Hmdb loader

Showing metabocard for PG(18:1(11Z)/16:1(9Z)) (HMDB0010616)

Jump To Section:
IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesenzymes (1) Show 1 proteinXML
enzymes (1) Show 1 protein
Record Information
Version5.0
StatusDetected and Quantified
Creation Date2008-09-25 13:34:32 UTC
Update Date2022-03-07 02:51:00 UTC
HMDB IDHMDB0010616
Secondary Accession Numbers
  • HMDB10616
Metabolite Identification
Common NamePG(18:1(11Z)/16:1(9Z))
DescriptionPG(18:1(11Z)/16:1(9Z)) is a phosphatidylglycerol or glycerophospholipid (PG or GP). It is a glycerophospholipid in which a phosphoglycerol moiety occupies a glycerol substitution site. As is the case with diacylglycerols, phosphatidylglycerols 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. PG(18:1(11Z)/16:1(9Z)), in particular, consists of one chain of vaccenic acid at the C-1 position and one chain of palmitoleic acid at the C-2 position. The vaccenic acid moiety is derived from butter fat and animal fat, while the palmitoleic acid moiety is derived from animal fats and vegetable oils. Phosphatidylglycerol is present at a level of 1-2% in most animal tissues, but it can be the second most abundant phospholipid in lung surfactant at up to 11% of the total. It is well established that the concentration of phosphatidylglycerol increases during fetal development. Phosphatidylglycerol may be present in animal tissues merely as a precursor for diphosphatidylglycerol (cardiolipin). Phosphatidylglycerol is formed from phosphatidic acid by a sequence of enzymatic reactions that proceeds via the intermediate, cytidine diphosphate diacylglycerol (CDP-diacylglycerol). Bioynthesis proceeds by condensation of phosphatidic acid and cytidine triphosphate with elimination of pyrophosphate via the action of phosphatidate cytidyltransferase (or CDP-synthase). CDP-diacylglycerol then reacts with glycerol-3-phosphate via phosphatidylglycerophosphate synthase to form 3-sn-phosphatidyl-1'-sn-glycerol 3'-phosphoric acid, with the release of cytidine monophosphate (CMP). Finally, phosphatidylglycerol is formed by the action of specific phosphatases. 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. PGs have a net charge of -1 at physiological pH and are found in high concentration in mitochondrial membranes and as components of pulmonary surfactant. PG also serves as a precursor for the synthesis of cardiolipin. PG is synthesized from CDP-diacylglycerol and glycerol-3-phosphate.
Structure
Data?1582752852
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))


  Mrv0541 02241201102D          

 53 52  0  0  1  0            999 V2000
   20.3760   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7009   -9.6360    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   19.0258   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0511   -9.6360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3506   -9.6360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1741  -10.4156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.7262   -9.2462    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   21.3365   -8.5710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.1160   -9.9213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.4014   -8.8564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0764   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7516   -8.8564    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   24.4267   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2887  -10.4453    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   25.0645   -8.8197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3279   -8.1715    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   23.1395   -8.1715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4901   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2046   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9190   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6335   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3480   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0625   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7770   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4914   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2059   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9204   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6348   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3493   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0638   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7783   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4928   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2072   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9217   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6362   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6362   -8.3985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7426  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4571  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1715  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8860  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6005  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3149  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0294  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7439  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4584  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1728  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8873  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6018  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3162  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0307  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7452  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4596  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4596  -11.6531    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
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  2  6  1  6  0  0  0
  7  4  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
  2 14  1  1  0  0  0
 13 15  1  0  0  0  0
 12 16  1  6  0  0  0
 12 17  1  1  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  1  0  0  0  0
 25 24  2  0  0  0  0
 26 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 27  1  0  0  0  0
 29 28  1  0  0  0  0
 30 29  1  0  0  0  0
 31 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 34  1  0  0  0  0
 36 35  2  0  0  0  0
  5 35  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52  6  1  0  0  0  0
 52 53  2  0  0  0  0
M  END
Download

3D MOL for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))

HMDB0010616
     RDKit          3D
PG(18:1(11Z)/16:1(9Z))
126125  0  0  0  0  0  0  0  0999 V2000
   -3.5261    1.9555   -0.9354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3856    2.7985   -1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8664    3.6204   -0.2605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9777    4.4927    0.2569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4997    5.3389    1.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3909    6.3154    1.0175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8247    7.2184   -0.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1931    7.3373   -1.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0259    6.6239   -1.5588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1415    7.5847   -1.9366 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3648    6.8339   -2.3133 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9686    6.0576   -1.1817 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2117    5.3116   -1.6415 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8405    4.6327   -0.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0422    3.8496   -0.8201 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9058    2.6883   -1.7269 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1440    1.5166   -1.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7257    1.6242   -0.9487 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9023    2.4095   -1.4368 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2347    0.7506    0.0076 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0070    0.5831    0.5431 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8392    0.2227   -0.2790 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3420    0.1147    0.7151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0427   -0.9507    1.5333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1970   -1.2223    2.7357 P   0  0  0  0  0  5  0  0  0  0  0  0
   -2.1683   -2.2984    2.3382 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    0.2159    3.0942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3694   -1.6836    4.1790 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7690   -2.3475    3.7527 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6604   -2.8485    4.8397 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7379   -3.5021    4.1879 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3243   -1.6809    5.5619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9652   -0.8425    4.6597 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9371   -0.9767   -1.0168 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6120   -1.0524   -2.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2154    0.0076   -2.9023 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7279   -2.3217   -3.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5520   -3.1168   -2.8130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7636   -2.3607   -3.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0799   -3.0318   -3.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2462   -4.3163   -3.7887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5905   -4.8768   -3.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1847   -5.3655   -2.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2457   -4.5002   -1.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8022   -4.8147   -0.0706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1889   -6.0852    0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8119   -5.9600    0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8066   -5.3119   -0.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4435   -5.2479    0.5963 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0907   -6.6459    0.9178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4876   -6.5039    1.5481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3462    1.5812    0.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4294    2.6057   -0.9183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7147    1.1243   -1.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5676    2.2346   -1.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7390    3.5449   -2.1960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6022    2.8326    0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9246    4.1250   -0.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4603    5.0801   -0.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7950    3.7810    0.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3582    5.8783    1.8344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0648    4.7314    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4264    5.8236    0.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2639    6.9717    1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7589    7.8218    0.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5952    8.0373   -1.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1999    6.0408   -2.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4470    5.9532   -0.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8274    8.1857   -2.8278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3653    8.2886   -1.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1267    7.4855   -2.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1488    6.0544   -3.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2663    6.7631   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2663    5.2813   -0.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0439    4.6464   -2.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9384    6.1063   -1.9598 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0988    4.0777    0.1229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2205    5.4961    0.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8486    4.5640   -1.1747 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4875    3.4680    0.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9679    2.3184   -1.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5194    3.0026   -2.7414 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3389    0.6914   -2.0223 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7285    1.1102   -0.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7394    1.5234    1.1439 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1060   -0.2007    1.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5416    1.0256   -0.9540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2941    0.0583    0.2022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2989    1.0330    1.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3762    0.7987    3.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117   -3.1398    3.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3718   -1.5599    3.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2284   -3.5788    5.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6088   -4.4665    4.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816   -1.1432    6.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312   -2.0631    6.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2725   -0.0416    5.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6237   -2.9167   -2.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7229   -2.1045   -4.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4555   -4.0542   -3.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -3.3780   -1.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6840   -2.0143   -4.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7702   -1.4080   -2.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3312   -3.1778   -1.9498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8814   -2.3342   -3.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4248   -5.0408   -3.5456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0558   -4.0439   -4.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3105   -4.1347   -4.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6671   -5.7580   -4.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2930   -5.5887   -2.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8320   -6.4120   -2.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6844   -3.5024   -1.3718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8882   -4.0734    0.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1220   -6.8443   -0.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8558   -6.5522    1.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4581   -7.0072    1.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8810   -5.4383    1.8430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1144   -4.2411   -0.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7138   -5.7856   -1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5044   -4.6753    1.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3008   -4.7539   -0.0379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5534   -7.1508    1.6677 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1832   -7.2514    0.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8104   -7.4947    1.9494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1922   -6.1780    0.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4991   -5.7237    2.3257 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  2  0
  8  9  1  0
  9 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  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  1  0
 25 26  2  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 22 34  1  0
 34 35  1  0
 35 36  2  0
 35 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  2  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
 50 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
  3 58  1  0
  4 59  1  0
  4 60  1  0
  5 61  1  0
  5 62  1  0
  6 63  1  0
  6 64  1  0
  7 65  1  0
  8 66  1  0
  9 67  1  0
  9 68  1  0
 10 69  1  0
 10 70  1  0
 11 71  1  0
 11 72  1  0
 12 73  1  0
 12 74  1  0
 13 75  1  0
 13 76  1  0
 14 77  1  0
 14 78  1  0
 15 79  1  0
 15 80  1  0
 16 81  1  0
 16 82  1  0
 17 83  1  0
 17 84  1  0
 21 85  1  0
 21 86  1  0
 22 87  1  6
 23 88  1  0
 23 89  1  0
 27 90  1  0
 29 91  1  0
 29 92  1  0
 30 93  1  1
 31 94  1  0
 32 95  1  0
 32 96  1  0
 33 97  1  0
 37 98  1  0
 37 99  1  0
 38100  1  0
 38101  1  0
 39102  1  0
 39103  1  0
 40104  1  0
 40105  1  0
 41106  1  0
 41107  1  0
 42108  1  0
 42109  1  0
 43110  1  0
 43111  1  0
 44112  1  0
 45113  1  0
 46114  1  0
 46115  1  0
 47116  1  0
 47117  1  0
 48118  1  0
 48119  1  0
 49120  1  0
 49121  1  0
 50122  1  0
 50123  1  0
 51124  1  0
 51125  1  0
 51126  1  0
M  END
Download

3D SDF for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))


  Mrv0541 02241201102D          

 53 52  0  0  1  0            999 V2000
   20.3760   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7009   -9.6360    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   19.0258   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0511   -9.6360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3506   -9.6360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1741  -10.4156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.7262   -9.2462    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   21.3365   -8.5710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.1160   -9.9213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.4014   -8.8564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0764   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7516   -8.8564    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   24.4267   -9.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2887  -10.4453    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   25.0645   -8.8197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3279   -8.1715    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   23.1395   -8.1715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4901   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2046   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9190   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6335   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3480   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0625   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7770   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4914   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2059   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9204   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6348   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3493   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0638   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7783   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4928   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2072   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9217   -9.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6362   -9.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6362   -8.3985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7426  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4571  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1715  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8860  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6005  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3149  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0294  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7439  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4584  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1728  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8873  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6018  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3162  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0307  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7452  -10.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4596  -10.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4596  -11.6531    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
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  2  6  1  6  0  0  0
  7  4  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
  2 14  1  1  0  0  0
 13 15  1  0  0  0  0
 12 16  1  6  0  0  0
 12 17  1  1  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  1  0  0  0  0
 25 24  2  0  0  0  0
 26 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 27  1  0  0  0  0
 29 28  1  0  0  0  0
 30 29  1  0  0  0  0
 31 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 34  1  0  0  0  0
 36 35  2  0  0  0  0
  5 35  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52  6  1  0  0  0  0
 52 53  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0010616

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C40H75O10P/c1-3-5-7-9-11-13-15-17-18-20-21-23-25-27-29-31-39(43)47-35-38(36-49-51(45,46)48-34-37(42)33-41)50-40(44)32-30-28-26-24-22-19-16-14-12-10-8-6-4-2/h13-16,37-38,41-42H,3-12,17-36H2,1-2H3,(H,45,46)/b15-13-,16-14-/t37-,38+/m0/s1

> <INCHI_KEY>
ICYKSOZJGJBBNU-GFJSAGKOSA-N

> <FORMULA>
C40H75O10P

> <MOLECULAR_WEIGHT>
746.9913

> <EXACT_MASS>
746.509785132

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
88.4855283747366

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S)-2,3-dihydroxypropoxy][(2R)-2-[(9Z)-hexadec-9-enoyloxy]-3-[(11Z)-octadec-11-enoyloxy]propoxy]phosphinic acid

> <ALOGPS_LOGP>
8.01

> <JCHEM_LOGP>
11.102345536

> <ALOGPS_LOGS>
-6.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.641245576372423

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8907737771908404

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9689647678483633

> <JCHEM_POLAR_SURFACE_AREA>
148.82000000000002

> <JCHEM_REFRACTIVITY>
206.74410000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
40

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.06e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,3-dihydroxypropoxy(2R)-2-[(9Z)-hexadec-9-enoyloxy]-3-[(11Z)-octadec-11-enoyloxy]propoxyphosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))

HMDB0010616
     RDKit          3D
PG(18:1(11Z)/16:1(9Z))
126125  0  0  0  0  0  0  0  0999 V2000
   -3.5261    1.9555   -0.9354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3856    2.7985   -1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8664    3.6204   -0.2605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9777    4.4927    0.2569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4997    5.3389    1.3805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3909    6.3154    1.0175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8247    7.2184   -0.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1931    7.3373   -1.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0259    6.6239   -1.5588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1415    7.5847   -1.9366 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3648    6.8339   -2.3133 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9686    6.0576   -1.1817 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2117    5.3116   -1.6415 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8405    4.6327   -0.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0422    3.8496   -0.8201 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9058    2.6883   -1.7269 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1440    1.5166   -1.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7257    1.6242   -0.9487 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9023    2.4095   -1.4368 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2347    0.7506    0.0076 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0070    0.5831    0.5431 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8392    0.2227   -0.2790 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3420    0.1147    0.7151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0427   -0.9507    1.5333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1970   -1.2223    2.7357 P   0  0  0  0  0  5  0  0  0  0  0  0
   -2.1683   -2.2984    2.3382 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    0.2159    3.0942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3694   -1.6836    4.1790 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7690   -2.3475    3.7527 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6604   -2.8485    4.8397 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7379   -3.5021    4.1879 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3243   -1.6809    5.5619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9652   -0.8425    4.6597 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9371   -0.9767   -1.0168 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6120   -1.0524   -2.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2154    0.0076   -2.9023 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7279   -2.3217   -3.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5520   -3.1168   -2.8130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7636   -2.3607   -3.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0799   -3.0318   -3.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2462   -4.3163   -3.7887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5905   -4.8768   -3.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1847   -5.3655   -2.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2457   -4.5002   -1.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8022   -4.8147   -0.0706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1889   -6.0852    0.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8119   -5.9600    0.8514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8066   -5.3119   -0.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4435   -5.2479    0.5963 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0907   -6.6459    0.9178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4876   -6.5039    1.5481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3462    1.5812    0.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4294    2.6057   -0.9183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7147    1.1243   -1.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5676    2.2346   -1.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7390    3.5449   -2.1960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6022    2.8326    0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9246    4.1250   -0.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4603    5.0801   -0.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7950    3.7810    0.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3582    5.8783    1.8344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0648    4.7314    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4264    5.8236    0.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2639    6.9717    1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7589    7.8218    0.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5952    8.0373   -1.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1999    6.0408   -2.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4470    5.9532   -0.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8274    8.1857   -2.8278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3653    8.2886   -1.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1267    7.4855   -2.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1488    6.0544   -3.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2663    6.7631   -0.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2663    5.2813   -0.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0439    4.6464   -2.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9384    6.1063   -1.9598 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0988    4.0777    0.1229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2205    5.4961    0.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8486    4.5640   -1.1747 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4875    3.4680    0.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9679    2.3184   -1.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5194    3.0026   -2.7414 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3389    0.6914   -2.0223 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7285    1.1102   -0.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7394    1.5234    1.1439 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1060   -0.2007    1.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5416    1.0256   -0.9540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2941    0.0583    0.2022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2989    1.0330    1.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3762    0.7987    3.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117   -3.1398    3.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3718   -1.5599    3.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2284   -3.5788    5.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6088   -4.4665    4.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816   -1.1432    6.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312   -2.0631    6.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2725   -0.0416    5.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6237   -2.9167   -2.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7229   -2.1045   -4.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4555   -4.0542   -3.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -3.3780   -1.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6840   -2.0143   -4.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7702   -1.4080   -2.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3312   -3.1778   -1.9498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8814   -2.3342   -3.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4248   -5.0408   -3.5456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0558   -4.0439   -4.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3105   -4.1347   -4.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6671   -5.7580   -4.4297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2930   -5.5887   -2.7007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8320   -6.4120   -2.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6844   -3.5024   -1.3718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8882   -4.0734    0.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1220   -6.8443   -0.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8558   -6.5522    1.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4581   -7.0072    1.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8810   -5.4383    1.8430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1144   -4.2411   -0.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7138   -5.7856   -1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5044   -4.6753    1.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3008   -4.7539   -0.0379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5534   -7.1508    1.6677 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1832   -7.2514    0.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8104   -7.4947    1.9494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1922   -6.1780    0.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4991   -5.7237    2.3257 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  2  0
  8  9  1  0
  9 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  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  1  0
 25 26  2  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 22 34  1  0
 34 35  1  0
 35 36  2  0
 35 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  2  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
 50 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
  3 58  1  0
  4 59  1  0
  4 60  1  0
  5 61  1  0
  5 62  1  0
  6 63  1  0
  6 64  1  0
  7 65  1  0
  8 66  1  0
  9 67  1  0
  9 68  1  0
 10 69  1  0
 10 70  1  0
 11 71  1  0
 11 72  1  0
 12 73  1  0
 12 74  1  0
 13 75  1  0
 13 76  1  0
 14 77  1  0
 14 78  1  0
 15 79  1  0
 15 80  1  0
 16 81  1  0
 16 82  1  0
 17 83  1  0
 17 84  1  0
 21 85  1  0
 21 86  1  0
 22 87  1  6
 23 88  1  0
 23 89  1  0
 27 90  1  0
 29 91  1  0
 29 92  1  0
 30 93  1  1
 31 94  1  0
 32 95  1  0
 32 96  1  0
 33 97  1  0
 37 98  1  0
 37 99  1  0
 38100  1  0
 38101  1  0
 39102  1  0
 39103  1  0
 40104  1  0
 40105  1  0
 41106  1  0
 41107  1  0
 42108  1  0
 42109  1  0
 43110  1  0
 43111  1  0
 44112  1  0
 45113  1  0
 46114  1  0
 46115  1  0
 47116  1  0
 47117  1  0
 48118  1  0
 48119  1  0
 49120  1  0
 49121  1  0
 50122  1  0
 50123  1  0
 51124  1  0
 51125  1  0
 51126  1  0
M  END
Download

PDB for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))

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      38.035 -17.260   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      36.775 -17.987   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      35.515 -17.260   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      39.295 -17.987   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      34.254 -17.987   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      35.792 -19.442   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      40.556 -17.260   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      39.828 -15.999   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      41.283 -18.520   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      41.816 -16.532   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      43.076 -17.260   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      44.336 -16.532   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      45.597 -17.260   0.000  0.00  0.00           C+0
HETATM   14  H   UNK     0      37.872 -19.498   0.000  0.00  0.00           H+0
HETATM   15  O   UNK     0      46.787 -16.463   0.000  0.00  0.00           O+0
HETATM   16  H   UNK     0      45.412 -15.253   0.000  0.00  0.00           H+0
HETATM   17  O   UNK     0      43.194 -15.253   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.248 -17.217   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.582 -17.987   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.915 -17.217   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.249 -17.987   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.583 -17.217   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.917 -17.987   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.250 -17.217   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      19.584 -17.217   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      20.918 -17.987   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      22.251 -17.217   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      23.585 -17.987   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      24.919 -17.217   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      26.252 -17.987   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      27.586 -17.217   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      28.920 -17.987   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      30.253 -17.217   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      31.587 -17.987   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      32.921 -17.217   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      32.921 -15.677   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      14.453 -20.212   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.787 -19.442   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      17.120 -20.212   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      18.454 -19.442   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      19.788 -20.212   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      21.121 -19.442   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      22.455 -20.212   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      23.789 -20.212   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      25.122 -19.442   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      26.456 -20.212   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      27.790 -19.442   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      29.123 -20.212   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      30.457 -19.442   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      31.791 -20.212   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      33.124 -19.442   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      34.458 -20.212   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      34.458 -21.752   0.000  0.00  0.00           O+0
CONECT    1    2    4                                                       
CONECT    2    1    3    6   14                                             
CONECT    3    2    5                                                       
CONECT    4    1    7                                                       
CONECT    5    3   35                                                       
CONECT    6    2   52                                                       
CONECT    7    4    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16   17                                             
CONECT   13   12   15                                                       
CONECT   14    2                                                            
CONECT   15   13                                                            
CONECT   16   12                                                            
CONECT   17   12                                                            
CONECT   18   19                                                            
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36    5                                                  
CONECT   36   35                                                            
CONECT   37   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                                                       
CONECT   52   51    6   53                                                  
CONECT   53   52                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  104    0
END
Download

3D PDB for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))

COMPND    HMDB0010616
HETATM    1  C1  UNL     1      -3.526   1.955  -0.935  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.386   2.799  -1.439  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.866   3.620  -0.260  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.978   4.493   0.257  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.500   5.339   1.381  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.391   6.315   1.018  1.00  0.00           C  
HETATM    7  C7  UNL     1      -1.825   7.218  -0.061  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.193   7.337  -1.187  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.026   6.624  -1.559  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.141   7.585  -1.937  1.00  0.00           C  
HETATM   11  C11 UNL     1       2.365   6.834  -2.313  1.00  0.00           C  
HETATM   12  C12 UNL     1       2.969   6.058  -1.182  1.00  0.00           C  
HETATM   13  C13 UNL     1       4.212   5.312  -1.642  1.00  0.00           C  
HETATM   14  C14 UNL     1       4.841   4.633  -0.452  1.00  0.00           C  
HETATM   15  C15 UNL     1       6.042   3.850  -0.820  1.00  0.00           C  
HETATM   16  C16 UNL     1       5.906   2.688  -1.727  1.00  0.00           C  
HETATM   17  C17 UNL     1       5.144   1.517  -1.256  1.00  0.00           C  
HETATM   18  C18 UNL     1       3.726   1.624  -0.949  1.00  0.00           C  
HETATM   19  O1  UNL     1       2.902   2.410  -1.437  1.00  0.00           O  
HETATM   20  O2  UNL     1       3.235   0.751   0.008  1.00  0.00           O  
HETATM   21  C19 UNL     1       2.007   0.583   0.543  1.00  0.00           C  
HETATM   22  C20 UNL     1       0.839   0.223  -0.279  1.00  0.00           C  
HETATM   23  C21 UNL     1      -0.342   0.115   0.715  1.00  0.00           C  
HETATM   24  O3  UNL     1      -0.043  -0.951   1.533  1.00  0.00           O  
HETATM   25  P1  UNL     1      -1.197  -1.222   2.736  1.00  0.00           P  
HETATM   26  O4  UNL     1      -2.168  -2.298   2.338  1.00  0.00           O  
HETATM   27  O5  UNL     1      -2.008   0.216   3.094  1.00  0.00           O  
HETATM   28  O6  UNL     1      -0.369  -1.684   4.179  1.00  0.00           O  
HETATM   29  C22 UNL     1       0.769  -2.348   3.753  1.00  0.00           C  
HETATM   30  C23 UNL     1       1.660  -2.848   4.840  1.00  0.00           C  
HETATM   31  O7  UNL     1       2.738  -3.502   4.188  1.00  0.00           O  
HETATM   32  C24 UNL     1       2.324  -1.681   5.562  1.00  0.00           C  
HETATM   33  O8  UNL     1       2.965  -0.842   4.660  1.00  0.00           O  
HETATM   34  O9  UNL     1       0.937  -0.977  -1.017  1.00  0.00           O  
HETATM   35  C25 UNL     1       0.612  -1.052  -2.358  1.00  0.00           C  
HETATM   36  O10 UNL     1       0.215   0.008  -2.902  1.00  0.00           O  
HETATM   37  C26 UNL     1       0.728  -2.322  -3.100  1.00  0.00           C  
HETATM   38  C27 UNL     1      -0.552  -3.117  -2.813  1.00  0.00           C  
HETATM   39  C28 UNL     1      -1.764  -2.361  -3.219  1.00  0.00           C  
HETATM   40  C29 UNL     1      -3.080  -3.032  -3.025  1.00  0.00           C  
HETATM   41  C30 UNL     1      -3.246  -4.316  -3.789  1.00  0.00           C  
HETATM   42  C31 UNL     1      -4.591  -4.877  -3.683  1.00  0.00           C  
HETATM   43  C32 UNL     1      -5.185  -5.365  -2.426  1.00  0.00           C  
HETATM   44  C33 UNL     1      -5.246  -4.500  -1.275  1.00  0.00           C  
HETATM   45  C34 UNL     1      -4.802  -4.815  -0.071  1.00  0.00           C  
HETATM   46  C35 UNL     1      -4.189  -6.085   0.283  1.00  0.00           C  
HETATM   47  C36 UNL     1      -2.812  -5.960   0.851  1.00  0.00           C  
HETATM   48  C37 UNL     1      -1.807  -5.312  -0.038  1.00  0.00           C  
HETATM   49  C38 UNL     1      -0.443  -5.248   0.596  1.00  0.00           C  
HETATM   50  C39 UNL     1       0.091  -6.646   0.918  1.00  0.00           C  
HETATM   51  C40 UNL     1       1.488  -6.504   1.548  1.00  0.00           C  
HETATM   52  H1  UNL     1      -3.346   1.581   0.077  1.00  0.00           H  
HETATM   53  H2  UNL     1      -4.429   2.606  -0.918  1.00  0.00           H  
HETATM   54  H3  UNL     1      -3.715   1.124  -1.659  1.00  0.00           H  
HETATM   55  H4  UNL     1      -1.568   2.235  -1.891  1.00  0.00           H  
HETATM   56  H5  UNL     1      -2.739   3.545  -2.196  1.00  0.00           H  
HETATM   57  H6  UNL     1      -1.602   2.833   0.516  1.00  0.00           H  
HETATM   58  H7  UNL     1      -0.925   4.125  -0.467  1.00  0.00           H  
HETATM   59  H8  UNL     1      -3.460   5.080  -0.558  1.00  0.00           H  
HETATM   60  H9  UNL     1      -3.795   3.781   0.586  1.00  0.00           H  
HETATM   61  H10 UNL     1      -3.358   5.878   1.834  1.00  0.00           H  
HETATM   62  H11 UNL     1      -2.065   4.731   2.220  1.00  0.00           H  
HETATM   63  H12 UNL     1      -0.426   5.824   0.894  1.00  0.00           H  
HETATM   64  H13 UNL     1      -1.264   6.972   1.932  1.00  0.00           H  
HETATM   65  H14 UNL     1      -2.759   7.822   0.139  1.00  0.00           H  
HETATM   66  H15 UNL     1      -1.595   8.037  -1.959  1.00  0.00           H  
HETATM   67  H16 UNL     1      -0.200   6.041  -2.488  1.00  0.00           H  
HETATM   68  H17 UNL     1       0.447   5.953  -0.820  1.00  0.00           H  
HETATM   69  H18 UNL     1       0.827   8.186  -2.828  1.00  0.00           H  
HETATM   70  H19 UNL     1       1.365   8.289  -1.116  1.00  0.00           H  
HETATM   71  H20 UNL     1       3.127   7.486  -2.824  1.00  0.00           H  
HETATM   72  H21 UNL     1       2.149   6.054  -3.113  1.00  0.00           H  
HETATM   73  H22 UNL     1       3.266   6.763  -0.402  1.00  0.00           H  
HETATM   74  H23 UNL     1       2.266   5.281  -0.859  1.00  0.00           H  
HETATM   75  H24 UNL     1       4.044   4.646  -2.486  1.00  0.00           H  
HETATM   76  H25 UNL     1       4.938   6.106  -1.960  1.00  0.00           H  
HETATM   77  H26 UNL     1       4.099   4.078   0.123  1.00  0.00           H  
HETATM   78  H27 UNL     1       5.221   5.496   0.189  1.00  0.00           H  
HETATM   79  H28 UNL     1       6.849   4.564  -1.175  1.00  0.00           H  
HETATM   80  H29 UNL     1       6.488   3.468   0.152  1.00  0.00           H  
HETATM   81  H30 UNL     1       6.968   2.318  -1.913  1.00  0.00           H  
HETATM   82  H31 UNL     1       5.519   3.003  -2.741  1.00  0.00           H  
HETATM   83  H32 UNL     1       5.339   0.691  -2.022  1.00  0.00           H  
HETATM   84  H33 UNL     1       5.729   1.110  -0.361  1.00  0.00           H  
HETATM   85  H34 UNL     1       1.739   1.523   1.144  1.00  0.00           H  
HETATM   86  H35 UNL     1       2.106  -0.201   1.370  1.00  0.00           H  
HETATM   87  H36 UNL     1       0.542   1.026  -0.954  1.00  0.00           H  
HETATM   88  H37 UNL     1      -1.294   0.058   0.202  1.00  0.00           H  
HETATM   89  H38 UNL     1      -0.299   1.033   1.327  1.00  0.00           H  
HETATM   90  H39 UNL     1      -1.376   0.799   3.623  1.00  0.00           H  
HETATM   91  H40 UNL     1       0.512  -3.140   3.024  1.00  0.00           H  
HETATM   92  H41 UNL     1       1.372  -1.560   3.205  1.00  0.00           H  
HETATM   93  H42 UNL     1       1.228  -3.579   5.519  1.00  0.00           H  
HETATM   94  H43 UNL     1       2.609  -4.466   4.164  1.00  0.00           H  
HETATM   95  H44 UNL     1       1.582  -1.143   6.145  1.00  0.00           H  
HETATM   96  H45 UNL     1       3.131  -2.063   6.250  1.00  0.00           H  
HETATM   97  H46 UNL     1       3.273  -0.042   5.134  1.00  0.00           H  
HETATM   98  H47 UNL     1       1.624  -2.917  -2.834  1.00  0.00           H  
HETATM   99  H48 UNL     1       0.723  -2.104  -4.203  1.00  0.00           H  
HETATM  100  H49 UNL     1      -0.456  -4.054  -3.392  1.00  0.00           H  
HETATM  101  H50 UNL     1      -0.584  -3.378  -1.740  1.00  0.00           H  
HETATM  102  H51 UNL     1      -1.684  -2.014  -4.288  1.00  0.00           H  
HETATM  103  H52 UNL     1      -1.770  -1.408  -2.613  1.00  0.00           H  
HETATM  104  H53 UNL     1      -3.331  -3.178  -1.950  1.00  0.00           H  
HETATM  105  H54 UNL     1      -3.881  -2.334  -3.402  1.00  0.00           H  
HETATM  106  H55 UNL     1      -2.425  -5.041  -3.546  1.00  0.00           H  
HETATM  107  H56 UNL     1      -3.056  -4.044  -4.865  1.00  0.00           H  
HETATM  108  H57 UNL     1      -5.310  -4.135  -4.206  1.00  0.00           H  
HETATM  109  H58 UNL     1      -4.667  -5.758  -4.430  1.00  0.00           H  
HETATM  110  H59 UNL     1      -6.293  -5.589  -2.701  1.00  0.00           H  
HETATM  111  H60 UNL     1      -4.832  -6.412  -2.195  1.00  0.00           H  
HETATM  112  H61 UNL     1      -5.684  -3.502  -1.372  1.00  0.00           H  
HETATM  113  H62 UNL     1      -4.888  -4.073   0.755  1.00  0.00           H  
HETATM  114  H63 UNL     1      -4.122  -6.844  -0.531  1.00  0.00           H  
HETATM  115  H64 UNL     1      -4.856  -6.552   1.098  1.00  0.00           H  
HETATM  116  H65 UNL     1      -2.458  -7.007   1.108  1.00  0.00           H  
HETATM  117  H66 UNL     1      -2.881  -5.438   1.843  1.00  0.00           H  
HETATM  118  H67 UNL     1      -2.114  -4.241  -0.193  1.00  0.00           H  
HETATM  119  H68 UNL     1      -1.714  -5.786  -1.022  1.00  0.00           H  
HETATM  120  H69 UNL     1      -0.504  -4.675   1.556  1.00  0.00           H  
HETATM  121  H70 UNL     1       0.301  -4.754  -0.038  1.00  0.00           H  
HETATM  122  H71 UNL     1      -0.553  -7.151   1.668  1.00  0.00           H  
HETATM  123  H72 UNL     1       0.183  -7.251   0.001  1.00  0.00           H  
HETATM  124  H73 UNL     1       1.810  -7.495   1.949  1.00  0.00           H  
HETATM  125  H74 UNL     1       2.192  -6.178   0.755  1.00  0.00           H  
HETATM  126  H75 UNL     1       1.499  -5.724   2.326  1.00  0.00           H  
CONECT    1    2   52   53   54
CONECT    2    3   55   56
CONECT    3    4   57   58
CONECT    4    5   59   60
CONECT    5    6   61   62
CONECT    6    7   63   64
CONECT    7    8    8   65
CONECT    8    9   66
CONECT    9   10   67   68
CONECT   10   11   69   70
CONECT   11   12   71   72
CONECT   12   13   73   74
CONECT   13   14   75   76
CONECT   14   15   77   78
CONECT   15   16   79   80
CONECT   16   17   81   82
CONECT   17   18   83   84
CONECT   18   19   19   20
CONECT   20   21
CONECT   21   22   85   86
CONECT   22   23   34   87
CONECT   23   24   88   89
CONECT   24   25
CONECT   25   26   26   27   28
CONECT   27   90
CONECT   28   29
CONECT   29   30   91   92
CONECT   30   31   32   93
CONECT   31   94
CONECT   32   33   95   96
CONECT   33   97
CONECT   34   35
CONECT   35   36   36   37
CONECT   37   38   98   99
CONECT   38   39  100  101
CONECT   39   40  102  103
CONECT   40   41  104  105
CONECT   41   42  106  107
CONECT   42   43  108  109
CONECT   43   44  110  111
CONECT   44   45   45  112
CONECT   45   46  113
CONECT   46   47  114  115
CONECT   47   48  116  117
CONECT   48   49  118  119
CONECT   49   50  120  121
CONECT   50   51  122  123
CONECT   51  124  125  126
END
Download

SMILES for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))

[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC
Download

INCHI for HMDB0010616 (PG(18:1(11Z)/16:1(9Z)))

InChI=1S/C40H75O10P/c1-3-5-7-9-11-13-15-17-18-20-21-23-25-27-29-31-39(43)47-35-38(36-49-51(45,46)48-34-37(42)33-41)50-40(44)32-30-28-26-24-22-19-16-14-12-10-8-6-4-2/h13-16,37-38,41-42H,3-12,17-36H2,1-2H3,(H,45,46)/b15-13-,16-14-/t37-,38+/m0/s1
Download
View in JSmolView Stereo Labels
Synonyms
ValueSource
1-(11Z-Octadecenoyl)-2-(9Z-hexadecenoyl)-sn-glycero-3-phospho-(1'-glycerol)HMDB
1-Vaccenoyl-2-palmitoleoyl-sn-glycero-3-phosphoglycerolHMDB
GPG(18:1/16:1)HMDB
GPG(18:1N7/16:1N7)HMDB
GPG(18:1W7/16:1W7)HMDB
GPG(34:2)HMDB
PG(18:1/16:1)HMDB
PG(18:1N7/16:1N7)HMDB
PG(18:1W7/16:1W7)HMDB
PG(34:2)HMDB
Phosphatidylglycerol(18:1/16:1)HMDB
Phosphatidylglycerol(18:1n7/16:1n7)HMDB
Phosphatidylglycerol(18:1W7/16:1W7)HMDB
Phosphatidylglycerol(34:2)HMDB
1-(11Z-Octadecenoyl)-2-(9Z-hexadecenoyl)-sn-glycero-3-phosphoglycerolHMDB
PG(18:1(11Z)/16:1(9Z))Lipid Annotator
Chemical FormulaC40H75O10P
Average Molecular Weight746.9913
Monoisotopic Molecular Weight746.509785132
IUPAC Name[(2S)-2,3-dihydroxypropoxy][(2R)-2-[(9Z)-hexadec-9-enoyloxy]-3-[(11Z)-octadec-11-enoyloxy]propoxy]phosphinic acid
Traditional Name(2S)-2,3-dihydroxypropoxy(2R)-2-[(9Z)-hexadec-9-enoyloxy]-3-[(11Z)-octadec-11-enoyloxy]propoxyphosphinic acid
CAS Registry NumberNot Available
SMILES
[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC
InChI Identifier
InChI=1S/C40H75O10P/c1-3-5-7-9-11-13-15-17-18-20-21-23-25-27-29-31-39(43)47-35-38(36-49-51(45,46)48-34-37(42)33-41)50-40(44)32-30-28-26-24-22-19-16-14-12-10-8-6-4-2/h13-16,37-38,41-42H,3-12,17-36H2,1-2H3,(H,45,46)/b15-13-,16-14-/t37-,38+/m0/s1
InChI KeyICYKSOZJGJBBNU-GFJSAGKOSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as phosphatidylglycerols. These are glycerophosphoglycerols in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages. As is the case with diacylglycerols, phosphatidylglycerols can have many different combinations of fatty acids of varying lengths and saturation attached to the C-1 and C-2 positions.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphoglycerols
Direct ParentPhosphatidylglycerols
Alternative Parents
Substituents
  • 1,2-diacylglycerophosphoglycerol
  • Fatty acid ester
  • Dialkyl phosphate
  • Dicarboxylic acid or derivatives
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • 1,2-diol
  • Carboxylic acid ester
  • Secondary alcohol
  • Carboxylic acid derivative
  • Organic oxide
  • Organooxygen compound
  • Alcohol
  • Organic oxygen compound
  • Primary alcohol
  • Carbonyl group
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
Process
Naturally occurring process
RoleNot Available
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 Solubility0.00011 g/LALOGPS
logP8.01ALOGPS
logP11.1ChemAxon
logS-6.8ALOGPS
pKa (Strongest Acidic)1.89ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area148.82 ŲChemAxon
Rotatable Bond Count40ChemAxon
Refractivity206.74 m³·mol⁻¹ChemAxon
Polarizability88.49 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
DarkChem[M+H]+284.78431661259
DarkChem[M-H]-271.00231661259
DeepCCS[M+H]+279.54930932474
DeepCCS[M-H]-277.39930932474
DeepCCS[M-2H]-310.63930932474
DeepCCS[M+Na]+285.46230932474
AllCCS[M+H]+281.832859911
AllCCS[M+H-H2O]+281.732859911
AllCCS[M+NH4]+281.932859911
AllCCS[M+Na]+281.932859911
AllCCS[M-H]-269.732859911
AllCCS[M+Na-2H]-276.132859911
AllCCS[M+HCOO]-283.132859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
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, 2022.9.49 minutes32390414
Predicted by Siyang on May 30, 202228.8746 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20222.0 minutes32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid82.9 seconds40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid5312.2 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid303.3 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid326.3 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid199.0 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid1058.4 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid1614.2 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid1147.3 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)266.0 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid3052.5 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid1100.1 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid2726.5 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid1186.1 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid686.8 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate365.7 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA573.3 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water9.4 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
PG(18:1(11Z)/16:1(9Z))[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC4708.9Standard polar33892256
PG(18:1(11Z)/16:1(9Z))[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC4522.9Standard non polar33892256
PG(18:1(11Z)/16:1(9Z))[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCC\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC5252.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TBDMS_1_1) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TBDMS_1_2) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - PG(18:1(11Z)/16:1(9Z)) GC-MS (TBDMS_1_3) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 10V, Positive-QTOFsplash10-00or-3190520500-b9b2250a97ef42e753ae2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 20V, Positive-QTOFsplash10-00or-4191311100-23d57e29501089b016eb2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 40V, Positive-QTOFsplash10-0ar9-9073231000-31ce03d5e86ca3fee0232015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 10V, Negative-QTOFsplash10-0gx1-0190200200-701c53e09b09bf0486562015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 20V, Negative-QTOFsplash10-01z9-4290100000-e48b747ecad89965d61e2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 40V, Negative-QTOFsplash10-004i-9030000000-a348c66bf164f3be20042015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 10V, Negative-QTOFsplash10-0002-0000000900-6a6a3edc7613adf015682021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 20V, Negative-QTOFsplash10-0uf1-0090300400-d377ddb6dd8dfe25475a2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PG(18:1(11Z)/16:1(9Z)) 40V, Negative-QTOFsplash10-0uf1-0190300400-5254bc3d1dcb8621b2862021-09-24Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-22Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Blood
Tissue Locations
  • All Tissues
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.080 +/- 0.010 uMAdult (>18 years old)BothNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB027766
KNApSAcK IDNot Available
Chemspider ID24768115
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53480615
PDB IDNot Available
ChEBI ID89271
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
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.

Enzymes

Enzyme Details
1. Acyl-CoA:lysophosphatidylglycerol acyltransferase 1
General function:
Involved in acyltransferase activity
Specific function:
Lysophoshatidylglycerol (LPG) specific acyltransferase that recognizes various acyl-CoAs and LPGs as substrates but demonstrates a clear preference for long chain saturated fatty acyl-CoAs and oleoyl-CoA as acyl donors. Prefers oleoyl-LPG over palmitoyl-LPG as an acyl receptor and oleoyl-CoA over lauroyl-CoA as an acyl donor
Gene Name:
LPGAT1
Uniprot ID:
Q92604
Molecular weight:
43089.1