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Record Information

Version

5.0

Status

Predicted

Creation Date

2021-09-12 01:52:41 UTC

Update Date

2022-11-30 19:53:45 UTC

HMDB ID

HMDB0260497

Secondary Accession Numbers

None

Metabolite Identification

Common Name

MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)

Description

MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) is an oxidized monoacyglycerol (MG). Oxidized monoacyglycerols are glycerolipids in which the fatty acyl chain has undergone oxidation. As all oxidized lipids, oxidized monoacyglycerols 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 other lipids, monoacyglycerols can be substituted by different fatty acids, with varying lengths, saturation and degrees of oxidation attached at the C-1, C-2 and C-3 positions. Lipids 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 lipids, the fatty acid distribution at the C-1 and C-2 positions of glycerol within oxidized lipids is continually in flux, owing to lipid degradation and the continuous lipid remodeling that occurs while these molecules are in membranes. Oxidized MGs can be synthesized via three different routes. In one route, the oxidized MG is synthetized de novo following the same mechanisms as for MGs but incorporating an oxidized acyl chain (PMID: 33329396 ). An alternative is the transacylation 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 MG backbone, mainly through the action of LOX (PMID: 33329396 ).

Structure

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

MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)
  Mrv1652309122103532D          

 31 30  0  0  1  0            999 V2000
   24.1444   -6.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1832   -7.0352    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.2217   -6.4803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1443   -5.3701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.2603   -7.0352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.1828   -8.1454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.5458   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5458   -5.8512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.8317   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1176   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4035   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6894   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8644   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1503   -7.0357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.1503   -7.8072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4362   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7221   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0079   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1829   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4688   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7547   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9297   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2156   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5015   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7874   -7.0357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.7874   -7.8072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0733   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3592   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5342   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8200   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1059   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  2  6  1  6  0  0  0
  3  2  1  0  0  0  0
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  7  5  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

HMDB0260497
     RDKit          3D
MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)
 69 68  0  0  0  0  0  0  0  0999 V2000
  -10.6460   -1.6659    1.5225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9934   -1.2532    0.2139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8854   -2.1318   -0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6626   -1.6162   -0.3384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3261   -0.2139   -0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7611    0.4245   -1.3976 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5249    1.7881   -0.9979 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6602   -0.2333   -1.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6483   -0.8171   -2.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5204   -1.4678   -2.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2853   -1.2547   -2.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2357   -0.2699   -1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7623   -0.8878    0.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -0.4044    0.9067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0783    0.8086    0.5154 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9109    1.2762    1.2363 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7009    2.4995    0.9481 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5215    2.8903    1.9336 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1667    2.4725   -0.4379 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3650    2.6655   -0.8512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5281    2.9498   -0.0339 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5656    1.8659   -0.3448 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9195    0.5302    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9647   -0.4798   -0.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7114   -1.4542   -0.9730 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2107   -0.2730    0.2679 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2609   -1.1590    0.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4659   -0.5639    0.7907 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1511   -0.5041    2.1513 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6106   -1.4985    0.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8313   -1.4444   -0.8788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9748   -2.2527    2.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5659   -2.2793    1.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9977   -0.7064    1.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8162   -1.4439   -0.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8105   -0.1832    0.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0526   -3.2048   -0.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9037   -2.3221   -0.6489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4046   -0.2340    0.5652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0181    0.4254    0.3974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6073    0.5739   -2.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2689    2.0662   -0.4181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8838    0.0951   -0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4403   -1.3700   -3.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4635   -2.2287   -3.5318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4148   -1.7833   -2.5355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9748    0.4805   -1.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3055    0.3789   -1.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2566   -1.8035    0.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5176   -0.9526    1.8302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3397    1.3503   -0.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1744    0.7207    2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8786    3.3375    0.9236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194    3.3680    2.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3691    2.2617   -1.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5679    2.6111   -1.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4232    2.8994    1.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0025    3.9252   -0.3534 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4413    2.0490    0.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8014    1.8739   -1.4246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9717    0.3546   -0.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972    0.5110    1.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4573   -1.2307   -1.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0522   -2.1868    0.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6467    0.4482    0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2728   -0.0913    2.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2764   -2.5436    0.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4890   -1.1835    1.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1640   -2.3089   -1.1475 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  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  6
  7 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 14 50  1  0
 15 51  1  0
 16 52  1  0
 17 53  1  6
 18 54  1  0
 19 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 27 63  1  0
 27 64  1  0
 28 65  1  6
 29 66  1  0
 30 67  1  0
 30 68  1  0
 31 69  1  0
M  END

MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)
  Mrv1652309122103532D          

 31 30  0  0  1  0            999 V2000
   24.1444   -6.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1832   -7.0352    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   22.2217   -6.4803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1443   -5.3701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.2603   -7.0352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.1828   -8.1454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.5458   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5458   -5.8512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.8317   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1176   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4035   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6894   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8644   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1503   -7.0357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.1503   -7.8072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4362   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7221   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0079   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1829   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4688   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7547   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9297   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2156   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5015   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7874   -7.0357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.7874   -7.8072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0733   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3592   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5342   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8200   -6.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1059   -7.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  2  6  1  6  0  0  0
  3  2  1  0  0  0  0
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  7  5  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0260497

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O6/c1-2-3-10-15-22(27)16-11-7-5-4-6-8-12-17-23(28)18-13-9-14-19-25(30)31-21-24(29)20-26/h3,5-8,10-13,16-18,22-24,26-29H,2,4,9,14-15,19-21H2,1H3/b7-5-,8-6-,10-3-,16-11+,17-12+,18-13-/t22-,23-,24+/m1/s1

> <INCHI_KEY>
LDHJHOGZZQKNEN-DHRKEDOKSA-N

> <FORMULA>
C25H38O6

> <MOLECULAR_WEIGHT>
434.573

> <EXACT_MASS>
434.266838944

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
49.79036889923938

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2,3-dihydroxypropyl (5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoate

> <ALOGPS_LOGP>
3.94

> <JCHEM_LOGP>
3.272207255666666

> <ALOGPS_LOGS>
-4.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.561713304155653

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.619245763933279

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4355784898997905

> <JCHEM_POLAR_SURFACE_AREA>
107.22

> <JCHEM_REFRACTIVITY>
131.2901

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.39e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,3-dihydroxypropyl (5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0260497
     RDKit          3D
MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)
 69 68  0  0  0  0  0  0  0  0999 V2000
  -10.6460   -1.6659    1.5225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9934   -1.2532    0.2139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8854   -2.1318   -0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6626   -1.6162   -0.3384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3261   -0.2139   -0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7611    0.4245   -1.3976 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5249    1.7881   -0.9979 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6602   -0.2333   -1.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6483   -0.8171   -2.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5204   -1.4678   -2.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2853   -1.2547   -2.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2357   -0.2699   -1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7623   -0.8878    0.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -0.4044    0.9067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0783    0.8086    0.5154 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9109    1.2762    1.2363 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7009    2.4995    0.9481 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5215    2.8903    1.9336 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1667    2.4725   -0.4379 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3650    2.6655   -0.8512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5281    2.9498   -0.0339 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5656    1.8659   -0.3448 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9195    0.5302    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9647   -0.4798   -0.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7114   -1.4542   -0.9730 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2107   -0.2730    0.2679 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2609   -1.1590    0.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4659   -0.5639    0.7907 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1511   -0.5041    2.1513 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6106   -1.4985    0.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8313   -1.4444   -0.8788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9748   -2.2527    2.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5659   -2.2793    1.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9977   -0.7064    1.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8162   -1.4439   -0.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8105   -0.1832    0.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0526   -3.2048   -0.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9037   -2.3221   -0.6489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4046   -0.2340    0.5652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0181    0.4254    0.3974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6073    0.5739   -2.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2689    2.0662   -0.4181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8838    0.0951   -0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4403   -1.3700   -3.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4635   -2.2287   -3.5318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4148   -1.7833   -2.5355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9748    0.4805   -1.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3055    0.3789   -1.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2566   -1.8035    0.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5176   -0.9526    1.8302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3397    1.3503   -0.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1744    0.7207    2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8786    3.3375    0.9236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194    3.3680    2.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3691    2.2617   -1.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5679    2.6111   -1.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4232    2.8994    1.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0025    3.9252   -0.3534 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4413    2.0490    0.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8014    1.8739   -1.4246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9717    0.3546   -0.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972    0.5110    1.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4573   -1.2307   -1.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0522   -2.1868    0.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6467    0.4482    0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2728   -0.0913    2.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2764   -2.5436    0.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4890   -1.1835    1.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1640   -2.3089   -1.1475 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  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  6
  7 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 14 50  1  0
 15 51  1  0
 16 52  1  0
 17 53  1  6
 18 54  1  0
 19 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 27 63  1  0
 27 64  1  0
 28 65  1  6
 29 66  1  0
 30 67  1  0
 30 68  1  0
 31 69  1  0
M  END

HEADER    PROTEIN                                 12-SEP-21   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-21         0                                  
HETATM    1  C   UNK     0      45.070 -12.096   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      43.275 -13.132   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      41.481 -12.097   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      45.069 -10.024   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      39.686 -13.132   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      43.275 -15.205   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      38.352 -12.362   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      38.352 -10.922   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      37.019 -13.133   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      35.686 -12.362   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      34.353 -13.133   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      33.020 -12.362   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      31.480 -12.362   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      30.147 -13.133   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      30.147 -14.573   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      28.814 -12.362   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      27.481 -13.133   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      26.148 -12.362   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.608 -12.362   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      23.275 -13.133   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.942 -12.362   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      20.402 -12.362   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.069 -13.133   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.736 -12.362   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      16.403 -13.133   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      16.403 -14.573   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      15.070 -12.362   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.737 -13.133   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.197 -13.133   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.864 -12.362   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.531 -13.133   0.000  0.00  0.00           C+0
CONECT    1    2    4                                                       
CONECT    2    1    6    3                                                  
CONECT    3    2    5                                                       
CONECT    4    1                                                            
CONECT    5    3    7                                                       
CONECT    6    2                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   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   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   60    0
END

COMPND    HMDB0260497
HETATM    1  C1  UNL     1     -10.646  -1.666   1.522  1.00  0.00           C  
HETATM    2  C2  UNL     1      -9.993  -1.253   0.214  1.00  0.00           C  
HETATM    3  C3  UNL     1      -8.885  -2.132  -0.198  1.00  0.00           C  
HETATM    4  C4  UNL     1      -7.663  -1.616  -0.338  1.00  0.00           C  
HETATM    5  C5  UNL     1      -7.326  -0.214  -0.115  1.00  0.00           C  
HETATM    6  C6  UNL     1      -6.761   0.424  -1.398  1.00  0.00           C  
HETATM    7  O1  UNL     1      -6.525   1.788  -0.998  1.00  0.00           O  
HETATM    8  C7  UNL     1      -5.660  -0.233  -1.864  1.00  0.00           C  
HETATM    9  C8  UNL     1      -4.648  -0.817  -2.268  1.00  0.00           C  
HETATM   10  C9  UNL     1      -3.520  -1.468  -2.718  1.00  0.00           C  
HETATM   11  C10 UNL     1      -2.285  -1.255  -2.175  1.00  0.00           C  
HETATM   12  C11 UNL     1      -2.236  -0.270  -1.069  1.00  0.00           C  
HETATM   13  C12 UNL     1      -1.762  -0.888   0.191  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.783  -0.404   0.907  1.00  0.00           C  
HETATM   15  C14 UNL     1      -0.078   0.809   0.515  1.00  0.00           C  
HETATM   16  C15 UNL     1       0.911   1.276   1.236  1.00  0.00           C  
HETATM   17  C16 UNL     1       1.701   2.500   0.948  1.00  0.00           C  
HETATM   18  O2  UNL     1       2.521   2.890   1.934  1.00  0.00           O  
HETATM   19  C17 UNL     1       2.167   2.473  -0.438  1.00  0.00           C  
HETATM   20  C18 UNL     1       3.365   2.666  -0.851  1.00  0.00           C  
HETATM   21  C19 UNL     1       4.528   2.950  -0.034  1.00  0.00           C  
HETATM   22  C20 UNL     1       5.566   1.866  -0.345  1.00  0.00           C  
HETATM   23  C21 UNL     1       4.919   0.530   0.052  1.00  0.00           C  
HETATM   24  C22 UNL     1       5.965  -0.480  -0.263  1.00  0.00           C  
HETATM   25  O3  UNL     1       5.711  -1.454  -0.973  1.00  0.00           O  
HETATM   26  O4  UNL     1       7.211  -0.273   0.268  1.00  0.00           O  
HETATM   27  C23 UNL     1       8.261  -1.159   0.033  1.00  0.00           C  
HETATM   28  C24 UNL     1       9.466  -0.564   0.791  1.00  0.00           C  
HETATM   29  O5  UNL     1       9.151  -0.504   2.151  1.00  0.00           O  
HETATM   30  C25 UNL     1      10.611  -1.498   0.512  1.00  0.00           C  
HETATM   31  O6  UNL     1      10.831  -1.444  -0.879  1.00  0.00           O  
HETATM   32  H1  UNL     1      -9.975  -2.253   2.173  1.00  0.00           H  
HETATM   33  H2  UNL     1     -11.566  -2.279   1.372  1.00  0.00           H  
HETATM   34  H3  UNL     1     -10.998  -0.706   1.989  1.00  0.00           H  
HETATM   35  H4  UNL     1     -10.816  -1.444  -0.562  1.00  0.00           H  
HETATM   36  H5  UNL     1      -9.810  -0.183   0.126  1.00  0.00           H  
HETATM   37  H6  UNL     1      -9.053  -3.205  -0.393  1.00  0.00           H  
HETATM   38  H7  UNL     1      -6.904  -2.322  -0.649  1.00  0.00           H  
HETATM   39  H8  UNL     1      -6.405  -0.234   0.565  1.00  0.00           H  
HETATM   40  H9  UNL     1      -8.018   0.425   0.397  1.00  0.00           H  
HETATM   41  H10 UNL     1      -7.607   0.574  -2.141  1.00  0.00           H  
HETATM   42  H11 UNL     1      -7.269   2.066  -0.418  1.00  0.00           H  
HETATM   43  H12 UNL     1      -4.884   0.095  -0.701  1.00  0.00           H  
HETATM   44  H13 UNL     1      -5.440  -1.370  -3.291  1.00  0.00           H  
HETATM   45  H14 UNL     1      -3.463  -2.229  -3.532  1.00  0.00           H  
HETATM   46  H15 UNL     1      -1.415  -1.783  -2.536  1.00  0.00           H  
HETATM   47  H16 UNL     1      -2.975   0.481  -1.009  1.00  0.00           H  
HETATM   48  H17 UNL     1      -1.306   0.379  -1.442  1.00  0.00           H  
HETATM   49  H18 UNL     1      -2.257  -1.803   0.533  1.00  0.00           H  
HETATM   50  H19 UNL     1      -0.518  -0.953   1.830  1.00  0.00           H  
HETATM   51  H20 UNL     1      -0.340   1.350  -0.343  1.00  0.00           H  
HETATM   52  H21 UNL     1       1.174   0.721   2.131  1.00  0.00           H  
HETATM   53  H22 UNL     1       0.879   3.338   0.924  1.00  0.00           H  
HETATM   54  H23 UNL     1       2.119   3.368   2.682  1.00  0.00           H  
HETATM   55  H24 UNL     1       1.369   2.262  -1.228  1.00  0.00           H  
HETATM   56  H25 UNL     1       3.568   2.611  -1.972  1.00  0.00           H  
HETATM   57  H26 UNL     1       4.423   2.899   1.060  1.00  0.00           H  
HETATM   58  H27 UNL     1       5.003   3.925  -0.353  1.00  0.00           H  
HETATM   59  H28 UNL     1       6.441   2.049   0.308  1.00  0.00           H  
HETATM   60  H29 UNL     1       5.801   1.874  -1.425  1.00  0.00           H  
HETATM   61  H30 UNL     1       3.972   0.355  -0.456  1.00  0.00           H  
HETATM   62  H31 UNL     1       4.797   0.511   1.175  1.00  0.00           H  
HETATM   63  H32 UNL     1       8.457  -1.231  -1.049  1.00  0.00           H  
HETATM   64  H33 UNL     1       8.052  -2.187   0.409  1.00  0.00           H  
HETATM   65  H34 UNL     1       9.647   0.448   0.409  1.00  0.00           H  
HETATM   66  H35 UNL     1       8.273  -0.091   2.303  1.00  0.00           H  
HETATM   67  H36 UNL     1      10.276  -2.544   0.768  1.00  0.00           H  
HETATM   68  H37 UNL     1      11.489  -1.183   1.098  1.00  0.00           H  
HETATM   69  H38 UNL     1      11.164  -2.309  -1.147  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3   35   36
CONECT    3    4    4   37
CONECT    4    5   38
CONECT    5    6   39   40
CONECT    6    7    8   41
CONECT    7   42
CONECT    8    9    9   43
CONECT    9   10   44
CONECT   10   11   11   45
CONECT   11   12   46
CONECT   12   13   47   48
CONECT   13   14   14   49
CONECT   14   15   50
CONECT   15   16   16   51
CONECT   16   17   52
CONECT   17   18   19   53
CONECT   18   54
CONECT   19   20   20   55
CONECT   20   21   56
CONECT   21   22   57   58
CONECT   22   23   59   60
CONECT   23   24   61   62
CONECT   24   25   25   26
CONECT   26   27
CONECT   27   28   63   64
CONECT   28   29   30   65
CONECT   29   66
CONECT   30   31   67   68
CONECT   31   69
END

HMDB0260497
     RDKit          3D
MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)
 69 68  0  0  0  0  0  0  0  0999 V2000
  -10.6460   -1.6659    1.5225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9934   -1.2532    0.2139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8854   -2.1318   -0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6626   -1.6162   -0.3384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3261   -0.2139   -0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7611    0.4245   -1.3976 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5249    1.7881   -0.9979 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6602   -0.2333   -1.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6483   -0.8171   -2.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5204   -1.4678   -2.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2853   -1.2547   -2.1749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2357   -0.2699   -1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7623   -0.8878    0.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -0.4044    0.9067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0783    0.8086    0.5154 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9109    1.2762    1.2363 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7009    2.4995    0.9481 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5215    2.8903    1.9336 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1667    2.4725   -0.4379 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3650    2.6655   -0.8512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5281    2.9498   -0.0339 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5656    1.8659   -0.3448 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9195    0.5302    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9647   -0.4798   -0.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7114   -1.4542   -0.9730 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2107   -0.2730    0.2679 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2609   -1.1590    0.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4659   -0.5639    0.7907 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1511   -0.5041    2.1513 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6106   -1.4985    0.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8313   -1.4444   -0.8788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9748   -2.2527    2.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5659   -2.2793    1.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9977   -0.7064    1.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8162   -1.4439   -0.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8105   -0.1832    0.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0526   -3.2048   -0.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9037   -2.3221   -0.6489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4046   -0.2340    0.5652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0181    0.4254    0.3974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6073    0.5739   -2.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2689    2.0662   -0.4181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8838    0.0951   -0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4403   -1.3700   -3.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4635   -2.2287   -3.5318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4148   -1.7833   -2.5355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9748    0.4805   -1.0085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3055    0.3789   -1.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2566   -1.8035    0.5328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5176   -0.9526    1.8302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3397    1.3503   -0.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1744    0.7207    2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8786    3.3375    0.9236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194    3.3680    2.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3691    2.2617   -1.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5679    2.6111   -1.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4232    2.8994    1.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0025    3.9252   -0.3534 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4413    2.0490    0.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8014    1.8739   -1.4246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9717    0.3546   -0.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972    0.5110    1.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4573   -1.2307   -1.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0522   -2.1868    0.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6467    0.4482    0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2728   -0.0913    2.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2764   -2.5436    0.7682 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4890   -1.1835    1.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1640   -2.3089   -1.1475 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  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  6
  7 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 14 50  1  0
 15 51  1  0
 16 52  1  0
 17 53  1  6
 18 54  1  0
 19 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 22 60  1  0
 23 61  1  0
 23 62  1  0
 27 63  1  0
 27 64  1  0
 28 65  1  6
 29 66  1  0
 30 67  1  0
 30 68  1  0
 31 69  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(2S)-2,3-Dihydroxypropyl (5Z,7S,8E,10Z,13Z,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoic acid	HMDB

Chemical Formula

C₂₅H₃₈O₆

Average Molecular Weight

434.573

Monoisotopic Molecular Weight

434.266838944

IUPAC Name

(2S)-2,3-dihydroxypropyl (5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoate

Traditional Name

(2S)-2,3-dihydroxypropyl (5Z,7S,8E,10Z,13Z,15E,17R,19Z)-7,17-dihydroxydocosa-5,8,10,13,15,19-hexaenoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C25H38O6/c1-2-3-10-15-22(27)16-11-7-5-4-6-8-12-17-23(28)18-13-9-14-19-25(30)31-21-24(29)20-26/h3,5-8,10-13,16-18,22-24,26-29H,2,4,9,14-15,19-21H2,1H3/b7-5-,8-6-,10-3-,16-11+,17-12+,18-13-/t22-,23-,24+/m1/s1

InChI Key

LDHJHOGZZQKNEN-DHRKEDOKSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Monoradylglycerol
Monoacylglycerol
1-acyl-sn-glycerol
Glycerolipid
Fatty acid ester
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0260497)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	3.94	ALOGPS
logP	3.27	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	13.62	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	131.29 m³·mol⁻¹	ChemAxon
Polarizability	49.79 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	214.172	32859911
AllCCS	[M+H-H2O]+	211.998	32859911
AllCCS	[M+Na]+	216.742	32859911
AllCCS	[M+NH4]+	216.171	32859911
AllCCS	[M-H]-	208.394	32859911
AllCCS	[M+Na-2H]-	211.488	32859911
AllCCS	[M+HCOO]-	215.043	32859911
DeepCCS	[M+H]+	204.107	30932474
DeepCCS	[M-H]-	201.711	30932474
DeepCCS	[M-2H]-	234.593	30932474
DeepCCS	[M+Na]+	210.019	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)	CC\C=C/C[C@@H](O)\C=C\C=C/C\C=C/C=C/[C@@H](O)\C=C/CCCC(=O)OC[C@@H](O)CO	4983.2	Standard polar	33892256
MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)	CC\C=C/C[C@@H](O)\C=C\C=C/C\C=C/C=C/[C@@H](O)\C=C/CCCC(=O)OC[C@@H](O)CO	3216.1	Standard non polar	33892256
MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0)	CC\C=C/C[C@@H](O)\C=C\C=C/C\C=C/C=C/[C@@H](O)\C=C/CCCC(=O)OC[C@@H](O)CO	3629.4	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (Non-derivatized) - 70eV, Positive	splash10-02t9-9023400000-0ed6c61360b1fd8e5046	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_3_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TMS_4_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-11-05	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

156963862

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 ]

Showing metabocard for MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0) (HMDB0260497)

MOL for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

3D MOL for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

3D SDF for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

3D-SDF for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

PDB for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

3D PDB for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

SMILES for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

INCHI for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

Structure for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

3D Structure for HMDB0260497 (MG(22:6(5Z,8E,10Z,13Z,15E,19Z)-2OH(7S, 17S)/0:0/0:0))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra