NP-MRD: Showing NP-Card for 1-18:3-2-18:1-phosphatidylcholine (NP0092274)

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Record Information

Version

2.0

Created at

2022-05-11 19:02:08 UTC

Updated at

2022-05-11 19:02:08 UTC

NP-MRD ID

NP0092274

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-18:3-2-18:1-phosphatidylcholine

Description

PC(18:3(9Z,12Z,15Z)/18:1(9Z)), also known as gpcho(18:3/18:1) Or phosphatidylcholine(18:3/18:1), 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. Thus, PC(18:3(9Z,12Z,15Z)/18:1(9Z)) is considered to be a glycerophosphocholine lipid molecule. A phosphatidylcholine 36:4 In which the acyl groups specified at positions 1 and 2 are (9Z,12Z,15Z)-octadecatrienoyl and (9Z)-octadecenoyl respectively. PC(18:3(9Z,12Z,15Z)/18:1(9Z)) is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. PC(18:3(9Z,12Z,15Z)/18:1(9Z)) exists in all eukaryotes, ranging from yeast to humans. Within humans, PC(18:3(9Z,12Z,15Z)/18:1(9Z)) participates in a number of enzymatic reactions. In particular, S-adenosylhomocysteine and PC(18:3(9Z,12Z,15Z)/18:1(9Z)) can be biosynthesized from S-adenosylmethionine and pe-nme2(18:3(9Z,12Z,15Z)/18:1(9Z)); which is catalyzed by the enzyme phosphatidylethanolamine N-methyltransferase. In addition, cytidine monophosphate and PC(18:3(9Z,12Z,15Z)/18:1(9Z)) can be biosynthesized from CDP-choline and DG(18:3(9Z,12Z,15Z)/18:1(9Z)/0:0) Through the action of the enzyme choline/ethanolaminephosphotransferase. In humans, PC(18:3(9Z,12Z,15Z)/18:1(9Z)) is involved in phosphatidylcholine biosynthesis. Outside of the human body, PC(18:3(9Z,12Z,15Z)/18:1(9Z)) has been detected, but not quantified in, several different foods, such as buffalo currants, narrowleaf cattails, wax gourds, horseradish, and soy beans. This could make PC(18:3(9Z,12Z,15Z)/18:1(9Z)) a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02231222102D          

 55 54  0  0  1  0            999 V2000
   25.0592   -7.8819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3540   -8.2890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.6488   -7.8819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7644   -8.2890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.9436   -8.2890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3540   -9.1032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4695   -7.8819    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   26.8767   -8.5870    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   26.0624   -7.1766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.1747   -7.4747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8799   -7.8819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5851   -7.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2902   -7.8819    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   28.8831   -8.5870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.9429   -7.0293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.9954   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0831   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7975   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5120   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2265   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9410   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6555   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3700   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0844   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7989   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5134   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2278   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9423   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6568   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3713   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0858   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8002   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5147   -8.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2292   -7.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2292   -7.0515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4934   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2079   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9223   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6368   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3513   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0658   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7803   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4948   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2092   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9237   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6382   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3526   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0672   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7816   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4961   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2106   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9250   -9.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6395   -9.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6395  -10.3408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.3886   -9.0260    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
 13 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  2  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  2  0  0  0  0
 24 23  1  0  0  0  0
 25 24  1  0  0  0  0
 26 25  2  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  2  0  0  0  0
  5 34  1  0  0  0  0
 37 36  1  0  0  0  0
 38 37  1  0  0  0  0
 39 38  1  0  0  0  0
 40 39  1  0  0  0  0
 41 40  1  0  0  0  0
 42 41  1  0  0  0  0
 43 42  1  0  0  0  0
 44 43  1  0  0  0  0
 45 44  2  0  0  0  0
 46 45  1  0  0  0  0
 47 46  1  0  0  0  0
 48 47  1  0  0  0  0
 49 48  1  0  0  0  0
 50 49  1  0  0  0  0
 51 50  1  0  0  0  0
 52 51  1  0  0  0  0
 53 52  1  0  0  0  0
 54 53  2  0  0  0  0
  6 53  1  0  0  0  0
  2 55  1  1  0  0  0
M  CHG  2   8  -1  13   1
M  END

