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Showing metabocard for PC(P-16:0/18:3(9Z,12Z,15Z)) (HMDB0011213)

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enzymes (71)transporters (1) Show 72 proteins
Record Information
Version5.0
StatusDetected and Quantified
Creation Date2008-12-10 02:05:42 UTC
Update Date2022-03-07 02:51:04 UTC
HMDB IDHMDB0011213
Secondary Accession Numbers
  • HMDB11213
Metabolite Identification
Common NamePC(P-16:0/18:3(9Z,12Z,15Z))
DescriptionPC(P-16:0/18:3(9Z,12Z,15Z)) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines 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. PC(P-16:0/18:3(9Z,12Z,15Z)), in particular, consists of one chain of plasmalogen 16:0 at the C-1 position and one chain of a-linolenic acid at the C-2 position. The plasmalogen 16:0 moiety is derived from animal fats, liver and kidney, while the a-linolenic acid moiety is derived from seed oils, especially canola and soybean oil. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC. Plasmalogens are glycerol ether phospholipids. They are of two types, alkyl ether (-O-CH2-) and alkenyl ether (-O-CH=CH-). Dihydroxyacetone phosphate (DHAP) serves as the glycerol precursor for the synthesis of plasmalogens. Three major classes of plasmalogens have been identified: choline, ethanolamine and serine derivatives. Ethanolamine plasmalogen is prevalent in myelin. Choline plasmalogen is abundant in cardiac tissue. Usually, the highest proportion of the plasmalogen form is in the ethanolamine class with rather less in choline, and commonly little or none in other phospholipids such as phosphatidylinositol. In choline plasmalogens of most tissues, a higher proportion is often of the O-alkyl rather than the O-alkenyl form, but the reverse tends to be true in heart lipids. In animal tissues, the alkyl and alkenyl moieties in both non-polar and phospholipids tend to be rather simple in composition with 16:0, 18:0 and 18:1 (double bond in position 9) predominating. Ether analogues of triacylglycerols, i.e. 1-alkyldiacyl-sn-glycerols, are present at trace levels only if at all in most animal tissues, but they can be major components of some marine lipids.
Structure
Data?1582752879
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))


  Mrv0541 02241201232D          

 52 51  0  0  1  0            999 V2000
   21.6686   -6.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9634   -6.7300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.2582   -6.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3738   -6.7300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.5530   -6.7300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0840   -6.3316    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   23.4880   -7.0364    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   22.6800   -5.6268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.7943   -5.9277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.4885   -6.3403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1988   -5.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9041   -6.3491    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   25.4914   -7.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.3167   -5.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.6092   -6.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5463   -7.2804    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   20.3578   -7.3295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.8360   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1190   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4019   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6848   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9678   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2507   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5337   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8281   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.6768   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9598   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2427   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.2131   -7.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   17.5000   -7.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2144   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9289   -7.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   19.6434   -8.5670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  1  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
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  2 16  1  1  0  0  0
  2 17  1  6  0  0  0
 19 18  2  0  0  0  0
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  5 18  1  0  0  0  0
 35 34  1  0  0  0  0
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 37 36  2  0  0  0  0
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 41 40  1  0  0  0  0
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 50 49  1  0  0  0  0
 51 50  1  0  0  0  0
 52 51  2  0  0  0  0
 17 51  1  0  0  0  0
M  CHG  2   7  -1  12   1
M  END
Download

3D MOL for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))

HMDB0011213
     RDKit          3D
PC(P-16:0/18:3(9Z,12Z,15Z))
129128  0  0  0  0  0  0  0  0999 V2000
    0.0515    1.7148   -6.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4266    1.3054   -7.0145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7240    1.2733   -8.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1425    0.2218   -9.1223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3854   -1.1197   -8.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8134   -1.4318   -8.7726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6856   -1.6414   -7.8319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2966   -1.5772   -6.3629 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0851   -0.0388   -3.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4504   -0.3221   -2.0354 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7038    0.5661    1.8094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0915    1.0024    2.9146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4982   -0.0968    1.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6466   -0.3240    2.8114 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6952    0.3422    2.6627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3807    0.0741    1.4821 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7411   -1.1756    1.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9729   -1.5835    1.0511 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1050   -0.6919    1.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.2402    0.2090    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7137   -3.1520    5.0721 P   0  0  0  0  0  5  0  0  0  0  0  0
   -0.4372   -3.5708    5.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0379   -2.9144    6.1337 O   0  0  0  0  0  1  0  0  0  0  0  0
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    2.7420   -6.1069    3.4831 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0498   -7.9636    4.8081 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4536   -6.8729    3.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1716   -8.1490    2.4886 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0907    0.1973    3.7659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3951    0.0178    3.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6114    1.4555    2.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9264   -1.8674    0.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2038   -2.5717    0.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7055   -1.2600    2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2120   -1.6369   -0.0501 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.3171    2.0122    0.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4911    2.1465    1.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4727    4.1117    0.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5456    5.5933    2.7152 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4717    3.3977    3.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3639    4.3575    0.8638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2611    5.2920    2.9071 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4299    3.6755    2.1636 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8960    6.3172    0.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2808    5.0602    1.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1143    4.6019   -0.7649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8605    3.3943   -0.2902 H   0  0  0  0  0  0  0  0  0  0  0  0
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 50124  1  0
 50125  1  0
 50126  1  0
 51127  1  0
 51128  1  0
 51129  1  0
M  CHG  2  44  -1  48   1
M  END
Download

3D SDF for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))


  Mrv0541 02241201232D          

 52 51  0  0  1  0            999 V2000
   21.6686   -6.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9634   -6.7300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.2582   -6.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3738   -6.7300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.5530   -6.7300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0840   -6.3316    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   23.4880   -7.0364    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   22.6800   -5.6268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.7943   -5.9277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.4885   -6.3403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1988   -5.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9041   -6.3491    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   25.4914   -7.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.3167   -5.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.6092   -6.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5463   -7.2804    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   20.3578   -7.3295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.8360   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   16.6848   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9678   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2507   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5337   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8281   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1110   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3939   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6768   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9598   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2427   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5257   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8087   -6.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0912   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4973   -7.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.6407   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3551   -7.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0697   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7841   -7.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4986   -7.3295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2131   -7.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9276   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6420   -7.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3565   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0710   -7.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7855   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5000   -7.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2144   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9289   -7.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6434   -7.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6434   -8.5670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
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 33 32  1  0  0  0  0
  5 18  1  0  0  0  0
 35 34  1  0  0  0  0
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 37 36  2  0  0  0  0
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 43 42  2  0  0  0  0
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 49 48  1  0  0  0  0
 50 49  1  0  0  0  0
 51 50  1  0  0  0  0
 52 51  2  0  0  0  0
 17 51  1  0  0  0  0
M  CHG  2   7  -1  12   1
M  END
> <DATABASE_ID>
HMDB0011213

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCCCCCCC\C=C/OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC

> <INCHI_IDENTIFIER>
InChI=1S/C42H78NO7P/c1-6-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-42(44)50-41(40-49-51(45,46)48-38-36-43(3,4)5)39-47-37-34-32-30-28-26-24-21-19-17-15-13-11-9-7-2/h8,10,14,16,20,22,34,37,41H,6-7,9,11-13,15,17-19,21,23-33,35-36,38-40H2,1-5H3/b10-8-,16-14-,22-20-,37-34-/t41-/m1/s1

> <INCHI_KEY>
WXQJKOUXCWEMOK-LUPMRSKMSA-N

> <FORMULA>
C42H78NO7P

> <MOLECULAR_WEIGHT>
740.045

> <EXACT_MASS>
739.551590367

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
89.93500027707526

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-3-[(1Z)-hexadec-1-en-1-yloxy]-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propyl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
5.80

> <JCHEM_LOGP>
8.30994338019492

> <ALOGPS_LOGS>
-7.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550574852835355

> <JCHEM_PKA_STRONGEST_BASIC>
-4.731743075587598

> <JCHEM_POLAR_SURFACE_AREA>
94.12

> <JCHEM_REFRACTIVITY>
228.75540000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
38

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.43e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-3-[(1Z)-hexadec-1-en-1-yloxy]-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propyl phosphonato]oxy}ethyl)trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))

HMDB0011213
     RDKit          3D
PC(P-16:0/18:3(9Z,12Z,15Z))
129128  0  0  0  0  0  0  0  0999 V2000
    0.0515    1.7148   -6.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4266    1.3054   -7.0145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7240    1.2733   -8.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1425    0.2218   -9.1223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3854   -1.1197   -8.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8134   -1.4318   -8.7726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6856   -1.6414   -7.8319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2966   -1.5772   -6.3629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5524   -2.8962   -5.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2901   -3.1487   -4.7726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0439   -2.3481   -3.8952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2028   -0.9218   -3.7662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0851   -0.0388   -3.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4504   -0.3221   -2.0354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3262    0.6840   -1.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5991    0.5103   -0.6253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5226    0.7474    0.5349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7038    0.5661    1.8094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0915    1.0024    2.9146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4982   -0.0968    1.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6466   -0.3240    2.8114 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6952    0.3422    2.6627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3807    0.0741    1.4821 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7411   -1.1756    1.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9729   -1.5835    1.0511 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1050   -0.6919    1.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0070   -0.5643    0.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2402    0.2090    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5966    2.2550    1.8075 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3116    4.5293    2.8657 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0949    4.9148    1.7687 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6172    4.7474    2.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7825    5.2144    0.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0790    4.4732   -0.4307 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1812    5.0227   -1.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2649    4.7962   -1.0834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5029   -1.7408    3.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4113   -1.6970    4.3439 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7137   -3.1520    5.0721 P   0  0  0  0  0  5  0  0  0  0  0  0
   -0.4372   -3.5708    5.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0379   -2.9144    6.1337 O   0  0  0  0  0  1  0  0  0  0  0  0
    1.1018   -4.4161    4.0602 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3512   -4.9498    4.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -6.1069    3.4831 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8417   -7.2214    3.5579 N   0  0  0  0  0  4  0  0  0  0  0  0
    2.0498   -7.9636    4.8081 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4536   -6.8729    3.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1716   -8.1490    2.4886 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2626    2.6617   -7.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3090    1.8169   -5.7789 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7082    0.9257   -7.2715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9967    2.0744   -6.4458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5617    0.3589   -6.4799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5786    2.2224   -9.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3220    0.3735  -10.2074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7382   -1.8074   -9.1860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0190   -1.2338   -7.5226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1774   -1.4946   -9.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7217   -1.8691   -8.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3324   -1.1515   -6.2664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1129   -0.8616   -5.9953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0473   -3.7569   -6.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3403   -4.2733   -4.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1418   -2.7721   -3.9553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8496   -2.7264   -2.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7896   -0.4545   -4.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0072   -0.7754   -2.9112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2791    0.0906   -4.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5344    1.0065   -3.2959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9731   -1.3239   -2.0567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1687   -0.1820   -1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7289    1.7221   -1.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6245    0.5077   -2.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1468   -0.5171   -0.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7529    1.2504   -0.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9219    1.7733    0.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3676    0.0407    0.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0907    0.1973    3.7659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3951    0.0178    3.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6114    1.4555    2.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9264   -1.8674    0.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2038   -2.5717    0.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7291    0.1832    1.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7055   -1.2600    2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2120   -1.6369   -0.0501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3765   -0.1776   -0.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9265   -0.0228   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8952   -0.2562    1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3171    2.0122    0.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7766    2.1940   -0.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9682    1.8308    2.7253 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4911    2.1465    1.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4727    4.1117    0.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9793    3.8717    1.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7695    4.2074    3.8195 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5456    5.5933    2.7152 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4717    3.3977    3.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5228    5.0851    3.8349 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3150    5.9869    1.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3639    4.3575    0.8638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2611    5.2920    2.9071 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4299    3.6755    2.1636 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8960    6.3172    0.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2808    5.0602    1.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1143    4.6019   -0.7649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8605    3.3943   -0.2902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3769    4.4900   -2.4761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3603    6.1070   -1.6578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3965    3.8481   -0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6077    5.6115   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9494    4.7703   -1.9677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3170   -2.4983    2.5396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4942   -1.9672    3.8180 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4359   -5.2030    5.4479 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0918   -4.1271    4.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8445   -5.7749    2.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7509   -6.4962    3.7793 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1465   -7.8920    5.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4426   -7.5372    5.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8211   -9.0214    4.6202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0974   -7.8086    3.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0126   -6.4903    4.3842 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3019   -6.1316    2.6436 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2330   -8.1065    2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9973   -9.1934    2.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4993   -7.9672    1.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  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
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 21 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  2  0
 42 44  1  0
 42 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 48 50  1  0
 48 51  1  0
  1 52  1  0
  1 53  1  0
  1 54  1  0
  2 55  1  0
  2 56  1  0
  3 57  1  0
  4 58  1  0
  5 59  1  0
  5 60  1  0
  6 61  1  0
  7 62  1  0
  8 63  1  0
  8 64  1  0
  9 65  1  0
 10 66  1  0
 11 67  1  0
 11 68  1  0
 12 69  1  0
 12 70  1  0
 13 71  1  0
 13 72  1  0
 14 73  1  0
 14 74  1  0
 15 75  1  0
 15 76  1  0
 16 77  1  0
 16 78  1  0
 17 79  1  0
 17 80  1  0
 21 81  1  1
 22 82  1  0
 22 83  1  0
 24 84  1  0
 25 85  1  0
 26 86  1  0
 26 87  1  0
 27 88  1  0
 27 89  1  0
 28 90  1  0
 28 91  1  0
 29 92  1  0
 29 93  1  0
 30 94  1  0
 30 95  1  0
 31 96  1  0
 31 97  1  0
 32 98  1  0
 32 99  1  0
 33100  1  0
 33101  1  0
 34102  1  0
 34103  1  0
 35104  1  0
 35105  1  0
 36106  1  0
 36107  1  0
 37108  1  0
 37109  1  0
 38110  1  0
 38111  1  0
 39112  1  0
 39113  1  0
 39114  1  0
 40115  1  0
 40116  1  0
 46117  1  0
 46118  1  0
 47119  1  0
 47120  1  0
 49121  1  0
 49122  1  0
 49123  1  0
 50124  1  0
 50125  1  0
 50126  1  0
 51127  1  0
 51128  1  0
 51129  1  0
M  CHG  2  44  -1  48   1
M  END
Download

PDB for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      40.448 -11.803   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      39.132 -12.563   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      37.815 -11.803   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      41.764 -12.563   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      36.499 -12.563   0.000  0.00  0.00           O+0
HETATM    6  P   UNK     0      43.090 -11.819   0.000  0.00  0.00           P+0
HETATM    7  O   UNK     0      43.844 -13.135   0.000  0.00  0.00           O-1
HETATM    8  O   UNK     0      42.336 -10.503   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      44.416 -11.065   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      45.712 -11.835   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      47.038 -11.092   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      48.354 -11.852   0.000  0.00  0.00           N+1
HETATM   13  C   UNK     0      47.584 -13.158   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      49.125 -10.545   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      49.671 -12.622   0.000  0.00  0.00           C+0
HETATM   16  H   UNK     0      40.220 -13.590   0.000  0.00  0.00           H+0
HETATM   17  O   UNK     0      38.001 -13.682   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      35.161 -11.801   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      33.822 -11.801   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      32.484 -12.563   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      31.145 -11.801   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      29.807 -12.563   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      28.468 -11.801   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      27.130 -12.563   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      25.812 -11.801   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      24.474 -12.563   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      23.135 -11.801   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      21.797 -12.563   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      20.458 -11.801   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      19.120 -12.563   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.781 -11.801   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.443 -12.563   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.104 -11.801   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.995 -14.452   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      15.329 -13.682   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.662 -14.452   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      17.996 -14.452   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      19.330 -13.682   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      20.663 -14.452   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      21.997 -14.452   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      23.331 -13.682   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      24.664 -14.452   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      25.998 -14.452   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      27.332 -13.682   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      28.665 -14.452   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      29.999 -13.682   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      31.333 -14.452   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      32.667 -13.682   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      34.000 -14.452   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      35.334 -13.682   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      36.668 -14.452   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      36.668 -15.992   0.000  0.00  0.00           O+0
CONECT    1    2    4                                                       
CONECT    2    1    3   16   17                                             
CONECT    3    2    5                                                       
CONECT    4    1    6                                                       
CONECT    5    3   18                                                       
CONECT    6    4    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12                                                            
CONECT   16    2                                                            
CONECT   17    2   51                                                       
CONECT   18   19    5                                                       
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                                                            
CONECT   34   35                                                            
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52   17                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  102    0
END
Download

3D PDB for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))

COMPND    HMDB0011213
HETATM    1  C1  UNL     1       0.051   1.715  -6.860  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.427   1.305  -7.014  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.724   1.273  -8.451  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.143   0.222  -9.122  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.385  -1.120  -8.522  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.813  -1.432  -8.773  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.686  -1.641  -7.832  1.00  0.00           C  
HETATM    8  C8  UNL     1      -4.297  -1.577  -6.363  1.00  0.00           C  
HETATM    9  C9  UNL     1      -4.552  -2.896  -5.794  1.00  0.00           C  
HETATM   10  C10 UNL     1      -5.290  -3.149  -4.773  1.00  0.00           C  
HETATM   11  C11 UNL     1      -6.044  -2.348  -3.895  1.00  0.00           C  
HETATM   12  C12 UNL     1      -6.203  -0.922  -3.766  1.00  0.00           C  
HETATM   13  C13 UNL     1      -5.085  -0.039  -3.395  1.00  0.00           C  
HETATM   14  C14 UNL     1      -4.450  -0.322  -2.035  1.00  0.00           C  
HETATM   15  C15 UNL     1      -3.326   0.684  -1.914  1.00  0.00           C  
HETATM   16  C16 UNL     1      -2.599   0.510  -0.625  1.00  0.00           C  
HETATM   17  C17 UNL     1      -3.523   0.747   0.535  1.00  0.00           C  
HETATM   18  C18 UNL     1      -2.704   0.566   1.809  1.00  0.00           C  
HETATM   19  O1  UNL     1      -3.091   1.002   2.915  1.00  0.00           O  
HETATM   20  O2  UNL     1      -1.498  -0.097   1.750  1.00  0.00           O  
HETATM   21  C19 UNL     1      -0.647  -0.324   2.811  1.00  0.00           C  
HETATM   22  C20 UNL     1       0.695   0.342   2.663  1.00  0.00           C  
HETATM   23  O3  UNL     1       1.381   0.074   1.482  1.00  0.00           O  
HETATM   24  C21 UNL     1       1.741  -1.176   1.078  1.00  0.00           C  
HETATM   25  C22 UNL     1       2.973  -1.584   1.051  1.00  0.00           C  
HETATM   26  C23 UNL     1       4.105  -0.692   1.469  1.00  0.00           C  
HETATM   27  C24 UNL     1       5.007  -0.564   0.293  1.00  0.00           C  
HETATM   28  C25 UNL     1       6.240   0.209   0.394  1.00  0.00           C  
HETATM   29  C26 UNL     1       6.228   1.658   0.599  1.00  0.00           C  
HETATM   30  C27 UNL     1       5.597   2.255   1.807  1.00  0.00           C  
HETATM   31  C28 UNL     1       5.877   3.772   1.718  1.00  0.00           C  
HETATM   32  C29 UNL     1       5.312   4.529   2.866  1.00  0.00           C  
HETATM   33  C30 UNL     1       3.822   4.405   2.997  1.00  0.00           C  
HETATM   34  C31 UNL     1       3.095   4.915   1.769  1.00  0.00           C  
HETATM   35  C32 UNL     1       1.617   4.747   2.000  1.00  0.00           C  
HETATM   36  C33 UNL     1       0.782   5.214   0.853  1.00  0.00           C  
HETATM   37  C34 UNL     1       1.079   4.473  -0.431  1.00  0.00           C  
HETATM   38  C35 UNL     1       0.181   5.023  -1.527  1.00  0.00           C  
HETATM   39  C36 UNL     1      -1.265   4.796  -1.083  1.00  0.00           C  
HETATM   40  C37 UNL     1      -0.503  -1.741   3.287  1.00  0.00           C  
HETATM   41  O4  UNL     1       0.411  -1.697   4.344  1.00  0.00           O  
HETATM   42  P1  UNL     1       0.714  -3.152   5.072  1.00  0.00           P  
HETATM   43  O5  UNL     1      -0.437  -3.571   5.987  1.00  0.00           O  
HETATM   44  O6  UNL     1       2.038  -2.914   6.134  1.00  0.00           O1-
HETATM   45  O7  UNL     1       1.102  -4.416   4.060  1.00  0.00           O  
HETATM   46  C38 UNL     1       2.351  -4.950   4.361  1.00  0.00           C  
HETATM   47  C39 UNL     1       2.742  -6.107   3.483  1.00  0.00           C  
HETATM   48  N1  UNL     1       1.842  -7.221   3.558  1.00  0.00           N1+
HETATM   49  C40 UNL     1       2.050  -7.964   4.808  1.00  0.00           C  
HETATM   50  C41 UNL     1       0.454  -6.873   3.434  1.00  0.00           C  
HETATM   51  C42 UNL     1       2.172  -8.149   2.489  1.00  0.00           C  
HETATM   52  H1  UNL     1       0.263   2.662  -7.356  1.00  0.00           H  
HETATM   53  H2  UNL     1       0.309   1.817  -5.779  1.00  0.00           H  
HETATM   54  H3  UNL     1       0.708   0.926  -7.271  1.00  0.00           H  
HETATM   55  H4  UNL     1      -1.997   2.074  -6.446  1.00  0.00           H  
HETATM   56  H5  UNL     1      -1.562   0.359  -6.480  1.00  0.00           H  
HETATM   57  H6  UNL     1      -1.579   2.222  -9.010  1.00  0.00           H  
HETATM   58  H7  UNL     1      -2.322   0.373 -10.207  1.00  0.00           H  
HETATM   59  H8  UNL     1      -1.738  -1.807  -9.186  1.00  0.00           H  
HETATM   60  H9  UNL     1      -2.019  -1.234  -7.523  1.00  0.00           H  
HETATM   61  H10 UNL     1      -4.177  -1.495  -9.810  1.00  0.00           H  
HETATM   62  H11 UNL     1      -5.722  -1.869  -8.098  1.00  0.00           H  
HETATM   63  H12 UNL     1      -3.332  -1.151  -6.266  1.00  0.00           H  
HETATM   64  H13 UNL     1      -5.113  -0.862  -5.995  1.00  0.00           H  
HETATM   65  H14 UNL     1      -4.047  -3.757  -6.310  1.00  0.00           H  
HETATM   66  H15 UNL     1      -5.340  -4.273  -4.537  1.00  0.00           H  
HETATM   67  H16 UNL     1      -7.142  -2.772  -3.955  1.00  0.00           H  
HETATM   68  H17 UNL     1      -5.850  -2.726  -2.781  1.00  0.00           H  
HETATM   69  H18 UNL     1      -6.790  -0.455  -4.609  1.00  0.00           H  
HETATM   70  H19 UNL     1      -7.007  -0.775  -2.911  1.00  0.00           H  
HETATM   71  H20 UNL     1      -4.279   0.091  -4.114  1.00  0.00           H  
HETATM   72  H21 UNL     1      -5.534   1.007  -3.296  1.00  0.00           H  
HETATM   73  H22 UNL     1      -3.973  -1.324  -2.057  1.00  0.00           H  
HETATM   74  H23 UNL     1      -5.169  -0.182  -1.228  1.00  0.00           H  
HETATM   75  H24 UNL     1      -3.729   1.722  -1.956  1.00  0.00           H  
HETATM   76  H25 UNL     1      -2.624   0.508  -2.784  1.00  0.00           H  
HETATM   77  H26 UNL     1      -2.147  -0.517  -0.553  1.00  0.00           H  
HETATM   78  H27 UNL     1      -1.753   1.250  -0.515  1.00  0.00           H  
HETATM   79  H28 UNL     1      -3.922   1.773   0.563  1.00  0.00           H  
HETATM   80  H29 UNL     1      -4.368   0.041   0.601  1.00  0.00           H  
HETATM   81  H30 UNL     1      -1.091   0.197   3.766  1.00  0.00           H  
HETATM   82  H31 UNL     1       1.395   0.018   3.496  1.00  0.00           H  
HETATM   83  H32 UNL     1       0.611   1.455   2.851  1.00  0.00           H  
HETATM   84  H33 UNL     1       0.926  -1.867   0.754  1.00  0.00           H  
HETATM   85  H34 UNL     1       3.204  -2.572   0.728  1.00  0.00           H  
HETATM   86  H35 UNL     1       3.729   0.183   1.957  1.00  0.00           H  
HETATM   87  H36 UNL     1       4.705  -1.260   2.252  1.00  0.00           H  
HETATM   88  H37 UNL     1       5.212  -1.637  -0.050  1.00  0.00           H  
HETATM   89  H38 UNL     1       4.377  -0.178  -0.575  1.00  0.00           H  
HETATM   90  H39 UNL     1       6.926  -0.023  -0.502  1.00  0.00           H  
HETATM   91  H40 UNL     1       6.895  -0.256   1.232  1.00  0.00           H  
HETATM   92  H41 UNL     1       7.317   2.012   0.561  1.00  0.00           H  
HETATM   93  H42 UNL     1       5.777   2.194  -0.314  1.00  0.00           H  
HETATM   94  H43 UNL     1       5.968   1.831   2.725  1.00  0.00           H  
HETATM   95  H44 UNL     1       4.491   2.146   1.726  1.00  0.00           H  
HETATM   96  H45 UNL     1       5.473   4.112   0.758  1.00  0.00           H  
HETATM   97  H46 UNL     1       6.979   3.872   1.723  1.00  0.00           H  
HETATM   98  H47 UNL     1       5.770   4.207   3.820  1.00  0.00           H  
HETATM   99  H48 UNL     1       5.546   5.593   2.715  1.00  0.00           H  
HETATM  100  H49 UNL     1       3.472   3.398   3.281  1.00  0.00           H  
HETATM  101  H50 UNL     1       3.523   5.085   3.835  1.00  0.00           H  
HETATM  102  H51 UNL     1       3.315   5.987   1.604  1.00  0.00           H  
HETATM  103  H52 UNL     1       3.364   4.357   0.864  1.00  0.00           H  
HETATM  104  H53 UNL     1       1.261   5.292   2.907  1.00  0.00           H  
HETATM  105  H54 UNL     1       1.430   3.675   2.164  1.00  0.00           H  
HETATM  106  H55 UNL     1       0.896   6.317   0.681  1.00  0.00           H  
HETATM  107  H56 UNL     1      -0.281   5.060   1.099  1.00  0.00           H  
HETATM  108  H57 UNL     1       2.114   4.602  -0.765  1.00  0.00           H  
HETATM  109  H58 UNL     1       0.860   3.394  -0.290  1.00  0.00           H  
HETATM  110  H59 UNL     1       0.377   4.490  -2.476  1.00  0.00           H  
HETATM  111  H60 UNL     1       0.360   6.107  -1.658  1.00  0.00           H  
HETATM  112  H61 UNL     1      -1.397   3.848  -0.538  1.00  0.00           H  
HETATM  113  H62 UNL     1      -1.608   5.611  -0.402  1.00  0.00           H  
HETATM  114  H63 UNL     1      -1.949   4.770  -1.968  1.00  0.00           H  
HETATM  115  H64 UNL     1      -0.317  -2.498   2.540  1.00  0.00           H  
HETATM  116  H65 UNL     1      -1.494  -1.967   3.818  1.00  0.00           H  
HETATM  117  H66 UNL     1       2.436  -5.203   5.448  1.00  0.00           H  
HETATM  118  H67 UNL     1       3.092  -4.127   4.201  1.00  0.00           H  
HETATM  119  H68 UNL     1       2.845  -5.775   2.445  1.00  0.00           H  
HETATM  120  H69 UNL     1       3.751  -6.496   3.779  1.00  0.00           H  
HETATM  121  H70 UNL     1       3.146  -7.892   5.019  1.00  0.00           H  
HETATM  122  H71 UNL     1       1.443  -7.537   5.623  1.00  0.00           H  
HETATM  123  H72 UNL     1       1.821  -9.021   4.620  1.00  0.00           H  
HETATM  124  H73 UNL     1      -0.097  -7.809   3.187  1.00  0.00           H  
HETATM  125  H74 UNL     1       0.013  -6.490   4.384  1.00  0.00           H  
HETATM  126  H75 UNL     1       0.302  -6.132   2.644  1.00  0.00           H  
HETATM  127  H76 UNL     1       3.233  -8.107   2.196  1.00  0.00           H  
HETATM  128  H77 UNL     1       1.997  -9.193   2.837  1.00  0.00           H  
HETATM  129  H78 UNL     1       1.499  -7.967   1.621  1.00  0.00           H  
CONECT    1    2   52   53   54
CONECT    2    3   55   56
CONECT    3    4    4   57
CONECT    4    5   58
CONECT    5    6   59   60
CONECT    6    7    7   61
CONECT    7    8   62
CONECT    8    9   63   64
CONECT    9   10   10   65
CONECT   10   11   66
CONECT   11   12   67   68
CONECT   12   13   69   70
CONECT   13   14   71   72
CONECT   14   15   73   74
CONECT   15   16   75   76
CONECT   16   17   77   78
CONECT   17   18   79   80
CONECT   18   19   19   20
CONECT   20   21
CONECT   21   22   40   81
CONECT   22   23   82   83
CONECT   23   24
CONECT   24   25   25   84
CONECT   25   26   85
CONECT   26   27   86   87
CONECT   27   28   88   89
CONECT   28   29   90   91
CONECT   29   30   92   93
CONECT   30   31   94   95
CONECT   31   32   96   97
CONECT   32   33   98   99
CONECT   33   34  100  101
CONECT   34   35  102  103
CONECT   35   36  104  105
CONECT   36   37  106  107
CONECT   37   38  108  109
CONECT   38   39  110  111
CONECT   39  112  113  114
CONECT   40   41  115  116
CONECT   41   42
CONECT   42   43   43   44   45
CONECT   45   46
CONECT   46   47  117  118
CONECT   47   48  119  120
CONECT   48   49   50   51
CONECT   49  121  122  123
CONECT   50  124  125  126
CONECT   51  127  128  129
END
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SMILES for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))

CCCCCCCCCCCCCC\C=C/OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC
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INCHI for HMDB0011213 (PC(P-16:0/18:3(9Z,12Z,15Z)))

InChI=1S/C42H78NO7P/c1-6-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-42(44)50-41(40-49-51(45,46)48-38-36-43(3,4)5)39-47-37-34-32-30-28-26-24-21-19-17-15-13-11-9-7-2/h8,10,14,16,20,22,34,37,41H,6-7,9,11-13,15,17-19,21,23-33,35-36,38-40H2,1-5H3/b10-8-,16-14-,22-20-,37-34-/t41-/m1/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
1-(1-Enyl-palmitoyl)-2-a-linolenoyl-sn-glycero-3-phosphocholineHMDB
1-(1-Enyl-palmitoyl)-2-alpha-linolenoyl-sn-glycero-3-phosphocholineHMDB
Gpcho(16:0/18:3)HMDB
Gpcho(16:0/18:3n3)HMDB
Gpcho(16:0/18:3W3)HMDB
Gpcho(34:3)HMDB
1-(1Z-Hexadecenyl)-2-alpha-linolenoyl-GPCHMDB
1-(1Z-Hexadecenyl)-2-alpha-linolenoyl-sn-glycero-3-phosphocholineHMDB
1-(1Z-Hexadecenyl)-2-alpha-linolenoyl-sn-glycero-phosphatidylcholineHMDB
GPC(16:1/18:3)HMDB
GPC(34:4)HMDB
GPC(O-16:1(1Z)/18:3(9Z,12Z,15Z))HMDB
GPC(O-16:1(1Z)/18:3n3)HMDB
GPC(O-16:1(1Z)/18:3W3)HMDB
GPC(p-16:0/18:3(9Z,12Z,15Z))HMDB
GPC(p-16:0/18:3n3)HMDB
GPC(p-16:0/18:3W3)HMDB
GPCho(16:1/18:3)HMDB
GPCho(34:4)HMDB
GPCho(O-16:1(1Z)/18:3(9Z,12Z,15Z))HMDB
GPCho(O-16:1(1Z)/18:3n3)HMDB
GPCho(O-16:1(1Z)/18:3W3)HMDB
GPCho(p-16:0/18:3(9Z,12Z,15Z))HMDB
GPCho(p-16:0/18:3n3)HMDB
GPCho(p-16:0/18:3W3)HMDB
PC(16:1/18:3)HMDB
PC(34:4)HMDB
PC(O-16:1(1Z)/18:3(9Z,12Z,15Z))HMDB
PC(O-16:1(1Z)/18:3n3)HMDB
PC(O-16:1(1Z)/18:3W3)HMDB
PC(p-16:0/18:3n3)HMDB
PC(p-16:0/18:3W3)HMDB
Phosphatidylcholine(16:1/18:3)HMDB
Phosphatidylcholine(34:4)HMDB
Phosphatidylcholine(O-16:1(1Z)/18:3(9Z,12Z,15Z))HMDB
Phosphatidylcholine(O-16:1(1Z)/18:3n3)HMDB
Phosphatidylcholine(O-16:1(1Z)/18:3W3)HMDB
Phosphatidylcholine(p-16:0/18:3(9Z,12Z,15Z))HMDB
Phosphatidylcholine(p-16:0/18:3n3)HMDB
Phosphatidylcholine(p-16:0/18:3W3)HMDB
Chemical FormulaC42H78NO7P
Average Molecular Weight740.045
Monoisotopic Molecular Weight739.551590367
IUPAC Name(2-{[(2R)-3-[(1Z)-hexadec-1-en-1-yloxy]-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propyl phosphonato]oxy}ethyl)trimethylazanium
Traditional Name(2-{[(2R)-3-[(1Z)-hexadec-1-en-1-yloxy]-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propyl phosphonato]oxy}ethyl)trimethylazanium
CAS Registry NumberNot Available
SMILES
CCCCCCCCCCCCCC\C=C/OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC
InChI Identifier
InChI=1S/C42H78NO7P/c1-6-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-42(44)50-41(40-49-51(45,46)48-38-36-43(3,4)5)39-47-37-34-32-30-28-26-24-21-19-17-15-13-11-9-7-2/h8,10,14,16,20,22,34,37,41H,6-7,9,11-13,15,17-19,21,23-33,35-36,38-40H2,1-5H3/b10-8-,16-14-,22-20-,37-34-/t41-/m1/s1
InChI KeyWXQJKOUXCWEMOK-LUPMRSKMSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 1-(1z-alkenyl),2-acyl-glycerophosphocholines. These are glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphocholines
Direct Parent1-(1Z-alkenyl),2-acyl-glycerophosphocholines
Alternative Parents
Substituents
  • 1-(1z-alkenyl),2-acyl-glycerophosphocholine
  • Phosphocholine
  • Glycerol vinyl ether
  • Fatty acid ester
  • Dialkyl phosphate
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • Quaternary ammonium salt
  • Tetraalkylammonium salt
  • Carboxylic acid ester
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Amine
  • Organic oxide
  • Organopnictogen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic salt
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Health effect
Disposition
Biological locationSource
Process
Naturally occurring process
Role
Biological roleIndustrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility3.4e-05 g/LALOGPS
logP5.8ALOGPS
logP8.31ChemAxon
logS-7.4ALOGPS
pKa (Strongest Acidic)1.86ChemAxon
pKa (Strongest Basic)-4.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area94.12 ŲChemAxon
Rotatable Bond Count38ChemAxon
Refractivity228.76 m³·mol⁻¹ChemAxon
Polarizability89.94 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+254.95930932474
DeepCCS[M-H]-253.13430932474
DeepCCS[M-2H]-286.37430932474
DeepCCS[M+Na]+260.56530932474
AllCCS[M+H]+284.632859911
AllCCS[M+H-H2O]+284.332859911
AllCCS[M+NH4]+284.732859911
AllCCS[M+Na]+284.832859911
AllCCS[M-H]-273.232859911
AllCCS[M+Na-2H]-278.032859911
AllCCS[M+HCOO]-283.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
PC(P-16:0/18:3(9Z,12Z,15Z))CCCCCCCCCCCCCC\C=C/OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC5242.8Standard polar33892256
PC(P-16:0/18:3(9Z,12Z,15Z))CCCCCCCCCCCCCC\C=C/OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC4239.7Standard non polar33892256
PC(P-16:0/18:3(9Z,12Z,15Z))CCCCCCCCCCCCCC\C=C/OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC4869.8Semi standard non polar33892256
Spectra

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 10V, Positive-QTOFsplash10-01q0-9170321300-7e65721430900e300b2b2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 20V, Positive-QTOFsplash10-03l9-3190111000-a6930dc592ed216c6e222017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 40V, Positive-QTOFsplash10-008i-5090011000-10f45870dac46a8b3b9b2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 10V, Negative-QTOFsplash10-000i-0090001500-dc7b388e0cb9b980c4db2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 20V, Negative-QTOFsplash10-002r-0090003000-7777b21befd5070e0f2a2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 40V, Negative-QTOFsplash10-004i-3090000000-5e0aa8c079eac98f4d392017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 10V, Negative-QTOFsplash10-000i-0000000900-0dd39b4f99d862ce6c4e2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 20V, Negative-QTOFsplash10-000i-0060023900-599dc2e110dcfa45823e2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 40V, Negative-QTOFsplash10-004i-4091100000-6839ec2e40b866645bdd2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 10V, Positive-QTOFsplash10-0006-0000000900-54661b3d39c121fe7f5f2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 20V, Positive-QTOFsplash10-001l-0900000500-484e6846e81d12d1a83b2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 40V, Positive-QTOFsplash10-001l-1900436900-3e4947b463d997d176fe2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 10V, Negative-QTOFsplash10-00di-0000000900-0fc35ac08cd5327ab7f72021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 20V, Negative-QTOFsplash10-00di-0000000900-0fc35ac08cd5327ab7f72021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(P-16:0/18:3(9Z,12Z,15Z)) 40V, Negative-QTOFsplash10-024j-0030911600-bb0419be959187e7fc872021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Blood
  • Feces
  • Saliva
  • Urine
Tissue Locations
  • All Tissues
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified2.8 (2.33-3.53) uMNewborn (0-30 days old)Not Available
Normal		 details
BloodDetected and Quantified11 (8.46-13.9) uMInfant (0-1 year old)Not Available
Normal		 details
BloodDetected and Quantified15.9 +/- 4.61 uMAdult (>18 years old)BothNormal details
BloodDetected and Quantified25.87(9.06) uMAdult (>18 years old)BothNormal details
FecesDetected and Quantified0.12 +/- 0.21 nmol/g wet fecesAdult (>18 years old)Both
Normal		 details
FecesDetected and Quantified0.39 +/- 0.47 nmol/g wet fecesAdult (>18 years old)Both
Normal		 details
SalivaDetected and Quantified0.016 +/- 0.005 uMAdult (>18 years old)Both
Normal
    • Zerihun T. Dame, ...
 details
UrineDetected and Quantified0.002 umol/mmol creatinineAdult (>18 years old)Both
Normal		 details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified13.2 +/- 4.8 uMChildren (1-13 years old)Both
Obesity
    • Metabolomics reve...
 details
BloodDetected and Quantified16.1 +/- 4.7 uMChildren (1-13 years old)Both
Obesity
    • Metabolomics reve...
 details
BloodDetected and Quantified14.688 (13.192) uMAdult (>18 years old)FemalePregnancy with fetus having congenital heart defect details
BloodDetected and Quantified26.705 (10.794) uMAdult (>18 years old)FemalePregnancy details
BloodDetected and Quantified20.04(6.27) uMAdult (>18 years old)BothHeart failure with preserved ejection fraction details
Predicted Concentrations
BiospecimenValueOriginal ageOriginal sexOriginal conditionComments
Blood25.051 +/- 9.685 uMAdult (>18 years old)BothNormal (Upper Limit)Concentration data updated from parsing Nick's...
Blood0.082 +/- 0.017 uMAdult (>18 years old)BothNormal (Most Probable)Concentration data updated from parsing Nick's...
Associated Disorders and Diseases
Disease References
Pregnancy
  1. Bahado-Singh RO, Ertl R, Mandal R, Bjorndahl TC, Syngelaki A, Han B, Dong E, Liu PB, Alpay-Savasan Z, Wishart DS, Nicolaides KH: Metabolomic prediction of fetal congenital heart defect in the first trimester. Am J Obstet Gynecol. 2014 Sep;211(3):240.e1-240.e14. doi: 10.1016/j.ajog.2014.03.056. Epub 2014 Apr 1. [PubMed:24704061 ]
Obesity
  1. Simone Wahl, Christina Holzapfel, Zhonghao Yu, Michaela Breier, Ivan Kondofersky, Christiane Fuchs, Paula Singmann, Cornelia Prehn, Jerzy Adamski, Harald Grallert, Thomas Illig, Rui Wang-Sattler, Thomas Reinehr (2013). Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children. Metabolomics.
Associated OMIM IDs
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB027968
KNApSAcK IDNot Available
Chemspider ID24767488
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound52923894
PDB IDNot Available
ChEBI ID89978
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDMDB00000805
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. 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 ]
  3. 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 ]
  4. 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 ]
  5. Divecha N, Irvine RF: Phospholipid signaling. Cell. 1995 Jan 27;80(2):269-78. [PubMed:7834746 ]
  6. Cevc, Gregor (1993). Phospholipids Handbook. Marcel Dekker.
  7. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Only showing the first 10 proteins. There are 72 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details
1. Calcium-dependent phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. This isozyme hydrolyzes more efficiently L-alpha-1-palmitoyl-2-oleoyl phosphatidylcholine than L-alpha-1-palmitoyl-2-arachidonyl phosphatidylcholine, L-alpha-1-palmitoyl-2-arachidonyl phosphatidylethanolamine, or L-alpha-1-stearoyl-2-arachidonyl phosphatidylinositol. May be involved in the production of lung surfactant, the remodeling or regulation of cardiac muscle.
Gene Name:
PLA2G5
Uniprot ID:
P39877
Molecular weight:
15674.065
Enzyme Details
2. Group IIF secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Hydrolyzes phosphatidylglycerol versus phosphatidylcholine with a 15-fold preference.
Gene Name:
PLA2G2F
Uniprot ID:
Q9BZM2
Molecular weight:
23256.29
Enzyme Details
3. Cytosolic phospholipase A2
General function:
Involved in metabolic process
Specific function:
Selectively hydrolyzes arachidonyl phospholipids in the sn-2 position releasing arachidonic acid. Together with its lysophospholipid activity, it is implicated in the initiation of the inflammatory response.
Gene Name:
PLA2G4A
Uniprot ID:
P47712
Molecular weight:
85210.19
Enzyme Details
4. Phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides.
Gene Name:
PLA2G1B
Uniprot ID:
P04054
Molecular weight:
16359.535
Enzyme Details
5. Group 10 secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a powerful potency for releasing arachidonic acid from cell membrane phospholipids. Prefers phosphatidylethanolamine and phosphatidylcholine liposomes to those of phosphatidylserine.
Gene Name:
PLA2G10
Uniprot ID:
O15496
Molecular weight:
18153.04
Enzyme Details
6. Group IIE secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a preference for arachidonic-containing phospholipids.
Gene Name:
PLA2G2E
Uniprot ID:
Q9NZK7
Molecular weight:
15988.525
Enzyme Details
7. Group XIIA secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Does not exhibit detectable activity toward sn-2-arachidonoyl- or linoleoyl-phosphatidylcholine or -phosphatidylethanolamine.
Gene Name:
PLA2G12A
Uniprot ID:
Q9BZM1
Molecular weight:
21066.99
Enzyme Details
8. 85/88 kDa calcium-independent phospholipase A2
General function:
Involved in metabolic process
Specific function:
Catalyzes the release of fatty acids from phospholipids. It has been implicated in normal phospholipid remodeling, nitric oxide-induced or vasopressin-induced arachidonic acid release and in leukotriene and prostaglandin production. May participate in fas mediated apoptosis and in regulating transmembrane ion flux in glucose-stimulated B-cells. Has a role in cardiolipin (CL) deacylation. Required for both speed and directionality of monocyte MCP1/CCL2-induced chemotaxis through regulation of F-actin polymerization at the pseudopods. Isoform ankyrin-iPLA2-1 and isoform ankyrin-iPLA2-2, which lack the catalytic domain, are probably involved in the negative regulation of iPLA2 activity.
Gene Name:
PLA2G6
Uniprot ID:
O60733
Molecular weight:
84092.635
Enzyme Details
9. Phosphatidylcholine-sterol acyltransferase
General function:
Involved in phosphatidylcholine-sterol O-acyltransferase activity
Specific function:
Central enzyme in the extracellular metabolism of plasma lipoproteins. Synthesized mainly in the liver and secreted into plasma where it converts cholesterol and phosphatidylcholines (lecithins) to cholesteryl esters and lysophosphatidylcholines on the surface of high and low density lipoproteins (HDLs and LDLs). The cholesterol ester is then transported back to the liver. Has a preference for plasma 16:0-18:2 or 18:O-18:2 phosphatidylcholines. Also produced in the brain by primary astrocytes, and esterifies free cholesterol on nascent APOE-containing lipoproteins secreted from glia and influences cerebral spinal fluid (CSF) APOE- and APOA1 levels. Together with APOE and the cholesterol transporter ABCA1, plays a key role in the maturation of glial-derived, nascent lipoproteins. Required for remodeling high-density lipoprotein particles into their spherical forms.
Gene Name:
LCAT
Uniprot ID:
P04180
Molecular weight:
49577.545
Enzyme Details
10. Phospholipase A2, membrane associated
General function:
Involved in phospholipase A2 activity
Specific function:
Thought to participate in the regulation of the phospholipid metabolism in biomembranes including eicosanoid biosynthesis. Catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides.
Gene Name:
PLA2G2A
Uniprot ID:
P14555
Molecular weight:
16082.525

Transporters

Enzyme Details
1. Multidrug resistance protein 3
General function:
Involved in ATP binding
Specific function:
Mediates ATP-dependent export of organic anions and drugs from the cytoplasm. Hydrolyzes ATP with low efficiency. Human MDR3 is not capable of conferring drug resistance. Mediates the translocation of phosphatidylcholine across the canalicular membrane of the hepatocyte
Gene Name:
ABCB4
Uniprot ID:
P21439
Molecular weight:
141521.8

Only showing the first 10 proteins. There are 72 proteins in total.

Show all enzymes and transporters