Hmdb loader

Showing metabocard for PC(16:0/14:0) (HMDB0007965)

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IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesenzymes (77)transporters (1) Show 78 proteinsXML
enzymes (77)transporters (1) Show 78 proteins
Record Information
Version5.0
StatusDetected and Quantified
Creation Date2008-09-12 01:29:05 UTC
Update Date2022-03-07 02:49:59 UTC
HMDB IDHMDB0007965
Secondary Accession Numbers
  • HMDB07965
Metabolite Identification
Common NamePC(16:0/14:0)
DescriptionPC(16:0/14:0) 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(16:0/14:0), in particular, consists of one chain of palmitic acid at the C-1 position and one chain of myristic acid at the C-2 position. The palmitic acid moiety is derived from fish oils, milk fats, vegetable oils and animal fats, while the myristic acid moiety is derived from nutmeg and butter. 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.
Structure
Data?1582752520
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0007965 (PC(16:0/14:0))


  Mrv0541 02231221542D          

 49 48  0  0  1  0            999 V2000
   17.9288  -11.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2235  -11.5497    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.5184  -11.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6339  -11.5497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8132  -11.5497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.2235  -12.3639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.3391  -11.1426    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   19.7463  -11.8477    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   18.9320  -10.4373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0443  -10.7354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7494  -11.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4547  -10.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1598  -11.1426    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   21.7527  -11.8477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8124  -10.2900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8650  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3817  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0962  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8107  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5251  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2396  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9541  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6685  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3830  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0975  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8119  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5264  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2409  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9553  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6698  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3843  -11.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0988  -11.1372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0988  -10.3122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2209  -12.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9353  -12.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6498  -12.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3643  -12.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0788  -12.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7933  -12.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5077  -12.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2222  -12.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9367  -12.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6511  -12.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3656  -12.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0801  -12.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7946  -12.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5091  -12.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5091  -13.6015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.0814  -12.1001    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  1  4  1  0  0  0  0
  3  5  1  0  0  0  0
  2  6  1  6  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
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 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
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 25 26  1  0  0  0  0
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 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32  5  1  0  0  0  0
 32 33  2  0  0  0  0
 34 35  1  0  0  0  0
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 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
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 39 40  1  0  0  0  0
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 46 47  1  0  0  0  0
 47  6  1  0  0  0  0
 47 48  2  0  0  0  0
  2 49  1  1  0  0  0
M  CHG  2   8  -1  13   1
M  END
Download

3D MOL for HMDB0007965 (PC(16:0/14:0))

HMDB0007965
     RDKit          3D
PC(16:0/14:0)
124123  0  0  0  0  0  0  0  0999 V2000
   -0.4435   -5.9385   -2.3831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3225   -7.4062   -2.2792 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6340   -8.1052   -3.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4635   -7.9977   -4.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5469   -6.7180   -5.3070 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8746   -5.9880   -5.1904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7881   -4.7037   -5.9427 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9896   -3.8780   -5.9747 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5835   -3.1989   -4.8192 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9901   -4.0223   -3.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7368   -3.2586   -2.5984 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9761   -2.1473   -1.9904 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6901   -2.5671   -1.3119 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9982   -2.7030    0.9620 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3219   -2.2671    2.0928 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0403   -1.9941    0.2359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5154   -0.8306    0.8052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5225   -0.1782   -0.0971 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9032    0.1517   -1.4617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9134    0.6376   -2.2574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4118    1.0407   -3.8018 P   0  0  0  0  0  5  0  0  0  0  0  0
   -1.2042   -0.2452   -4.5762 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6870    1.8702   -4.5832 O   0  0  0  0  0  1  0  0  0  0  0  0
    0.0157    1.9053   -3.8611 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1600    3.2760   -3.6717 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2058    3.9215   -3.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1629    5.3391   -3.5716 N   0  0  0  0  0  4  0  0  0  0  0  0
    1.8151    5.6845   -2.3186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1782    5.8817   -3.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9346    5.9861   -4.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0751    0.9813    0.4796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4275    1.1041    0.6729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1865    0.1612    0.3161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0638    2.2957    1.2859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0896    2.9796    2.2542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7210    4.1809    2.8762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9536    4.9736    3.8309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4745    4.4830    5.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5407    3.3612    5.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2896    3.2401    6.7893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3481    2.1066    7.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9984    2.2497    6.4546 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7270    3.4913    6.9238 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9338    3.4741    8.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6602    4.7310    8.8281 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9074    5.9902    8.4788 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208   -5.4662   -2.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2765   -5.5902   -3.0320 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5165   -9.2082   -2.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5457   -8.4554   -4.8587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -5.9918   -5.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2160   -5.8676   -4.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6559   -6.6063   -5.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8698   -4.1110   -5.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4681   -5.0146   -7.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8136   -4.4834   -6.5435 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7850   -3.1002   -6.8263 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4390   -2.5706   -5.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8335   -2.3864   -4.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0283   -4.2959   -3.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4565   -4.9542   -3.9746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0527   -3.9565   -1.7969 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6616   -2.8770   -3.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6216   -1.7289   -1.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7965   -1.2837   -2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3063   -1.6340   -0.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9547   -2.9817   -2.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5676   -3.0787    0.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281   -4.4388   -0.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7960   -4.6965    1.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0015   -4.3197   -0.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9622   -1.1004    1.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2600   -0.0658    1.0254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3469   -0.9008   -0.2968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0306    0.7986   -1.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5247   -0.8282   -1.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6561    3.4432   -2.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6107    3.6583   -4.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5353    5.7538   -5.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9828    5.6307   -4.5766 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9681    7.0762   -4.4219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3474    2.9896    0.4728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9571    2.0238    1.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2100    3.2520    1.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7014    2.2509    2.9745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9479    4.8782    1.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6010    5.8984    4.0652 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3415    4.2788    5.8333 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  CHG  2  25  -1  29   1
M  END
Download

3D SDF for HMDB0007965 (PC(16:0/14:0))


  Mrv0541 02231221542D          

 49 48  0  0  1  0            999 V2000
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  2 49  1  1  0  0  0
M  CHG  2   8  -1  13   1
M  END
> <DATABASE_ID>
HMDB0007965

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C38H76NO8P/c1-6-8-10-12-14-16-18-19-21-22-24-26-28-30-37(40)44-34-36(35-46-48(42,43)45-33-32-39(3,4)5)47-38(41)31-29-27-25-23-20-17-15-13-11-9-7-2/h36H,6-35H2,1-5H3/t36-/m1/s1

> <INCHI_KEY>
UIXXHROAQSBBOV-PSXMRANNSA-N

> <FORMULA>
C38H76NO8P

> <MOLECULAR_WEIGHT>
705.9857

> <EXACT_MASS>
705.530854925

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
87.05566999568006

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
4.95

> <JCHEM_LOGP>
7.224659049194919

> <ALOGPS_LOGS>
-7.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309169687

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
206.66310000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
38

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.39e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lecithin

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0007965 (PC(16:0/14:0))

HMDB0007965
     RDKit          3D
PC(16:0/14:0)
124123  0  0  0  0  0  0  0  0999 V2000
   -0.4435   -5.9385   -2.3831 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2160   -5.8676   -4.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6559   -6.6063   -5.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8698   -4.1110   -5.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4681   -5.0146   -7.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8136   -4.4834   -6.5435 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7850   -3.1002   -6.8263 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4390   -2.5706   -5.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8335   -2.3864   -4.5122 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0283   -4.2959   -3.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4565   -4.9542   -3.9746 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0527   -3.9565   -1.7969 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6616   -2.8770   -3.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6216   -1.7289   -1.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7965   -1.2837   -2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3063   -1.6340   -0.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9547   -2.9817   -2.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5676   -3.0787    0.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5281   -4.4388   -0.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7960   -4.6965    1.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0015   -4.3197   -0.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9622   -1.1004    1.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2600   -0.0658    1.0254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3469   -0.9008   -0.2968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0306    0.7986   -1.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5247   -0.8282   -1.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6561    3.4432   -2.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893    3.6302   -4.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6107    3.6583   -4.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8473    3.4377   -3.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4468    4.8141   -1.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4796    6.5450   -2.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0768    5.8680   -1.5078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6639    5.4789   -2.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7560    5.7171   -4.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0754    6.9837   -3.3764 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5353    5.7538   -5.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9828    5.6307   -4.5766 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9681    7.0762   -4.4219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3474    2.9896    0.4728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9571    2.0238    1.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2100    3.2520    1.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7014    2.2509    2.9745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9479    4.8782    1.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7757    3.9493    3.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6010    5.8984    4.0652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1157    5.4737    3.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3415    4.2788    5.8333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9821    5.3712    5.6411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9086    2.3462    5.0160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5336    3.5498    4.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2654    3.0092    7.2627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9563    4.2149    7.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8187    1.1992    6.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3205    1.8416    8.1476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9221    2.2817    5.3697 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5953    1.3455    6.7034 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7313    3.4567    6.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2275    4.4012    6.5938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5246    2.6133    8.7506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9811    3.4549    8.9821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6633    4.8174    8.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8555    4.7657    9.9232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1821    6.8346    9.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8217    5.7704    8.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0341    6.2945    7.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  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  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 23 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
 20 33  1  0
 33 34  1  0
 34 35  2  0
 34 36  1  0
 36 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  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  2 52  1  0
  2 53  1  0
  3 54  1  0
  3 55  1  0
  4 56  1  0
  4 57  1  0
  5 58  1  0
  5 59  1  0
  6 60  1  0
  6 61  1  0
  7 62  1  0
  7 63  1  0
  8 64  1  0
  8 65  1  0
  9 66  1  0
  9 67  1  0
 10 68  1  0
 10 69  1  0
 11 70  1  0
 11 71  1  0
 12 72  1  0
 12 73  1  0
 13 74  1  0
 13 75  1  0
 14 76  1  0
 14 77  1  0
 15 78  1  0
 15 79  1  0
 19 80  1  0
 19 81  1  0
 20 82  1  6
 21 83  1  0
 21 84  1  0
 27 85  1  0
 27 86  1  0
 28 87  1  0
 28 88  1  0
 30 89  1  0
 30 90  1  0
 30 91  1  0
 31 92  1  0
 31 93  1  0
 31 94  1  0
 32 95  1  0
 32 96  1  0
 32 97  1  0
 36 98  1  0
 36 99  1  0
 37100  1  0
 37101  1  0
 38102  1  0
 38103  1  0
 39104  1  0
 39105  1  0
 40106  1  0
 40107  1  0
 41108  1  0
 41109  1  0
 42110  1  0
 42111  1  0
 43112  1  0
 43113  1  0
 44114  1  0
 44115  1  0
 45116  1  0
 45117  1  0
 46118  1  0
 46119  1  0
 47120  1  0
 47121  1  0
 48122  1  0
 48123  1  0
 48124  1  0
M  CHG  2  25  -1  29   1
M  END
Download

PDB for HMDB0007965 (PC(16:0/14:0))

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      33.467 -20.800   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      32.151 -21.559   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      30.834 -20.800   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      34.783 -21.559   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      29.518 -21.559   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      32.151 -23.079   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      36.100 -20.800   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      36.860 -22.116   0.000  0.00  0.00           O-1
HETATM    9  O   UNK     0      35.340 -19.483   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      37.416 -20.039   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      38.732 -20.800   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      40.049 -20.039   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      41.365 -20.800   0.000  0.00  0.00           N+1
HETATM   14  C   UNK     0      40.605 -22.116   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      42.583 -19.208   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      42.681 -21.559   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.179 -21.559   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.513 -20.789   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.847 -21.559   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.180 -20.789   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.514 -21.559   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.848 -20.789   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.181 -21.559   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.515 -20.789   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.849 -21.559   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      20.182 -20.789   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      21.516 -21.559   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      22.850 -20.789   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      24.183 -21.559   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      25.517 -20.789   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      26.851 -21.559   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      28.184 -20.789   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      28.184 -19.249   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      13.479 -23.079   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.813 -23.849   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.146 -23.079   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      17.480 -23.849   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      18.814 -23.079   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      20.147 -23.849   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      21.481 -23.079   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      22.815 -23.849   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      24.149 -23.079   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      25.482 -23.849   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      26.816 -23.079   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      28.150 -23.849   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      29.483 -23.079   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      30.817 -23.849   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      30.817 -25.389   0.000  0.00  0.00           O+0
HETATM   49  H   UNK     0      33.752 -22.587   0.000  0.00  0.00           H+0
CONECT    1    2    4                                                       
CONECT    2    1    3    6   49                                             
CONECT    3    2    5                                                       
CONECT    4    1    7                                                       
CONECT    5    3   32                                                       
CONECT    6    2   47                                                       
CONECT    7    4    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13                                                            
CONECT   17   18                                                            
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    5   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    6   48                                                  
CONECT   48   47                                                            
CONECT   49    2                                                            
MASTER        0    0    0    0    0    0    0    0   49    0   96    0
END
Download

3D PDB for HMDB0007965 (PC(16:0/14:0))

COMPND    HMDB0007965
HETATM    1  C1  UNL     1      -0.444  -5.939  -2.383  1.00  0.00           C  
HETATM    2  C2  UNL     1      -0.323  -7.406  -2.279  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.634  -8.105  -3.166  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.463  -7.998  -4.619  1.00  0.00           C  
HETATM    5  C5  UNL     1       0.547  -6.718  -5.307  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.875  -5.988  -5.190  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.788  -4.704  -5.943  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.990  -3.878  -5.975  1.00  0.00           C  
HETATM    9  C9  UNL     1       3.584  -3.199  -4.819  1.00  0.00           C  
HETATM   10  C10 UNL     1       3.990  -4.022  -3.685  1.00  0.00           C  
HETATM   11  C11 UNL     1       4.737  -3.259  -2.598  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.976  -2.147  -1.990  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.690  -2.567  -1.312  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.974  -3.550  -0.184  1.00  0.00           C  
HETATM   15  C15 UNL     1       1.628  -3.928   0.445  1.00  0.00           C  
HETATM   16  C16 UNL     1       0.998  -2.703   0.962  1.00  0.00           C  
HETATM   17  O1  UNL     1       1.322  -2.267   2.093  1.00  0.00           O  
HETATM   18  O2  UNL     1       0.040  -1.994   0.236  1.00  0.00           O  
HETATM   19  C17 UNL     1      -0.515  -0.831   0.805  1.00  0.00           C  
HETATM   20  C18 UNL     1      -1.523  -0.178  -0.097  1.00  0.00           C  
HETATM   21  C19 UNL     1      -0.903   0.152  -1.462  1.00  0.00           C  
HETATM   22  O3  UNL     1      -1.913   0.638  -2.257  1.00  0.00           O  
HETATM   23  P1  UNL     1      -1.412   1.041  -3.802  1.00  0.00           P  
HETATM   24  O4  UNL     1      -1.204  -0.245  -4.576  1.00  0.00           O  
HETATM   25  O5  UNL     1      -2.687   1.870  -4.583  1.00  0.00           O1-
HETATM   26  O6  UNL     1       0.016   1.905  -3.861  1.00  0.00           O  
HETATM   27  C20 UNL     1      -0.160   3.276  -3.672  1.00  0.00           C  
HETATM   28  C21 UNL     1       1.206   3.921  -3.751  1.00  0.00           C  
HETATM   29  N1  UNL     1       1.163   5.339  -3.572  1.00  0.00           N1+
HETATM   30  C22 UNL     1       1.815   5.685  -2.319  1.00  0.00           C  
HETATM   31  C23 UNL     1      -0.178   5.882  -3.522  1.00  0.00           C  
HETATM   32  C24 UNL     1       1.935   5.986  -4.633  1.00  0.00           C  
HETATM   33  O7  UNL     1      -2.075   0.981   0.480  1.00  0.00           O  
HETATM   34  C25 UNL     1      -3.427   1.104   0.673  1.00  0.00           C  
HETATM   35  O8  UNL     1      -4.186   0.161   0.316  1.00  0.00           O  
HETATM   36  C26 UNL     1      -4.064   2.296   1.286  1.00  0.00           C  
HETATM   37  C27 UNL     1      -3.090   2.980   2.254  1.00  0.00           C  
HETATM   38  C28 UNL     1      -3.721   4.181   2.876  1.00  0.00           C  
HETATM   39  C29 UNL     1      -2.954   4.974   3.831  1.00  0.00           C  
HETATM   40  C30 UNL     1      -2.474   4.483   5.109  1.00  0.00           C  
HETATM   41  C31 UNL     1      -1.541   3.361   5.255  1.00  0.00           C  
HETATM   42  C32 UNL     1      -1.290   3.240   6.789  1.00  0.00           C  
HETATM   43  C33 UNL     1      -0.348   2.107   7.073  1.00  0.00           C  
HETATM   44  C34 UNL     1       0.998   2.250   6.455  1.00  0.00           C  
HETATM   45  C35 UNL     1       1.727   3.491   6.924  1.00  0.00           C  
HETATM   46  C36 UNL     1       1.934   3.474   8.424  1.00  0.00           C  
HETATM   47  C37 UNL     1       2.660   4.731   8.828  1.00  0.00           C  
HETATM   48  C38 UNL     1       1.907   5.990   8.479  1.00  0.00           C  
HETATM   49  H1  UNL     1       0.521  -5.466  -2.561  1.00  0.00           H  
HETATM   50  H2  UNL     1      -1.276  -5.590  -3.032  1.00  0.00           H  
HETATM   51  H3  UNL     1      -0.759  -5.561  -1.358  1.00  0.00           H  
HETATM   52  H4  UNL     1      -1.373  -7.825  -2.357  1.00  0.00           H  
HETATM   53  H5  UNL     1      -0.047  -7.662  -1.211  1.00  0.00           H  
HETATM   54  H6  UNL     1       1.698  -7.920  -2.824  1.00  0.00           H  
HETATM   55  H7  UNL     1       0.516  -9.208  -2.918  1.00  0.00           H  
HETATM   56  H8  UNL     1       1.173  -8.743  -5.091  1.00  0.00           H  
HETATM   57  H9  UNL     1      -0.546  -8.455  -4.859  1.00  0.00           H  
HETATM   58  H10 UNL     1      -0.256  -5.992  -5.114  1.00  0.00           H  
HETATM   59  H11 UNL     1       0.457  -6.926  -6.418  1.00  0.00           H  
HETATM   60  H12 UNL     1       2.216  -5.868  -4.199  1.00  0.00           H  
HETATM   61  H13 UNL     1       2.656  -6.606  -5.746  1.00  0.00           H  
HETATM   62  H14 UNL     1       0.870  -4.111  -5.627  1.00  0.00           H  
HETATM   63  H15 UNL     1       1.468  -5.015  -7.004  1.00  0.00           H  
HETATM   64  H16 UNL     1       3.814  -4.483  -6.543  1.00  0.00           H  
HETATM   65  H17 UNL     1       2.785  -3.100  -6.826  1.00  0.00           H  
HETATM   66  H18 UNL     1       4.439  -2.571  -5.228  1.00  0.00           H  
HETATM   67  H19 UNL     1       2.834  -2.386  -4.512  1.00  0.00           H  
HETATM   68  H20 UNL     1       3.028  -4.296  -3.122  1.00  0.00           H  
HETATM   69  H21 UNL     1       4.457  -4.954  -3.975  1.00  0.00           H  
HETATM   70  H22 UNL     1       5.053  -3.957  -1.797  1.00  0.00           H  
HETATM   71  H23 UNL     1       5.662  -2.877  -3.072  1.00  0.00           H  
HETATM   72  H24 UNL     1       4.622  -1.729  -1.164  1.00  0.00           H  
HETATM   73  H25 UNL     1       3.796  -1.284  -2.659  1.00  0.00           H  
HETATM   74  H26 UNL     1       2.306  -1.634  -0.804  1.00  0.00           H  
HETATM   75  H27 UNL     1       1.955  -2.982  -2.001  1.00  0.00           H  
HETATM   76  H28 UNL     1       3.568  -3.079   0.623  1.00  0.00           H  
HETATM   77  H29 UNL     1       3.528  -4.439  -0.528  1.00  0.00           H  
HETATM   78  H30 UNL     1       1.796  -4.696   1.240  1.00  0.00           H  
HETATM   79  H31 UNL     1       1.002  -4.320  -0.361  1.00  0.00           H  
HETATM   80  H32 UNL     1      -0.962  -1.100   1.779  1.00  0.00           H  
HETATM   81  H33 UNL     1       0.260  -0.066   1.025  1.00  0.00           H  
HETATM   82  H34 UNL     1      -2.347  -0.901  -0.297  1.00  0.00           H  
HETATM   83  H35 UNL     1      -0.031   0.799  -1.376  1.00  0.00           H  
HETATM   84  H36 UNL     1      -0.525  -0.828  -1.877  1.00  0.00           H  
HETATM   85  H37 UNL     1      -0.656   3.443  -2.698  1.00  0.00           H  
HETATM   86  H38 UNL     1      -0.789   3.630  -4.528  1.00  0.00           H  
HETATM   87  H39 UNL     1       1.611   3.658  -4.771  1.00  0.00           H  
HETATM   88  H40 UNL     1       1.847   3.438  -3.016  1.00  0.00           H  
HETATM   89  H41 UNL     1       2.447   4.814  -1.974  1.00  0.00           H  
HETATM   90  H42 UNL     1       2.480   6.545  -2.400  1.00  0.00           H  
HETATM   91  H43 UNL     1       1.077   5.868  -1.508  1.00  0.00           H  
HETATM   92  H44 UNL     1      -0.664   5.479  -2.612  1.00  0.00           H  
HETATM   93  H45 UNL     1      -0.756   5.717  -4.435  1.00  0.00           H  
HETATM   94  H46 UNL     1      -0.075   6.984  -3.376  1.00  0.00           H  
HETATM   95  H47 UNL     1       1.535   5.754  -5.643  1.00  0.00           H  
HETATM   96  H48 UNL     1       2.983   5.631  -4.577  1.00  0.00           H  
HETATM   97  H49 UNL     1       1.968   7.076  -4.422  1.00  0.00           H  
HETATM   98  H50 UNL     1      -4.347   2.990   0.473  1.00  0.00           H  
HETATM   99  H51 UNL     1      -4.957   2.024   1.854  1.00  0.00           H  
HETATM  100  H52 UNL     1      -2.210   3.252   1.603  1.00  0.00           H  
HETATM  101  H53 UNL     1      -2.701   2.251   2.975  1.00  0.00           H  
HETATM  102  H54 UNL     1      -3.948   4.878   1.995  1.00  0.00           H  
HETATM  103  H55 UNL     1      -4.776   3.949   3.226  1.00  0.00           H  
HETATM  104  H56 UNL     1      -3.601   5.898   4.065  1.00  0.00           H  
HETATM  105  H57 UNL     1      -2.116   5.474   3.234  1.00  0.00           H  
HETATM  106  H58 UNL     1      -3.342   4.279   5.833  1.00  0.00           H  
HETATM  107  H59 UNL     1      -1.982   5.371   5.641  1.00  0.00           H  
HETATM  108  H60 UNL     1      -1.909   2.346   5.016  1.00  0.00           H  
HETATM  109  H61 UNL     1      -0.534   3.550   4.833  1.00  0.00           H  
HETATM  110  H62 UNL     1      -2.265   3.009   7.263  1.00  0.00           H  
HETATM  111  H63 UNL     1      -0.956   4.215   7.177  1.00  0.00           H  
HETATM  112  H64 UNL     1      -0.819   1.199   6.586  1.00  0.00           H  
HETATM  113  H65 UNL     1      -0.320   1.842   8.148  1.00  0.00           H  
HETATM  114  H66 UNL     1       0.922   2.282   5.370  1.00  0.00           H  
HETATM  115  H67 UNL     1       1.595   1.346   6.703  1.00  0.00           H  
HETATM  116  H68 UNL     1       2.731   3.457   6.456  1.00  0.00           H  
HETATM  117  H69 UNL     1       1.228   4.401   6.594  1.00  0.00           H  
HETATM  118  H70 UNL     1       2.525   2.613   8.751  1.00  0.00           H  
HETATM  119  H71 UNL     1       0.981   3.455   8.982  1.00  0.00           H  
HETATM  120  H72 UNL     1       3.663   4.817   8.341  1.00  0.00           H  
HETATM  121  H73 UNL     1       2.856   4.766   9.923  1.00  0.00           H  
HETATM  122  H74 UNL     1       2.182   6.835   9.166  1.00  0.00           H  
HETATM  123  H75 UNL     1       0.822   5.770   8.628  1.00  0.00           H  
HETATM  124  H76 UNL     1       2.034   6.295   7.428  1.00  0.00           H  
CONECT    1    2   49   50   51
CONECT    2    3   52   53
CONECT    3    4   54   55
CONECT    4    5   56   57
CONECT    5    6   58   59
CONECT    6    7   60   61
CONECT    7    8   62   63
CONECT    8    9   64   65
CONECT    9   10   66   67
CONECT   10   11   68   69
CONECT   11   12   70   71
CONECT   12   13   72   73
CONECT   13   14   74   75
CONECT   14   15   76   77
CONECT   15   16   78   79
CONECT   16   17   17   18
CONECT   18   19
CONECT   19   20   80   81
CONECT   20   21   33   82
CONECT   21   22   83   84
CONECT   22   23
CONECT   23   24   24   25   26
CONECT   26   27
CONECT   27   28   85   86
CONECT   28   29   87   88
CONECT   29   30   31   32
CONECT   30   89   90   91
CONECT   31   92   93   94
CONECT   32   95   96   97
CONECT   33   34
CONECT   34   35   35   36
CONECT   36   37   98   99
CONECT   37   38  100  101
CONECT   38   39  102  103
CONECT   39   40  104  105
CONECT   40   41  106  107
CONECT   41   42  108  109
CONECT   42   43  110  111
CONECT   43   44  112  113
CONECT   44   45  114  115
CONECT   45   46  116  117
CONECT   46   47  118  119
CONECT   47   48  120  121
CONECT   48  122  123  124
END
Download

SMILES for HMDB0007965 (PC(16:0/14:0))

[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
Download

INCHI for HMDB0007965 (PC(16:0/14:0))

InChI=1S/C38H76NO8P/c1-6-8-10-12-14-16-18-19-21-22-24-26-28-30-37(40)44-34-36(35-46-48(42,43)45-33-32-39(3,4)5)47-38(41)31-29-27-25-23-20-17-15-13-11-9-7-2/h36H,6-35H2,1-5H3/t36-/m1/s1
Download
View in JSmolView Stereo Labels
Synonyms
ValueSource
1-Hexadecanoyl-2-tetradecanoyl-sn-glycero-3-phosphocholineChEBI
1-Hexadecanoyl-2-tetradecanoyl-sn-phosphatidylcholineChEBI
Phosphatidylcholine(16:0/14:0)HMDB
PC(30:0)HMDB
1-Palmitoyl-2-myristoyl-sn-glycero-3-phosphocholineHMDB
GPCho(16:0/14:0)HMDB
LecithinHMDB
Phosphatidylcholine(30:0)HMDB
GPCho(30:0)HMDB
PC(16:0/14:0)Lipid Annotator
Chemical FormulaC38H76NO8P
Average Molecular Weight705.9857
Monoisotopic Molecular Weight705.530854925
IUPAC Name(2-{[(2R)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium
Traditional Namelecithin
CAS Registry NumberNot Available
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
InChI Identifier
InChI=1S/C38H76NO8P/c1-6-8-10-12-14-16-18-19-21-22-24-26-28-30-37(40)44-34-36(35-46-48(42,43)45-33-32-39(3,4)5)47-38(41)31-29-27-25-23-20-17-15-13-11-9-7-2/h36H,6-35H2,1-5H3/t36-/m1/s1
InChI KeyUIXXHROAQSBBOV-PSXMRANNSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphocholines
Direct ParentPhosphatidylcholines
Alternative Parents
Substituents
  • Diacylglycero-3-phosphocholine
  • Phosphocholine
  • Fatty acid ester
  • Dialkyl phosphate
  • Dicarboxylic acid or derivatives
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • Quaternary ammonium salt
  • Tetraalkylammonium salt
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Amine
  • Organic salt
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Health effectOrganoleptic effect
Disposition
Biological locationRoute of exposureSource
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
logP4.95ALOGPS
logP7.22ChemAxon
logS-7.4ALOGPS
pKa (Strongest Acidic)1.86ChemAxon
pKa (Strongest Basic)-6.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area111.19 ŲChemAxon
Rotatable Bond Count38ChemAxon
Refractivity206.66 m³·mol⁻¹ChemAxon
Polarizability87.06 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]+277.58130932474
DeepCCS[M-H]-274.28830932474
DeepCCS[M-2H]-308.54430932474
DeepCCS[M+Na]+285.04530932474
AllCCS[M+H]+283.732859911
AllCCS[M+H-H2O]+283.532859911
AllCCS[M+NH4]+283.932859911
AllCCS[M+Na]+283.932859911
AllCCS[M-H]-273.332859911
AllCCS[M+Na-2H]-276.932859911
AllCCS[M+HCOO]-280.832859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
PC(16:0/14:0)[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC4480.1Standard polar33892256
PC(16:0/14:0)[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC4033.5Standard non polar33892256
PC(16:0/14:0)[H][C@@](COC(=O)CCCCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC4561.0Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - PC(16:0/14:0) GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-13Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 10V, Positive-QTOFsplash10-0a4i-0000000900-f318d9d8bc7d6908f79a2017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 20V, Positive-QTOFsplash10-0a59-0600000900-3affddc5190d74346fce2017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 40V, Positive-QTOFsplash10-001i-1900412100-ae77033ea12adc91c4aa2017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 10V, Negative-QTOFsplash10-0pbi-0090000200-d74121390b891133305f2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 20V, Negative-QTOFsplash10-0a4i-0090001000-d973cea29e92b1876bea2017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 40V, Negative-QTOFsplash10-0a6r-4190000000-907977833484f97072242017-10-06Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 10V, Positive-QTOFsplash10-004i-0000000900-b00a0ca4532ff91820942021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 20V, Positive-QTOFsplash10-004i-0000001900-4bbfc80efe35c8e1c7e52021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 40V, Positive-QTOFsplash10-0002-0600491100-d3be2cced1b82ac1c4552021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 10V, Negative-QTOFsplash10-0006-0000000900-4857d5d4f8976860ccc22021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 20V, Negative-QTOFsplash10-0006-0030000900-80adb7a66fc0aee6315e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 40V, Negative-QTOFsplash10-0a96-0090000400-5f272dc8d69ac17f55ec2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 10V, Negative-QTOFsplash10-0udi-0000000900-c6fb3bc05eaaa84c86e62021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 20V, Negative-QTOFsplash10-0zfr-0090012500-774e232fd1625079230e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 40V, Negative-QTOFsplash10-0a6r-2291000000-6411d42ac7ef868fb6ea2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 10V, Positive-QTOFsplash10-0a4i-0000000900-ce96887ed69b9e85f7a82021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 20V, Positive-QTOFsplash10-0a59-0600000900-fe4e7280392995d009f02021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 40V, Positive-QTOFsplash10-001i-1900412100-713da14b61754e31d3042021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 10V, Positive-QTOFsplash10-03di-0000000900-7615039fbfae408d95f12021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 20V, Positive-QTOFsplash10-03di-0000001900-984ab4028567ba2b66bb2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(16:0/14:0) 40V, Positive-QTOFsplash10-004i-0101791100-97808bd3a382a5e63f972021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Blood
  • Feces
Tissue Locations
  • All Tissues
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified2.99 (2.39-3.84) uMInfant (0-1 year old)Not Available
Normal		 details
BloodDetected and Quantified2.26 (0.33-4.11) uMAdolescent (13-18 years old)Both
Normal		 details
BloodDetected and Quantified5.12(2.19) uMAdult (>18 years old)BothNormal details
BloodDetected and Quantified2.95 (2.53-3.44) uMNewborn (0-30 days old)Not Available
Normal		 details
BloodDetected and Quantified4.73 +/- 1.65 uMAdult (>18 years old)BothNormal details
FecesDetected and Quantified0.77 +/- 0.6 nmol/g wet fecesAdult (>18 years old)Both
Normal		 details
FecesDetected and Quantified1.06 +/- 1.14 nmol/g wet fecesAdult (>18 years old)Both
Normal		 details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified4.01(1.5) uMAdult (>18 years old)BothHeart failure with preserved ejection fraction details
BloodDetected and Quantified4.18(1.8) uMAdult (>18 years old)BothHeart failure with reduced ejection fraction details
BloodDetected and Quantified3.5667 (3.29) uMAdult (>18 years old)FemalePregnancy with fetus having congenital heart defect details
BloodDetected and Quantified6.0819 (2.7436) uMAdult (>18 years old)FemalePregnancy details
BloodDetected and Quantified2.79 (1.9-6.47) uMAdolescent (13-18 years old)Both
Pain or fever		 details
BloodDetected and Quantified3.35 (2.43-10.45) uMAdolescent (13-18 years old)Both
Acetaminophen overdose		 details
BloodDetected and Quantified3.17 +/- 1.32 uMChildren (1-13 years old)Both
Obesity
    • Metabolomics reve...
 details
BloodDetected and Quantified3.77 +/- 1.18 uMChildren (1-13 years old)Both
Obesity
    • Metabolomics reve...
 details
Predicted Concentrations
BiospecimenValueOriginal ageOriginal sexOriginal conditionComments
Blood3.103 +/- 0.808 uMAdult (>18 years old)BothNormal (Most Probable)Calculated using MetaboAnalyst
Blood16.900 +/- 3.727 uMAdult (>18 years old)BothNormal (Upper Limit)Calculated using MetaboAnalyst
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 IDFDB025157
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound24778679
PDB IDNot Available
ChEBI ID75304
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDMDB00000527
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Only showing the first 10 proteins. There are 78 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details
1. Acyl-protein thioesterase 1
General function:
Involved in hydrolase activity
Specific function:
Hydrolyzes fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins or HRAS. Has depalmitoylating activity and also low lysophospholipase activity.
Gene Name:
LYPLA1
Uniprot ID:
O75608
Molecular weight:
24669.355
Enzyme Details
2. Group XV phospholipase A2
General function:
Involved in phosphatidylcholine-sterol O-acyltransferase activity
Specific function:
Has transacylase and calcium-independent phospholipase A2 activity. Catalyzes the formation of 1-O-acyl-N-acetylsphingosine and the concomitant release of a lyso-phospholipid (By similarity). May have weak lysophospholipase activity.
Gene Name:
PLA2G15
Uniprot ID:
Q8NCC3
Molecular weight:
Not Available
Enzyme Details
3. 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
4. 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
5. 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
6. 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
7. Group XIIB secretory phospholipase A2-like protein
General function:
Involved in phospholipase A2 activity
Specific function:
Not known; does not seem to have catalytic activity.
Gene Name:
PLA2G12B
Uniprot ID:
Q9BX93
Molecular weight:
Not Available
Enzyme Details
8. 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
9. 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
10. Acyl-protein thioesterase 2
General function:
Involved in hydrolase activity
Specific function:
May hydrolyze fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins or HRAS. Has lysophospholipase activity (By similarity). Deacylates GAP43.
Gene Name:
LYPLA2
Uniprot ID:
O95372
Molecular weight:
24736.71

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 78 proteins in total.

Show all enzymes and transporters