     RDKit          3D

134133  0  0  0  0  0  0  0  0999 V2000
    8.4988   -6.6794   -4.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0123   -5.2798   -4.5827 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7717   -3.2339   -3.8515 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3160   -2.9427   -5.1697 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9831   -2.9064   -5.6602 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8631   -3.1609   -5.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4486   -3.5983   -3.8546 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2443   -3.9430   -2.7295 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1974   -3.2729   -1.5830 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3535   -2.1089   -1.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1091   -0.8671   -0.9753 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3892    0.3756   -0.7042 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4915    0.5640    0.4247 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2687   -0.2238    0.6374 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2427   -0.1977   -0.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0301   -0.9648   -0.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2559   -2.3793    0.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3272   -2.9881    0.1150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7705   -3.1567    0.8597 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6213   -4.5143    1.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0122   -4.8948    1.8017 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0128   -4.7524    0.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7423   -5.5864   -0.3894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9378   -5.3190   -1.5750 P   0  0  1  0  0  5  0  0  0  0  0  0
   -3.2860   -5.0645   -2.9317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8726   -6.7444   -1.6857 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.9207   -4.0469   -1.1280 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6649   -2.8621   -1.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6280   -1.8332   -1.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4774   -0.5297   -1.8655 N   0  0  1  0  0  4  0  0  0  0  0  0
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   -5.1935   -0.6213   -3.2730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7114    0.2048   -1.6660 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5907   -5.2448    4.6770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9340   -2.8809    4.8688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7122   -2.3533    5.5258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8000   -1.0469    6.2097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8950    0.1686    5.3510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9891    0.3066    4.4010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1619    1.5967    3.6808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0967    2.1282    2.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539    2.5861    3.4283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4194    3.8458    3.2910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1016    4.9118    2.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1705    5.3415    1.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7651    6.4225    0.5361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2379    6.7386   -0.5726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2629    7.8092   -1.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.1468   -5.3655   -4.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6115   -2.9177   -3.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9295   -4.8285   -2.6807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8595   -3.6158   -0.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5061   -2.0204   -1.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8961   -2.4027   -0.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8273   -0.6729   -1.8412 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8459   -1.0404   -0.1223 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8790    0.7845   -1.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2078    1.1859   -0.5878 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0858    0.4833    1.3995 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1588    1.6682    0.5077 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3864   -1.2355    1.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7307    0.3005    1.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0105   -4.9931    1.1207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9560   -3.7008    0.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.6678   -2.1818   -1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6361    1.3074   -1.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5037    0.0795   -1.8320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2685   -0.1541   -0.1694 H   0  0  0  0  0  0  0  0  0  0  0  0
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 34100  1  0
 34101  1  0
M  CHG  2  27  -1  31   1
M  END


  Mrv0541 02231222102D          

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 53 52  1  0  0  0  0
 54 53  2  0  0  0  0
  6 53  1  0  0  0  0
  2 55  1  1  0  0  0
M  CHG  2   8  -1  13   1
M  END
> <DATABASE_ID>
NP0092274

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C44H80NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h8,10,14,16,20-23,42H,6-7,9,11-13,15,17-19,24-41H2,1-5H3/b10-8-,16-14-,22-20-,23-21-/t42-/m1/s1

> <INCHI_KEY>
LPDGUCIMNBNWEJ-BXZVQSHESA-N

> <FORMULA>
C44H80NO8P

> <MOLECULAR_WEIGHT>
782.0817

> <EXACT_MASS>
781.562155053

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
93.2744799033859

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
trimethyl(2-{[(2R)-2-[(9Z)-octadec-9-enoyloxy]-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propyl phosphonato]oxy}ethyl)azanium

> <ALOGPS_LOGP>
5.69

> <JCHEM_LOGP>
8.444384412528256

> <ALOGPS_LOGS>
-7.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309169755

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
238.7355000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
40

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.16e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lecithin

> <JCHEM_VEBER_RULE>
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      46.777 -14.713   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      45.461 -15.473   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      44.144 -14.713   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      48.094 -15.473   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      42.828 -15.473   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      45.461 -16.993   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      49.410 -14.713   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      50.170 -16.029   0.000  0.00  0.00           O-1
HETATM    9  O   UNK     0      48.650 -13.396   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      50.726 -13.953   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      52.042 -14.713   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      53.359 -13.953   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      54.675 -14.713   0.000  0.00  0.00           N+1
HETATM   14  C   UNK     0      53.915 -16.029   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      55.893 -13.121   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      55.991 -15.473   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.822 -14.703   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.155 -15.473   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.489 -14.703   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.823 -14.703   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      24.157 -15.473   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      25.490 -14.703   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      26.824 -14.703   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      28.158 -15.473   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      29.491 -14.703   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      30.825 -14.703   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      32.159 -15.473   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      33.492 -14.703   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      34.826 -15.473   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      36.160 -14.703   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      37.493 -15.473   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      38.827 -14.703   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      40.161 -15.473   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      41.495 -14.703   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      41.495 -13.163   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      21.454 -17.763   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      22.788 -16.993   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      24.122 -17.763   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      25.455 -16.993   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      26.789 -17.763   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      28.123 -16.993   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      29.457 -17.763   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      30.790 -16.993   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      32.124 -17.763   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      33.458 -17.763   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      34.791 -16.993   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      36.125 -17.763   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      37.459 -16.993   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      38.792 -17.763   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      40.126 -16.993   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      41.460 -17.763   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      42.793 -16.993   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      44.127 -17.763   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      44.127 -19.303   0.000  0.00  0.00           O+0
HETATM   55  H   UNK     0      47.392 -16.849   0.000  0.00  0.00           H+0
CONECT    1    2    4                                                       
CONECT    2    1    3    6   55                                             
CONECT    3    2    5                                                       
CONECT    4    1    7                                                       
CONECT    5    3   34                                                       
CONECT    6    2   53                                                       
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   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35    5                                                  
CONECT   35   34                                                            
CONECT   36   37                                                            
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54    6                                                  
CONECT   54   53                                                            
CONECT   55    2                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  108    0
END

View in JSmol

Synonyms

Value	Source
1-alpha-Linolenoyl-2-oleoyl-sn-glycero-3-phosphocholine	ChEBI
GPCho(18:3/18:1)	ChEBI
GPCho(18:3n3/18:1n9)	ChEBI
GPCho(18:3W3/18:1W9)	ChEBI
PC(18:3/18:1)	ChEBI
PC(18:3n3/18:1n9)	ChEBI
PC(18:3W3/18:1W9)	ChEBI
Phosphatidylcholine(18:3/18:1)	ChEBI
Phosphatidylcholine(18:3n3/18:1n9)	ChEBI
Phosphatidylcholine(18:3W3/18:1W9)	ChEBI
1-a-Linolenoyl-2-oleoyl-sn-glycero-3-phosphocholine	Generator
1-Α-linolenoyl-2-oleoyl-sn-glycero-3-phosphocholine	Generator
Phosphatidylcholine(36:4)	HMDB
PC(36:4)	HMDB
Lecithin	HMDB
1-(9Z,12Z,15Z-Octadeatrienoyl)-2-(9Z-octadecenoyl)-sn-glycero-3-phosphocholine	HMDB
GPCho(36:4)	HMDB
PC(18:3(9Z,12Z,15Z)/18:1(9Z))	Lipid Annotator, ChEBI

Chemical Formula

C₄₄H₈₀NO₈P

Average Mass

782.0817 Da

Monoisotopic Mass

781.56216 Da

IUPAC Name

trimethyl(2-{[(2R)-2-[(9Z)-octadec-9-enoyloxy]-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propyl phosphonato]oxy}ethyl)azanium

Traditional Name

lecithin

CAS Registry Number

Not Available

SMILES

CCCCCCCC\C=C/CCCCCCCC(=O)O[C@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)COP([O-])(=O)OCC[N+](C)(C)C

InChI Identifier

InChI=1S/C44H80NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h8,10,14,16,20-23,42H,6-7,9,11-13,15,17-19,24-41H2,1-5H3/b10-8-,16-14-,22-20-,23-21-/t42-/m1/s1

InChI Key

LPDGUCIMNBNWEJ-BXZVQSHESA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

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.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphocholines

Direct Parent

Phosphatidylcholines

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 Framework

Aliphatic acyclic compounds

External Descriptors

phosphatidylcholine 36:4 (CHEBI:86127 )
Diacylglycerophosphocholines (LMGP01010955 )

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.69	ALOGPS
logP	8.44	ChemAxon
logS	-7.4	ALOGPS
pKa (Strongest Acidic)	1.86	ChemAxon
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	111.19 Å²	ChemAxon
Rotatable Bond Count	40	ChemAxon
Refractivity	238.74 m³·mol⁻¹	ChemAxon
Polarizability	93.27 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0008203

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB030234

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24778989

PDB ID

Not Available

ChEBI ID

86127

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 1-18:3-2-18:1-phosphatidylcholine (NP0092274)

MOL for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

3D MOL for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

3D SDF for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

3D-SDF for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

PDB for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

3D PDB for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

SMILES for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

INCHI for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

Structure for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)

3D Structure for NP0092274 (1-18:3-2-18:1-phosphatidylcholine)