Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (43) Show 43 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2008-09-12 01:44:03 UTC

Update Date

2022-11-30 19:03:19 UTC

HMDB ID

HMDB0008855

Secondary Accession Numbers

HMDB08855

Metabolite Identification

Common Name

PE(14:1(9Z)/14:1(9Z))

Description

PE(14:1(9Z)/14:1(9Z)) is a phosphatidylethanolamine (PE or GPEtn). It is a glycerophospholipid in which a phosphorylethanolamine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphoethanolamines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PE(14:1(9Z)/14:1(9Z)), in particular, consists of two chains of myristoleic acid at the C-1 and C-2 positions. The myristoleic acid moieties are derived from milk fats. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PEs are neutral zwitterions at physiological pH. They mostly have palmitic or stearic acid on carbon 1 and a long chain unsaturated fatty acid (e.g. 18:2, 20:4 and 22:6) on carbon 2. PE synthesis can occur via two pathways. The first requires that ethanolamine be activated by phosphorylation and then coupled to CDP. The ethanolamine is then transferred from CDP-ethanolamine to phosphatidic acid to yield PE. The second involves the decarboxylation of PS.

Structure

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


  Mrv0541 02231222552D          

 44 43  0  0  1  0            999 V2000
   24.9626   -5.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2875   -5.9431    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.6124   -5.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.6378   -5.9431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.9373   -5.9431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.7607   -6.7227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.3128   -5.5534    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   25.9231   -4.8782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.7026   -6.2284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.9880   -5.1636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.6631   -5.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3382   -5.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.0133   -5.5534    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.8753   -6.7524    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9346   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6490   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3635   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0780   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7925   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5070   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2214   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9359   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6504   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3648   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0793   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7938   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5083   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2228   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2228   -4.7056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7580   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4725   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1870   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9014   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6160   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3304   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.0449   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7594   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4738   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.1883   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9028   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6172   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3318   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0462   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0462   -7.9602    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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28  5  1  0  0  0  0
 28 29  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43  6  1  0  0  0  0
 43 44  2  0  0  0  0
M  END

HMDB0008855
     RDKit          3D
PE(14:1(9Z)/14:1(9Z))
105104  0  0  0  0  0  0  0  0999 V2000
   11.1329    5.1663   -3.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5266    3.8594   -3.5978 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4518    2.9236   -2.4158 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6034    3.5057   -1.2756 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5155    2.5924   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3964    2.0878    0.3289 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0959    2.4147   -0.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3573    1.2112   -0.8020 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0652    0.1497    0.1880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2310    0.6409    1.3196 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9066    1.1611    0.7899 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0545    1.6518    1.9179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7605    0.5616    2.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0030   -0.5273    2.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685   -0.3948    1.0908 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.6799    2.9644 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1245   -2.8062    2.5625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3398   -2.6467    2.3852 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9820   -3.9356    1.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7681   -4.9993    2.6761 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4430   -6.4310    2.1548 P   0  0  0  0  0  5  0  0  0  0  0  0
   -0.5379   -7.5481    2.6973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9674   -6.7134    2.8297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4865   -6.6230    0.4945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7060   -6.3679   -0.0803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6523   -6.5647   -1.5844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9027   -6.3091   -2.2314 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6591   -1.6699    1.4317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5244   -0.5999    1.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9613   -0.5802    2.8935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8662    0.4019    0.7424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8440    1.3927    1.2736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1391    0.8088    1.7276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8678    0.0705    0.6004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1208   -0.5156    1.1874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8945   -1.2574    0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3846   -0.3087   -0.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2542    0.6718   -0.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1069    1.9609   -0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0362    2.6699   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7419    3.6448   -1.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6075    2.8594   -2.8177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8385    1.8792   -3.6650 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3151    5.9159   -3.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8517    5.4427   -4.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6583    5.0667   -2.2358 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1359    3.3330   -4.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4803    3.9791   -3.9690 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9772    1.9853   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4656    2.7400   -1.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7078    3.9618   -1.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2422    4.3810   -0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4406    2.2782    0.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4582    1.3941    1.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0558    3.2106   -0.9886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4510    2.7801    0.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4244    1.5648   -1.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9304    0.7326   -1.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9857   -0.3845    0.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4833   -0.6451   -0.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7656    1.4066    1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0291   -0.2472    1.9805 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0928    2.0653    0.1324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4535    0.3866    0.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6052    2.4708    2.4410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0926    2.0687    1.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1289    0.9959    3.7366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6913    0.1561    3.3566 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -3.6227    3.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6282   -3.1763    1.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8569   -2.3625    3.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0413   -3.6961    1.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4943   -4.1305    0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4059   -5.8926    3.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5654   -6.8802    0.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8974   -5.2624    0.0529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8811   -5.9288   -2.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3789   -7.6349   -1.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6111   -6.0365   -1.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2359   -7.1272   -2.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2935   -0.1524   -0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9719    0.9713    0.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3999    1.9376    2.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0539    2.1921    0.5079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0468    0.1928    2.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7850    1.6852    2.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9961    0.7510   -0.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2143   -0.7713    0.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8969   -1.1315    2.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7385    0.3618    1.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1844   -1.9863   -0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7549   -1.8251    0.5918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0359   -0.8860   -1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5049    0.1036   -1.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1098    0.2502    0.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8247    2.5686    0.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4112    3.2605   -0.2049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4042    2.0601   -1.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3918    4.3270   -1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9866    4.2168   -2.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3495    2.3109   -2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1635    3.5875   -3.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1376    0.8370   -3.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7511    1.9855   -3.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1080    2.0573   -4.7466 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 18 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  2  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  2 48  1  0
  3 49  1  0
  3 50  1  0
  4 51  1  0
  4 52  1  0
  5 53  1  0
  6 54  1  0
  7 55  1  0
  7 56  1  0
  8 57  1  0
  8 58  1  0
  9 59  1  0
  9 60  1  0
 10 61  1  0
 10 62  1  0
 11 63  1  0
 11 64  1  0
 12 65  1  0
 12 66  1  0
 13 67  1  0
 13 68  1  0
 17 69  1  0
 17 70  1  0
 18 71  1  1
 19 72  1  0
 19 73  1  0
 23 74  1  0
 25 75  1  0
 25 76  1  0
 26 77  1  0
 26 78  1  0
 27 79  1  0
 27 80  1  0
 31 81  1  0
 31 82  1  0
 32 83  1  0
 32 84  1  0
 33 85  1  0
 33 86  1  0
 34 87  1  0
 34 88  1  0
 35 89  1  0
 35 90  1  0
 36 91  1  0
 36 92  1  0
 37 93  1  0
 37 94  1  0
 38 95  1  0
 39 96  1  0
 40 97  1  0
 40 98  1  0
 41 99  1  0
 41100  1  0
 42101  1  0
 42102  1  0
 43103  1  0
 43104  1  0
 43105  1  0
M  END


  Mrv0541 02231222552D          

 44 43  0  0  1  0            999 V2000
   24.9626   -5.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2875   -5.9431    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.6124   -5.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.6378   -5.9431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.9373   -5.9431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.7607   -6.7227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.3128   -5.5534    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   25.9231   -4.8782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.7026   -6.2284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.9880   -5.1636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.6631   -5.5534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3382   -5.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.0133   -5.5534    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.8753   -6.7524    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9346   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6490   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3635   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0780   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7925   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5070   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2214   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9359   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6504   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3648   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0793   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7938   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5083   -5.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2228   -5.5306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2228   -4.7056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7580   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4725   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1870   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9014   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6160   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3304   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.0449   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7594   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4738   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.1883   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9028   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.6172   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3318   -6.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0462   -7.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0462   -7.9602    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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28  5  1  0  0  0  0
 28 29  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43  6  1  0  0  0  0
 43 44  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0008855

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C33H62NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-32(35)39-29-31(30-41-43(37,38)40-28-27-34)42-33(36)26-24-22-20-18-16-14-12-10-8-6-4-2/h9-12,31H,3-8,13-30,34H2,1-2H3,(H,37,38)/b11-9-,12-10-/t31-/m1/s1

> <INCHI_KEY>
NMAFIXDXWCNTFK-HFQSORNJSA-N

> <FORMULA>
C33H62NO8P

> <MOLECULAR_WEIGHT>
631.821

> <EXACT_MASS>
631.421304477

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
74.06435682874206

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-aminoethoxy)[(2R)-2,3-bis[(9Z)-tetradec-9-enoyloxy]propoxy]phosphinic acid

> <ALOGPS_LOGP>
6.86

> <JCHEM_LOGP>
7.948797385803423

> <ALOGPS_LOGS>
-6.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8688003136581992

> <JCHEM_PKA_STRONGEST_BASIC>
9.999929336362278

> <JCHEM_POLAR_SURFACE_AREA>
134.38

> <JCHEM_REFRACTIVITY>
174.8331

> <JCHEM_ROTATABLE_BOND_COUNT>
33

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.47e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-aminoethoxy(2R)-2,3-bis[(9Z)-tetradec-9-enoyloxy]propoxyphosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0008855
     RDKit          3D
PE(14:1(9Z)/14:1(9Z))
105104  0  0  0  0  0  0  0  0999 V2000
   11.1329    5.1663   -3.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5266    3.8594   -3.5978 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4518    2.9236   -2.4158 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6034    3.5057   -1.2756 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5155    2.5924   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3964    2.0878    0.3289 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0959    2.4147   -0.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3573    1.2112   -0.8020 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0652    0.1497    0.1880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2310    0.6409    1.3196 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9066    1.1611    0.7899 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0545    1.6518    1.9179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7605    0.5616    2.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0030   -0.5273    2.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685   -0.3948    1.0908 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.6799    2.9644 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1245   -2.8062    2.5625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3398   -2.6467    2.3852 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9820   -3.9356    1.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7681   -4.9993    2.6761 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4430   -6.4310    2.1548 P   0  0  0  0  0  5  0  0  0  0  0  0
   -0.5379   -7.5481    2.6973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9674   -6.7134    2.8297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4865   -6.6230    0.4945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7060   -6.3679   -0.0803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6523   -6.5647   -1.5844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9027   -6.3091   -2.2314 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6591   -1.6699    1.4317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5244   -0.5999    1.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9613   -0.5802    2.8935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8662    0.4019    0.7424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8440    1.3927    1.2736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1391    0.8088    1.7276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8678    0.0705    0.6004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1208   -0.5156    1.1874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8945   -1.2574    0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3846   -0.3087   -0.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2542    0.6718   -0.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1069    1.9609   -0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0362    2.6699   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7419    3.6448   -1.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6075    2.8594   -2.8177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8385    1.8792   -3.6650 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3151    5.9159   -3.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8517    5.4427   -4.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6583    5.0667   -2.2358 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1359    3.3330   -4.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4803    3.9791   -3.9690 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9772    1.9853   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4656    2.7400   -1.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7078    3.9618   -1.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2422    4.3810   -0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4406    2.2782    0.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4582    1.3941    1.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0558    3.2106   -0.9886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4510    2.7801    0.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4244    1.5648   -1.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9304    0.7326   -1.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9857   -0.3845    0.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4833   -0.6451   -0.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7656    1.4066    1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0291   -0.2472    1.9805 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0928    2.0653    0.1324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4535    0.3866    0.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6052    2.4708    2.4410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0926    2.0687    1.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1289    0.9959    3.7366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6913    0.1561    3.3566 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -3.6227    3.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6282   -3.1763    1.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8569   -2.3625    3.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0413   -3.6961    1.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4943   -4.1305    0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4059   -5.8926    3.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5654   -6.8802    0.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8974   -5.2624    0.0529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8811   -5.9288   -2.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3789   -7.6349   -1.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6111   -6.0365   -1.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2359   -7.1272   -2.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2935   -0.1524   -0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9719    0.9713    0.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3999    1.9376    2.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0539    2.1921    0.5079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0468    0.1928    2.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7850    1.6852    2.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9961    0.7510   -0.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2143   -0.7713    0.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8969   -1.1315    2.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7385    0.3618    1.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1844   -1.9863   -0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7549   -1.8251    0.5918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0359   -0.8860   -1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5049    0.1036   -1.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1098    0.2502    0.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8247    2.5686    0.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4112    3.2605   -0.2049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4042    2.0601   -1.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3918    4.3270   -1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9866    4.2168   -2.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3495    2.3109   -2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1635    3.5875   -3.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1376    0.8370   -3.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7511    1.9855   -3.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1080    2.0573   -4.7466 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 18 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  2  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  2 48  1  0
  3 49  1  0
  3 50  1  0
  4 51  1  0
  4 52  1  0
  5 53  1  0
  6 54  1  0
  7 55  1  0
  7 56  1  0
  8 57  1  0
  8 58  1  0
  9 59  1  0
  9 60  1  0
 10 61  1  0
 10 62  1  0
 11 63  1  0
 11 64  1  0
 12 65  1  0
 12 66  1  0
 13 67  1  0
 13 68  1  0
 17 69  1  0
 17 70  1  0
 18 71  1  1
 19 72  1  0
 19 73  1  0
 23 74  1  0
 25 75  1  0
 25 76  1  0
 26 77  1  0
 26 78  1  0
 27 79  1  0
 27 80  1  0
 31 81  1  0
 31 82  1  0
 32 83  1  0
 32 84  1  0
 33 85  1  0
 33 86  1  0
 34 87  1  0
 34 88  1  0
 35 89  1  0
 35 90  1  0
 36 91  1  0
 36 92  1  0
 37 93  1  0
 37 94  1  0
 38 95  1  0
 39 96  1  0
 40 97  1  0
 40 98  1  0
 41 99  1  0
 41100  1  0
 42101  1  0
 42102  1  0
 43103  1  0
 43104  1  0
 43105  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      46.597 -10.366   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      45.337 -11.094   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      44.076 -10.366   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      47.857 -11.094   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      42.816 -11.094   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      44.353 -12.549   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      49.117 -10.366   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      48.390  -9.106   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      49.845 -11.626   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      50.378  -9.639   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      51.638 -10.366   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      52.898  -9.639   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      54.158 -10.366   0.000  0.00  0.00           N+0
HETATM   14  H   UNK     0      46.434 -12.604   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0      24.145 -10.324   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      25.478 -11.094   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.812 -10.324   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.146 -11.094   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      29.479 -10.324   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      30.813 -10.324   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      32.147 -11.094   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      33.480 -10.324   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      34.814 -11.094   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      36.148 -10.324   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      37.481 -11.094   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      38.815 -10.324   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      40.149 -11.094   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      41.483 -10.324   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      41.483  -8.784   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      25.682 -13.319   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      27.015 -12.549   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      28.349 -13.319   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      29.683 -12.549   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      31.017 -13.319   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      32.350 -13.319   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      33.684 -12.549   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      35.018 -13.319   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      36.351 -12.549   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      37.685 -13.319   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      39.019 -12.549   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      40.352 -13.319   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      41.686 -12.549   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      43.020 -13.319   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      43.020 -14.859   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   28                                                       
CONECT    6    2   43                                                       
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    5   29                                                  
CONECT   29   28                                                            
CONECT   30   31                                                            
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42    6   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   86    0
END

COMPND    HMDB0008855
HETATM    1  C1  UNL     1      11.133   5.166  -3.210  1.00  0.00           C  
HETATM    2  C2  UNL     1      10.527   3.859  -3.598  1.00  0.00           C  
HETATM    3  C3  UNL     1      10.452   2.924  -2.416  1.00  0.00           C  
HETATM    4  C4  UNL     1       9.603   3.506  -1.276  1.00  0.00           C  
HETATM    5  C5  UNL     1       9.516   2.592  -0.146  1.00  0.00           C  
HETATM    6  C6  UNL     1       8.396   2.088   0.329  1.00  0.00           C  
HETATM    7  C7  UNL     1       7.096   2.415  -0.260  1.00  0.00           C  
HETATM    8  C8  UNL     1       6.357   1.211  -0.802  1.00  0.00           C  
HETATM    9  C9  UNL     1       6.065   0.150   0.188  1.00  0.00           C  
HETATM   10  C10 UNL     1       5.231   0.641   1.320  1.00  0.00           C  
HETATM   11  C11 UNL     1       3.907   1.161   0.790  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.055   1.652   1.918  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.760   0.562   2.894  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.003  -0.527   2.241  1.00  0.00           C  
HETATM   15  O1  UNL     1       1.569  -0.395   1.091  1.00  0.00           O  
HETATM   16  O2  UNL     1       1.808  -1.680   2.964  1.00  0.00           O  
HETATM   17  C15 UNL     1       1.124  -2.806   2.562  1.00  0.00           C  
HETATM   18  C16 UNL     1      -0.340  -2.647   2.385  1.00  0.00           C  
HETATM   19  C17 UNL     1      -0.982  -3.936   1.850  1.00  0.00           C  
HETATM   20  O3  UNL     1      -0.768  -4.999   2.676  1.00  0.00           O  
HETATM   21  P1  UNL     1      -1.443  -6.431   2.155  1.00  0.00           P  
HETATM   22  O4  UNL     1      -0.538  -7.548   2.697  1.00  0.00           O  
HETATM   23  O5  UNL     1      -2.967  -6.713   2.830  1.00  0.00           O  
HETATM   24  O6  UNL     1      -1.486  -6.623   0.494  1.00  0.00           O  
HETATM   25  C18 UNL     1      -2.706  -6.368  -0.080  1.00  0.00           C  
HETATM   26  C19 UNL     1      -2.652  -6.565  -1.584  1.00  0.00           C  
HETATM   27  N1  UNL     1      -3.903  -6.309  -2.231  1.00  0.00           N  
HETATM   28  O7  UNL     1      -0.659  -1.670   1.432  1.00  0.00           O  
HETATM   29  C20 UNL     1      -1.524  -0.600   1.741  1.00  0.00           C  
HETATM   30  O8  UNL     1      -1.961  -0.580   2.893  1.00  0.00           O  
HETATM   31  C21 UNL     1      -1.866   0.402   0.742  1.00  0.00           C  
HETATM   32  C22 UNL     1      -2.844   1.393   1.274  1.00  0.00           C  
HETATM   33  C23 UNL     1      -4.139   0.809   1.728  1.00  0.00           C  
HETATM   34  C24 UNL     1      -4.868   0.071   0.600  1.00  0.00           C  
HETATM   35  C25 UNL     1      -6.121  -0.516   1.187  1.00  0.00           C  
HETATM   36  C26 UNL     1      -6.895  -1.257   0.156  1.00  0.00           C  
HETATM   37  C27 UNL     1      -7.385  -0.309  -0.930  1.00  0.00           C  
HETATM   38  C28 UNL     1      -8.254   0.672  -0.230  1.00  0.00           C  
HETATM   39  C29 UNL     1      -8.107   1.961  -0.224  1.00  0.00           C  
HETATM   40  C30 UNL     1      -7.036   2.670  -0.930  1.00  0.00           C  
HETATM   41  C31 UNL     1      -7.742   3.645  -1.886  1.00  0.00           C  
HETATM   42  C32 UNL     1      -8.607   2.859  -2.818  1.00  0.00           C  
HETATM   43  C33 UNL     1      -7.839   1.879  -3.665  1.00  0.00           C  
HETATM   44  H1  UNL     1      10.315   5.916  -3.132  1.00  0.00           H  
HETATM   45  H2  UNL     1      11.852   5.443  -4.023  1.00  0.00           H  
HETATM   46  H3  UNL     1      11.658   5.067  -2.236  1.00  0.00           H  
HETATM   47  H4  UNL     1      11.136   3.333  -4.368  1.00  0.00           H  
HETATM   48  H5  UNL     1       9.480   3.979  -3.969  1.00  0.00           H  
HETATM   49  H6  UNL     1       9.977   1.985  -2.769  1.00  0.00           H  
HETATM   50  H7  UNL     1      11.466   2.740  -1.997  1.00  0.00           H  
HETATM   51  H8  UNL     1       8.708   3.962  -1.659  1.00  0.00           H  
HETATM   52  H9  UNL     1      10.242   4.381  -0.916  1.00  0.00           H  
HETATM   53  H10 UNL     1      10.441   2.278   0.377  1.00  0.00           H  
HETATM   54  H11 UNL     1       8.458   1.394   1.203  1.00  0.00           H  
HETATM   55  H12 UNL     1       7.056   3.211  -0.989  1.00  0.00           H  
HETATM   56  H13 UNL     1       6.451   2.780   0.600  1.00  0.00           H  
HETATM   57  H14 UNL     1       5.424   1.565  -1.271  1.00  0.00           H  
HETATM   58  H15 UNL     1       6.930   0.733  -1.636  1.00  0.00           H  
HETATM   59  H16 UNL     1       6.986  -0.384   0.541  1.00  0.00           H  
HETATM   60  H17 UNL     1       5.483  -0.645  -0.348  1.00  0.00           H  
HETATM   61  H18 UNL     1       5.766   1.407   1.909  1.00  0.00           H  
HETATM   62  H19 UNL     1       5.029  -0.247   1.980  1.00  0.00           H  
HETATM   63  H20 UNL     1       4.093   2.065   0.132  1.00  0.00           H  
HETATM   64  H21 UNL     1       3.453   0.387   0.180  1.00  0.00           H  
HETATM   65  H22 UNL     1       3.605   2.471   2.441  1.00  0.00           H  
HETATM   66  H23 UNL     1       2.093   2.069   1.508  1.00  0.00           H  
HETATM   67  H24 UNL     1       2.129   0.996   3.737  1.00  0.00           H  
HETATM   68  H25 UNL     1       3.691   0.156   3.357  1.00  0.00           H  
HETATM   69  H26 UNL     1       1.364  -3.623   3.303  1.00  0.00           H  
HETATM   70  H27 UNL     1       1.628  -3.176   1.624  1.00  0.00           H  
HETATM   71  H28 UNL     1      -0.857  -2.362   3.340  1.00  0.00           H  
HETATM   72  H29 UNL     1      -2.041  -3.696   1.643  1.00  0.00           H  
HETATM   73  H30 UNL     1      -0.494  -4.130   0.874  1.00  0.00           H  
HETATM   74  H31 UNL     1      -3.406  -5.893   3.158  1.00  0.00           H  
HETATM   75  H32 UNL     1      -3.565  -6.880   0.366  1.00  0.00           H  
HETATM   76  H33 UNL     1      -2.897  -5.262   0.053  1.00  0.00           H  
HETATM   77  H34 UNL     1      -1.881  -5.929  -2.052  1.00  0.00           H  
HETATM   78  H35 UNL     1      -2.379  -7.635  -1.783  1.00  0.00           H  
HETATM   79  H36 UNL     1      -4.611  -6.037  -1.520  1.00  0.00           H  
HETATM   80  H37 UNL     1      -4.236  -7.127  -2.775  1.00  0.00           H  
HETATM   81  H38 UNL     1      -2.293  -0.152  -0.140  1.00  0.00           H  
HETATM   82  H39 UNL     1      -0.972   0.971   0.397  1.00  0.00           H  
HETATM   83  H40 UNL     1      -2.400   1.938   2.146  1.00  0.00           H  
HETATM   84  H41 UNL     1      -3.054   2.192   0.508  1.00  0.00           H  
HETATM   85  H42 UNL     1      -4.047   0.193   2.612  1.00  0.00           H  
HETATM   86  H43 UNL     1      -4.785   1.685   2.050  1.00  0.00           H  
HETATM   87  H44 UNL     1      -4.996   0.751  -0.226  1.00  0.00           H  
HETATM   88  H45 UNL     1      -4.214  -0.771   0.229  1.00  0.00           H  
HETATM   89  H46 UNL     1      -5.897  -1.131   2.090  1.00  0.00           H  
HETATM   90  H47 UNL     1      -6.739   0.362   1.530  1.00  0.00           H  
HETATM   91  H48 UNL     1      -6.184  -1.986  -0.332  1.00  0.00           H  
HETATM   92  H49 UNL     1      -7.755  -1.825   0.592  1.00  0.00           H  
HETATM   93  H50 UNL     1      -8.036  -0.886  -1.632  1.00  0.00           H  
HETATM   94  H51 UNL     1      -6.505   0.104  -1.407  1.00  0.00           H  
HETATM   95  H52 UNL     1      -9.110   0.250   0.339  1.00  0.00           H  
HETATM   96  H53 UNL     1      -8.825   2.569   0.343  1.00  0.00           H  
HETATM   97  H54 UNL     1      -6.411   3.261  -0.205  1.00  0.00           H  
HETATM   98  H55 UNL     1      -6.404   2.060  -1.573  1.00  0.00           H  
HETATM   99  H56 UNL     1      -8.392   4.327  -1.290  1.00  0.00           H  
HETATM  100  H57 UNL     1      -6.987   4.217  -2.460  1.00  0.00           H  
HETATM  101  H58 UNL     1      -9.349   2.311  -2.196  1.00  0.00           H  
HETATM  102  H59 UNL     1      -9.163   3.587  -3.461  1.00  0.00           H  
HETATM  103  H60 UNL     1      -8.138   0.837  -3.459  1.00  0.00           H  
HETATM  104  H61 UNL     1      -6.751   1.985  -3.580  1.00  0.00           H  
HETATM  105  H62 UNL     1      -8.108   2.057  -4.747  1.00  0.00           H  
CONECT    1    2   44   45   46
CONECT    2    3   47   48
CONECT    3    4   49   50
CONECT    4    5   51   52
CONECT    5    6    6   53
CONECT    6    7   54
CONECT    7    8   55   56
CONECT    8    9   57   58
CONECT    9   10   59   60
CONECT   10   11   61   62
CONECT   11   12   63   64
CONECT   12   13   65   66
CONECT   13   14   67   68
CONECT   14   15   15   16
CONECT   16   17
CONECT   17   18   69   70
CONECT   18   19   28   71
CONECT   19   20   72   73
CONECT   20   21
CONECT   21   22   22   23   24
CONECT   23   74
CONECT   24   25
CONECT   25   26   75   76
CONECT   26   27   77   78
CONECT   27   79   80
CONECT   28   29
CONECT   29   30   30   31
CONECT   31   32   81   82
CONECT   32   33   83   84
CONECT   33   34   85   86
CONECT   34   35   87   88
CONECT   35   36   89   90
CONECT   36   37   91   92
CONECT   37   38   93   94
CONECT   38   39   39   95
CONECT   39   40   96
CONECT   40   41   97   98
CONECT   41   42   99  100
CONECT   42   43  101  102
CONECT   43  103  104  105
END

HMDB0008855
     RDKit          3D
PE(14:1(9Z)/14:1(9Z))
105104  0  0  0  0  0  0  0  0999 V2000
   11.1329    5.1663   -3.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5266    3.8594   -3.5978 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4518    2.9236   -2.4158 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6034    3.5057   -1.2756 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5155    2.5924   -0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3964    2.0878    0.3289 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0959    2.4147   -0.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3573    1.2112   -0.8020 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0652    0.1497    0.1880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2310    0.6409    1.3196 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9066    1.1611    0.7899 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0545    1.6518    1.9179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7605    0.5616    2.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0030   -0.5273    2.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685   -0.3948    1.0908 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077   -1.6799    2.9644 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1245   -2.8062    2.5625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3398   -2.6467    2.3852 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9820   -3.9356    1.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7681   -4.9993    2.6761 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4430   -6.4310    2.1548 P   0  0  0  0  0  5  0  0  0  0  0  0
   -0.5379   -7.5481    2.6973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9674   -6.7134    2.8297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4865   -6.6230    0.4945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7060   -6.3679   -0.0803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6523   -6.5647   -1.5844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9027   -6.3091   -2.2314 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6591   -1.6699    1.4317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5244   -0.5999    1.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9613   -0.5802    2.8935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8662    0.4019    0.7424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8440    1.3927    1.2736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1391    0.8088    1.7276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8678    0.0705    0.6004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1208   -0.5156    1.1874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8945   -1.2574    0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3846   -0.3087   -0.9297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2542    0.6718   -0.2303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1069    1.9609   -0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0362    2.6699   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7419    3.6448   -1.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6075    2.8594   -2.8177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8385    1.8792   -3.6650 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3151    5.9159   -3.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8517    5.4427   -4.0226 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6583    5.0667   -2.2358 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1359    3.3330   -4.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4803    3.9791   -3.9690 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9772    1.9853   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4656    2.7400   -1.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7078    3.9618   -1.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2422    4.3810   -0.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4406    2.2782    0.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4582    1.3941    1.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0558    3.2106   -0.9886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4510    2.7801    0.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4244    1.5648   -1.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9304    0.7326   -1.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9857   -0.3845    0.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4833   -0.6451   -0.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7656    1.4066    1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0291   -0.2472    1.9805 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0928    2.0653    0.1324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4535    0.3866    0.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6052    2.4708    2.4410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0926    2.0687    1.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1289    0.9959    3.7366 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6913    0.1561    3.3566 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3642   -3.6227    3.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6282   -3.1763    1.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8569   -2.3625    3.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0413   -3.6961    1.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4943   -4.1305    0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4059   -5.8926    3.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5654   -6.8802    0.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8974   -5.2624    0.0529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8811   -5.9288   -2.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3789   -7.6349   -1.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6111   -6.0365   -1.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2359   -7.1272   -2.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2935   -0.1524   -0.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9719    0.9713    0.3973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3999    1.9376    2.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0539    2.1921    0.5079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0468    0.1928    2.6120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7850    1.6852    2.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9961    0.7510   -0.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2143   -0.7713    0.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8969   -1.1315    2.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7385    0.3618    1.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1844   -1.9863   -0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7549   -1.8251    0.5918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0359   -0.8860   -1.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5049    0.1036   -1.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1098    0.2502    0.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8247    2.5686    0.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4112    3.2605   -0.2049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4042    2.0601   -1.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3918    4.3270   -1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9866    4.2168   -2.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3495    2.3109   -2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1635    3.5875   -3.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1376    0.8370   -3.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7511    1.9855   -3.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1080    2.0573   -4.7466 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 18 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  2  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  2 48  1  0
  3 49  1  0
  3 50  1  0
  4 51  1  0
  4 52  1  0
  5 53  1  0
  6 54  1  0
  7 55  1  0
  7 56  1  0
  8 57  1  0
  8 58  1  0
  9 59  1  0
  9 60  1  0
 10 61  1  0
 10 62  1  0
 11 63  1  0
 11 64  1  0
 12 65  1  0
 12 66  1  0
 13 67  1  0
 13 68  1  0
 17 69  1  0
 17 70  1  0
 18 71  1  1
 19 72  1  0
 19 73  1  0
 23 74  1  0
 25 75  1  0
 25 76  1  0
 26 77  1  0
 26 78  1  0
 27 79  1  0
 27 80  1  0
 31 81  1  0
 31 82  1  0
 32 83  1  0
 32 84  1  0
 33 85  1  0
 33 86  1  0
 34 87  1  0
 34 88  1  0
 35 89  1  0
 35 90  1  0
 36 91  1  0
 36 92  1  0
 37 93  1  0
 37 94  1  0
 38 95  1  0
 39 96  1  0
 40 97  1  0
 40 98  1  0
 41 99  1  0
 41100  1  0
 42101  1  0
 42102  1  0
 43103  1  0
 43104  1  0
 43105  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
PE(14:1/14:1)	HMDB
1,2-Dimyristoleoyl-rac-glycero-3-phosphoethanolamine	HMDB
GPEtn(14:1/14:1)	HMDB
GPEtn(28:2)	HMDB
Phophatidylethanolamine(14:1/14:1)	HMDB
PE(28:2)	HMDB
1,2-Di(9Z-tetradecenoyl)-rac-glycero-3-phosphoethanolamine	HMDB
Phophatidylethanolamine(28:2)	HMDB
PE(14:1(9Z)/14:1(9Z))	Lipid Annotator

Chemical Formula

C₃₃H₆₂NO₈P

Average Molecular Weight

631.821

Monoisotopic Molecular Weight

631.421304477

IUPAC Name

(2-aminoethoxy)[(2R)-2,3-bis[(9Z)-tetradec-9-enoyloxy]propoxy]phosphinic acid

Traditional Name

2-aminoethoxy(2R)-2,3-bis[(9Z)-tetradec-9-enoyloxy]propoxyphosphinic acid

CAS Registry Number

Not Available

SMILES

[H][C@@](COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCC

InChI Identifier

InChI=1S/C33H62NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-32(35)39-29-31(30-41-43(37,38)40-28-27-34)42-33(36)26-24-22-20-18-16-14-12-10-8-6-4-2/h9-12,31H,3-8,13-30,34H2,1-2H3,(H,37,38)/b11-9-,12-10-/t31-/m1/s1

InChI Key

NMAFIXDXWCNTFK-HFQSORNJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phosphatidylethanolamines. These are glycerophosphoetahnolamines in which two fatty acids are bonded to the glycerol moiety through ester linkages.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoethanolamines

Direct Parent

Phosphatidylethanolamines

Alternative Parents

Substituents

Diacylglycero-3-phosphoethanolamine
Phosphoethanolamine
Fatty acid ester
Dialkyl phosphate
Dicarboxylic acid or derivatives
Organic phosphoric acid derivative
Phosphoric acid ester
Alkyl phosphate
Fatty acyl
Amino acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Amine
Primary aliphatic amine
Organic nitrogen compound
Primary amine
Carbonyl group
Organic oxide
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Diacylglycerophosphoethanolamines (LMGP02011238 )

Ontology

Physiological effect

Health effect

Diabetes mellitus type 2 (PMID: 30402908)
Non-alcoholic fatty liver disease (PMID: 26811286)
Parkinson's disease (PMID: 26811286)

Nervous system disorder

Central nervous system disorder

Alzheimer's Disease (PMID: 26811286)

Organoleptic effect

Touch

Smooth (HMDB: HMDB0008855)

Disposition

Biological location

Cellular substructure

Organelle

endoplasmic reticulum (HMDB: HMDB0008855)

golgi apparatus membrane (HMDB: HMDB0008855)
cell membrane (HMDB: HMDB0008855)
Membrane (HMDB: HMDB0008855)
Extracellular (HMDB: HMDB0008855)

Cell

All cells and tissues (HMDB: HMDB0008855)

Cell membrane (HMDB: HMDB0008855)
Intracellular membrane (HMDB: HMDB0008855)
Nervous system (HMDB: HMDB0008855)

Biofluid or Excreta

Blood (HMDB: HMDB0008855)

Tissue substructure

All tissues (HMDB: HMDB0008855)

Tissue

All Tissues (HMDB: HMDB0008855)

Organ

Brain (HMDB: HMDB0008855)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0008855)

Source

Endogenous

Endogenous (HMDB: HMDB0008855)

Animal

Animal (HMDB: HMDB0008855)

Exogenous

Food

Food (HMDB: HMDB0008855)

Animal origin

Poultry

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

Role

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	0.00025 g/L	ALOGPS
logP	6.86	ALOGPS
logP	7.95	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	1.87	ChemAxon
pKa (Strongest Basic)	10	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	134.38 Å²	ChemAxon
Rotatable Bond Count	33	ChemAxon
Refractivity	174.83 m³·mol⁻¹	ChemAxon
Polarizability	74.06 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	261.067	31661259
DarkChem	[M-H]-	247.728	31661259
DeepCCS	[M+H]+	244.877	30932474
DeepCCS	[M-H]-	242.519	30932474
DeepCCS	[M-2H]-	275.404	30932474
DeepCCS	[M+Na]+	250.97	30932474
AllCCS	[M+H]+	257.1	32859911
AllCCS	[M+H-H2O]+	256.6	32859911
AllCCS	[M+NH4]+	257.5	32859911
AllCCS	[M+Na]+	257.6	32859911
AllCCS	[M-H]-	237.8	32859911
AllCCS	[M+Na-2H]-	243.0	32859911
AllCCS	[M+HCOO]-	248.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
PE(14:1(9Z)/14:1(9Z))	[H][C@@](COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCC	4288.5	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z))	[H][C@@](COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCC	4119.9	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z))	[H][C@@](COC(=O)CCCCCCC\C=C/CCCC)(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C/CCCC	4418.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
PE(14:1(9Z)/14:1(9Z)),1TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4359.6	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	3827.5	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	6022.2	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4495.8	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4068.3	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	5912.0	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4388.1	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4013.8	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4831.2	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4647.1	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4073.0	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	5571.0	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),3TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4553.0	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),3TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4030.9	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),3TMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4665.8	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TBDMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4594.3	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TBDMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	3900.3	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TBDMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	5987.4	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TBDMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4701.7	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TBDMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4162.4	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),1TBDMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	5815.8	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TBDMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4864.4	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TBDMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4214.9	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TBDMS,isomer #1	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4898.5	Standard polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TBDMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	5160.8	Semi standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TBDMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	4247.5	Standard non polar	33892256
PE(14:1(9Z)/14:1(9Z)),2TBDMS,isomer #2	CCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCC/C=C\CCCC	5437.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - PE(14:1(9Z)/14:1(9Z)) GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2022-08-08	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 - PE(14:1(9Z)/14:1(9Z)) 10V, Negative-QTOF	splash10-001i-0010009000-e89d5deca08c3c1c4faa	2017-10-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 20V, Negative-QTOF	splash10-001i-0010009000-e89d5deca08c3c1c4faa	2017-10-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 40V, Negative-QTOF	splash10-0059-0390306000-a1d1dcf840908615bcf4	2017-10-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 10V, Positive-QTOF	splash10-001i-0000109000-6ccc893fb7f9528c2607	2017-10-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 20V, Positive-QTOF	splash10-000x-0010905000-d0238f6581a8470ec342	2017-10-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 40V, Positive-QTOF	splash10-0006-0010902000-f181701b8af12cf7bc34	2017-10-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 10V, Positive-QTOF	splash10-0udi-0000019000-20020144971e8864ee29	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 20V, Positive-QTOF	splash10-0w29-0000019000-b35b8feef510de7c7475	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 40V, Positive-QTOF	splash10-03di-0101019000-e49787485265a53c5019	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 10V, Negative-QTOF	splash10-001i-0010009000-ae17da6119a6f38b1c64	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 20V, Negative-QTOF	splash10-001i-0010009000-ae17da6119a6f38b1c64	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 40V, Negative-QTOF	splash10-0059-0390306000-a85647cc3a52577f726f	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 10V, Positive-QTOF	splash10-001i-0000109000-b3f8f95899d59073a897	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 20V, Positive-QTOF	splash10-000x-0010905000-244dbd303e9b061bba8f	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PE(14:1(9Z)/14:1(9Z)) 40V, Positive-QTOF	splash10-0006-0010902000-f5ea9f11de40b179d64a	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

All Tissues
Brain

Pathways

Name	SMPDB/PathBank	KEGG
Phosphatidylcholine Biosynthesis PC(14:1(9Z)/14:1(9Z))		Not Available
Phosphatidylethanolamine Biosynthesis PE(14:1(9Z)/14:1(9Z))		Not Available

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Predicted Concentrations

Biospecimen	Value	Original age	Original sex	Original condition	Comments
Blood	0.001 +/- 0.001 uM	Adult (>18 years old)	Both	Normal (Most Probable)	Calculated using MetaboAnalyst
Blood	0.283 +/- 0.144 uM	Adult (>18 years old)	Both	Normal (Upper Limit)	Calculated using MetaboAnalyst

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

FDB026045

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

52924935

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

Not Available

Only showing the first 10 proteins. There are 43 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details

1. Calcium-dependent phospholipase A2

General function:: Involved in phospholipase A2 activity
Specific function:: PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. This isozyme hydrolyzes more efficiently L-alpha-1-palmitoyl-2-oleoyl phosphatidylcholine than L-alpha-1-palmitoyl-2-arachidonyl phosphatidylcholine, L-alpha-1-palmitoyl-2-arachidonyl phosphatidylethanolamine, or L-alpha-1-stearoyl-2-arachidonyl phosphatidylinositol. May be involved in the production of lung surfactant, the remodeling or regulation of cardiac muscle.
Gene Name:: PLA2G5
Uniprot ID:: P39877
Molecular weight:: 15674.065

Enzyme Details

2. Group IIF secretory phospholipase A2

General function:: Involved in phospholipase A2 activity
Specific function:: PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Hydrolyzes phosphatidylglycerol versus phosphatidylcholine with a 15-fold preference.
Gene Name:: PLA2G2F
Uniprot ID:: Q9BZM2
Molecular weight:: 23256.29

Enzyme Details

3. Cytosolic phospholipase A2

General function:: Involved in metabolic process
Specific function:: Selectively hydrolyzes arachidonyl phospholipids in the sn-2 position releasing arachidonic acid. Together with its lysophospholipid activity, it is implicated in the initiation of the inflammatory response.
Gene Name:: PLA2G4A
Uniprot ID:: P47712
Molecular weight:: 85210.19

Enzyme Details

4. Phospholipase A2

General function:: Involved in phospholipase A2 activity
Specific function:: PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides.
Gene Name:: PLA2G1B
Uniprot ID:: P04054
Molecular weight:: 16359.535

Enzyme Details

5. Group XIIB secretory phospholipase A2-like protein

General function:: Involved in phospholipase A2 activity
Specific function:: Not known; does not seem to have catalytic activity.
Gene Name:: PLA2G12B
Uniprot ID:: Q9BX93
Molecular weight:: Not Available

Enzyme Details

6. Group 10 secretory phospholipase A2

General function:: Involved in phospholipase A2 activity
Specific function:: PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a powerful potency for releasing arachidonic acid from cell membrane phospholipids. Prefers phosphatidylethanolamine and phosphatidylcholine liposomes to those of phosphatidylserine.
Gene Name:: PLA2G10
Uniprot ID:: O15496
Molecular weight:: 18153.04

Enzyme Details

7. Group IIE secretory phospholipase A2

General function:: Involved in phospholipase A2 activity
Specific function:: PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a preference for arachidonic-containing phospholipids.
Gene Name:: PLA2G2E
Uniprot ID:: Q9NZK7
Molecular weight:: 15988.525

Enzyme Details

8. 85/88 kDa calcium-independent phospholipase A2

General function:: Involved in metabolic process
Specific function:: Catalyzes the release of fatty acids from phospholipids. It has been implicated in normal phospholipid remodeling, nitric oxide-induced or vasopressin-induced arachidonic acid release and in leukotriene and prostaglandin production. May participate in fas mediated apoptosis and in regulating transmembrane ion flux in glucose-stimulated B-cells. Has a role in cardiolipin (CL) deacylation. Required for both speed and directionality of monocyte MCP1/CCL2-induced chemotaxis through regulation of F-actin polymerization at the pseudopods. Isoform ankyrin-iPLA2-1 and isoform ankyrin-iPLA2-2, which lack the catalytic domain, are probably involved in the negative regulation of iPLA2 activity.
Gene Name:: PLA2G6
Uniprot ID:: O60733
Molecular weight:: 84092.635

Enzyme Details

9. Group IID secretory phospholipase A2

General function:: Involved in phospholipase A2 activity
Specific function:: PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. L-alpha-1-palmitoyl-2-linoleoyl phosphatidylethanolamine is more efficiently hydrolyzed than the other phospholipids examined.
Gene Name:: PLA2G2D
Uniprot ID:: Q9UNK4
Molecular weight:: 16546.1

Enzyme Details

10. Phospholipase D2

General function:: Involved in protein binding
Specific function:: May have a role in signal-induced cytoskeletal regulation and/or endocytosis (By similarity).
Gene Name:: PLD2
Uniprot ID:: O14939
Molecular weight:: 104656.485

Only showing the first 10 proteins. There are 43 proteins in total.

Show all enzymes and transporters

Showing metabocard for PE(14:1(9Z)/14:1(9Z)) (HMDB0008855)

MOL for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

3D MOL for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

3D SDF for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

3D-SDF for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

PDB for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

3D PDB for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

SMILES for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

INCHI for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

Structure for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

3D Structure for HMDB0008855 (PE(14:1(9Z)/14:1(9Z)))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes