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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (8) Show 8 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2009-01-08 17:24:38 UTC

Update Date

2022-11-30 19:04:00 UTC

HMDB ID

HMDB0011560

Secondary Accession Numbers

HMDB11560

Metabolite Identification

Common Name

MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)

Description

MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) is a monoacylglyceride. A monoglyceride, more correctly known as a monoacylglycerol, is a glyceride consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage. Monoacylglycerol can be broadly divided into two groups; 1-monoacylglycerols (or 3-monoacylglycerols) and 2-monoacylglycerols, depending on the position of the ester bond on the glycerol moiety. Normally the 1-/3-isomers are not distinguished from each other and are termed 'alpha-monoacylglycerols', while the 2-isomers are beta-monoacylglycerols. Monoacylglycerols are formed biochemically via release of a fatty acid from diacylglycerol by diacylglycerol lipase or hormone sensitive lipase. Monoacylglycerols are broken down by monoacylglycerol lipase. They tend to be minor components only of most plant and animal tissues, and indeed would not be expected to accumulate because their strong detergent properties would have a disruptive effect on membranes. 2-Monoacylglycerols are a major end product of the intestinal digestion of dietary fats in animals via the enzyme pancreatic lipase. They are taken up directly by the intestinal cells and converted to triacylglycerols via the monoacylglycerol pathway before being transported in lymph to the liver. Mono- and Diglycerides are commonly added to commercial food products in small quantities. They act as emulsifiers, helping to mix ingredients such as oil and water that would not otherwise blend well.

Structure

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

MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)
  Mrv1652307191923492D          

 33 32  0  0  0  0            999 V2000
   24.1437   -6.4800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1826   -7.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2214   -6.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1436   -5.3702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.2601   -7.0350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.4325   -8.1450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9378   -8.1588    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   21.7180   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7180   -9.3289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.0039   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2898   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5756   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8615   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1474   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3224   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6083   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8942   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0692   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3551   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6409   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8159   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1018   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3877   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5627   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8486   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1344   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3094   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5953   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8812   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0562   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6279   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9138   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  2  6  1  0  0  0  0
  2  7  1  0  0  0  0
  3  2  1  0  0  0  0
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  8  6  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

HMDB0011560
     RDKit          3D
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)
 76 75  0  0  0  0  0  0  0  0999 V2000
    9.2518   -1.4305   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5279   -0.3262   -0.7365 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4027    0.2627   -1.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    1.3088   -0.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5489    1.3949   -0.5129 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4293    0.5218   -0.7905 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5447   -0.6381   -1.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3505   -1.8683   -1.2599 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9596   -2.3598    0.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7037   -3.1023   -0.0572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5835   -2.9404    0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1568   -2.0202    1.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0658   -1.1085    2.1826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    0.1859    2.1945 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1455    1.1288    1.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0348    0.6842    0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2532    0.8973    1.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7537    1.6114    2.2002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5020    2.8528    2.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7847    3.5296    1.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475    3.2728   -0.3816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7612    3.1191   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5496    1.9814   -0.6069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8531    1.8355   -1.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6064    0.6979   -0.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2903    0.8500    0.2676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5605   -0.5359   -1.4175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2756   -1.6548   -0.8817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2797   -2.7663   -0.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3548   -2.2849    0.3683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2381   -2.1461   -1.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1297   -1.1274   -2.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6291   -2.1325   -0.6370 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5826   -1.9859   -2.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1425   -1.1002   -1.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2354    0.4648   -0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0702   -0.7267    0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8536   -0.6030   -1.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9956    0.7382   -2.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4327    2.1633   -0.4887 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2432    2.3066    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8523    0.2679    0.1545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6475    1.2026   -1.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7852   -0.4676   -2.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4842   -2.6520   -2.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861   -3.0874    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9844   -1.5654    0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7549   -3.9452   -0.8494 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537   -3.6851    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -1.5863    1.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8636   -2.7584    2.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9006   -1.5767    2.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062    0.6579    2.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8011    1.8052    0.9311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7881    1.8564    2.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2293    0.1301   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9618    0.4374    0.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5113    0.8895    2.7344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9882    1.6853    3.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9016    3.3021    3.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985    4.4865    1.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9334    4.2113   -0.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7958    2.4464   -0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3519    4.0578   -1.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5591    2.9863   -2.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6881    2.0836    0.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9541    1.0480   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5949    1.6192   -2.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3906    2.7963   -1.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8124   -1.3600    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6692   -2.9444   -1.5034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8013   -3.6635   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8592   -1.6523    0.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8022   -3.0204   -1.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6445   -2.4573   -2.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1548   -0.4977   -1.5120 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  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 28 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  0
 20 61  1  0
 21 62  1  0
 21 63  1  0
 22 64  1  0
 22 65  1  0
 23 66  1  0
 23 67  1  0
 24 68  1  0
 24 69  1  0
 28 70  1  0
 29 71  1  0
 29 72  1  0
 30 73  1  0
 31 74  1  0
 31 75  1  0
 32 76  1  0
M  END

MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)
  Mrv1652307191923492D          

 33 32  0  0  0  0            999 V2000
   24.1437   -6.4800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1826   -7.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2214   -6.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1436   -5.3702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.2601   -7.0350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.4325   -8.1450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9378   -8.1588    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   21.7180   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7180   -9.3289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.0039   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2898   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5756   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8615   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1474   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3224   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6083   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8942   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0692   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3551   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6409   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8159   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1018   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3877   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5627   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8486   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1344   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3094   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5953   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8812   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0562   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6279   -8.1444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9138   -8.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  2  6  1  0  0  0  0
  2  7  1  0  0  0  0
  3  2  1  0  0  0  0
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  8  6  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0011560

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C28H44O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-28(31)32-27(25-29)26-30/h4-5,7-8,10-11,13-14,16-17,19-20,27,29-30H,2-3,6,9,12,15,18,21-26H2,1H3/b5-4-,8-7-,11-10-,14-13-,17-16-,20-19-

> <INCHI_KEY>
AVASJSIRAIRDIT-JDPCYWKWSA-N

> <FORMULA>
C28H44O4

> <MOLECULAR_WEIGHT>
444.656

> <EXACT_MASS>
444.323959897

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
53.770321229934794

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,3-dihydroxypropan-2-yl (6Z,9Z,12Z,15Z,18Z,21Z)-pentacosa-6,9,12,15,18,21-hexaenoate

> <ALOGPS_LOGP>
6.62

> <JCHEM_LOGP>
6.911627924666668

> <ALOGPS_LOGS>
-6.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.97961936953455

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.278372843548581

> <JCHEM_PKA_STRONGEST_BASIC>
-2.982769198128425

> <JCHEM_POLAR_SURFACE_AREA>
66.75999999999999

> <JCHEM_REFRACTIVITY>
142.21610000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
21

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.94e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,3-dihydroxypropan-2-yl (6Z,9Z,12Z,15Z,18Z,21Z)-pentacosa-6,9,12,15,18,21-hexaenoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0011560
     RDKit          3D
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)
 76 75  0  0  0  0  0  0  0  0999 V2000
    9.2518   -1.4305   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5279   -0.3262   -0.7365 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4027    0.2627   -1.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    1.3088   -0.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5489    1.3949   -0.5129 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4293    0.5218   -0.7905 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5447   -0.6381   -1.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3505   -1.8683   -1.2599 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9596   -2.3598    0.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7037   -3.1023   -0.0572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5835   -2.9404    0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1568   -2.0202    1.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0658   -1.1085    2.1826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    0.1859    2.1945 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1455    1.1288    1.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0348    0.6842    0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2532    0.8973    1.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7537    1.6114    2.2002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5020    2.8528    2.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7847    3.5296    1.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475    3.2728   -0.3816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7612    3.1191   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5496    1.9814   -0.6069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8531    1.8355   -1.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6064    0.6979   -0.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2903    0.8500    0.2676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5605   -0.5359   -1.4175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2756   -1.6548   -0.8817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2797   -2.7663   -0.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3548   -2.2849    0.3683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2381   -2.1461   -1.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1297   -1.1274   -2.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6291   -2.1325   -0.6370 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5826   -1.9859   -2.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1425   -1.1002   -1.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2354    0.4648   -0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0702   -0.7267    0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8536   -0.6030   -1.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9956    0.7382   -2.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4327    2.1633   -0.4887 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2432    2.3066    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8523    0.2679    0.1545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6475    1.2026   -1.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7852   -0.4676   -2.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4842   -2.6520   -2.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861   -3.0874    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9844   -1.5654    0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7549   -3.9452   -0.8494 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537   -3.6851    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -1.5863    1.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8636   -2.7584    2.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9006   -1.5767    2.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062    0.6579    2.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8011    1.8052    0.9311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7881    1.8564    2.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2293    0.1301   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9618    0.4374    0.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5113    0.8895    2.7344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9882    1.6853    3.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9016    3.3021    3.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985    4.4865    1.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9334    4.2113   -0.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7958    2.4464   -0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3519    4.0578   -1.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5591    2.9863   -2.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6881    2.0836    0.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9541    1.0480   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5949    1.6192   -2.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3906    2.7963   -1.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8124   -1.3600    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6692   -2.9444   -1.5034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8013   -3.6635   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8592   -1.6523    0.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8022   -3.0204   -1.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6445   -2.4573   -2.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1548   -0.4977   -1.5120 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  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 28 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  0
 20 61  1  0
 21 62  1  0
 21 63  1  0
 22 64  1  0
 22 65  1  0
 23 66  1  0
 23 67  1  0
 24 68  1  0
 24 69  1  0
 28 70  1  0
 29 71  1  0
 29 72  1  0
 30 73  1  0
 31 74  1  0
 31 75  1  0
 32 76  1  0
M  END

HEADER    PROTEIN                                 19-JUL-19   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)           
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUL-19         0                                  
HETATM    1  C   UNK     0      45.068 -12.096   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      43.274 -13.132   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      41.480 -12.096   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      45.068 -10.024   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      39.686 -13.132   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      41.874 -15.204   0.000  0.00  0.00           O+0
HETATM    7  H   UNK     0      44.684 -15.230   0.000  0.00  0.00           H+0
HETATM    8  C   UNK     0      40.540 -15.974   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      40.540 -17.414   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      39.207 -15.203   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      37.874 -15.974   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      36.541 -15.203   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      35.208 -15.974   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      33.875 -15.203   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      32.335 -15.203   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      31.002 -15.974   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      29.669 -15.203   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.129 -15.203   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      26.796 -15.974   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.463 -15.203   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      23.923 -15.203   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      22.590 -15.974   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.257 -15.203   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      19.717 -15.203   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.384 -15.974   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      17.051 -15.203   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.511 -15.203   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.178 -15.974   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.845 -15.203   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.305 -15.203   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.972 -15.974   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.639 -15.203   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.306 -15.974   0.000  0.00  0.00           C+0
CONECT    1    2    4                                                       
CONECT    2    1    6    7    3                                             
CONECT    3    2    5                                                       
CONECT    4    1                                                            
CONECT    5    3                                                            
CONECT    6    2    8                                                       
CONECT    7    2                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
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   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   64    0
END

COMPND    HMDB0011560
HETATM    1  C1  UNL     1       9.252  -1.430  -1.436  1.00  0.00           C  
HETATM    2  C2  UNL     1       8.528  -0.326  -0.736  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.403   0.263  -1.651  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.789   1.309  -0.861  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.549   1.395  -0.513  1.00  0.00           C  
HETATM    6  C6  UNL     1       4.429   0.522  -0.791  1.00  0.00           C  
HETATM    7  C7  UNL     1       4.545  -0.638  -1.630  1.00  0.00           C  
HETATM    8  C8  UNL     1       4.350  -1.868  -1.260  1.00  0.00           C  
HETATM    9  C9  UNL     1       3.960  -2.360   0.124  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.704  -3.102  -0.057  1.00  0.00           C  
HETATM   11  C11 UNL     1       1.583  -2.940   0.536  1.00  0.00           C  
HETATM   12  C12 UNL     1       1.157  -2.020   1.565  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.066  -1.108   2.183  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.060   0.186   2.195  1.00  0.00           C  
HETATM   15  C15 UNL     1       1.146   1.129   1.589  1.00  0.00           C  
HETATM   16  C16 UNL     1       0.035   0.684   0.780  1.00  0.00           C  
HETATM   17  C17 UNL     1      -1.253   0.897   1.047  1.00  0.00           C  
HETATM   18  C18 UNL     1      -1.754   1.611   2.200  1.00  0.00           C  
HETATM   19  C19 UNL     1      -2.502   2.853   2.074  1.00  0.00           C  
HETATM   20  C20 UNL     1      -2.785   3.530   1.005  1.00  0.00           C  
HETATM   21  C21 UNL     1      -2.448   3.273  -0.382  1.00  0.00           C  
HETATM   22  C22 UNL     1      -3.761   3.119  -1.167  1.00  0.00           C  
HETATM   23  C23 UNL     1      -4.550   1.981  -0.607  1.00  0.00           C  
HETATM   24  C24 UNL     1      -5.853   1.835  -1.379  1.00  0.00           C  
HETATM   25  C25 UNL     1      -6.606   0.698  -0.795  1.00  0.00           C  
HETATM   26  O1  UNL     1      -7.290   0.850   0.268  1.00  0.00           O  
HETATM   27  O2  UNL     1      -6.560  -0.536  -1.418  1.00  0.00           O  
HETATM   28  C26 UNL     1      -7.276  -1.655  -0.882  1.00  0.00           C  
HETATM   29  C27 UNL     1      -6.280  -2.766  -0.570  1.00  0.00           C  
HETATM   30  O3  UNL     1      -5.355  -2.285   0.368  1.00  0.00           O  
HETATM   31  C28 UNL     1      -8.238  -2.146  -1.932  1.00  0.00           C  
HETATM   32  O4  UNL     1      -9.130  -1.127  -2.269  1.00  0.00           O  
HETATM   33  H1  UNL     1       9.629  -2.133  -0.637  1.00  0.00           H  
HETATM   34  H2  UNL     1       8.583  -1.986  -2.105  1.00  0.00           H  
HETATM   35  H3  UNL     1      10.143  -1.100  -1.999  1.00  0.00           H  
HETATM   36  H4  UNL     1       9.235   0.465  -0.452  1.00  0.00           H  
HETATM   37  H5  UNL     1       8.070  -0.727   0.183  1.00  0.00           H  
HETATM   38  H6  UNL     1       6.854  -0.603  -1.950  1.00  0.00           H  
HETATM   39  H7  UNL     1       7.996   0.738  -2.471  1.00  0.00           H  
HETATM   40  H8  UNL     1       7.433   2.163  -0.489  1.00  0.00           H  
HETATM   41  H9  UNL     1       5.243   2.307   0.127  1.00  0.00           H  
HETATM   42  H10 UNL     1       3.852   0.268   0.155  1.00  0.00           H  
HETATM   43  H11 UNL     1       3.647   1.203  -1.312  1.00  0.00           H  
HETATM   44  H12 UNL     1       4.785  -0.468  -2.713  1.00  0.00           H  
HETATM   45  H13 UNL     1       4.484  -2.652  -2.042  1.00  0.00           H  
HETATM   46  H14 UNL     1       4.786  -3.087   0.398  1.00  0.00           H  
HETATM   47  H15 UNL     1       3.984  -1.565   0.837  1.00  0.00           H  
HETATM   48  H16 UNL     1       2.755  -3.945  -0.849  1.00  0.00           H  
HETATM   49  H17 UNL     1       0.754  -3.685   0.167  1.00  0.00           H  
HETATM   50  H18 UNL     1       0.137  -1.586   1.344  1.00  0.00           H  
HETATM   51  H19 UNL     1       0.864  -2.758   2.459  1.00  0.00           H  
HETATM   52  H20 UNL     1       2.901  -1.577   2.785  1.00  0.00           H  
HETATM   53  H21 UNL     1       2.906   0.658   2.770  1.00  0.00           H  
HETATM   54  H22 UNL     1       1.801   1.805   0.931  1.00  0.00           H  
HETATM   55  H23 UNL     1       0.788   1.856   2.366  1.00  0.00           H  
HETATM   56  H24 UNL     1       0.229   0.130  -0.171  1.00  0.00           H  
HETATM   57  H25 UNL     1      -1.962   0.437   0.324  1.00  0.00           H  
HETATM   58  H26 UNL     1      -2.511   0.889   2.734  1.00  0.00           H  
HETATM   59  H27 UNL     1      -0.988   1.685   3.036  1.00  0.00           H  
HETATM   60  H28 UNL     1      -2.902   3.302   3.055  1.00  0.00           H  
HETATM   61  H29 UNL     1      -3.398   4.487   1.163  1.00  0.00           H  
HETATM   62  H30 UNL     1      -1.933   4.211  -0.838  1.00  0.00           H  
HETATM   63  H31 UNL     1      -1.796   2.446  -0.578  1.00  0.00           H  
HETATM   64  H32 UNL     1      -4.352   4.058  -1.025  1.00  0.00           H  
HETATM   65  H33 UNL     1      -3.559   2.986  -2.248  1.00  0.00           H  
HETATM   66  H34 UNL     1      -4.688   2.084   0.468  1.00  0.00           H  
HETATM   67  H35 UNL     1      -3.954   1.048  -0.803  1.00  0.00           H  
HETATM   68  H36 UNL     1      -5.595   1.619  -2.422  1.00  0.00           H  
HETATM   69  H37 UNL     1      -6.391   2.796  -1.252  1.00  0.00           H  
HETATM   70  H38 UNL     1      -7.812  -1.360   0.028  1.00  0.00           H  
HETATM   71  H39 UNL     1      -5.669  -2.944  -1.503  1.00  0.00           H  
HETATM   72  H40 UNL     1      -6.801  -3.663  -0.233  1.00  0.00           H  
HETATM   73  H41 UNL     1      -5.859  -1.652   0.944  1.00  0.00           H  
HETATM   74  H42 UNL     1      -8.802  -3.020  -1.523  1.00  0.00           H  
HETATM   75  H43 UNL     1      -7.644  -2.457  -2.827  1.00  0.00           H  
HETATM   76  H44 UNL     1      -9.155  -0.498  -1.512  1.00  0.00           H  
CONECT    1    2   33   34   35
CONECT    2    3   36   37
CONECT    3    4   38   39
CONECT    4    5    5   40
CONECT    5    6   41
CONECT    6    7   42   43
CONECT    7    8    8   44
CONECT    8    9   45
CONECT    9   10   46   47
CONECT   10   11   11   48
CONECT   11   12   49
CONECT   12   13   50   51
CONECT   13   14   14   52
CONECT   14   15   53
CONECT   15   16   54   55
CONECT   16   17   17   56
CONECT   17   18   57
CONECT   18   19   58   59
CONECT   19   20   20   60
CONECT   20   21   61
CONECT   21   22   62   63
CONECT   22   23   64   65
CONECT   23   24   66   67
CONECT   24   25   68   69
CONECT   25   26   26   27
CONECT   27   28
CONECT   28   29   31   70
CONECT   29   30   71   72
CONECT   30   73
CONECT   31   32   74   75
CONECT   32   76
END

HMDB0011560
     RDKit          3D
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)
 76 75  0  0  0  0  0  0  0  0999 V2000
    9.2518   -1.4305   -1.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5279   -0.3262   -0.7365 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4027    0.2627   -1.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    1.3088   -0.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5489    1.3949   -0.5129 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4293    0.5218   -0.7905 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5447   -0.6381   -1.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3505   -1.8683   -1.2599 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9596   -2.3598    0.1243 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7037   -3.1023   -0.0572 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5835   -2.9404    0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1568   -2.0202    1.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0658   -1.1085    2.1826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0599    0.1859    2.1945 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1455    1.1288    1.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0348    0.6842    0.7798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2532    0.8973    1.0467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7537    1.6114    2.2002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5020    2.8528    2.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7847    3.5296    1.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475    3.2728   -0.3816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7612    3.1191   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5496    1.9814   -0.6069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8531    1.8355   -1.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6064    0.6979   -0.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2903    0.8500    0.2676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5605   -0.5359   -1.4175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2756   -1.6548   -0.8817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2797   -2.7663   -0.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3548   -2.2849    0.3683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2381   -2.1461   -1.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1297   -1.1274   -2.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6291   -2.1325   -0.6370 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5826   -1.9859   -2.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1425   -1.1002   -1.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2354    0.4648   -0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0702   -0.7267    0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8536   -0.6030   -1.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9956    0.7382   -2.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4327    2.1633   -0.4887 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2432    2.3066    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8523    0.2679    0.1545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6475    1.2026   -1.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7852   -0.4676   -2.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4842   -2.6520   -2.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861   -3.0874    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9844   -1.5654    0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7549   -3.9452   -0.8494 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537   -3.6851    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365   -1.5863    1.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8636   -2.7584    2.4588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9006   -1.5767    2.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062    0.6579    2.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8011    1.8052    0.9311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7881    1.8564    2.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2293    0.1301   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9618    0.4374    0.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5113    0.8895    2.7344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9882    1.6853    3.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9016    3.3021    3.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3985    4.4865    1.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9334    4.2113   -0.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7958    2.4464   -0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3519    4.0578   -1.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5591    2.9863   -2.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6881    2.0836    0.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9541    1.0480   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5949    1.6192   -2.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3906    2.7963   -1.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8124   -1.3600    0.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6692   -2.9444   -1.5034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8013   -3.6635   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8592   -1.6523    0.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8022   -3.0204   -1.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6445   -2.4573   -2.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1548   -0.4977   -1.5120 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  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 28 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  0
 20 61  1  0
 21 62  1  0
 21 63  1  0
 22 64  1  0
 22 65  1  0
 23 66  1  0
 23 67  1  0
 24 68  1  0
 24 69  1  0
 28 70  1  0
 29 71  1  0
 29 72  1  0
 30 73  1  0
 31 74  1  0
 31 75  1  0
 32 76  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Glycerolipid	HMDB
2-(6Z,9Z,12Z,15Z,18Z,21Z-Tetracosahexaenoyl)-sn-glycerol	HMDB
Glycerolipid(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)	HMDB
1-Monoacylglyceride	HMDB
1-Monoacylglycerol	HMDB
MG(24:6)	HMDB
MAG(24:6)	HMDB
MG(0:0/24:6/0:0)	HMDB
MAG(0:0/24:6/0:0)	HMDB
1,3-Dihydroxypropan-2-yl (6Z,9Z,15Z,21Z)-pentacosa-6,9,12,15,18,21-hexaenoic acid	HMDB

Chemical Formula

C₂₈H₄₄O₄

Average Molecular Weight

444.656

Monoisotopic Molecular Weight

444.323959897

IUPAC Name

1,3-dihydroxypropan-2-yl (6Z,9Z,12Z,15Z,18Z,21Z)-pentacosa-6,9,12,15,18,21-hexaenoate

Traditional Name

1,3-dihydroxypropan-2-yl (6Z,9Z,12Z,15Z,18Z,21Z)-pentacosa-6,9,12,15,18,21-hexaenoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C28H44O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-28(31)32-27(25-29)26-30/h4-5,7-8,10-11,13-14,16-17,19-20,27,29-30H,2-3,6,9,12,15,18,21-26H2,1H3/b5-4-,8-7-,11-10-,14-13-,17-16-,20-19-

InChI Key

AVASJSIRAIRDIT-JDPCYWKWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-monoacylglycerols. These are monoacylglycerols containing a glycerol acylated at the 2-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Monoradylglycerols

Direct Parent

2-monoacylglycerols

Alternative Parents

Substituents

2-acyl-sn-glycerol
Fatty acid ester
Fatty acyl
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

All Tissues (HMDB: HMDB0011560)

Cellular substructure

Membrane (HMDB: HMDB0011560)
Extracellular (HMDB: HMDB0011560)

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

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

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

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

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

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00049 g/L	ALOGPS
logP	6.62	ALOGPS
logP	6.91	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	14.28	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	21	ChemAxon
Refractivity	142.22 m³·mol⁻¹	ChemAxon
Polarizability	53.77 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	217.455	30932474
DeepCCS	[M-H]-	215.097	30932474
DeepCCS	[M-2H]-	249.086	30932474
DeepCCS	[M+Na]+	224.565	30932474
AllCCS	[M+H]+	219.5	32859911
AllCCS	[M+H-H2O]+	217.5	32859911
AllCCS	[M+NH4]+	221.4	32859911
AllCCS	[M+Na]+	221.9	32859911
AllCCS	[M-H]-	215.7	32859911
AllCCS	[M+Na-2H]-	219.5	32859911
AllCCS	[M+HCOO]-	223.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)	[H]C(CO)(CO)OC(=O)CCCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC	3705.9	Standard polar	33892256
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)	[H]C(CO)(CO)OC(=O)CCCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC	2879.6	Standard non polar	33892256
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0)	[H]C(CO)(CO)OC(=O)CCCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC	3389.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0),1TMS,isomer #1	CCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC(CO)CO[Si](C)(C)C	3458.2	Semi standard non polar	33892256
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0),2TMS,isomer #1	CCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC(CO[Si](C)(C)C)CO[Si](C)(C)C	3437.3	Semi standard non polar	33892256
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0),1TBDMS,isomer #1	CCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC(CO)CO[Si](C)(C)C(C)(C)C	3680.3	Semi standard non polar	33892256
MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0),2TBDMS,isomer #1	CCC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCC(=O)OC(CO[Si](C)(C)C(C)(C)C)CO[Si](C)(C)C(C)(C)C	3913.7	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) GC-MS (2 TMS) - 70eV, Positive	splash10-0g4i-6495030000-23c50fb33226b9725d81	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 10V, Positive-QTOF	splash10-03di-0000900000-430fbfe1364f2ab6f250	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 20V, Positive-QTOF	splash10-01ox-0000900000-abcf76f39fe195907bdb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 40V, Positive-QTOF	splash10-000o-0007900000-60722dcec83a2e9f08d9	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 10V, Negative-QTOF	splash10-006x-9003500000-54e8002ffc66f61652bd	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 20V, Negative-QTOF	splash10-0avl-9002100000-5e741449ddaf50ac1db6	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 40V, Negative-QTOF	splash10-0kmi-9037000000-bfb88760aff1a9f44e73	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 10V, Positive-QTOF	splash10-0002-0000900000-1a957e83c4ea14ce17c5	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 20V, Positive-QTOF	splash10-00dk-0007900000-9a4aedf9ec6d035ec3ba	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 40V, Positive-QTOF	splash10-05i0-0009500000-93fa8d182d48dca380d6	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 10V, Positive-QTOF	splash10-014i-0000900000-d3bcf1701b80aa546f62	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 20V, Positive-QTOF	splash10-014i-0000900000-d3bcf1701b80aa546f62	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) 40V, Positive-QTOF	splash10-0aox-0005900000-034951b97628254a0ce6	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

All Tissues

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB028273

KNApSAcK ID

Not Available

Chemspider ID

24765784

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53480974

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Ghosh S, Strum JC, Bell RM: Lipid biochemistry: functions of glycerolipids and sphingolipids in cellular signaling. FASEB J. 1997 Jan;11(1):45-50. [PubMed:9034165 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Enzymes

Enzyme Details

1. Monoglyceride lipase

General function:: Lipid transport and metabolism
Specific function:: Converts monoacylglycerides to free fatty acids and glycerol. Hydrolyzes the endocannabinoid 2-arachidonoylglycerol, and thereby contributes to the regulation of endocannabinoid signaling, nociperception and perception of pain (By similarity). Regulates the levels of fatty acids that serve as signaling molecules and promote cancer cell migration, invasion and tumor growth.
Gene Name:: MGLL
Uniprot ID:: Q99685
Molecular weight:: Not Available

Enzyme Details

2. Hormone-sensitive lipase

General function:: Involved in hydrolase activity
Specific function:: In adipose tissue and heart, it primarily hydrolyzes stored triglycerides to free fatty acids, while in steroidogenic tissues, it principally converts cholesteryl esters to free cholesterol for steroid hormone production.
Gene Name:: LIPE
Uniprot ID:: Q05469
Molecular weight:: 116596.715

Enzyme Details

3. 2-acylglycerol O-acyltransferase 2

General function:: Involved in transferase activity, transferring acyl groups other than amino-acyl groups
Specific function:: Catalyzes the formation of diacylglycerol from 2-monoacylglycerol and fatty acyl-CoA. Has a preference toward monoacylglycerols containing unsaturated fatty acids in an order of C18:3 > C18:2 > C18:1 > C18:0. Plays a central role in absorption of dietary fat in the small intestine by catalyzing the resynthesis of triacylglycerol in enterocytes. May play a role in diet-induced obesity.
Gene Name:: MOGAT2
Uniprot ID:: Q3SYC2
Molecular weight:: 38195.285

Enzyme Details

4. 2-acylglycerol O-acyltransferase 1

General function:: Involved in transferase activity, transferring acyl groups other than amino-acyl groups
Specific function:: Catalyzes the formation of diacylglycerol from 2-monoacylglycerol and fatty acyl-CoA. Probably not involved in absorption of dietary fat in the small intestine (By similarity).
Gene Name:: MOGAT1
Uniprot ID:: Q96PD6
Molecular weight:: 38812.19

Enzyme Details

5. 2-acylglycerol O-acyltransferase 3

General function:: Involved in transferase activity, transferring acyl groups other than amino-acyl groups
Specific function:: Catalyzes the formation of diacylglycerol from 2-monoacylglycerol and fatty acyl-CoA. Also able to catalyze the terminal step in triacylglycerol synthesis by using diacylglycerol and fatty acyl-CoA as substrates. Has a preference toward palmitoyl-CoA and oleoyl-CoA. May be involved in absorption of dietary fat in the small intestine by catalyzing the resynthesis of triacylglycerol in enterocytes.
Gene Name:: MOGAT3
Uniprot ID:: Q86VF5
Molecular weight:: 38729.84

Enzyme Details

6. Lysophosphatidic acid phosphatase type 6

General function:: Involved in acid phosphatase activity
Specific function:: Hydrolyzes lysophosphatidic acid to monoacylglycerol.
Gene Name:: ACP6
Uniprot ID:: Q9NPH0
Molecular weight:: 48853.955

Enzyme Details

7. Acylglycerol kinase, mitochondrial

General function:: Involved in NAD+ kinase activity
Specific function:: Lipid kinase that can phosphorylate both monoacylglycerol and diacylglycerol to form lysophosphatidic acid (LPA) and phosphatidic acid (PA), respectively. Does not phosphorylate sphingosine. Overexpression increases the formation and secretion of LPA, resulting in transactivation of EGFR and activation of the downstream MAPK signaling pathway, leading to increased cell growth
Gene Name:: AGK
Uniprot ID:: Q53H12
Molecular weight:: 47136.8

Enzyme Details

8. Ectonucleotide pyrophosphatase/phosphodiesterase family member 6

General function:: Involved in catalytic activity
Specific function:: Choline-specific glycerophosphodiester phosphodiesterase. The preferred substrate may be lysosphingomyelin (By similarity). Hydrolyzes lysophosphatidylcholine (LPC) to form monoacylglycerol and phosphorylcholine but not lysophosphatidic acid, showing it has a lysophospholipase C activity. Has a preference for LPC with short (12:0 and 14:0) or polyunsaturated (18:2 and 20:4) fatty acids. Also hydrolyzes glycerophosphorylcholine and sphingosylphosphorylcholine efficiently. Hydrolyzes the classical substrate for phospholipase C, p-nitrophenyl phosphorylcholine in vitro, while it does not hydrolyze the classical nucleotide phosphodiesterase substrate, p-nitrophenyl thymidine 5'-monophosphate. Does not hydrolyze diacyl phospholipids such as phosphatidylethanolamine, phosphatidylinositol, phosphatidylserine, phosphatidylglycerol and phosphatidic acid.
Gene Name:: ENPP6
Uniprot ID:: Q6UWR7
Molecular weight:: 50240.625

Showing metabocard for MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0) (HMDB0011560)

MOL for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

3D MOL for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

3D SDF for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

3D-SDF for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

PDB for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

3D PDB for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

SMILES for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

INCHI for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

Structure for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

3D Structure for HMDB0011560 (MG(0:0/24:6(6Z,9Z,12Z,15Z,18Z,21Z)/0:0))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes