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Record Information

Version

5.0

Status

Predicted

Creation Date

2021-09-12 11:49:26 UTC

Update Date

2022-11-30 19:56:26 UTC

HMDB ID

HMDB0266771

Secondary Accession Numbers

None

Metabolite Identification

Common Name

PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))

Description

PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) is an oxidized phosphatidic acid (PA). Oxidized phosphatidic acids are glycerophospholipids in which a phosphate moiety occupies a glycerol substitution site and at least one of the fatty acyl chains has undergone oxidation. As all oxidized lipids, oxidized phosphatidic acids belong to a group of biomolecules that have a role as signaling molecules. The biosynthesis of oxidized lipids is mediated by several enzymatic families, including cyclooxygenases (COX), lipoxygenases (LOX) and cytochrome P450s (CYP). Non-enzymatically oxidized lipids are produced by uncontrolled oxidation through free radicals and are considered harmful to human health (PMID: 33329396 ). As is the case with diacylglycerols, phosphatidic acids can have many different combinations of fatty acids of varying lengths, saturation and degrees of oxidation attached at the C-1 and C-2 positions. PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)), in particular, consists of one chain of one 1Z-hexadecenyl at the C-1 position and one chain of 14-hydroxy-docosahexaenoyl at the C-2 position. Phospholipids are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling. Similarly to what occurs with phospholipids, the fatty acid distribution at the C-1 and C-2 positions of glycerol within oxidized phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. Oxidized PAs can be synthesized via three different routes. In one route, the oxidized PA is synthetized de novo following the same mechanisms as for PAs but incorporating oxidized acyl chains (PMID: 33329396 ). An alternative is the transacylation of one of the non-oxidized acyl chains with an oxidized acylCoA (PMID: 33329396 ). The third pathway results from the oxidation of the acyl chain while still attached to the PA backbone, mainly through the action of LOX (PMID: 33329396 ).

Structure

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

PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))
  Mrv1652309122113492D          

 51 50  0  0  1  0            999 V2000
   -3.8020    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9591    0.3596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2447    0.7720    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6571    1.4866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1679    0.0575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    1.1846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0969    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    0.3590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6679    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9699   -0.3554    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7950   -0.3554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5121    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2262    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9403    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6544    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3686    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0827    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7968    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5109    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2250    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9391    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6532    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3673    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0815    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7956    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5097    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2239    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.5394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2236   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9377   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6518   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4768   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1910   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9051   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7301   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4442   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1583   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9833   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6974   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4115   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1256   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1256   -1.5394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8397   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5539   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.3789   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.0930   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.8071   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.6321   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.3462   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -19.0603   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 12  1  0  0  0  0
  2  9  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  3  1  0  0  0  0
  7  1  1  0  0  0  0
  8  7  1  0  0  0  0
  8 10  1  1  0  0  0
  8 11  1  0  0  0  0
  9  8  1  0  0  0  0
 11 28  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  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  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 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
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END

HMDB0266771
     RDKit          3D
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))
119118  0  0  0  0  0  0  0  0999 V2000
   15.2428   -3.2542    1.6098 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9515   -1.9482    0.8457 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7379   -2.2634   -0.5745 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6530   -2.0565   -1.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3917   -1.5000   -0.8382 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1114   -1.0914    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8163    0.0917    0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7149    1.2717    0.0784 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2672    1.7807    0.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0834    2.8707   -0.5589 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3922    0.6306   -0.0363 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2326    0.8034   -0.6976 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3713   -0.3107   -0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2408   -0.3087   -1.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5576    0.8015   -2.1759 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1170    2.1121   -2.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6542    3.1552   -1.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881    3.3000   -0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6589    2.1698   -0.4048 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3791    2.0805   -0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5445    3.0795   -1.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3836    3.5118   -0.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3719    2.2544   -0.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7323    1.5650   -1.1796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6161    1.9355    1.1288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3312    0.7080    1.4094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4584    1.0493    2.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3173    0.0466    2.6963 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1148   -0.6588    1.8327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7515   -1.5057    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7835   -2.1693    0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5649   -1.7317   -1.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5278   -2.3437   -2.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9677   -2.0584   -2.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3399   -0.6052   -2.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8011   -0.4072   -1.7936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2541   -0.9183   -0.4586 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7937   -0.6728   -0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2300   -1.1573    1.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6664   -1.1457    1.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4728    0.0795    1.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7093    0.7442    0.0078 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5933    1.9826    0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.8136    2.6134   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2630   -0.1295    2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7215   -1.3529    2.5109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4533   -2.2835    3.2857 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.1816   -2.4954    4.7463 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9902   -1.6015    3.0988 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4736   -3.8072    2.5399 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0237   -3.1099    2.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.5662   -4.0082    0.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3294   -3.5721    2.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.2664   -1.3224    1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.0100   -1.4572    0.8558 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.6273   -2.7358   -1.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.7141   -2.3709   -2.3259 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1300   -0.6382   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5605   -2.2522   -1.1911 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064   -1.8899    1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6220    0.2639    2.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3922    2.0897    0.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8813    1.1417   -0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1681    2.1050    1.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9316    2.7070   -1.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6319   -0.3793    0.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0498    1.8217   -0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7311   -1.3160   -0.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7086   -1.3270   -1.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5689    0.5063   -3.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4407    0.7530   -2.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0423    2.3223   -2.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2475    4.1104   -1.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8547    4.1877   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9073    3.7586    0.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294    1.3242    0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8808    1.1411   -0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0142    3.9596   -1.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596    2.5437   -2.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6915    4.0608    0.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2667    4.1535   -1.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5941    0.2745    0.4382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0089    1.9163    1.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0857    1.5361    3.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -0.4831    1.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7075   -1.7190    0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5770   -3.2636    0.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7705   -1.8989    0.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5455   -1.9788   -1.6611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6498   -0.6195   -1.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3711   -3.4498   -2.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2613   -1.9746   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3208   -2.5175   -1.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5550   -2.5629   -2.8545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1114   -0.1748   -3.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7548   -0.0343   -1.2934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0050    0.6929   -1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3827   -0.8973   -2.6075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7423   -0.3635    0.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1292   -2.0078   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8708    0.4497   -0.4133 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3310   -1.1092   -1.1593 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8114   -2.2251    1.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6812   -0.5913    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7729   -1.5684    2.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2173   -1.9652    0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.4786   -0.1684    1.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0239    0.8424    2.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3832    0.0887   -0.6046 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8539    1.0985   -0.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.5164    1.6202    0.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0407    2.6554    0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.3792    3.5602   -1.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.4573    1.8916   -1.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8772    2.6976   -1.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0436    0.4410    3.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5885   -0.2869    1.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1234   -1.4652    2.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1806   -3.8715    1.8242 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  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 30 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  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 26 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  2  0
 47 49  1  0
 47 50  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  0
  2 55  1  0
  3 56  1  0
  4 57  1  0
  5 58  1  0
  5 59  1  0
  6 60  1  0
  7 61  1  0
  8 62  1  0
  8 63  1  0
  9 64  1  0
 10 65  1  0
 11 66  1  0
 12 67  1  0
 13 68  1  0
 14 69  1  0
 15 70  1  0
 15 71  1  0
 16 72  1  0
 17 73  1  0
 18 74  1  0
 18 75  1  0
 19 76  1  0
 20 77  1  0
 21 78  1  0
 21 79  1  0
 22 80  1  0
 22 81  1  0
 26 82  1  6
 27 83  1  0
 27 84  1  0
 29 85  1  0
 30 86  1  0
 31 87  1  0
 31 88  1  0
 32 89  1  0
 32 90  1  0
 33 91  1  0
 33 92  1  0
 34 93  1  0
 34 94  1  0
 35 95  1  0
 35 96  1  0
 36 97  1  0
 36 98  1  0
 37 99  1  0
 37100  1  0
 38101  1  0
 38102  1  0
 39103  1  0
 39104  1  0
 40105  1  0
 40106  1  0
 41107  1  0
 41108  1  0
 42109  1  0
 42110  1  0
 43111  1  0
 43112  1  0
 44113  1  0
 44114  1  0
 44115  1  0
 45116  1  0
 45117  1  0
 49118  1  0
 50119  1  0
M  END

PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))
  Mrv1652309122113492D          

 51 50  0  0  1  0            999 V2000
   -3.8020    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9591    0.3596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2447    0.7720    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6571    1.4866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1679    0.0575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    1.1846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0969    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    0.3590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6679    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9699   -0.3554    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7950   -0.3554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5121    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2262    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9403    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6544    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3686    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0827    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7968    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5109    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2250    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9391    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6532    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3673    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0815    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7956    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5097    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2239    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.5394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2236   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9377   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6518   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4768   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1910   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9051   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7301   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4442   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1583   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9833   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6974   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4115   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1256   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1256   -1.5394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8397   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5539   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.3789   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.0930   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.8071   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.6321   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.3462   -0.3549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -19.0603   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 12  1  0  0  0  0
  2  9  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  3  1  0  0  0  0
  7  1  1  0  0  0  0
  8  7  1  0  0  0  0
  8 10  1  1  0  0  0
  8 11  1  0  0  0  0
  9  8  1  0  0  0  0
 11 28  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  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  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 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
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0266771

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C41H69O8P/c1-3-5-7-9-11-12-13-14-15-18-21-24-28-32-36-47-37-40(38-48-50(44,45)46)49-41(43)35-31-27-23-20-17-16-19-22-26-30-34-39(42)33-29-25-10-8-6-4-2/h6,8,16-17,22-23,25-27,29-30,32,34,36,39-40,42H,3-5,7,9-15,18-21,24,28,31,33,35,37-38H2,1-2H3,(H2,44,45,46)/b8-6-,17-16-,26-22-,27-23-,29-25-,34-30+,36-32+/t39?,40-/m1/s1

> <INCHI_KEY>
ZOWQHWPWNUYGHV-TZNQBFAOSA-N

> <FORMULA>
C41H69O8P

> <MOLECULAR_WEIGHT>
720.969

> <EXACT_MASS>
720.47300618

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
85.56971979159887

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R)-3-[(1E)-hexadec-1-en-1-yloxy]-2-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxy]phosphonic acid

> <ALOGPS_LOGP>
8.57

> <JCHEM_LOGP>
11.537373374666668

> <ALOGPS_LOGS>
-6.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.343600820101842

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.3182867815193506

> <JCHEM_PKA_STRONGEST_BASIC>
-1.608900435247551

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000002

> <JCHEM_REFRACTIVITY>
214.7314

> <JCHEM_ROTATABLE_BOND_COUNT>
35

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.95e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-3-[(1E)-hexadec-1-en-1-yloxy]-2-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0266771
     RDKit          3D
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))
119118  0  0  0  0  0  0  0  0999 V2000
   15.2428   -3.2542    1.6098 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9515   -1.9482    0.8457 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7379   -2.2634   -0.5745 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6530   -2.0565   -1.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3917   -1.5000   -0.8382 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1114   -1.0914    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8163    0.0917    0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7149    1.2717    0.0784 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2672    1.7807    0.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0834    2.8707   -0.5589 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3922    0.6306   -0.0363 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2326    0.8034   -0.6976 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3713   -0.3107   -0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2408   -0.3087   -1.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5576    0.8015   -2.1759 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1170    2.1121   -2.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6542    3.1552   -1.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881    3.3000   -0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6589    2.1698   -0.4048 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3791    2.0805   -0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5445    3.0795   -1.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3836    3.5118   -0.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3719    2.2544   -0.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7323    1.5650   -1.1796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6161    1.9355    1.1288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3312    0.7080    1.4094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4584    1.0493    2.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3173    0.0466    2.6963 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1148   -0.6588    1.8327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7515   -1.5057    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7835   -2.1693    0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5649   -1.7317   -1.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5278   -2.3437   -2.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9677   -2.0584   -2.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3399   -0.6052   -2.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8011   -0.4072   -1.7936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2541   -0.9183   -0.4586 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7937   -0.6728   -0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2300   -1.1573    1.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6664   -1.1457    1.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4728    0.0795    1.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7093    0.7442    0.0078 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5933    1.9826    0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.8136    2.6134   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2630   -0.1295    2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7215   -1.3529    2.5109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4533   -2.2835    3.2857 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.1816   -2.4954    4.7463 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9902   -1.6015    3.0988 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4736   -3.8072    2.5399 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0237   -3.1099    2.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.5662   -4.0082    0.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3294   -3.5721    2.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.2664   -1.3224    1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.0100   -1.4572    0.8558 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.6273   -2.7358   -1.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.7141   -2.3709   -2.3259 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1300   -0.6382   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5605   -2.2522   -1.1911 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064   -1.8899    1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6220    0.2639    2.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3922    2.0897    0.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8813    1.1417   -0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1681    2.1050    1.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9316    2.7070   -1.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6319   -0.3793    0.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0498    1.8217   -0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7311   -1.3160   -0.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7086   -1.3270   -1.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5689    0.5063   -3.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4407    0.7530   -2.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0423    2.3223   -2.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2475    4.1104   -1.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8547    4.1877   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9073    3.7586    0.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294    1.3242    0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8808    1.1411   -0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0142    3.9596   -1.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596    2.5437   -2.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6915    4.0608    0.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2667    4.1535   -1.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5941    0.2745    0.4382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0089    1.9163    1.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0857    1.5361    3.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -0.4831    1.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7075   -1.7190    0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5770   -3.2636    0.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7705   -1.8989    0.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5455   -1.9788   -1.6611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6498   -0.6195   -1.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3711   -3.4498   -2.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2613   -1.9746   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3208   -2.5175   -1.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5550   -2.5629   -2.8545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1114   -0.1748   -3.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7548   -0.0343   -1.2934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0050    0.6929   -1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3827   -0.8973   -2.6075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7423   -0.3635    0.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1292   -2.0078   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8708    0.4497   -0.4133 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3310   -1.1092   -1.1593 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8114   -2.2251    1.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6812   -0.5913    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7729   -1.5684    2.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2173   -1.9652    0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.4786   -0.1684    1.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0239    0.8424    2.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3832    0.0887   -0.6046 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8539    1.0985   -0.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.5164    1.6202    0.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0407    2.6554    0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.3792    3.5602   -1.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.4573    1.8916   -1.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8772    2.6976   -1.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0436    0.4410    3.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5885   -0.2869    1.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1234   -1.4652    2.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1806   -3.8715    1.8242 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
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M  END

HEADER    PROTEIN                                 12-SEP-21   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))     
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-21         0                                  
HETATM    1  O   UNK     0      -7.097   0.673   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      -1.790   0.671   0.000  0.00  0.00           O+0
HETATM    3  P   UNK     0      -0.457   1.441   0.000  0.00  0.00           P+0
HETATM    4  O   UNK     0      -1.227   2.775   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       0.313   0.107   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       0.877   2.211   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -5.781   1.440   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.447   0.670   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.113   1.440   0.000  0.00  0.00           C+0
HETATM   10  H   UNK     0      -3.677  -0.663   0.000  0.00  0.00           H+0
HETATM   11  O   UNK     0      -5.217  -0.663   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -8.423   1.436   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -9.756   0.665   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -11.089   1.436   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -12.422   0.665   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -13.755   1.436   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -15.088   0.665   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -16.421   1.436   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -17.754   0.665   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -19.087   1.436   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -20.420   0.665   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -21.753   1.436   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -23.086   0.665   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -24.419   1.436   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -25.752   0.665   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -27.085   1.436   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -28.418   0.665   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.551  -1.433   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.551  -2.873   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -7.884  -0.662   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -9.217  -1.433   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -10.550  -0.662   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -12.090  -0.662   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -13.423  -1.433   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -14.756  -0.662   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -16.296  -0.662   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -17.629  -1.433   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -18.962  -0.662   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -20.502  -0.662   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -21.835  -1.433   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -23.168  -0.662   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0     -24.501  -1.433   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0     -24.501  -2.873   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0     -25.834  -0.662   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -27.167  -1.433   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -28.707  -1.433   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -30.040  -0.662   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0     -31.373  -1.433   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0     -32.913  -1.433   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0     -34.246  -0.662   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0     -35.579  -1.433   0.000  0.00  0.00           C+0
CONECT    1   12    7                                                       
CONECT    2    9    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3                                                            
CONECT    7    1    8                                                       
CONECT    8    7   10   11    9                                             
CONECT    9    2    8                                                       
CONECT   10    8                                                            
CONECT   11    8   28                                                       
CONECT   12    1   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   11   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   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   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  100    0
END

COMPND    HMDB0266771
HETATM    1  C1  UNL     1      15.243  -3.254   1.610  1.00  0.00           C  
HETATM    2  C2  UNL     1      14.952  -1.948   0.846  1.00  0.00           C  
HETATM    3  C3  UNL     1      14.738  -2.263  -0.574  1.00  0.00           C  
HETATM    4  C4  UNL     1      13.653  -2.056  -1.237  1.00  0.00           C  
HETATM    5  C5  UNL     1      12.392  -1.500  -0.838  1.00  0.00           C  
HETATM    6  C6  UNL     1      12.111  -1.091   0.515  1.00  0.00           C  
HETATM    7  C7  UNL     1      11.816   0.092   0.947  1.00  0.00           C  
HETATM    8  C8  UNL     1      11.715   1.272   0.078  1.00  0.00           C  
HETATM    9  C9  UNL     1      10.267   1.781   0.240  1.00  0.00           C  
HETATM   10  O1  UNL     1      10.083   2.871  -0.559  1.00  0.00           O  
HETATM   11  C10 UNL     1       9.392   0.631  -0.036  1.00  0.00           C  
HETATM   12  C11 UNL     1       8.233   0.803  -0.698  1.00  0.00           C  
HETATM   13  C12 UNL     1       7.371  -0.311  -0.972  1.00  0.00           C  
HETATM   14  C13 UNL     1       6.241  -0.309  -1.594  1.00  0.00           C  
HETATM   15  C14 UNL     1       5.558   0.801  -2.176  1.00  0.00           C  
HETATM   16  C15 UNL     1       6.117   2.112  -2.195  1.00  0.00           C  
HETATM   17  C16 UNL     1       5.654   3.155  -1.584  1.00  0.00           C  
HETATM   18  C17 UNL     1       4.488   3.300  -0.730  1.00  0.00           C  
HETATM   19  C18 UNL     1       3.659   2.170  -0.405  1.00  0.00           C  
HETATM   20  C19 UNL     1       2.379   2.080  -0.689  1.00  0.00           C  
HETATM   21  C20 UNL     1       1.544   3.079  -1.374  1.00  0.00           C  
HETATM   22  C21 UNL     1       0.384   3.512  -0.469  1.00  0.00           C  
HETATM   23  C22 UNL     1      -0.372   2.254  -0.198  1.00  0.00           C  
HETATM   24  O2  UNL     1      -0.732   1.565  -1.180  1.00  0.00           O  
HETATM   25  O3  UNL     1      -0.616   1.935   1.129  1.00  0.00           O  
HETATM   26  C23 UNL     1      -1.331   0.708   1.409  1.00  0.00           C  
HETATM   27  C24 UNL     1      -2.458   1.049   2.313  1.00  0.00           C  
HETATM   28  O4  UNL     1      -3.317   0.047   2.696  1.00  0.00           O  
HETATM   29  C25 UNL     1      -4.115  -0.659   1.833  1.00  0.00           C  
HETATM   30  C26 UNL     1      -3.751  -1.506   0.905  1.00  0.00           C  
HETATM   31  C27 UNL     1      -4.784  -2.169   0.071  1.00  0.00           C  
HETATM   32  C28 UNL     1      -4.565  -1.732  -1.353  1.00  0.00           C  
HETATM   33  C29 UNL     1      -5.528  -2.344  -2.311  1.00  0.00           C  
HETATM   34  C30 UNL     1      -6.968  -2.058  -2.042  1.00  0.00           C  
HETATM   35  C31 UNL     1      -7.340  -0.605  -2.061  1.00  0.00           C  
HETATM   36  C32 UNL     1      -8.801  -0.407  -1.794  1.00  0.00           C  
HETATM   37  C33 UNL     1      -9.254  -0.918  -0.459  1.00  0.00           C  
HETATM   38  C34 UNL     1     -10.794  -0.673  -0.319  1.00  0.00           C  
HETATM   39  C35 UNL     1     -11.230  -1.157   1.011  1.00  0.00           C  
HETATM   40  C36 UNL     1     -12.666  -1.146   1.330  1.00  0.00           C  
HETATM   41  C37 UNL     1     -13.473   0.080   1.302  1.00  0.00           C  
HETATM   42  C38 UNL     1     -13.709   0.744   0.008  1.00  0.00           C  
HETATM   43  C39 UNL     1     -14.593   1.983   0.288  1.00  0.00           C  
HETATM   44  C40 UNL     1     -14.814   2.613  -1.073  1.00  0.00           C  
HETATM   45  C41 UNL     1      -0.263  -0.129   2.124  1.00  0.00           C  
HETATM   46  O5  UNL     1      -0.721  -1.353   2.511  1.00  0.00           O  
HETATM   47  P1  UNL     1       0.453  -2.284   3.286  1.00  0.00           P  
HETATM   48  O6  UNL     1       0.182  -2.495   4.746  1.00  0.00           O  
HETATM   49  O7  UNL     1       1.990  -1.602   3.099  1.00  0.00           O  
HETATM   50  O8  UNL     1       0.474  -3.807   2.540  1.00  0.00           O  
HETATM   51  H1  UNL     1      16.024  -3.110   2.370  1.00  0.00           H  
HETATM   52  H2  UNL     1      15.566  -4.008   0.896  1.00  0.00           H  
HETATM   53  H3  UNL     1      14.329  -3.572   2.147  1.00  0.00           H  
HETATM   54  H4  UNL     1      14.266  -1.322   1.358  1.00  0.00           H  
HETATM   55  H5  UNL     1      16.010  -1.457   0.856  1.00  0.00           H  
HETATM   56  H6  UNL     1      15.627  -2.736  -1.120  1.00  0.00           H  
HETATM   57  H7  UNL     1      13.714  -2.371  -2.326  1.00  0.00           H  
HETATM   58  H8  UNL     1      12.130  -0.638  -1.543  1.00  0.00           H  
HETATM   59  H9  UNL     1      11.560  -2.252  -1.191  1.00  0.00           H  
HETATM   60  H10 UNL     1      12.106  -1.890   1.312  1.00  0.00           H  
HETATM   61  H11 UNL     1      11.622   0.264   2.018  1.00  0.00           H  
HETATM   62  H12 UNL     1      12.392   2.090   0.458  1.00  0.00           H  
HETATM   63  H13 UNL     1      11.881   1.142  -0.984  1.00  0.00           H  
HETATM   64  H14 UNL     1      10.168   2.105   1.306  1.00  0.00           H  
HETATM   65  H15 UNL     1       9.932   2.707  -1.501  1.00  0.00           H  
HETATM   66  H16 UNL     1       9.632  -0.379   0.271  1.00  0.00           H  
HETATM   67  H17 UNL     1       8.050   1.822  -0.953  1.00  0.00           H  
HETATM   68  H18 UNL     1       7.731  -1.316  -0.591  1.00  0.00           H  
HETATM   69  H19 UNL     1       5.709  -1.327  -1.695  1.00  0.00           H  
HETATM   70  H20 UNL     1       5.569   0.506  -3.350  1.00  0.00           H  
HETATM   71  H21 UNL     1       4.441   0.753  -2.063  1.00  0.00           H  
HETATM   72  H22 UNL     1       7.042   2.322  -2.837  1.00  0.00           H  
HETATM   73  H23 UNL     1       6.247   4.110  -1.734  1.00  0.00           H  
HETATM   74  H24 UNL     1       3.855   4.188  -1.083  1.00  0.00           H  
HETATM   75  H25 UNL     1       4.907   3.759   0.247  1.00  0.00           H  
HETATM   76  H26 UNL     1       4.129   1.324   0.143  1.00  0.00           H  
HETATM   77  H27 UNL     1       1.881   1.141  -0.373  1.00  0.00           H  
HETATM   78  H28 UNL     1       2.014   3.960  -1.763  1.00  0.00           H  
HETATM   79  H29 UNL     1       1.060   2.544  -2.232  1.00  0.00           H  
HETATM   80  H30 UNL     1       0.691   4.061   0.410  1.00  0.00           H  
HETATM   81  H31 UNL     1      -0.267   4.153  -1.092  1.00  0.00           H  
HETATM   82  H32 UNL     1      -1.594   0.274   0.438  1.00  0.00           H  
HETATM   83  H33 UNL     1      -3.009   1.916   1.818  1.00  0.00           H  
HETATM   84  H34 UNL     1      -2.086   1.536   3.268  1.00  0.00           H  
HETATM   85  H35 UNL     1      -5.221  -0.483   1.941  1.00  0.00           H  
HETATM   86  H36 UNL     1      -2.707  -1.719   0.765  1.00  0.00           H  
HETATM   87  H37 UNL     1      -4.577  -3.264   0.144  1.00  0.00           H  
HETATM   88  H38 UNL     1      -5.770  -1.899   0.441  1.00  0.00           H  
HETATM   89  H39 UNL     1      -3.545  -1.979  -1.661  1.00  0.00           H  
HETATM   90  H40 UNL     1      -4.650  -0.620  -1.377  1.00  0.00           H  
HETATM   91  H41 UNL     1      -5.371  -3.450  -2.359  1.00  0.00           H  
HETATM   92  H42 UNL     1      -5.261  -1.975  -3.339  1.00  0.00           H  
HETATM   93  H43 UNL     1      -7.321  -2.517  -1.094  1.00  0.00           H  
HETATM   94  H44 UNL     1      -7.555  -2.563  -2.855  1.00  0.00           H  
HETATM   95  H45 UNL     1      -7.111  -0.175  -3.041  1.00  0.00           H  
HETATM   96  H46 UNL     1      -6.755  -0.034  -1.293  1.00  0.00           H  
HETATM   97  H47 UNL     1      -9.005   0.693  -1.901  1.00  0.00           H  
HETATM   98  H48 UNL     1      -9.383  -0.897  -2.608  1.00  0.00           H  
HETATM   99  H49 UNL     1      -8.742  -0.363   0.339  1.00  0.00           H  
HETATM  100  H50 UNL     1      -9.129  -2.008  -0.382  1.00  0.00           H  
HETATM  101  H51 UNL     1     -10.871   0.450  -0.413  1.00  0.00           H  
HETATM  102  H52 UNL     1     -11.331  -1.109  -1.159  1.00  0.00           H  
HETATM  103  H53 UNL     1     -10.811  -2.225   1.089  1.00  0.00           H  
HETATM  104  H54 UNL     1     -10.681  -0.591   1.836  1.00  0.00           H  
HETATM  105  H55 UNL     1     -12.773  -1.568   2.400  1.00  0.00           H  
HETATM  106  H56 UNL     1     -13.217  -1.965   0.739  1.00  0.00           H  
HETATM  107  H57 UNL     1     -14.479  -0.168   1.749  1.00  0.00           H  
HETATM  108  H58 UNL     1     -13.024   0.842   2.010  1.00  0.00           H  
HETATM  109  H59 UNL     1     -14.383   0.089  -0.605  1.00  0.00           H  
HETATM  110  H60 UNL     1     -12.854   1.098  -0.548  1.00  0.00           H  
HETATM  111  H61 UNL     1     -15.516   1.620   0.757  1.00  0.00           H  
HETATM  112  H62 UNL     1     -14.041   2.655   0.944  1.00  0.00           H  
HETATM  113  H63 UNL     1     -15.379   3.560  -1.036  1.00  0.00           H  
HETATM  114  H64 UNL     1     -15.457   1.892  -1.653  1.00  0.00           H  
HETATM  115  H65 UNL     1     -13.877   2.698  -1.639  1.00  0.00           H  
HETATM  116  H66 UNL     1       0.044   0.441   3.026  1.00  0.00           H  
HETATM  117  H67 UNL     1       0.589  -0.287   1.416  1.00  0.00           H  
HETATM  118  H68 UNL     1       2.123  -1.465   2.107  1.00  0.00           H  
HETATM  119  H69 UNL     1      -0.181  -3.872   1.824  1.00  0.00           H  
CONECT    1    2   51   52   53
CONECT    2    3   54   55
CONECT    3    4    4   56
CONECT    4    5   57
CONECT    5    6   58   59
CONECT    6    7    7   60
CONECT    7    8   61
CONECT    8    9   62   63
CONECT    9   10   11   64
CONECT   10   65
CONECT   11   12   12   66
CONECT   12   13   67
CONECT   13   14   14   68
CONECT   14   15   69
CONECT   15   16   70   71
CONECT   16   17   17   72
CONECT   17   18   73
CONECT   18   19   74   75
CONECT   19   20   20   76
CONECT   20   21   77
CONECT   21   22   78   79
CONECT   22   23   80   81
CONECT   23   24   24   25
CONECT   25   26
CONECT   26   27   45   82
CONECT   27   28   83   84
CONECT   28   29
CONECT   29   30   30   85
CONECT   30   31   86
CONECT   31   32   87   88
CONECT   32   33   89   90
CONECT   33   34   91   92
CONECT   34   35   93   94
CONECT   35   36   95   96
CONECT   36   37   97   98
CONECT   37   38   99  100
CONECT   38   39  101  102
CONECT   39   40  103  104
CONECT   40   41  105  106
CONECT   41   42  107  108
CONECT   42   43  109  110
CONECT   43   44  111  112
CONECT   44  113  114  115
CONECT   45   46  116  117
CONECT   46   47
CONECT   47   48   48   49   50
CONECT   49  118
CONECT   50  119
END

HMDB0266771
     RDKit          3D
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))
119118  0  0  0  0  0  0  0  0999 V2000
   15.2428   -3.2542    1.6098 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9515   -1.9482    0.8457 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7379   -2.2634   -0.5745 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6530   -2.0565   -1.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3917   -1.5000   -0.8382 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1114   -1.0914    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8163    0.0917    0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7149    1.2717    0.0784 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2672    1.7807    0.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0834    2.8707   -0.5589 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3922    0.6306   -0.0363 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2326    0.8034   -0.6976 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3713   -0.3107   -0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2408   -0.3087   -1.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5576    0.8015   -2.1759 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1170    2.1121   -2.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6542    3.1552   -1.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881    3.3000   -0.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6589    2.1698   -0.4048 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3791    2.0805   -0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5445    3.0795   -1.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3836    3.5118   -0.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3719    2.2544   -0.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7323    1.5650   -1.1796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6161    1.9355    1.1288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3312    0.7080    1.4094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4584    1.0493    2.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3173    0.0466    2.6963 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1148   -0.6588    1.8327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7515   -1.5057    0.9053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7835   -2.1693    0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5649   -1.7317   -1.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5278   -2.3437   -2.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9677   -2.0584   -2.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3399   -0.6052   -2.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8011   -0.4072   -1.7936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2541   -0.9183   -0.4586 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7937   -0.6728   -0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2300   -1.1573    1.0113 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6664   -1.1457    1.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4728    0.0795    1.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7093    0.7442    0.0078 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5933    1.9826    0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.8136    2.6134   -1.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2630   -0.1295    2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7215   -1.3529    2.5109 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4533   -2.2835    3.2857 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.1816   -2.4954    4.7463 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9902   -1.6015    3.0988 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4736   -3.8072    2.5399 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0237   -3.1099    2.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.5662   -4.0082    0.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3294   -3.5721    2.1466 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.2664   -1.3224    1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.0100   -1.4572    0.8558 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.6273   -2.7358   -1.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.7141   -2.3709   -2.3259 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1300   -0.6382   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5605   -2.2522   -1.1911 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1064   -1.8899    1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6220    0.2639    2.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3922    2.0897    0.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8813    1.1417   -0.9839 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1681    2.1050    1.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9316    2.7070   -1.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6319   -0.3793    0.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0498    1.8217   -0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7311   -1.3160   -0.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7086   -1.3270   -1.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5689    0.5063   -3.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4407    0.7530   -2.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0423    2.3223   -2.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2475    4.1104   -1.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8547    4.1877   -1.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9073    3.7586    0.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294    1.3242    0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8808    1.1411   -0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0142    3.9596   -1.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596    2.5437   -2.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6915    4.0608    0.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2667    4.1535   -1.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5941    0.2745    0.4382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0089    1.9163    1.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0857    1.5361    3.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2206   -0.4831    1.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7075   -1.7190    0.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5770   -3.2636    0.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7705   -1.8989    0.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5455   -1.9788   -1.6611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6498   -0.6195   -1.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3711   -3.4498   -2.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2613   -1.9746   -3.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3208   -2.5175   -1.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5550   -2.5629   -2.8545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1114   -0.1748   -3.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7548   -0.0343   -1.2934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0050    0.6929   -1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3827   -0.8973   -2.6075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7423   -0.3635    0.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1292   -2.0078   -0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8708    0.4497   -0.4133 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3310   -1.1092   -1.1593 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8114   -2.2251    1.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6812   -0.5913    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7729   -1.5684    2.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2173   -1.9652    0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.4786   -0.1684    1.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0239    0.8424    2.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3832    0.0887   -0.6046 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8539    1.0985   -0.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.5164    1.6202    0.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0407    2.6554    0.9440 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.3792    3.5602   -1.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.4573    1.8916   -1.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8772    2.6976   -1.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0436    0.4410    3.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5885   -0.2869    1.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1234   -1.4652    2.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1806   -3.8715    1.8242 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
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 50119  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
[(2R)-3-[(1E)-Hexadec-1-en-1-yloxy]-2-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxy]phosphonate	Generator

Chemical Formula

C₄₁H₆₉O₈P

Average Molecular Weight

720.969

Monoisotopic Molecular Weight

720.47300618

IUPAC Name

[(2R)-3-[(1E)-hexadec-1-en-1-yloxy]-2-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxy]phosphonic acid

Traditional Name

(2R)-3-[(1E)-hexadec-1-en-1-yloxy]-2-{[(4Z,7Z,10Z,12E,16Z,19Z)-14-hydroxydocosa-4,7,10,12,16,19-hexaenoyl]oxy}propoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C41H69O8P/c1-3-5-7-9-11-12-13-14-15-18-21-24-28-32-36-47-37-40(38-48-50(44,45)46)49-41(43)35-31-27-23-20-17-16-19-22-26-30-34-39(42)33-29-25-10-8-6-4-2/h6,8,16-17,22-23,25-27,29-30,32,34,36,39-40,42H,3-5,7,9-15,18-21,24,28,31,33,35,37-38H2,1-2H3,(H2,44,45,46)/b8-6-,17-16-,26-22-,27-23-,29-25-,34-30+,36-32+/t39?,40-/m1/s1

InChI Key

ZOWQHWPWNUYGHV-TZNQBFAOSA-N

Chemical Taxonomy

Classification

Not classified

Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	8.57	ALOGPS
logP	11.54	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Acidic)	1.32	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	122.52 Å²	ChemAxon
Rotatable Bond Count	35	ChemAxon
Refractivity	214.73 m³·mol⁻¹	ChemAxon
Polarizability	85.57 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
AllCCS	[M+H]+	273.321	32859911
AllCCS	[M+H-H2O]+	272.925	32859911
AllCCS	[M+Na]+	273.748	32859911
AllCCS	[M+NH4]+	273.657	32859911
AllCCS	[M-H]-	271.971	32859911
AllCCS	[M+Na-2H]-	278.909	32859911
AllCCS	[M+HCOO]-	286.565	32859911
DeepCCS	[M+H]+	264.428	30932474
DeepCCS	[M-H]-	262.033	30932474
DeepCCS	[M-2H]-	294.917	30932474
DeepCCS	[M+Na]+	270.324	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))	[H][C@@](CO\C=C\CCCCCCCCCCCCCC)(COP(O)(O)=O)OC(=O)CC\C=C/C\C=C/C\C=C/C=C/C(O)C\C=C/C\C=C/CC	5794.3	Standard polar	33892256
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))	[H][C@@](CO\C=C\CCCCCCCCCCCCCC)(COP(O)(O)=O)OC(=O)CC\C=C/C\C=C/C\C=C/C=C/C(O)C\C=C/C\C=C/CC	4362.5	Standard non polar	33892256
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))	[H][C@@](CO\C=C\CCCCCCCCCCCCCC)(COP(O)(O)=O)OC(=O)CC\C=C/C\C=C/C\C=C/C=C/C(O)C\C=C/C\C=C/CC	5320.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)),2TMS,isomer #1	CC/C=C\C/C=C\CC(/C=C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](CO/C=C/CCCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	5295.2	Semi standard non polar	33892256
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)),2TMS,isomer #1	CC/C=C\C/C=C\CC(/C=C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](CO/C=C/CCCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	4637.7	Standard non polar	33892256
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)),2TMS,isomer #1	CC/C=C\C/C=C\CC(/C=C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](CO/C=C/CCCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	5292.0	Standard polar	33892256
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)),2TMS,isomer #2	CC/C=C\C/C=C\CC(O)/C=C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](CO/C=C/CCCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	5266.8	Semi standard non polar	33892256
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)),2TMS,isomer #2	CC/C=C\C/C=C\CC(O)/C=C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](CO/C=C/CCCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4683.5	Standard non polar	33892256
PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)),2TMS,isomer #2	CC/C=C\C/C=C\CC(O)/C=C/C=C\C/C=C\C/C=C\CCC(=O)O[C@H](CO/C=C/CCCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	5246.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	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 - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) 10V, Positive-QTOF	splash10-0kmi-1002019400-297e3437fde7c2e35747	2021-10-18	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) 20V, Positive-QTOF	splash10-0lz9-3000029100-aaffd511e4c768e92503	2021-10-18	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) 40V, Positive-QTOF	splash10-056r-0479100000-81e247905d5d25feda61	2021-10-18	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) 10V, Negative-QTOF	splash10-014i-2001000900-5f6f116ad20b3ffc5501	2021-10-18	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) 20V, Negative-QTOF	splash10-004j-9001000100-35d54a014e598a1e30a4	2021-10-18	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) 40V, Negative-QTOF	splash10-004j-9113000000-866815c2ea08bf7d9fb5	2021-10-18	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

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

Hajeyah AA, Griffiths WJ, Wang Y, Finch AJ, O'Donnell VB: The Biosynthesis of Enzymatically Oxidized Lipids. Front Endocrinol (Lausanne). 2020 Nov 19;11:591819. doi: 10.3389/fendo.2020.591819. eCollection 2020. [PubMed:33329396 ]

Only showing the first 10 proteins. There are 50 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details

1. 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

Enzyme Details

2. Diacylglycerol kinase gamma

General function:: Involved in diacylglycerol kinase activity
Specific function:: Reverses the normal flow of glycerolipid biosynthesis by phosphorylating diacylglycerol back to phosphatidic acid
Gene Name:: DGKG
Uniprot ID:: P49619
Molecular weight:: 89095.3

Enzyme Details

3. Lipid phosphate phosphohydrolase 2

General function:: Involved in catalytic activity
Specific function:: Catalyzes the conversion of phosphatidic acid (PA) to diacylglycerol (DG). In addition it hydrolyzes lysophosphatidic acid (LPA), ceramide-1-phosphate (C-1-P) and sphingosine-1-phosphate (S-1-P). The relative catalytic efficiency is PA > C-1-P > LPA > S-1-P.
Gene Name:: PPAP2C
Uniprot ID:: O43688
Molecular weight:: 32573.435

Enzyme Details

4. Lipid phosphate phosphohydrolase 1

General function:: Involved in catalytic activity
Specific function:: Broad-specificity phosphohydrolase that dephosphorylates exogenous bioactive glycerolipids and sphingolipids. Catalyzes the conversion of phosphatidic acid (PA) to diacylglycerol (DG). Pivotal regulator of lysophosphatidic acid (LPA) signaling in the cardiovascular system. Major enzyme responsible of dephosphorylating LPA in platelets, which terminates signaling actions of LPA. May control circulating, and possibly also regulate localized, LPA levels resulting from platelet activation. It has little activity towards ceramide-1-phosphate (C-1-P) and sphingosine-1-phosphate (S-1-P). The relative catalytic efficiency is LPA > PA > S-1-P > C-1-P. It's down-regulation may contribute to the development of colon adenocarcinoma.
Gene Name:: PPAP2A
Uniprot ID:: O14494
Molecular weight:: 32155.715

Enzyme Details

5. Lipid phosphate phosphohydrolase 3

General function:: Involved in catalytic activity
Specific function:: Catalyzes the conversion of phosphatidic acid (PA) to diacylglycerol (DG). In addition it hydrolyzes lysophosphatidic acid (LPA), ceramide-1-phosphate (C-1-P) and sphingosine-1-phosphate (S-1-P). The relative catalytic efficiency is LPA = PA > C-1-P > S-1-P. May be involved in cell adhesion and in cell-cell interactions.
Gene Name:: PPAP2B
Uniprot ID:: O14495
Molecular weight:: 35115.61

Enzyme Details

6. Phospholipase DDHD1

General function:: Involved in metal ion binding
Specific function:: Probable phospholipase that hydrolyzes phosphatidic acid. The different isoforms may change the substrate specificity
Gene Name:: DDHD1
Uniprot ID:: Q8NEL9
Molecular weight:: 100434.4

Enzyme Details

7. cAMP-specific 3',5'-cyclic phosphodiesterase 4D

General function:: Involved in catalytic activity
Specific function:: Hydrolyzes the second messenger cAMP, which is a key regulator of many important physiological processes.
Gene Name:: PDE4D
Uniprot ID:: Q08499
Molecular weight:: 91114.1

Enzyme Details

8. Probable phospholipid-transporting ATPase IG

General function:: Involved in ATP binding
Specific function:: ATP + H(2)O + phospholipid(In) = ADP + phosphate + phospholipid(Out)
Gene Name:: ATP11C
Uniprot ID:: Q8NB49
Molecular weight:: 129476.0

Enzyme Details

9. Probable phospholipid-transporting ATPase IH

General function:: Involved in ATP binding
Specific function:: ATP + H(2)O + phospholipid(In) = ADP + phosphate + phospholipid(Out)
Gene Name:: ATP11A
Uniprot ID:: P98196
Molecular weight:: 129754.6

Enzyme Details

10. Probable phospholipid-transporting ATPase VA

General function:: Involved in ATP binding
Specific function:: ATP + H(2)O + phospholipid(In) = ADP + phosphate + phospholipid(Out)
Gene Name:: ATP10A
Uniprot ID:: O60312
Molecular weight:: 167686.6

Only showing the first 10 proteins. There are 50 proteins in total.

Show all enzymes and transporters

Showing metabocard for PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) (HMDB0266771)

MOL for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

3D MOL for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

3D SDF for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

3D-SDF for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

PDB for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

3D PDB for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

SMILES for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

INCHI for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

Structure for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

3D Structure for HMDB0266771 (PA(P-16:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes