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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-08-27 18:26:59 UTC

Update Date

2021-09-14 15:42:57 UTC

HMDB ID

HMDB0242160

Secondary Accession Numbers

None

Metabolite Identification

Common Name

1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-)

Description

1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-) belongs to the class of organic compounds known as 1-acyl-sn-glycerol-3-phosphoinositols. These are glycerophosphoinositols where the glycerol is acylated only at position O-1 with a fatty acid. Based on a literature review a significant number of articles have been published on 1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-).

Structure

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

  Mrv1652308272120372D          

 49 49  0  0  1  0            999 V2000
    8.5737   16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   14.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   13.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4315   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762    9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   10.7250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.8618    9.4875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618   11.1375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.1473    9.9000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.1473   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    9.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907    9.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618    8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   11.9625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328    9.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1309   10.0105    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   15.3059   11.4395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   10.7250    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   11.9625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   11.1375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   11.5500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473    9.0750    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   11.5500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 20 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 17  1  0  0  0  0
 23 22  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 27 26  1  0  0  0  0
 20 28  1  1  0  0  0
 29 21  2  0  0  0  0
 30 22  1  0  0  0  0
 23 31  1  6  0  0  0
 24 32  1  6  0  0  0
 25 33  1  1  0  0  0
 26 34  1  1  0  0  0
 37 18  1  0  0  0  0
 37 21  1  0  0  0  0
 38 19  1  0  0  0  0
 39 27  1  0  0  0  0
 40 35  1  0  0  0  0
 40 36  2  0  0  0  0
 40 38  1  0  0  0  0
 40 39  1  0  0  0  0
 41  9  1  0  0  0  0
 42 10  1  0  0  0  0
 20 43  1  1  0  0  0
 44 22  1  0  0  0  0
 23 45  1  1  0  0  0
 24 46  1  1  0  0  0
 25 47  1  1  0  0  0
 26 48  1  6  0  0  0
 49 27  1  0  0  0  0
M  CHG  1  35  -1
M  END

HMDB0242160
     RDKit          3D
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-)
 90 90  0  0  0  0  0  0  0  0999 V2000
   10.2402   -2.4089    0.3308 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7866   -1.4620    1.4441 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3192   -1.5875    1.6817 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6713   -0.7738    2.6966 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4090    0.6344    2.7167 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2822    1.7696    2.5728 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9983    2.1527    1.3527 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1686    2.4746    0.1421 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3756    1.3601   -0.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0534    1.2738   -0.4617 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3902    2.8753   -1.3006 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2398   -1.4204   -2.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2212   -1.8096   -1.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2062   -2.7633   -2.3755 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5454   -3.9025   -2.8586 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.1266   -2.5101    0.2521 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.7058   -3.7247    1.0499 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.3705   -1.1755    1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5321   -0.5408    0.8978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2845    0.8934    0.4394 C   0  0  2  0  0  0  0  0  0  0  0  0
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  -10.7395    0.8235    0.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.8431    0.0384    2.1409 O   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.0352   -1.6957    2.3998 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3805   -3.0387    0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1185   -2.9943    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7980    3.7845   -1.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0207    0.9758   -2.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8897    2.3380   -2.6645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9045    1.0319    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7863    2.2369   -0.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0013   -3.8867   -1.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.3601    0.8625   -0.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4984    2.6359    1.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.3197   -2.3660    2.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
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 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 30  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  2 44  1  0
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  3 46  1  0
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  4 48  1  0
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  8 56  1  0
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 12 63  1  0
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 16 70  1  0
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 17 73  1  0
 21 74  1  0
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 22 76  1  6
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 30 80  1  0
 31 81  1  6
 32 82  1  0
 33 83  1  6
 34 84  1  0
 35 85  1  0
 36 86  1  0
 37 87  1  1
 38 88  1  0
 39 89  1  1
 40 90  1  0
M  CHG  1  28  -1
M  END

  Mrv1652308272120372D          

 49 49  0  0  1  0            999 V2000
    8.5737   16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4302   12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   10.3125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4315   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762    9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   10.7250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.8618    9.4875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618   11.1375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.1473    9.9000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.1473   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    9.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907    9.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618    8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   11.9625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328    9.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1309   10.0105    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   15.3059   11.4395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   10.7250    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   11.9625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   11.1375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   11.5500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473    9.0750    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   10.3125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   11.5500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 20 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 17  1  0  0  0  0
 23 22  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 27 26  1  0  0  0  0
 20 28  1  1  0  0  0
 29 21  2  0  0  0  0
 30 22  1  0  0  0  0
 23 31  1  6  0  0  0
 24 32  1  6  0  0  0
 25 33  1  1  0  0  0
 26 34  1  1  0  0  0
 37 18  1  0  0  0  0
 37 21  1  0  0  0  0
 38 19  1  0  0  0  0
 39 27  1  0  0  0  0
 40 35  1  0  0  0  0
 40 36  2  0  0  0  0
 40 38  1  0  0  0  0
 40 39  1  0  0  0  0
 41  9  1  0  0  0  0
 42 10  1  0  0  0  0
 20 43  1  1  0  0  0
 44 22  1  0  0  0  0
 23 45  1  1  0  0  0
 24 46  1  1  0  0  0
 25 47  1  1  0  0  0
 26 48  1  6  0  0  0
 49 27  1  0  0  0  0
M  CHG  1  35  -1
M  END
> <DATABASE_ID>
HMDB0242160

> <DATABASE_NAME>
hmdb

> <SMILES>
[H]\C(CCCCCCCC)=C(/[H])CCCCCCCC(=O)OC[C@@]([H])(O)COP([O-])(=O)OC1([H])[C@]([H])(O)[C@@]([H])(O)C([H])(O)[C@@]([H])(O)[C@@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C27H51O12P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(29)37-18-20(28)19-38-40(35,36)39-27-25(33)23(31)22(30)24(32)26(27)34/h9-10,20,22-28,30-34H,2-8,11-19H2,1H3,(H,35,36)/p-1/b10-9-/t20-,22?,23-,24+,25-,26-,27?/m1/s1

> <INCHI_KEY>
UGDOFRYHDCDVHD-GFMLYYSJSA-M

> <FORMULA>
C27H50O12P

> <MOLECULAR_WEIGHT>
597.659

> <EXACT_MASS>
597.304537628

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
63.75964393348255

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
-1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-hydroxy-3-{[(2R,3R,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl phosphono]oxy}propyl (9Z)-octadec-9-enoate

> <ALOGPS_LOGP>
3.32

> <JCHEM_LOGP>
2.6002176609999994

> <ALOGPS_LOGS>
-3.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.339055972873332

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.833538640840655

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4040034470113856

> <JCHEM_POLAR_SURFACE_AREA>
206.26999999999998

> <JCHEM_REFRACTIVITY>
146.1733

> <JCHEM_ROTATABLE_BOND_COUNT>
23

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.26e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-hydroxy-3-{[(2R,3R,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl phosphono]oxy}propyl (9Z)-octadec-9-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242160
     RDKit          3D
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-)
 90 90  0  0  0  0  0  0  0  0999 V2000
   10.2402   -2.4089    0.3308 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7866   -1.4620    1.4441 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3192   -1.5875    1.6817 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6713   -0.7738    2.6966 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4090    0.6344    2.7167 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2822    1.7696    2.5728 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9983    2.1527    1.3527 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1686    2.4746    0.1421 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3756    1.3601   -0.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0534    1.2738   -0.4617 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1958    2.4075   -0.1128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3902    2.8753   -1.3006 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4530    1.8086   -1.8453 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4613    1.3609   -0.8335 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5466    0.3144   -1.4127 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7998    0.8948   -2.5842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1795   -0.0708   -3.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2392   -0.5166   -2.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3367   -0.1442   -1.0648 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2398   -1.4204   -2.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2212   -1.8096   -1.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2062   -2.7633   -2.3755 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5454   -3.9025   -2.8586 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2738   -3.1723   -1.3708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9545   -2.0728   -0.8792 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1266   -2.5101    0.2521 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.7058   -3.7247    1.0499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6084   -2.8998   -0.4614 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.3705   -1.1755    1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5321   -0.5408    0.8978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2845    0.8934    0.4394 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.0705    1.7492    1.5080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4765    1.3068   -0.3945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.3289    0.6541   -1.6236 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7395    0.8235    0.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2991   -0.2573   -0.4724 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5907    0.5246    1.7042 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.8431    0.0384    2.1409 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5245   -0.4540    2.0445 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.0352   -1.6957    2.3998 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3805   -3.0387    0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1185   -2.9943    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5864   -1.7728   -0.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1332   -0.4771    1.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2747   -1.8017    2.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1490   -2.6861    1.9920 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7724   -1.5732    0.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6260   -1.2813    2.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2043   -1.0256    3.7158 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4047    0.8968    2.1846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9569    0.8062    3.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6913    2.7236    2.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0434    1.7594    3.4689 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8582    1.5511    1.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4633    3.2029    1.6221 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9346    2.6823   -0.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6262    3.4218    0.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9475    0.4476   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6087    0.3293   -0.8475 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5190    2.0667    0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7785    3.2321    0.3099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0772    3.1412   -2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7980    3.7845   -1.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0207    0.9758   -2.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8897    2.3380   -2.6645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9045    1.0319    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7863    2.2369   -0.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2349   -0.4929   -1.8117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8974   -0.1469   -0.6417 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2534    1.7773   -2.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5389    1.1106   -3.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6676    0.3587   -4.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4137   -0.9502   -3.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6790   -2.3922   -0.9445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7075   -0.9799   -1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7159   -2.2854   -3.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5644   -3.7764   -2.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7209   -3.6992   -0.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0013   -3.8867   -1.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0066   -1.0846    0.0649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3601    0.8625   -0.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4984    2.6359    1.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4850    2.4130   -0.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5061    1.3062   -2.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5019    1.6327    0.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1850   -0.4951   -0.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4561    1.5026    2.2202 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9553   -0.9136    1.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9796   -0.0620    2.9486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3197   -2.3660    2.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
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  9 10  2  0
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 12 13  1  0
 13 14  1  0
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 18 20  1  0
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 37 87  1  1
 38 88  1  0
 39 89  1  1
 40 90  1  0
M  CHG  1  28  -1
M  END

HEADER    PROTEIN                                 27-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-AUG-21         0                                  
HETATM    1  C   UNK     0      16.004  30.800   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.004  29.260   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.670  28.490   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.670  26.950   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.337  26.180   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.337  24.640   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.003  23.870   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.003  22.330   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669  21.560   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669  20.020   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.003  19.250   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.337  20.020   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.670  19.250   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.004  20.020   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.338  19.250   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      18.672  20.020   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.005  19.250   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      24.006  20.020   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      26.674  20.020   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.340  19.250   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.339  20.020   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      34.676  18.480   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      34.676  20.020   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      33.342  17.710   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      33.342  20.790   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      32.008  18.480   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      32.008  20.020   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      25.340  17.710   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      21.339  21.560   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      36.009  17.710   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      36.009  20.790   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      33.342  16.170   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      33.342  22.330   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      30.675  17.710   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      30.111  18.686   0.000  0.00  0.00           O-1
HETATM   36  O   UNK     0      28.571  21.354   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      22.673  19.250   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      28.007  19.250   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      30.675  20.790   0.000  0.00  0.00           O+0
HETATM   40  P   UNK     0      29.341  20.020   0.000  0.00  0.00           P+0
HETATM   41  H   UNK     0       9.336  22.330   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       9.336  19.250   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0      25.340  20.790   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0      36.009  19.250   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0      34.676  21.560   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0      32.008  16.940   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0      33.342  19.250   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0      30.675  19.250   0.000  0.00  0.00           H+0
HETATM   49  H   UNK     0      32.008  21.560   0.000  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   41                                                  
CONECT   10    9   11   42                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   21                                                       
CONECT   18   20   37                                                       
CONECT   19   20   38                                                       
CONECT   20   18   19   28   43                                             
CONECT   21   17   29   37                                                  
CONECT   22   23   24   30   44                                             
CONECT   23   22   25   31   45                                             
CONECT   24   22   26   32   46                                             
CONECT   25   23   27   33   47                                             
CONECT   26   24   27   34   48                                             
CONECT   27   25   26   39   49                                             
CONECT   28   20                                                            
CONECT   29   21                                                            
CONECT   30   22                                                            
CONECT   31   23                                                            
CONECT   32   24                                                            
CONECT   33   25                                                            
CONECT   34   26                                                            
CONECT   35   40                                                            
CONECT   36   40                                                            
CONECT   37   18   21                                                       
CONECT   38   19   40                                                       
CONECT   39   27   40                                                       
CONECT   40   35   36   38   39                                             
CONECT   41    9                                                            
CONECT   42   10                                                            
CONECT   43   20                                                            
CONECT   44   22                                                            
CONECT   45   23                                                            
CONECT   46   24                                                            
CONECT   47   25                                                            
CONECT   48   26                                                            
CONECT   49   27                                                            
MASTER        0    0    0    0    0    0    0    0   49    0   98    0
END

COMPND    HMDB0242160
HETATM    1  C1  UNL     1      10.240  -2.409   0.331  1.00  0.00           C  
HETATM    2  C2  UNL     1       9.787  -1.462   1.444  1.00  0.00           C  
HETATM    3  C3  UNL     1       8.319  -1.588   1.682  1.00  0.00           C  
HETATM    4  C4  UNL     1       7.671  -0.774   2.697  1.00  0.00           C  
HETATM    5  C5  UNL     1       7.409   0.634   2.717  1.00  0.00           C  
HETATM    6  C6  UNL     1       8.282   1.770   2.573  1.00  0.00           C  
HETATM    7  C7  UNL     1       8.998   2.153   1.353  1.00  0.00           C  
HETATM    8  C8  UNL     1       8.169   2.475   0.142  1.00  0.00           C  
HETATM    9  C9  UNL     1       7.376   1.360  -0.327  1.00  0.00           C  
HETATM   10  C10 UNL     1       6.053   1.274  -0.462  1.00  0.00           C  
HETATM   11  C11 UNL     1       5.196   2.408  -0.113  1.00  0.00           C  
HETATM   12  C12 UNL     1       4.390   2.875  -1.301  1.00  0.00           C  
HETATM   13  C13 UNL     1       3.453   1.809  -1.845  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.461   1.361  -0.834  1.00  0.00           C  
HETATM   15  C15 UNL     1       1.547   0.314  -1.413  1.00  0.00           C  
HETATM   16  C16 UNL     1       0.800   0.895  -2.584  1.00  0.00           C  
HETATM   17  C17 UNL     1      -0.180  -0.071  -3.204  1.00  0.00           C  
HETATM   18  C18 UNL     1      -1.239  -0.517  -2.264  1.00  0.00           C  
HETATM   19  O1  UNL     1      -1.337  -0.144  -1.065  1.00  0.00           O  
HETATM   20  O2  UNL     1      -2.240  -1.420  -2.683  1.00  0.00           O  
HETATM   21  C19 UNL     1      -3.221  -1.810  -1.744  1.00  0.00           C  
HETATM   22  C20 UNL     1      -4.206  -2.763  -2.375  1.00  0.00           C  
HETATM   23  O3  UNL     1      -3.545  -3.902  -2.859  1.00  0.00           O  
HETATM   24  C21 UNL     1      -5.274  -3.172  -1.371  1.00  0.00           C  
HETATM   25  O4  UNL     1      -5.955  -2.073  -0.879  1.00  0.00           O  
HETATM   26  P1  UNL     1      -7.127  -2.510   0.252  1.00  0.00           P  
HETATM   27  O5  UNL     1      -6.706  -3.725   1.050  1.00  0.00           O  
HETATM   28  O6  UNL     1      -8.608  -2.900  -0.461  1.00  0.00           O1-
HETATM   29  O7  UNL     1      -7.371  -1.176   1.256  1.00  0.00           O  
HETATM   30  C22 UNL     1      -8.532  -0.541   0.898  1.00  0.00           C  
HETATM   31  C23 UNL     1      -8.285   0.893   0.439  1.00  0.00           C  
HETATM   32  O8  UNL     1      -8.071   1.749   1.508  1.00  0.00           O  
HETATM   33  C24 UNL     1      -9.477   1.307  -0.395  1.00  0.00           C  
HETATM   34  O9  UNL     1      -9.329   0.654  -1.624  1.00  0.00           O  
HETATM   35  C25 UNL     1     -10.739   0.823   0.240  1.00  0.00           C  
HETATM   36  O10 UNL     1     -11.299  -0.257  -0.472  1.00  0.00           O  
HETATM   37  C26 UNL     1     -10.591   0.525   1.704  1.00  0.00           C  
HETATM   38  O11 UNL     1     -11.843   0.038   2.141  1.00  0.00           O  
HETATM   39  C27 UNL     1      -9.524  -0.454   2.044  1.00  0.00           C  
HETATM   40  O12 UNL     1     -10.035  -1.696   2.400  1.00  0.00           O  
HETATM   41  H1  UNL     1       9.380  -3.039   0.058  1.00  0.00           H  
HETATM   42  H2  UNL     1      11.119  -2.994   0.699  1.00  0.00           H  
HETATM   43  H3  UNL     1      10.586  -1.773  -0.501  1.00  0.00           H  
HETATM   44  H4  UNL     1      10.133  -0.477   1.262  1.00  0.00           H  
HETATM   45  H5  UNL     1      10.275  -1.802   2.414  1.00  0.00           H  
HETATM   46  H6  UNL     1       8.149  -2.686   1.992  1.00  0.00           H  
HETATM   47  H7  UNL     1       7.772  -1.573   0.681  1.00  0.00           H  
HETATM   48  H8  UNL     1       6.626  -1.281   2.896  1.00  0.00           H  
HETATM   49  H9  UNL     1       8.204  -1.026   3.716  1.00  0.00           H  
HETATM   50  H10 UNL     1       6.405   0.897   2.185  1.00  0.00           H  
HETATM   51  H11 UNL     1       6.957   0.806   3.832  1.00  0.00           H  
HETATM   52  H12 UNL     1       7.691   2.724   2.910  1.00  0.00           H  
HETATM   53  H13 UNL     1       9.043   1.759   3.469  1.00  0.00           H  
HETATM   54  H14 UNL     1       9.858   1.551   1.023  1.00  0.00           H  
HETATM   55  H15 UNL     1       9.463   3.203   1.622  1.00  0.00           H  
HETATM   56  H16 UNL     1       8.935   2.682  -0.679  1.00  0.00           H  
HETATM   57  H17 UNL     1       7.626   3.422   0.353  1.00  0.00           H  
HETATM   58  H18 UNL     1       7.948   0.448  -0.612  1.00  0.00           H  
HETATM   59  H19 UNL     1       5.609   0.329  -0.848  1.00  0.00           H  
HETATM   60  H20 UNL     1       4.519   2.067   0.721  1.00  0.00           H  
HETATM   61  H21 UNL     1       5.778   3.232   0.310  1.00  0.00           H  
HETATM   62  H22 UNL     1       5.077   3.141  -2.129  1.00  0.00           H  
HETATM   63  H23 UNL     1       3.798   3.785  -1.070  1.00  0.00           H  
HETATM   64  H24 UNL     1       4.021   0.976  -2.275  1.00  0.00           H  
HETATM   65  H25 UNL     1       2.890   2.338  -2.665  1.00  0.00           H  
HETATM   66  H26 UNL     1       2.905   1.032   0.129  1.00  0.00           H  
HETATM   67  H27 UNL     1       1.786   2.237  -0.586  1.00  0.00           H  
HETATM   68  H28 UNL     1       2.235  -0.493  -1.812  1.00  0.00           H  
HETATM   69  H29 UNL     1       0.897  -0.147  -0.642  1.00  0.00           H  
HETATM   70  H30 UNL     1       0.253   1.777  -2.251  1.00  0.00           H  
HETATM   71  H31 UNL     1       1.539   1.111  -3.395  1.00  0.00           H  
HETATM   72  H32 UNL     1      -0.668   0.359  -4.079  1.00  0.00           H  
HETATM   73  H33 UNL     1       0.414  -0.950  -3.581  1.00  0.00           H  
HETATM   74  H34 UNL     1      -2.679  -2.392  -0.945  1.00  0.00           H  
HETATM   75  H35 UNL     1      -3.708  -0.980  -1.225  1.00  0.00           H  
HETATM   76  H36 UNL     1      -4.716  -2.285  -3.226  1.00  0.00           H  
HETATM   77  H37 UNL     1      -2.564  -3.776  -2.815  1.00  0.00           H  
HETATM   78  H38 UNL     1      -4.721  -3.699  -0.557  1.00  0.00           H  
HETATM   79  H39 UNL     1      -6.001  -3.887  -1.794  1.00  0.00           H  
HETATM   80  H40 UNL     1      -9.007  -1.085   0.065  1.00  0.00           H  
HETATM   81  H41 UNL     1      -7.360   0.863  -0.201  1.00  0.00           H  
HETATM   82  H42 UNL     1      -8.498   2.636   1.323  1.00  0.00           H  
HETATM   83  H43 UNL     1      -9.485   2.413  -0.543  1.00  0.00           H  
HETATM   84  H44 UNL     1      -9.506   1.306  -2.345  1.00  0.00           H  
HETATM   85  H45 UNL     1     -11.502   1.633   0.156  1.00  0.00           H  
HETATM   86  H46 UNL     1     -12.185  -0.495  -0.095  1.00  0.00           H  
HETATM   87  H47 UNL     1     -10.456   1.503   2.220  1.00  0.00           H  
HETATM   88  H48 UNL     1     -11.955  -0.914   1.964  1.00  0.00           H  
HETATM   89  H49 UNL     1      -8.980  -0.062   2.949  1.00  0.00           H  
HETATM   90  H50 UNL     1      -9.320  -2.366   2.473  1.00  0.00           H  
CONECT    1    2   41   42   43
CONECT    2    3   44   45
CONECT    3    4   46   47
CONECT    4    5   48   49
CONECT    5    6   50   51
CONECT    6    7   52   53
CONECT    7    8   54   55
CONECT    8    9   56   57
CONECT    9   10   10   58
CONECT   10   11   59
CONECT   11   12   60   61
CONECT   12   13   62   63
CONECT   13   14   64   65
CONECT   14   15   66   67
CONECT   15   16   68   69
CONECT   16   17   70   71
CONECT   17   18   72   73
CONECT   18   19   19   20
CONECT   20   21
CONECT   21   22   74   75
CONECT   22   23   24   76
CONECT   23   77
CONECT   24   25   78   79
CONECT   25   26
CONECT   26   27   27   28   29
CONECT   29   30
CONECT   30   31   39   80
CONECT   31   32   33   81
CONECT   32   82
CONECT   33   34   35   83
CONECT   34   84
CONECT   35   36   37   85
CONECT   36   86
CONECT   37   38   39   87
CONECT   38   88
CONECT   39   40   89
CONECT   40   90
END

HMDB0242160
     RDKit          3D
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-)
 90 90  0  0  0  0  0  0  0  0999 V2000
   10.2402   -2.4089    0.3308 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7866   -1.4620    1.4441 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3192   -1.5875    1.6817 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6713   -0.7738    2.6966 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4090    0.6344    2.7167 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2822    1.7696    2.5728 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9983    2.1527    1.3527 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1686    2.4746    0.1421 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3756    1.3601   -0.3266 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0534    1.2738   -0.4617 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1958    2.4075   -0.1128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3902    2.8753   -1.3006 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4530    1.8086   -1.8453 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4613    1.3609   -0.8335 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5466    0.3144   -1.4127 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7998    0.8948   -2.5842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1795   -0.0708   -3.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2392   -0.5166   -2.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3367   -0.1442   -1.0648 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2398   -1.4204   -2.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2212   -1.8096   -1.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2062   -2.7633   -2.3755 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5454   -3.9025   -2.8586 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2738   -3.1723   -1.3708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9545   -2.0728   -0.8792 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1266   -2.5101    0.2521 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.7058   -3.7247    1.0499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6084   -2.8998   -0.4614 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.3705   -1.1755    1.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5321   -0.5408    0.8978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2845    0.8934    0.4394 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.0705    1.7492    1.5080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4765    1.3068   -0.3945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.3289    0.6541   -1.6236 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7395    0.8235    0.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2991   -0.2573   -0.4724 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5907    0.5246    1.7042 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.8431    0.0384    2.1409 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5245   -0.4540    2.0445 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.0352   -1.6957    2.3998 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3805   -3.0387    0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1185   -2.9943    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5864   -1.7728   -0.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1332   -0.4771    1.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2747   -1.8017    2.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1490   -2.6861    1.9920 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7724   -1.5732    0.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6260   -1.2813    2.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2043   -1.0256    3.7158 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4047    0.8968    2.1846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9569    0.8062    3.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6913    2.7236    2.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0434    1.7594    3.4689 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8582    1.5511    1.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4633    3.2029    1.6221 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9346    2.6823   -0.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6262    3.4218    0.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9475    0.4476   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6087    0.3293   -0.8475 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5190    2.0667    0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7785    3.2321    0.3099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0772    3.1412   -2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7980    3.7845   -1.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0207    0.9758   -2.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8897    2.3380   -2.6645 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9045    1.0319    0.1291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7863    2.2369   -0.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2349   -0.4929   -1.8117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8974   -0.1469   -0.6417 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2534    1.7773   -2.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5389    1.1106   -3.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6676    0.3587   -4.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4137   -0.9502   -3.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6790   -2.3922   -0.9445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7075   -0.9799   -1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7159   -2.2854   -3.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5644   -3.7764   -2.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7209   -3.6992   -0.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0013   -3.8867   -1.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0066   -1.0846    0.0649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3601    0.8625   -0.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4984    2.6359    1.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4850    2.4130   -0.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5061    1.3062   -2.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5019    1.6327    0.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1850   -0.4951   -0.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4561    1.5026    2.2202 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9553   -0.9136    1.9637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9796   -0.0620    2.9486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3197   -2.3660    2.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 30  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  2 44  1  0
  2 45  1  0
  3 46  1  0
  3 47  1  0
  4 48  1  0
  4 49  1  0
  5 50  1  0
  5 51  1  0
  6 52  1  0
  6 53  1  0
  7 54  1  0
  7 55  1  0
  8 56  1  0
  8 57  1  0
  9 58  1  0
 10 59  1  0
 11 60  1  0
 11 61  1  0
 12 62  1  0
 12 63  1  0
 13 64  1  0
 13 65  1  0
 14 66  1  0
 14 67  1  0
 15 68  1  0
 15 69  1  0
 16 70  1  0
 16 71  1  0
 17 72  1  0
 17 73  1  0
 21 74  1  0
 21 75  1  0
 22 76  1  6
 23 77  1  0
 24 78  1  0
 24 79  1  0
 30 80  1  0
 31 81  1  6
 32 82  1  0
 33 83  1  6
 34 84  1  0
 35 85  1  0
 36 86  1  0
 37 87  1  1
 38 88  1  0
 39 89  1  1
 40 90  1  0
M  CHG  1  28  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₇H₅₀O₁₂P

Average Molecular Weight

597.659

Monoisotopic Molecular Weight

597.304537628

IUPAC Name

(2R)-2-hydroxy-3-{[(2R,3R,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl phosphono]oxy}propyl (9Z)-octadec-9-enoate

Traditional Name

(2R)-2-hydroxy-3-{[(2R,3R,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl phosphono]oxy}propyl (9Z)-octadec-9-enoate

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCCCCC)=C(/[H])CCCCCCCC(=O)OC[C@@]([H])(O)COP([O-])(=O)OC1([H])[C@]([H])(O)[C@@]([H])(O)C([H])(O)[C@@]([H])(O)[C@@]1([H])O

InChI Identifier

InChI=1S/C27H51O12P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(29)37-18-20(28)19-38-40(35,36)39-27-25(33)23(31)22(30)24(32)26(27)34/h9-10,20,22-28,30-34H,2-8,11-19H2,1H3,(H,35,36)/p-1/b10-9-/t20-,22?,23-,24+,25-,26-,27?/m1/s1

InChI Key

UGDOFRYHDCDVHD-GFMLYYSJSA-M

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-acyl-sn-glycerol-3-phosphoinositols. These are glycerophosphoinositols where the glycerol is acylated only at position O-1 with a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoinositols

Direct Parent

1-acyl-sn-glycerol-3-phosphoinositols

Alternative Parents

Substituents

1-acyl-sn-glycerol-3-phosphoinositol
Inositol phosphate
Dialkyl phosphate
Fatty acid ester
Cyclohexanol
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Cyclitol or derivatives
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Organic anion
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

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	3.32	ALOGPS
logP	2.6	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	1.83	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	206.27 Å²	ChemAxon
Rotatable Bond Count	23	ChemAxon
Refractivity	146.17 m³·mol⁻¹	ChemAxon
Polarizability	63.76 Å³	ChemAxon
Number of Rings	1	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
DeepCCS	[M+H]+	218.183	30932474
DeepCCS	[M-H]-	216.477	30932474
DeepCCS	[M-2H]-	250.512	30932474
DeepCCS	[M+Na]+	224.285	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-)	[H]\C(CCCCCCCC)=C(/[H])CCCCCCCC(=O)OC[C@@]([H])(O)COP([O-])(=O)OC1([H])[C@]([H])(O)[C@@]([H])(O)C([H])(O)[C@@]([H])(O)[C@@]1([H])O	4637.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-)	[H]\C(CCCCCCCC)=C(/[H])CCCCCCCC(=O)OC[C@@]([H])(O)COP([O-])(=O)OC1([H])[C@]([H])(O)[C@@]([H])(O)C([H])(O)[C@@]([H])(O)[C@@]1([H])O	4010.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-)	[H]\C(CCCCCCCC)=C(/[H])CCCCCCCC(=O)OC[C@@]([H])(O)COP([O-])(=O)OC1([H])[C@]([H])(O)[C@@]([H])(O)C([H])(O)[C@@]([H])(O)[C@@]1([H])O	4405.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4309.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4059.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	6172.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O	4257.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O	4025.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O	6036.2	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O	4264.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O	4022.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O	6023.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O	4250.5	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O	4048.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O	6039.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	4264.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	4022.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	6023.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4257.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4025.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	6036.2	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4223.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4063.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	5727.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4202.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4027.3	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5631.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	4226.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	3999.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	5574.8	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4222.3	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4038.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	5598.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4187.9	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4039.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	5629.6	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O	4202.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O	4027.3	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O	5631.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4195.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4026.1	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5613.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4243.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4053.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	5717.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C	4208.9	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C	4081.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C	5743.3	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4243.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4053.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	5717.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4223.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4063.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5727.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O	4195.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O	4026.1	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O	5613.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4187.9	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4039.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5629.6	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	4222.3	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	4038.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	5598.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4196.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4007.2	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	5616.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4167.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	4040.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C	5349.5	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4167.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4040.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5349.5	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4139.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4010.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5286.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	4170.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	4010.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O	5219.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4155.3	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	4005.6	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C	5248.3	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4149.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3989.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	5278.6	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4158.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4018.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5273.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #16	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4155.3	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #16	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4005.6	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #16	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5248.3	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #17	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4158.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #17	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4018.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #17	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	5273.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #18	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4158.2	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #18	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3991.2	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #18	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5279.2	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #19	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4170.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #19	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4010.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #19	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5219.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4157.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4055.3	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5376.5	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #20	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4139.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #20	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4010.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #20	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5286.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4185.5	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4055.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	5341.2	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4156.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4029.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5356.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4174.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4044.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	5377.3	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4200.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4016.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	5314.4	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4185.5	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4055.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5341.2	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4157.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4055.3	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5376.5	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C	4174.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C	4044.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),3TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C	5377.3	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4124.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	3996.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5027.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4124.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	3996.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5027.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4118.5	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3940.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	4934.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4106.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3957.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4932.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4121.2	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3960.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4862.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4118.5	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3940.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4934.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4106.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3957.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4932.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4148.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4004.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4957.6	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4140.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	3996.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4987.4	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4129.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	3968.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5027.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4135.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4008.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5023.5	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4140.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	3996.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4987.4	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4135.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4008.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	5023.5	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	4139.0	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	3975.3	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)O[Si](C)(C)C	5023.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4148.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4004.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),4TMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C)C(O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)O[Si](C)(C)C	4957.6	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4492.0	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4249.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	6095.4	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O	4440.9	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O	4227.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O	5989.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O	4450.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O	4222.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O	5975.8	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4458.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4243.1	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	6001.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4450.8	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4222.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5975.8	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4440.9	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4227.9	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),1TBDMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5989.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4612.5	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4428.4	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #1	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	5697.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4602.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4397.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #10	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5633.4	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4600.1	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4370.5	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #11	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5576.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4602.3	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4410.2	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #12	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5600.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4594.2	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4408.1	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #13	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5631.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4602.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4397.0	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #14	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5633.4	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4587.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4397.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #15	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	5615.6	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4621.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4419.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #2	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	5686.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4624.0	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	4445.3	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #3	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)O[Si](C)(C)C(C)(C)C	5715.0	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C	4621.4	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C	4419.7	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #4	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)O[Si](C)(C)C(C)(C)C	5686.1	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4612.5	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4428.4	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #5	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OC1[C@H](O)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	5697.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O	4587.7	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O	4397.8	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #6	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C(O)[C@@H](O)[C@H]1O	5615.6	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4594.2	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4408.1	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #7	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O)[C@H](O)C(O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5631.7	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4602.3	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4410.2	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #8	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5600.9	Standard polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4590.6	Semi standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4381.2	Standard non polar	33892256
1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-),2TBDMS,isomer #9	CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@@H](O)COP(=O)([O-])OC1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C(O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5617.3	Standard polar	33892256

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-) 10V, Negative-QTOF	splash10-0002-0000090000-3f928c8b251245456479	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-) 20V, Negative-QTOF	splash10-0002-0000090000-3f928c8b251245456479	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-) 40V, Negative-QTOF	splash10-0fsm-0394130000-f21c91e8f198de1aea3c	2021-10-12	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

86289644

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

Kong SW, Hernandez-Ferrer C: Assessment of coverage for endogenous metabolites and exogenous chemical compounds using an untargeted metabolomics platform. Pac Symp Biocomput. 2020;25:587-598. [PubMed:31797630 ]

Showing metabocard for 1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-) (HMDB0242160)

MOL for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

3D MOL for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

3D SDF for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

3D-SDF for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

PDB for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

3D PDB for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

SMILES for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

INCHI for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

Structure for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

3D Structure for HMDB0242160 (1-Oleoyl-sn-glycero-3-phospho-D-myo-inositol(1-))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

MS/MS Spectra