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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (61) Show 61 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2017-09-09 05:30:16 UTC

Update Date

2022-11-30 19:26:18 UTC

HMDB ID

HMDB0115680

Secondary Accession Numbers

None

Metabolite Identification

Common Name

PA(8:0/a-13:0)

Description

PA(8:0/a-13:0) is a phosphatidic acid. It is a glycerophospholipid in which a phosphate moiety occupies a glycerol substitution site. As is the case with diacylglycerols, phosphatidic acids can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PA(8:0/a-13:0), in particular, consists of one chain of caprylic acid at the C-1 position and one chain of anteisotridecanoic acid at the C-2 position. Phosphatidic acids are quite rare but are extremely important as intermediates in the biosynthesis of triacylglycerols and phospholipids.

Structure

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

PA(8:0/a-13:0)
  Mrv1652309161705352D          

 34 33  0  0  1  0            999 V2000
   -0.1691    0.3607    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8792    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5896    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2414   -0.3495    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5796   -0.3495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5412    0.7708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2515    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0098    0.3436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2621    0.6480    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    1.9003    0.0209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2621    1.3958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2997    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2997    1.5410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0138    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7279    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4421    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1562    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8703    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5845    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2986    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3236   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3236   -1.5406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0377   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7518   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4660   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8942   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6084   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3225   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0367   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7508   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4649   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4649    0.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1791   -0.3573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  5  1  0  0  0  0
  1  4  1  1  0  0  0
  2  3  1  0  0  0  0
  3 12  1  0  0  0  0
  6  1  1  0  0  0  0
  7  6  1  0  0  0  0
  9  8  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  9  7  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21  5  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END

HMDB0115680
     RDKit          3D
PA(8:0/a-13:0)
 80 79  0  0  0  0  0  0  0  0999 V2000
    9.3957   -0.4876   -4.4902 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0024   -0.8116   -4.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0372   -1.3580   -2.6561 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6083   -0.4264   -1.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8210    0.8617   -1.5496 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3912    0.6385   -1.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2437   -0.0334    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7817   -0.2288    0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9501    0.1646   -0.3636 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3655   -0.8209    1.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0177   -1.0184    1.9626 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2786    0.2843    2.0742 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8875    1.1334    3.1737 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7796    0.4766    4.3938 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4666    1.4504    5.5858 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.0491    2.6919    4.9905 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6545    0.5254    6.3632 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2323    1.8055    6.7024 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9029    0.0714    2.3965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0405    0.5811    1.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3535    1.2000    0.5077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5079    0.4130    1.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9536   -0.7181    0.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4241   -0.9560    1.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1903    0.2687    0.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6886    0.1147    0.8713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2074   -0.9766   -0.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6930   -1.1522    0.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4808    0.0649   -0.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2357    0.5018   -1.6938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0488    1.7322   -2.0291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4106   -0.5915   -2.6945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7773   -1.1892   -2.7115 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5366   -0.6415   -5.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0894   -1.1486   -3.9645 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6311    0.5661   -4.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2893    0.0274   -4.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6168   -1.6242   -4.7091 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0443   -1.7122   -2.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6974   -2.2620   -2.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6547   -0.1445   -1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5913   -0.9219   -0.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2985    1.4539   -0.7252 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9129    1.4570   -2.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.0610   -1.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9042    1.6423   -1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7279   -1.0154    0.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7107    0.5915    0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5416   -1.6509    1.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9874   -1.5736    2.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3800    0.8518    1.1370 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9492    1.3337    2.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3114    2.0664    3.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417    0.8070    6.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0742    2.7709    6.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210    0.2209    2.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9601    1.3877    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3828   -1.6430    1.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7951   -0.4486   -0.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7562   -1.8650    0.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5373   -1.2326    2.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9499    0.6840   -0.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9175    1.0560    1.4898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9875   -0.0843    1.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1303    1.1016    0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8651   -0.8947   -1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7703   -1.9465    0.3695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9628   -1.5124    1.0942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9727   -1.9558   -0.6197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3113    0.9350    0.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5558   -0.1981   -0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1593    0.8185   -1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4399    2.5221   -2.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4618    2.1313   -1.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9204    1.4626   -2.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6643   -1.3792   -2.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2477   -0.1229   -3.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0584   -1.4715   -3.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5681   -0.5385   -2.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7966   -2.1722   -2.1601 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  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 12 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  6 46  1  0
  7 47  1  0
  7 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  6
 13 52  1  0
 13 53  1  0
 17 54  1  0
 18 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  0
 23 59  1  0
 24 60  1  0
 24 61  1  0
 25 62  1  0
 25 63  1  0
 26 64  1  0
 26 65  1  0
 27 66  1  0
 27 67  1  0
 28 68  1  0
 28 69  1  0
 29 70  1  0
 29 71  1  0
 30 72  1  0
 31 73  1  0
 31 74  1  0
 31 75  1  0
 32 76  1  0
 32 77  1  0
 33 78  1  0
 33 79  1  0
 33 80  1  0
M  END

PA(8:0/a-13:0)
  Mrv1652309161705352D          

 34 33  0  0  1  0            999 V2000
   -0.1691    0.3607    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8792    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5896    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2414   -0.3495    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5796   -0.3495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5412    0.7708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2515    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0098    0.3436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2621    0.6480    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    1.9003    0.0209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2621    1.3958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2997    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2997    1.5410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0138    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7279    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4421    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1562    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8703    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5845    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2986    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3236   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3236   -1.5406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0377   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7518   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4660   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8942   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6084   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3225   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0367   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7508   -0.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4649   -0.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4649    0.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1791   -0.3573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  5  1  0  0  0  0
  1  4  1  1  0  0  0
  2  3  1  0  0  0  0
  3 12  1  0  0  0  0
  6  1  1  0  0  0  0
  7  6  1  0  0  0  0
  9  8  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  9  7  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21  5  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0115680

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@](COC(=O)CCCCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCC(C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C24H47O8P/c1-4-6-7-10-14-17-23(25)30-19-22(20-31-33(27,28)29)32-24(26)18-15-12-9-8-11-13-16-21(3)5-2/h21-22H,4-20H2,1-3H3,(H2,27,28,29)/t21?,22-/m1/s1

> <INCHI_KEY>
JQLHVVRKTDFQPB-FOIFJWKZSA-N

> <FORMULA>
C24H47O8P

> <MOLECULAR_WEIGHT>
494.606

> <EXACT_MASS>
494.300855471

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
56.81998852024432

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R)-2-[(10-methyldodecanoyl)oxy]-3-(octanoyloxy)propoxy]phosphonic acid

> <ALOGPS_LOGP>
5.13

> <JCHEM_LOGP>
6.831722867

> <ALOGPS_LOGS>
-5.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.343234649149876

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.3174060830586427

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159310865115

> <JCHEM_POLAR_SURFACE_AREA>
119.35999999999999

> <JCHEM_REFRACTIVITY>
127.90839999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.13e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(10-methyldodecanoyl)oxy]-3-(octanoyloxy)propoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0115680
     RDKit          3D
PA(8:0/a-13:0)
 80 79  0  0  0  0  0  0  0  0999 V2000
    9.3957   -0.4876   -4.4902 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0024   -0.8116   -4.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0372   -1.3580   -2.6561 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6083   -0.4264   -1.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8210    0.8617   -1.5496 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3912    0.6385   -1.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2437   -0.0334    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7817   -0.2288    0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9501    0.1646   -0.3636 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3655   -0.8209    1.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0177   -1.0184    1.9626 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2786    0.2843    2.0742 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8875    1.1334    3.1737 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7796    0.4766    4.3938 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4666    1.4504    5.5858 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.0491    2.6919    4.9905 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6545    0.5254    6.3632 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2323    1.8055    6.7024 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9029    0.0714    2.3965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0405    0.5811    1.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3535    1.2000    0.5077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5079    0.4130    1.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9536   -0.7181    0.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4241   -0.9560    1.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1903    0.2687    0.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6886    0.1147    0.8713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2074   -0.9766   -0.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6930   -1.1522    0.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4808    0.0649   -0.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2357    0.5018   -1.6938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0488    1.7322   -2.0291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4106   -0.5915   -2.6945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7773   -1.1892   -2.7115 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5366   -0.6415   -5.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0894   -1.1486   -3.9645 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6311    0.5661   -4.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2893    0.0274   -4.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0443   -1.7122   -2.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6974   -2.2620   -2.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.9129    1.4570   -2.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.0610   -1.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9042    1.6423   -1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7279   -1.0154    0.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7107    0.5915    0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5416   -1.6509    1.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9874   -1.5736    2.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3800    0.8518    1.1370 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9492    1.3337    2.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3114    2.0664    3.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417    0.8070    6.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0742    2.7709    6.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210    0.2209    2.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9601    1.3877    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3828   -1.6430    1.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7951   -0.4486   -0.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7562   -1.8650    0.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5373   -1.2326    2.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9499    0.6840   -0.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9175    1.0560    1.4898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9875   -0.0843    1.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1303    1.1016    0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8651   -0.8947   -1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7703   -1.9465    0.3695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9628   -1.5124    1.0942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9727   -1.9558   -0.6197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3113    0.9350    0.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5558   -0.1981   -0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1593    0.8185   -1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4399    2.5221   -2.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4618    2.1313   -1.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9204    1.4626   -2.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6643   -1.3792   -2.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2477   -0.1229   -3.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0584   -1.4715   -3.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5681   -0.5385   -2.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7966   -2.1722   -2.1601 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  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 12 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  6 46  1  0
  7 47  1  0
  7 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  6
 13 52  1  0
 13 53  1  0
 17 54  1  0
 18 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  0
 23 59  1  0
 24 60  1  0
 24 61  1  0
 25 62  1  0
 25 63  1  0
 26 64  1  0
 26 65  1  0
 27 66  1  0
 27 67  1  0
 28 68  1  0
 28 69  1  0
 29 70  1  0
 29 71  1  0
 30 72  1  0
 31 73  1  0
 31 74  1  0
 31 75  1  0
 32 76  1  0
 32 77  1  0
 33 78  1  0
 33 79  1  0
 33 80  1  0
M  END

HEADER    PROTEIN                                 16-SEP-17   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: PA(8:0/a-13:0)                                    
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-SEP-17         0                                  
HETATM    1  C   UNK     0      -0.316   0.673   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.641   1.436   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.967   0.673   0.000  0.00  0.00           O+0
HETATM    4  H   UNK     0       0.451  -0.652   0.000  0.00  0.00           H+0
HETATM    5  O   UNK     0      -1.082  -0.652   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.010   1.439   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.336   0.673   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       5.618   0.641   0.000  0.00  0.00           O+0
HETATM    9  P   UNK     0       4.223   1.210   0.000  0.00  0.00           P+0
HETATM   10  O   UNK     0       3.547   0.039   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       4.223   2.606   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.293   1.436   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.293   2.876   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -5.626   0.665   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.959   1.436   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.292   0.665   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.625   1.436   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -10.958   0.665   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -12.291   1.436   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -13.624   0.665   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.471  -1.436   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.471  -2.876   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -3.804  -0.665   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.137  -1.436   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.470  -0.665   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -7.803  -1.436   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -9.136  -0.665   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -10.469  -1.436   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -11.802  -0.665   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -13.135  -1.436   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -14.468  -0.665   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -15.801  -1.436   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -15.801   0.104   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -17.134  -0.667   0.000  0.00  0.00           C+0
CONECT    1    2    5    4    6                                             
CONECT    2    1    3                                                       
CONECT    3    2   12                                                       
CONECT    4    1                                                            
CONECT    5    1   21                                                       
CONECT    6    1    7                                                       
CONECT    7    6    9                                                       
CONECT    8    9                                                            
CONECT    9    8   10   11    7                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    3   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21    5   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   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   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   66    0
END

COMPND    HMDB0115680
HETATM    1  C1  UNL     1       9.396  -0.488  -4.490  1.00  0.00           C  
HETATM    2  C2  UNL     1       8.002  -0.812  -4.052  1.00  0.00           C  
HETATM    3  C3  UNL     1       8.037  -1.358  -2.656  1.00  0.00           C  
HETATM    4  C4  UNL     1       8.608  -0.426  -1.637  1.00  0.00           C  
HETATM    5  C5  UNL     1       7.821   0.862  -1.550  1.00  0.00           C  
HETATM    6  C6  UNL     1       6.391   0.639  -1.175  1.00  0.00           C  
HETATM    7  C7  UNL     1       6.244  -0.033   0.164  1.00  0.00           C  
HETATM    8  C8  UNL     1       4.782  -0.229   0.473  1.00  0.00           C  
HETATM    9  O1  UNL     1       3.950   0.165  -0.364  1.00  0.00           O  
HETATM   10  O2  UNL     1       4.366  -0.821   1.638  1.00  0.00           O  
HETATM   11  C9  UNL     1       3.018  -1.018   1.963  1.00  0.00           C  
HETATM   12  C10 UNL     1       2.279   0.284   2.074  1.00  0.00           C  
HETATM   13  C11 UNL     1       2.887   1.133   3.174  1.00  0.00           C  
HETATM   14  O3  UNL     1       2.780   0.477   4.394  1.00  0.00           O  
HETATM   15  P1  UNL     1       3.467   1.450   5.586  1.00  0.00           P  
HETATM   16  O4  UNL     1       4.049   2.692   4.991  1.00  0.00           O  
HETATM   17  O5  UNL     1       4.654   0.525   6.363  1.00  0.00           O  
HETATM   18  O6  UNL     1       2.232   1.805   6.702  1.00  0.00           O  
HETATM   19  O7  UNL     1       0.903   0.071   2.396  1.00  0.00           O  
HETATM   20  C12 UNL     1      -0.041   0.581   1.525  1.00  0.00           C  
HETATM   21  O8  UNL     1       0.353   1.200   0.508  1.00  0.00           O  
HETATM   22  C13 UNL     1      -1.508   0.413   1.766  1.00  0.00           C  
HETATM   23  C14 UNL     1      -1.954  -0.718   0.873  1.00  0.00           C  
HETATM   24  C15 UNL     1      -3.424  -0.956   1.072  1.00  0.00           C  
HETATM   25  C16 UNL     1      -4.190   0.269   0.722  1.00  0.00           C  
HETATM   26  C17 UNL     1      -5.689   0.115   0.871  1.00  0.00           C  
HETATM   27  C18 UNL     1      -6.207  -0.977  -0.012  1.00  0.00           C  
HETATM   28  C19 UNL     1      -7.693  -1.152   0.103  1.00  0.00           C  
HETATM   29  C20 UNL     1      -8.481   0.065  -0.268  1.00  0.00           C  
HETATM   30  C21 UNL     1      -8.236   0.502  -1.694  1.00  0.00           C  
HETATM   31  C22 UNL     1      -9.049   1.732  -2.029  1.00  0.00           C  
HETATM   32  C23 UNL     1      -8.411  -0.592  -2.694  1.00  0.00           C  
HETATM   33  C24 UNL     1      -9.777  -1.189  -2.711  1.00  0.00           C  
HETATM   34  H1  UNL     1       9.537  -0.642  -5.595  1.00  0.00           H  
HETATM   35  H2  UNL     1      10.089  -1.149  -3.964  1.00  0.00           H  
HETATM   36  H3  UNL     1       9.631   0.566  -4.242  1.00  0.00           H  
HETATM   37  H4  UNL     1       7.289   0.027  -4.159  1.00  0.00           H  
HETATM   38  H5  UNL     1       7.617  -1.624  -4.709  1.00  0.00           H  
HETATM   39  H6  UNL     1       7.044  -1.712  -2.313  1.00  0.00           H  
HETATM   40  H7  UNL     1       8.697  -2.262  -2.678  1.00  0.00           H  
HETATM   41  H8  UNL     1       9.655  -0.145  -1.867  1.00  0.00           H  
HETATM   42  H9  UNL     1       8.591  -0.922  -0.664  1.00  0.00           H  
HETATM   43  H10 UNL     1       8.299   1.454  -0.725  1.00  0.00           H  
HETATM   44  H11 UNL     1       7.913   1.457  -2.459  1.00  0.00           H  
HETATM   45  H12 UNL     1       5.841   0.061  -1.951  1.00  0.00           H  
HETATM   46  H13 UNL     1       5.904   1.642  -1.132  1.00  0.00           H  
HETATM   47  H14 UNL     1       6.728  -1.015   0.156  1.00  0.00           H  
HETATM   48  H15 UNL     1       6.711   0.591   0.942  1.00  0.00           H  
HETATM   49  H16 UNL     1       2.542  -1.651   1.157  1.00  0.00           H  
HETATM   50  H17 UNL     1       2.987  -1.574   2.925  1.00  0.00           H  
HETATM   51  H18 UNL     1       2.380   0.852   1.137  1.00  0.00           H  
HETATM   52  H19 UNL     1       3.949   1.334   2.915  1.00  0.00           H  
HETATM   53  H20 UNL     1       2.311   2.066   3.235  1.00  0.00           H  
HETATM   54  H21 UNL     1       5.542   0.807   6.035  1.00  0.00           H  
HETATM   55  H22 UNL     1       2.074   2.771   6.762  1.00  0.00           H  
HETATM   56  H23 UNL     1      -1.721   0.221   2.830  1.00  0.00           H  
HETATM   57  H24 UNL     1      -1.960   1.388   1.471  1.00  0.00           H  
HETATM   58  H25 UNL     1      -1.383  -1.643   1.114  1.00  0.00           H  
HETATM   59  H26 UNL     1      -1.795  -0.449  -0.196  1.00  0.00           H  
HETATM   60  H27 UNL     1      -3.756  -1.865   0.528  1.00  0.00           H  
HETATM   61  H28 UNL     1      -3.537  -1.233   2.162  1.00  0.00           H  
HETATM   62  H29 UNL     1      -3.950   0.684  -0.252  1.00  0.00           H  
HETATM   63  H30 UNL     1      -3.917   1.056   1.490  1.00  0.00           H  
HETATM   64  H31 UNL     1      -5.988  -0.084   1.913  1.00  0.00           H  
HETATM   65  H32 UNL     1      -6.130   1.102   0.595  1.00  0.00           H  
HETATM   66  H33 UNL     1      -5.865  -0.895  -1.049  1.00  0.00           H  
HETATM   67  H34 UNL     1      -5.770  -1.947   0.370  1.00  0.00           H  
HETATM   68  H35 UNL     1      -7.963  -1.512   1.094  1.00  0.00           H  
HETATM   69  H36 UNL     1      -7.973  -1.956  -0.620  1.00  0.00           H  
HETATM   70  H37 UNL     1      -8.311   0.935   0.382  1.00  0.00           H  
HETATM   71  H38 UNL     1      -9.556  -0.198  -0.169  1.00  0.00           H  
HETATM   72  H39 UNL     1      -7.159   0.819  -1.737  1.00  0.00           H  
HETATM   73  H40 UNL     1      -8.440   2.522  -2.511  1.00  0.00           H  
HETATM   74  H41 UNL     1      -9.462   2.131  -1.081  1.00  0.00           H  
HETATM   75  H42 UNL     1      -9.920   1.463  -2.660  1.00  0.00           H  
HETATM   76  H43 UNL     1      -7.664  -1.379  -2.558  1.00  0.00           H  
HETATM   77  H44 UNL     1      -8.248  -0.123  -3.707  1.00  0.00           H  
HETATM   78  H45 UNL     1     -10.058  -1.471  -3.766  1.00  0.00           H  
HETATM   79  H46 UNL     1     -10.568  -0.538  -2.318  1.00  0.00           H  
HETATM   80  H47 UNL     1      -9.797  -2.172  -2.160  1.00  0.00           H  
CONECT    1    2   34   35   36
CONECT    2    3   37   38
CONECT    3    4   39   40
CONECT    4    5   41   42
CONECT    5    6   43   44
CONECT    6    7   45   46
CONECT    7    8   47   48
CONECT    8    9    9   10
CONECT   10   11
CONECT   11   12   49   50
CONECT   12   13   19   51
CONECT   13   14   52   53
CONECT   14   15
CONECT   15   16   16   17   18
CONECT   17   54
CONECT   18   55
CONECT   19   20
CONECT   20   21   21   22
CONECT   22   23   56   57
CONECT   23   24   58   59
CONECT   24   25   60   61
CONECT   25   26   62   63
CONECT   26   27   64   65
CONECT   27   28   66   67
CONECT   28   29   68   69
CONECT   29   30   70   71
CONECT   30   31   32   72
CONECT   31   73   74   75
CONECT   32   33   76   77
CONECT   33   78   79   80
END

HMDB0115680
     RDKit          3D
PA(8:0/a-13:0)
 80 79  0  0  0  0  0  0  0  0999 V2000
    9.3957   -0.4876   -4.4902 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0024   -0.8116   -4.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0372   -1.3580   -2.6561 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6083   -0.4264   -1.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8210    0.8617   -1.5496 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3912    0.6385   -1.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2437   -0.0334    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7817   -0.2288    0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9501    0.1646   -0.3636 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3655   -0.8209    1.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0177   -1.0184    1.9626 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2786    0.2843    2.0742 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8875    1.1334    3.1737 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7796    0.4766    4.3938 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4666    1.4504    5.5858 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.0491    2.6919    4.9905 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6545    0.5254    6.3632 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2323    1.8055    6.7024 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9029    0.0714    2.3965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0405    0.5811    1.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3535    1.2000    0.5077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5079    0.4130    1.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9536   -0.7181    0.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4241   -0.9560    1.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1903    0.2687    0.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6886    0.1147    0.8713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2074   -0.9766   -0.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6930   -1.1522    0.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4808    0.0649   -0.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2357    0.5018   -1.6938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0488    1.7322   -2.0291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4106   -0.5915   -2.6945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7773   -1.1892   -2.7115 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5366   -0.6415   -5.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0894   -1.1486   -3.9645 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6311    0.5661   -4.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2893    0.0274   -4.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6168   -1.6242   -4.7091 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0443   -1.7122   -2.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6974   -2.2620   -2.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6547   -0.1445   -1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5913   -0.9219   -0.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2985    1.4539   -0.7252 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9129    1.4570   -2.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.0610   -1.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9042    1.6423   -1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7279   -1.0154    0.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7107    0.5915    0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5416   -1.6509    1.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9874   -1.5736    2.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3800    0.8518    1.1370 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9492    1.3337    2.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3114    2.0664    3.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417    0.8070    6.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0742    2.7709    6.7619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210    0.2209    2.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9601    1.3877    1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3828   -1.6430    1.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7951   -0.4486   -0.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7562   -1.8650    0.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5373   -1.2326    2.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9499    0.6840   -0.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9175    1.0560    1.4898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9875   -0.0843    1.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1303    1.1016    0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8651   -0.8947   -1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7703   -1.9465    0.3695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9628   -1.5124    1.0942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9727   -1.9558   -0.6197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3113    0.9350    0.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5558   -0.1981   -0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1593    0.8185   -1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4399    2.5221   -2.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4618    2.1313   -1.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9204    1.4626   -2.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6643   -1.3792   -2.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2477   -0.1229   -3.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0584   -1.4715   -3.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5681   -0.5385   -2.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7966   -2.1722   -2.1601 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  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 15 18  1  0
 12 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  6 46  1  0
  7 47  1  0
  7 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  6
 13 52  1  0
 13 53  1  0
 17 54  1  0
 18 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  0
 23 59  1  0
 24 60  1  0
 24 61  1  0
 25 62  1  0
 25 63  1  0
 26 64  1  0
 26 65  1  0
 27 66  1  0
 27 67  1  0
 28 68  1  0
 28 69  1  0
 29 70  1  0
 29 71  1  0
 30 72  1  0
 31 73  1  0
 31 74  1  0
 31 75  1  0
 32 76  1  0
 32 77  1  0
 33 78  1  0
 33 79  1  0
 33 80  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-Capryloyl-2-anteisotridecanoyl-sn-glycero-3-phosphate	HMDB
1-Capryloyl-2-anteisotridecanoyl-sn-phosphatidic acid	HMDB
PA(21:0)	HMDB
Phosphatidic acid(8:0/a-13:0)	HMDB
Phosphatidic acid(21:0)	HMDB
Phosphatidate(8:0/A-13:0)	HMDB
Phosphatidate(21:0)	HMDB
[(2R)-2-[(10-Methyldodecanoyl)oxy]-3-(octanoyloxy)propoxy]phosphonate	HMDB
PA(8:0/a-13:0)	SMPDB

Chemical Formula

C₂₄H₄₇O₈P

Average Molecular Weight

494.606

Monoisotopic Molecular Weight

494.300855471

IUPAC Name

[(2R)-2-[(10-methyldodecanoyl)oxy]-3-(octanoyloxy)propoxy]phosphonic acid

Traditional Name

(2R)-2-[(10-methyldodecanoyl)oxy]-3-(octanoyloxy)propoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

[H][C@@](COC(=O)CCCCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCC(C)CC

InChI Identifier

InChI=1S/C24H47O8P/c1-4-6-7-10-14-17-23(25)30-19-22(20-31-33(27,28)29)32-24(26)18-15-12-9-8-11-13-16-21(3)5-2/h21-22H,4-20H2,1-3H3,(H2,27,28,29)/t21?,22-/m1/s1

InChI Key

JQLHVVRKTDFQPB-FOIFJWKZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-diacylglycerol-3-phosphates. These are glycerol-3-phosphates in which the glycerol moiety is bonded to two aliphatic chains through ester linkages.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphates

Direct Parent

1,2-diacylglycerol-3-phosphates

Alternative Parents

Substituents

1,2-diacylglycerol-3-phosphate
Fatty acid ester
Monoalkyl phosphate
Dicarboxylic acid or derivatives
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Carboxylic acid ester
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0115680)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/a-25:0) (PathBank: SMP0102906)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-15:0) (PathBank: SMP0102910)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-18:0) (PathBank: SMP0102913)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-20:0) (PathBank: SMP0102915)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-24:0) (PathBank: SMP0102918)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/a-17:0) (PathBank: SMP0106509)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-16:0) (PathBank: SMP0106516)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-17:0) (PathBank: SMP0106517)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/a-21:0) (PathBank: SMP0110217)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-19:0) (PathBank: SMP0110226)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-22:0) (PathBank: SMP0110229)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-12:0) (PathBank: SMP0102907)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-14:0) (PathBank: SMP0102909)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-21:0) (PathBank: SMP0102916)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/a-15:0) (PathBank: SMP0106508)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/a-13:0) (PathBank: SMP0110214)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/i-13:0) (PathBank: SMP0110220)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/10:0) (PathBank: SMP0037372)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/12:0) (PathBank: SMP0037373)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/13:0) (PathBank: SMP0037374)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/14:0) (PathBank: SMP0037375)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/15:0) (PathBank: SMP0037376)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/16:0) (PathBank: SMP0037377)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/17:0) (PathBank: SMP0037378)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/18:0) (PathBank: SMP0037379)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/19:0) (PathBank: SMP0037380)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/20:0) (PathBank: SMP0037381)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/21:0) (PathBank: SMP0037382)
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/22:0) (PathBank: SMP0037383)

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
logP	5.13	ALOGPS
logP	6.83	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	1.32	ChemAxon
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	127.91 m³·mol⁻¹	ChemAxon
Polarizability	56.82 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	222.803	31661259
DarkChem	[M-H]-	215.518	31661259
DeepCCS	[M+H]+	211.784	30932474
DeepCCS	[M-H]-	209.426	30932474
DeepCCS	[M-2H]-	243.218	30932474
DeepCCS	[M+Na]+	218.44	30932474
AllCCS	[M+H]+	228.4	32859911
AllCCS	[M+H-H2O]+	227.0	32859911
AllCCS	[M+NH4]+	229.6	32859911
AllCCS	[M+Na]+	229.9	32859911
AllCCS	[M-H]-	214.9	32859911
AllCCS	[M+Na-2H]-	217.8	32859911
AllCCS	[M+HCOO]-	221.2	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	11.19 minutes	32390414
Predicted by Siyang on May 30, 2022	18.3462 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.3 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	3209.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	271.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	241.2 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	173.7 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	628.6 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	1036.1 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	978.2 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	162.9 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1835.3 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	735.2 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1830.4 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	679.9 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	478.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	300.6 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	396.2 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	18.2 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
PA(8:0/a-13:0)	[H][C@@](COC(=O)CCCCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCC(C)CC	3670.2	Standard polar	33892256
PA(8:0/a-13:0)	[H][C@@](COC(=O)CCCCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCC(C)CC	2981.4	Standard non polar	33892256
PA(8:0/a-13:0)	[H][C@@](COC(=O)CCCCCCC)(COP(O)(O)=O)OC(=O)CCCCCCCCC(C)CC	3393.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
PA(8:0/a-13:0),1TMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)OC(=O)CCCCCCCCC(C)CC	3374.7	Semi standard non polar	33892256
PA(8:0/a-13:0),1TMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)OC(=O)CCCCCCCCC(C)CC	2987.4	Standard non polar	33892256
PA(8:0/a-13:0),1TMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C)OC(=O)CCCCCCCCC(C)CC	4355.0	Standard polar	33892256
PA(8:0/a-13:0),2TMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCCCC(C)CC	3400.5	Semi standard non polar	33892256
PA(8:0/a-13:0),2TMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCCCC(C)CC	3023.4	Standard non polar	33892256
PA(8:0/a-13:0),2TMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CCCCCCCCC(C)CC	3770.5	Standard polar	33892256
PA(8:0/a-13:0),1TBDMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCCCC(C)CC	3619.7	Semi standard non polar	33892256
PA(8:0/a-13:0),1TBDMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCCCC(C)CC	3150.5	Standard non polar	33892256
PA(8:0/a-13:0),1TBDMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCCCC(C)CC	4405.3	Standard polar	33892256
PA(8:0/a-13:0),2TBDMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCCCC(C)CC	3874.8	Semi standard non polar	33892256
PA(8:0/a-13:0),2TBDMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCCCC(C)CC	3293.8	Standard non polar	33892256
PA(8:0/a-13:0),2TBDMS,isomer #1	CCCCCCCC(=O)OC[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(=O)CCCCCCCCC(C)CC	3901.3	Standard polar	33892256

Spectra

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/10:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/12:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/13:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/14:0)		Not Available
De Novo Triacylglycerol Biosynthesis TG(8:0/a-13:0/15:0)		Not Available

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

74877418

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131822336

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Only showing the first 10 proteins. There are 61 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details

1. Phospholipase D2

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

Enzyme Details

2. Diacylglycerol kinase theta

General function:: Involved in diacylglycerol kinase activity
Specific function:: Phosphorylates diacylglycerol (DAG) to generate phosphatidic acid (PA). May regulate the activity of protein kinase C by controlling the balance between these two signaling lipids. Activated in the nucleus in response to alpha-thrombin and nerve growth factor. May be involved in cAMP- induced activation of NR5A1 and subsequent steroidogenic gene transcription by delivering PA as ligand for NR5A1. Acts synergistically with NR5A1 on CYP17 transcriptional activity
Gene Name:: DGKQ
Uniprot ID:: P52824
Molecular weight:: 101154.0

Enzyme Details

3. Diacylglycerol kinase gamma

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

Enzyme Details

4. Lipid phosphate phosphohydrolase 2

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

Enzyme Details

5. Diacylglycerol kinase alpha

General function:: Involved in diacylglycerol kinase activity
Specific function:: Upon cell stimulation converts the second messenger diacylglycerol into phosphatidate, initiating the resynthesis of phosphatidylinositols and attenuating protein kinase C activity
Gene Name:: DGKA
Uniprot ID:: P23743
Molecular weight:: 82629.5

Enzyme Details

6. Diacylglycerol kinase delta

General function:: Involved in diacylglycerol kinase activity
Specific function:: Isoform 2 may be involved in cell growth and tumorigenesis. Involved in clathrin-dependent endocytosis
Gene Name:: DGKD
Uniprot ID:: Q16760
Molecular weight:: 134524.2

Enzyme Details

7. Lipid phosphate phosphohydrolase 1

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

Enzyme Details

8. Diacylglycerol kinase beta

General function:: Involved in diacylglycerol kinase activity
Specific function:: Exhibits high phosphorylation activity for long-chain diacylglycerols
Gene Name:: DGKB
Uniprot ID:: Q9Y6T7
Molecular weight:: 90594.7

Enzyme Details

9. Diacylglycerol kinase iota

General function:: Involved in diacylglycerol kinase activity
Specific function:: ATP + 1,2-diacylglycerol = ADP + 1,2-diacyl- sn-glycerol 3-phosphate
Gene Name:: DGKI
Uniprot ID:: O75912
Molecular weight:: 116996.2

Enzyme Details

10. Lipid phosphate phosphohydrolase 3

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

Only showing the first 10 proteins. There are 61 proteins in total.

Show all enzymes and transporters

Showing metabocard for PA(8:0/a-13:0) (HMDB0115680)

MOL for HMDB0115680 (PA(8:0/a-13:0))

3D MOL for HMDB0115680 (PA(8:0/a-13:0))

3D SDF for HMDB0115680 (PA(8:0/a-13:0))

3D-SDF for HMDB0115680 (PA(8:0/a-13:0))

PDB for HMDB0115680 (PA(8:0/a-13:0))

3D PDB for HMDB0115680 (PA(8:0/a-13:0))

SMILES for HMDB0115680 (PA(8:0/a-13:0))

INCHI for HMDB0115680 (PA(8:0/a-13:0))

Structure for HMDB0115680 (PA(8:0/a-13:0))

3D Structure for HMDB0115680 (PA(8:0/a-13:0))

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

Enzymes