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7598   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4743  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1888  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9033   -9.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6178  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3322  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0467   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7612  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4757   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.1902  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9046   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6191  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.3336   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0480  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0480  -11.1326    0.0000 O   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  1  1  0  0  0  0
  5  3  1  0  0  0  0
  2  6  1  6  0  0  0
  7  4  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
  2 14  1  1  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  2  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  2  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  2  0  0  0  0
 25 24  1  0  0  0  0
 26 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 27  1  0  0  0  0
 29 28  1  0  0  0  0
 30 29  1  0  0  0  0
 31 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 32  2  0  0  0  0
  6 32  1  0  0  0  0
M  END

HMDB0011479
     RDKit          3D
LysoPE(0:0/18:3(9Z,12Z,15Z))
 74 73  0  0  0  0  0  0  0  0999 V2000
   -8.4833   -0.8348   -3.4109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1104   -0.6411   -2.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3141    0.8002   -1.8605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8000    1.5599   -0.9438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8916    1.0220    0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5944    1.7054    0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4634    1.1073   -0.2104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2742   -0.2996   -0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4388   -1.1081    0.4468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7704   -0.7407    1.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7328    0.5831    2.0674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5376    1.4206    2.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3289    1.0017    2.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6487   -0.1985    2.2708 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6157   -0.5332    3.0727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2454   -1.7470    2.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6337   -1.5611    1.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6252   -0.4688    0.9143 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1294    0.1842    1.8485 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -0.0632   -0.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0224    0.9460   -0.5436 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5273    2.1211   -1.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1154    1.7582   -2.6189 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3112    0.4708   -1.1714 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598   -0.4860   -0.2946 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3148   -1.0940   -0.8952 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.7113   -0.2359   -2.0827 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1922   -2.6736   -1.4278 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5539   -0.9019    0.2598 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7602   -0.9678   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8645   -0.7949    0.6173 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1350   -0.8570   -0.0499 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3133   -0.9037   -4.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9197   -1.7837   -3.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8384    0.0452   -3.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1225   -1.1216   -2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4457   -1.1389   -1.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9781    1.2971   -2.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0283    2.6398   -0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8581   -0.0446    0.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3257    1.3908    1.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5600    2.8148    0.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5149    1.7375   -0.2782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2860   -0.8139   -0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9682   -0.4850   -1.5334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3440   -2.2135    0.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2391   -1.6048    2.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8835    0.3395    3.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6560    1.2074    1.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1794    1.7202    1.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8741    2.4197    2.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5168    0.8740    3.9500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6019    1.8660    2.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2070   -1.1117    2.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3420    0.0752    1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2896    0.3096    3.1571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3090   -0.7972    4.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140   -2.6578    2.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2004   -1.9147    3.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1229   -2.4869    0.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7211   -1.3992    0.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3007    1.3525    0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4066    2.8001   -1.4830 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7730    2.7322   -0.8009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1472    2.6045   -3.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9943    1.3054   -1.3345 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0729   -0.0805   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5039   -3.1701   -0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8933   -0.1411   -1.1452 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8911   -1.9147   -0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7460   -1.5500    1.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6853    0.2022    1.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9038   -0.4361    0.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1000   -0.4371   -0.9956 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 14 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 21 62  1  1
 22 63  1  0
 22 64  1  0
 23 65  1  0
 24 66  1  0
 24 67  1  0
 28 68  1  0
 30 69  1  0
 30 70  1  0
 31 71  1  0
 31 72  1  0
 32 73  1  0
 32 74  1  0
M  END


  Mrv0541 02241201412D          

 33 32  0  0  1  0            999 V2000
   25.9644   -8.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.2893   -9.1155    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   24.6142   -8.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.6396   -9.1155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9390   -9.1155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.7625   -9.8951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.3146   -8.7257    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   26.9249   -8.0505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.7044   -9.4008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.9898   -8.3359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.6649   -8.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.3400   -8.3359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0151   -8.7257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.8771   -9.9248    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9019  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6164   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3309  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0453  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7598   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4743  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1888  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9033   -9.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6178  -10.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3322  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0467   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7612  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4757   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.1902  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9046   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6191  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.3336   -9.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0480  -10.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0480  -11.1326    0.0000 O   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  1  1  0  0  0  0
  5  3  1  0  0  0  0
  2  6  1  6  0  0  0
  7  4  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
  2 14  1  1  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  2  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  2  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  2  0  0  0  0
 25 24  1  0  0  0  0
 26 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 27  1  0  0  0  0
 29 28  1  0  0  0  0
 30 29  1  0  0  0  0
 31 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 32  2  0  0  0  0
  6 32  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0011479

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@](CO)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC

> <INCHI_IDENTIFIER>
InChI=1S/C23H42NO7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-23(26)31-22(20-25)21-30-32(27,28)29-19-18-24/h3-4,6-7,9-10,22,25H,2,5,8,11-21,24H2,1H3,(H,27,28)/b4-3-,7-6-,10-9-/t22-/m1/s1

> <INCHI_KEY>
JGWWMNVPHKMUCV-WOBXFXBNSA-N

> <FORMULA>
C23H42NO7P

> <MOLECULAR_WEIGHT>
475.5558

> <EXACT_MASS>
475.269889215

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
52.34249679615983

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-aminoethoxy)[(2R)-3-hydroxy-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy]phosphinic acid

> <ALOGPS_LOGP>
4.34

> <JCHEM_LOGP>
3.333233815327011

> <ALOGPS_LOGS>
-5.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.579269652388977

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8688048676175866

> <JCHEM_PKA_STRONGEST_BASIC>
9.999917895738319

> <JCHEM_POLAR_SURFACE_AREA>
128.31

> <JCHEM_REFRACTIVITY>
129.9643

> <JCHEM_ROTATABLE_BOND_COUNT>
22

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.27e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-aminoethoxy(2R)-3-hydroxy-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxyphosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0011479
     RDKit          3D
LysoPE(0:0/18:3(9Z,12Z,15Z))
 74 73  0  0  0  0  0  0  0  0999 V2000
   -8.4833   -0.8348   -3.4109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1104   -0.6411   -2.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3141    0.8002   -1.8605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8000    1.5599   -0.9438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8916    1.0220    0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5944    1.7054    0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4634    1.1073   -0.2104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2742   -0.2996   -0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4388   -1.1081    0.4468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7704   -0.7407    1.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7328    0.5831    2.0674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5376    1.4206    2.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3289    1.0017    2.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6487   -0.1985    2.2708 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6157   -0.5332    3.0727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2454   -1.7470    2.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6337   -1.5611    1.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6252   -0.4688    0.9143 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1294    0.1842    1.8485 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -0.0632   -0.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0224    0.9460   -0.5436 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5273    2.1211   -1.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1154    1.7582   -2.6189 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3112    0.4708   -1.1714 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598   -0.4860   -0.2946 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3148   -1.0940   -0.8952 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.7113   -0.2359   -2.0827 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1922   -2.6736   -1.4278 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5539   -0.9019    0.2598 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7602   -0.9678   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8645   -0.7949    0.6173 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1350   -0.8570   -0.0499 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3133   -0.9037   -4.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9197   -1.7837   -3.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8384    0.0452   -3.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1225   -1.1216   -2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4457   -1.1389   -1.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9781    1.2971   -2.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0283    2.6398   -0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8581   -0.0446    0.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3257    1.3908    1.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5600    2.8148    0.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5149    1.7375   -0.2782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2860   -0.8139   -0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9682   -0.4850   -1.5334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3440   -2.2135    0.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2391   -1.6048    2.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8835    0.3395    3.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6560    1.2074    1.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1794    1.7202    1.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8741    2.4197    2.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5168    0.8740    3.9500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6019    1.8660    2.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2070   -1.1117    2.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3420    0.0752    1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2896    0.3096    3.1571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3090   -0.7972    4.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140   -2.6578    2.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2004   -1.9147    3.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1229   -2.4869    0.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7211   -1.3992    0.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3007    1.3525    0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4066    2.8001   -1.4830 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7730    2.7322   -0.8009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1472    2.6045   -3.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9943    1.3054   -1.3345 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0729   -0.0805   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5039   -3.1701   -0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8933   -0.1411   -1.1452 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8911   -1.9147   -0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7460   -1.5500    1.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6853    0.2022    1.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9038   -0.4361    0.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1000   -0.4371   -0.9956 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 14 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 21 62  1  1
 22 63  1  0
 22 64  1  0
 23 65  1  0
 24 66  1  0
 24 67  1  0
 28 68  1  0
 30 69  1  0
 30 70  1  0
 31 71  1  0
 31 72  1  0
 32 73  1  0
 32 74  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      48.467 -16.288   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      47.207 -17.016   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      45.947 -16.288   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      49.727 -17.016   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      44.686 -17.016   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      46.223 -18.471   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      50.987 -16.288   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      50.260 -15.028   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      51.715 -17.548   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      52.248 -15.560   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      53.508 -16.288   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      54.768 -15.560   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      56.028 -16.288   0.000  0.00  0.00           N+0
HETATM   14  H   UNK     0      48.304 -18.526   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0      22.217 -19.241   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      23.551 -18.471   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      24.884 -19.241   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      26.218 -19.241   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      27.552 -18.471   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      28.885 -19.241   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      30.219 -19.241   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      31.553 -18.471   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      32.887 -19.241   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      34.220 -19.241   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      35.554 -18.471   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      36.888 -19.241   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      38.221 -18.471   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      39.555 -19.241   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      40.889 -18.471   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      42.222 -19.241   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      43.556 -18.471   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      44.890 -19.241   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      44.890 -20.781   0.000  0.00  0.00           O+0
CONECT    1    2    4                                                       
CONECT    2    1    3    6   14                                             
CONECT    3    2    5                                                       
CONECT    4    1    7                                                       
CONECT    5    3                                                            
CONECT    6    2   32                                                       
CONECT    7    4    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    2                                                            
CONECT   15   16                                                            
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33    6                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   64    0
END

COMPND    HMDB0011479
HETATM    1  C1  UNL     1      -8.483  -0.835  -3.411  1.00  0.00           C  
HETATM    2  C2  UNL     1      -9.110  -0.641  -2.023  1.00  0.00           C  
HETATM    3  C3  UNL     1      -9.314   0.800  -1.860  1.00  0.00           C  
HETATM    4  C4  UNL     1      -8.800   1.560  -0.944  1.00  0.00           C  
HETATM    5  C5  UNL     1      -7.892   1.022   0.107  1.00  0.00           C  
HETATM    6  C6  UNL     1      -6.594   1.705   0.018  1.00  0.00           C  
HETATM    7  C7  UNL     1      -5.463   1.107  -0.210  1.00  0.00           C  
HETATM    8  C8  UNL     1      -5.274  -0.300  -0.414  1.00  0.00           C  
HETATM    9  C9  UNL     1      -4.439  -1.108   0.447  1.00  0.00           C  
HETATM   10  C10 UNL     1      -3.770  -0.741   1.513  1.00  0.00           C  
HETATM   11  C11 UNL     1      -3.733   0.583   2.067  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.538   1.421   2.114  1.00  0.00           C  
HETATM   13  C13 UNL     1      -1.329   1.002   2.840  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.649  -0.198   2.271  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.616  -0.533   3.073  1.00  0.00           C  
HETATM   16  C16 UNL     1       1.245  -1.747   2.479  1.00  0.00           C  
HETATM   17  C17 UNL     1       1.634  -1.561   1.044  1.00  0.00           C  
HETATM   18  C18 UNL     1       2.625  -0.469   0.914  1.00  0.00           C  
HETATM   19  O1  UNL     1       3.129   0.184   1.848  1.00  0.00           O  
HETATM   20  O2  UNL     1       3.099  -0.063  -0.347  1.00  0.00           O  
HETATM   21  C19 UNL     1       4.022   0.946  -0.544  1.00  0.00           C  
HETATM   22  C20 UNL     1       3.527   2.121  -1.338  1.00  0.00           C  
HETATM   23  O3  UNL     1       3.115   1.758  -2.619  1.00  0.00           O  
HETATM   24  C21 UNL     1       5.311   0.471  -1.171  1.00  0.00           C  
HETATM   25  O4  UNL     1       5.860  -0.486  -0.295  1.00  0.00           O  
HETATM   26  P1  UNL     1       7.315  -1.094  -0.895  1.00  0.00           P  
HETATM   27  O5  UNL     1       7.711  -0.236  -2.083  1.00  0.00           O  
HETATM   28  O6  UNL     1       7.192  -2.674  -1.428  1.00  0.00           O  
HETATM   29  O7  UNL     1       8.554  -0.902   0.260  1.00  0.00           O  
HETATM   30  C22 UNL     1       9.760  -0.968  -0.423  1.00  0.00           C  
HETATM   31  C23 UNL     1      10.865  -0.795   0.617  1.00  0.00           C  
HETATM   32  N1  UNL     1      12.135  -0.857  -0.050  1.00  0.00           N  
HETATM   33  H1  UNL     1      -9.313  -0.904  -4.141  1.00  0.00           H  
HETATM   34  H2  UNL     1      -7.920  -1.784  -3.432  1.00  0.00           H  
HETATM   35  H3  UNL     1      -7.838   0.045  -3.613  1.00  0.00           H  
HETATM   36  H4  UNL     1     -10.122  -1.122  -2.047  1.00  0.00           H  
HETATM   37  H5  UNL     1      -8.446  -1.139  -1.329  1.00  0.00           H  
HETATM   38  H6  UNL     1      -9.978   1.297  -2.599  1.00  0.00           H  
HETATM   39  H7  UNL     1      -9.028   2.640  -0.922  1.00  0.00           H  
HETATM   40  H8  UNL     1      -7.858  -0.045   0.203  1.00  0.00           H  
HETATM   41  H9  UNL     1      -8.326   1.391   1.117  1.00  0.00           H  
HETATM   42  H10 UNL     1      -6.560   2.815   0.154  1.00  0.00           H  
HETATM   43  H11 UNL     1      -4.515   1.737  -0.278  1.00  0.00           H  
HETATM   44  H12 UNL     1      -6.286  -0.814  -0.440  1.00  0.00           H  
HETATM   45  H13 UNL     1      -4.968  -0.485  -1.533  1.00  0.00           H  
HETATM   46  H14 UNL     1      -4.344  -2.213   0.167  1.00  0.00           H  
HETATM   47  H15 UNL     1      -3.239  -1.605   2.018  1.00  0.00           H  
HETATM   48  H16 UNL     1      -3.884   0.340   3.245  1.00  0.00           H  
HETATM   49  H17 UNL     1      -4.656   1.207   1.973  1.00  0.00           H  
HETATM   50  H18 UNL     1      -2.179   1.720   1.070  1.00  0.00           H  
HETATM   51  H19 UNL     1      -2.874   2.420   2.575  1.00  0.00           H  
HETATM   52  H20 UNL     1      -1.517   0.874   3.950  1.00  0.00           H  
HETATM   53  H21 UNL     1      -0.602   1.866   2.817  1.00  0.00           H  
HETATM   54  H22 UNL     1      -1.207  -1.112   2.201  1.00  0.00           H  
HETATM   55  H23 UNL     1      -0.342   0.075   1.217  1.00  0.00           H  
HETATM   56  H24 UNL     1       1.290   0.310   3.157  1.00  0.00           H  
HETATM   57  H25 UNL     1       0.309  -0.797   4.132  1.00  0.00           H  
HETATM   58  H26 UNL     1       0.614  -2.658   2.623  1.00  0.00           H  
HETATM   59  H27 UNL     1       2.200  -1.915   3.072  1.00  0.00           H  
HETATM   60  H28 UNL     1       2.123  -2.487   0.630  1.00  0.00           H  
HETATM   61  H29 UNL     1       0.721  -1.399   0.436  1.00  0.00           H  
HETATM   62  H30 UNL     1       4.301   1.352   0.470  1.00  0.00           H  
HETATM   63  H31 UNL     1       4.407   2.800  -1.483  1.00  0.00           H  
HETATM   64  H32 UNL     1       2.773   2.732  -0.801  1.00  0.00           H  
HETATM   65  H33 UNL     1       3.147   2.605  -3.158  1.00  0.00           H  
HETATM   66  H34 UNL     1       5.994   1.305  -1.334  1.00  0.00           H  
HETATM   67  H35 UNL     1       5.073  -0.081  -2.114  1.00  0.00           H  
HETATM   68  H36 UNL     1       6.504  -3.170  -0.940  1.00  0.00           H  
HETATM   69  H37 UNL     1       9.893  -0.141  -1.145  1.00  0.00           H  
HETATM   70  H38 UNL     1       9.891  -1.915  -0.973  1.00  0.00           H  
HETATM   71  H39 UNL     1      10.746  -1.550   1.404  1.00  0.00           H  
HETATM   72  H40 UNL     1      10.685   0.202   1.089  1.00  0.00           H  
HETATM   73  H41 UNL     1      12.904  -0.436   0.540  1.00  0.00           H  
HETATM   74  H42 UNL     1      12.100  -0.437  -0.996  1.00  0.00           H  
CONECT    1    2   33   34   35
CONECT    2    3   36   37
CONECT    3    4    4   38
CONECT    4    5   39
CONECT    5    6   40   41
CONECT    6    7    7   42
CONECT    7    8   43
CONECT    8    9   44   45
CONECT    9   10   10   46
CONECT   10   11   47
CONECT   11   12   48   49
CONECT   12   13   50   51
CONECT   13   14   52   53
CONECT   14   15   54   55
CONECT   15   16   56   57
CONECT   16   17   58   59
CONECT   17   18   60   61
CONECT   18   19   19   20
CONECT   20   21
CONECT   21   22   24   62
CONECT   22   23   63   64
CONECT   23   65
CONECT   24   25   66   67
CONECT   25   26
CONECT   26   27   27   28   29
CONECT   28   68
CONECT   29   30
CONECT   30   31   69   70
CONECT   31   32   71   72
CONECT   32   73   74
END

HMDB0011479
     RDKit          3D
LysoPE(0:0/18:3(9Z,12Z,15Z))
 74 73  0  0  0  0  0  0  0  0999 V2000
   -8.4833   -0.8348   -3.4109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1104   -0.6411   -2.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3141    0.8002   -1.8605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8000    1.5599   -0.9438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8916    1.0220    0.1073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5944    1.7054    0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4634    1.1073   -0.2104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2742   -0.2996   -0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4388   -1.1081    0.4468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7704   -0.7407    1.5126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7328    0.5831    2.0674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5376    1.4206    2.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3289    1.0017    2.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6487   -0.1985    2.2708 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6157   -0.5332    3.0727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2454   -1.7470    2.4791 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6337   -1.5611    1.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6252   -0.4688    0.9143 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1294    0.1842    1.8485 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0992   -0.0632   -0.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0224    0.9460   -0.5436 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5273    2.1211   -1.3379 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1154    1.7582   -2.6189 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3112    0.4708   -1.1714 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598   -0.4860   -0.2946 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3148   -1.0940   -0.8952 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.7113   -0.2359   -2.0827 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1922   -2.6736   -1.4278 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5539   -0.9019    0.2598 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7602   -0.9678   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8645   -0.7949    0.6173 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1350   -0.8570   -0.0499 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3133   -0.9037   -4.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9197   -1.7837   -3.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8384    0.0452   -3.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1225   -1.1216   -2.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4457   -1.1389   -1.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9781    1.2971   -2.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0283    2.6398   -0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8581   -0.0446    0.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3257    1.3908    1.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5600    2.8148    0.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5149    1.7375   -0.2782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2860   -0.8139   -0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9682   -0.4850   -1.5334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3440   -2.2135    0.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2391   -1.6048    2.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8835    0.3395    3.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6560    1.2074    1.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1794    1.7202    1.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8741    2.4197    2.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5168    0.8740    3.9500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6019    1.8660    2.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2070   -1.1117    2.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3420    0.0752    1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2896    0.3096    3.1571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3090   -0.7972    4.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140   -2.6578    2.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2004   -1.9147    3.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1229   -2.4869    0.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7211   -1.3992    0.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3007    1.3525    0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4066    2.8001   -1.4830 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7730    2.7322   -0.8009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1472    2.6045   -3.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9943    1.3054   -1.3345 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0729   -0.0805   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5039   -3.1701   -0.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8933   -0.1411   -1.1452 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8911   -1.9147   -0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7460   -1.5500    1.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6853    0.2022    1.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9038   -0.4361    0.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1000   -0.4371   -0.9956 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  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  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 14 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 21 62  1  1
 22 63  1  0
 22 64  1  0
 23 65  1  0
 24 66  1  0
 24 67  1  0
 28 68  1  0
 30 69  1  0
 30 70  1  0
 31 71  1  0
 31 72  1  0
 32 73  1  0
 32 74  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(9Z,12Z,15Z-Octadeatrienoyl)-lysophosphatidylethanolamine	HMDB
1-Hydroxy-2-a-linolenoyl-sn-glycero-3-phosphoethanolamine	HMDB
1-Hydroxy-2-alpha-linolenoyl-sn-glycero-3-phosphoethanolamine	HMDB
LPE(0:0/18:3)	HMDB
LPE(0:0/18:3n3)	HMDB
LPE(0:0/18:3W3)	HMDB
LPE(18:3)	HMDB
Lyso-pe(0:0/18:3)	HMDB
Lyso-pe(0:0/18:3n3)	HMDB
Lyso-pe(0:0/18:3W3)	HMDB
Lyso-pe(18:3)	HMDB
LysoPE(0:0/18:3)	HMDB
LysoPE(0:0/18:3n3)	HMDB
LysoPE(0:0/18:3W3)	HMDB
LysoPE(18:3)	HMDB
Lysophosphatidylethanolamine(0:0/18:3)	HMDB
Lysophosphatidylethanolamine(0:0/18:3n3)	HMDB
Lysophosphatidylethanolamine(0:0/18:3W3)	HMDB
Lysophosphatidylethanolamine(18:3)	HMDB
1-Hydroxy-2-(9Z,12Z,15Z-octadeatrienoyl)-sn-glycero-3-phosphoethanolamine	HMDB
LysoPE(0:0/18:3(9Z,12Z,15Z))	Lipid Annotator

Chemical Formula

C₂₃H₄₂NO₇P

Average Molecular Weight

475.5558

Monoisotopic Molecular Weight

475.269889215

IUPAC Name

(2-aminoethoxy)[(2R)-3-hydroxy-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy]phosphinic acid

Traditional Name

2-aminoethoxy(2R)-3-hydroxy-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxyphosphinic acid

CAS Registry Number

Not Available

SMILES

[H][C@@](CO)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC

InChI Identifier

InChI=1S/C23H42NO7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-23(26)31-22(20-25)21-30-32(27,28)29-19-18-24/h3-4,6-7,9-10,22,25H,2,5,8,11-21,24H2,1H3,(H,27,28)/b4-3-,7-6-,10-9-/t22-/m1/s1

InChI Key

JGWWMNVPHKMUCV-WOBXFXBNSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-acyl-sn-glycero-3-phosphoethanolamines. These are glycerophoethanolamines in which the glycerol is esterified with a fatty acid at O-2 position, and linked at position 3 to a phosphoethanolamine.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoethanolamines

Direct Parent

2-acyl-sn-glycero-3-phosphoethanolamines

Alternative Parents

Substituents

2-monoacyl-sn-glycero-3-phosphoethanolamine
Phosphoethanolamine
Fatty acid ester
Dialkyl phosphate
Organic phosphoric acid derivative
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Amino acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Alcohol
Primary aliphatic amine
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Amine
Primary amine
Primary alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

All Tissues (HMDB: HMDB0011479)

Cellular substructure

Membrane (HMDB: HMDB0011479)
Extracellular (HMDB: HMDB0011479)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

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
Water Solubility	0.0043 g/L	ALOGPS
logP	4.34	ALOGPS
logP	3.33	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	1.87	ChemAxon
pKa (Strongest Basic)	10	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	128.31 Å²	ChemAxon
Rotatable Bond Count	22	ChemAxon
Refractivity	129.96 m³·mol⁻¹	ChemAxon
Polarizability	52.34 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
DarkChem	[M+H]+	221.698	31661259
DarkChem	[M-H]-	217.527	31661259
DeepCCS	[M+H]+	203.252	30932474
DeepCCS	[M-H]-	200.894	30932474
DeepCCS	[M-2H]-	234.616	30932474
DeepCCS	[M+Na]+	209.428	30932474
AllCCS	[M+H]+	218.3	32859911
AllCCS	[M+H-H2O]+	216.6	32859911
AllCCS	[M+NH4]+	220.0	32859911
AllCCS	[M+Na]+	220.4	32859911
AllCCS	[M-H]-	212.9	32859911
AllCCS	[M+Na-2H]-	216.2	32859911
AllCCS	[M+HCOO]-	219.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
LysoPE(0:0/18:3(9Z,12Z,15Z))	[H][C@@](CO)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC	3740.3	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z))	[H][C@@](CO)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC	3083.3	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z))	[H][C@@](CO)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC	3528.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
LysoPE(0:0/18:3(9Z,12Z,15Z)),1TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(O)OCCN	3574.5	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),1TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN)O[Si](C)(C)C	3508.4	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),1TMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN[Si](C)(C)C	3625.6	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN)O[Si](C)(C)C	3517.7	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN)O[Si](C)(C)C	3090.9	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN)O[Si](C)(C)C	4612.5	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(O)OCCN[Si](C)(C)C	3612.0	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(O)OCCN[Si](C)(C)C	3333.0	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(O)OCCN[Si](C)(C)C	4632.9	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3576.6	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3369.1	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	4235.4	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #4	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	3784.7	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #4	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	3410.4	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TMS,isomer #4	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	4779.1	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3555.3	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3313.6	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3881.1	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	3758.4	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	3393.7	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	4389.3	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3734.7	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3428.3	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4052.0	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),4TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3718.9	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),4TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3365.9	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),4TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3728.9	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),1TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(O)OCCN	3785.3	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),1TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C	3703.4	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),1TBDMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C	3827.1	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C	3955.3	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C	3324.0	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C	4599.9	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C	4040.7	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C	3614.0	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C	4589.2	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4000.4	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3606.9	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4267.7	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #4	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4183.8	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #4	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3665.0	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),2TBDMS,isomer #4	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4672.3	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4212.1	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3687.7	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3964.3	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4423.7	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3773.8	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO[Si](C)(C)C(C)(C)C)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4331.3	Standard polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4341.6	Semi standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3761.1	Standard non polar	33892256
LysoPE(0:0/18:3(9Z,12Z,15Z)),3TBDMS,isomer #3	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)O[C@H](CO)COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4085.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) GC-MS (Non-derivatized) - 70eV, Positive	splash10-001j-6940200000-c0d2a199619f8bbf2258	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) GC-MS (1 TMS) - 70eV, Positive	splash10-0089-9680120000-505f27bac2e997e05294	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 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
Experimental LC-MS/MS	LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 36V, Positive-QTOF	splash10-004i-0090000000-0cbbcb1bbcf4b053f6ab	2021-09-20	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 10V, Positive-QTOF	splash10-0006-9120200000-a8aaf5c3d6fb630adb66	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 20V, Positive-QTOF	splash10-0006-9120000000-c36b7857bdf239910c00	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 40V, Positive-QTOF	splash10-0006-9020000000-b64d57cb848c0fe93b72	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 10V, Negative-QTOF	splash10-00fr-2570900000-c85ea10b9d03e90f3fd4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 20V, Negative-QTOF	splash10-004l-9530200000-f5addd53867e157fe86a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 40V, Negative-QTOF	splash10-01t9-9110000000-9649510b732e394dab24	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 10V, Negative-QTOF	splash10-00di-1400900000-ee766484cc8b65e58684	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 20V, Negative-QTOF	splash10-004i-9720100000-91f11b635af478d1bba9	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 40V, Negative-QTOF	splash10-004i-9310000000-62dc0898ac111adcda8b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 10V, Positive-QTOF	splash10-005i-3006900000-e92eff46230e77a571f2	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 20V, Positive-QTOF	splash10-01q3-9227700000-2da6ebfbb0bc5140449c	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(0:0/18:3(9Z,12Z,15Z)) 40V, Positive-QTOF	splash10-0006-9410000000-9a6dd6cdadc467e33e3d	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

All Tissues

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

FDB028195

KNApSAcK ID

Not Available

Chemspider ID

24769360

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53480928

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

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 ]
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.

Enzymes

Enzyme Details

1. Ectonucleotide pyrophosphatase/phosphodiesterase family member 2

General function:: Involved in catalytic activity
Specific function:: Hydrolyzes lysophospholipids to produce lysophosphatidic acid (LPA) in extracellular fluids. Major substrate is lysophosphatidylcholine. Also can act on sphingosylphosphphorylcholine producing sphingosine-1-phosphate, a modulator of cell motility. Can hydrolyze, in vitro, bis-pNPP, to some extent pNP-TMP, and barely ATP. Involved in several motility-related processes such as angiogenesis and neurite outgrowth. Acts as an angiogenic factor by stimulating migration of smooth muscle cells and microtubule formation. Stimulates migration of melanoma cells, probably via a pertussis toxin-sensitive G protein. May have a role in induction of parturition. Possible involvement in cell proliferation and adipose tissue development. Tumor cell motility-stimulating factor.
Gene Name:: ENPP2
Uniprot ID:: Q13822
Molecular weight:: 98992.78

Showing metabocard for LysoPE(0:0/18:3(9Z,12Z,15Z)) (HMDB0011479)

MOL for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

3D MOL for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

3D SDF for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

3D-SDF for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

PDB for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

3D PDB for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

SMILES for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

INCHI for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

Structure for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

3D Structure for HMDB0011479 (LysoPE(0:0/18:3(9Z,12Z,15Z)))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes