NP-MRD: Showing NP-Card for PGP(16:0/22:4(7Z,10Z,13Z,16Z)) (NP0339276)

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Record Information

Version

2.0

Created at

2024-09-11 20:49:39 UTC

Updated at

2024-09-11 20:49:40 UTC

NP-MRD ID

NP0339276

Secondary Accession Numbers

None

Natural Product Identification

Common Name

PGP(16:0/22:4(7Z,10Z,13Z,16Z))

Description

PGP(16:0/22:4(7Z,10Z,13Z,16Z)), also known as PGP(16:0/22:4) Or PGP(38:4), Belongs to the class of organic compounds known as phosphatidylglycerophosphates. These are glycerophosphoglycerophosphates in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages. Fatty acids containing 16, 18 and 20 carbons are the most common. 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. Bioynthesis proceeds by condensation of phosphatidic acid and cytidine triphosphate with elimination of pyrophosphate via the action of phosphatidate cytidyltransferase (or CDP-synthase). PGP(16:0/22:4(7Z,10Z,13Z,16Z)) is an extremely weak basic (essentially neutral) compound (based on its pKa). Phosphatidylglycerolphosphate may be present in animal tissues merely as a precursor for diphosphatidylglycerol (cardiolipin). It is well established that the concentration of Phosphatidylglycerolphosphate increases during fetal development. PGP also serves as a precursor for the synthesis of cardiolipin. 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. The palmitic acid moiety is derived from fish oils, milk fats, vegetable oils and animal fats, while the adrenic acid moiety is derived from animal fats.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652303252017072D          

 61 60  0  0  1  0            999 V2000
   22.6003   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9252   -3.5882    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.2501   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2754   -3.5882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.5749   -3.5882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.3984   -4.3678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9505   -3.1984    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   23.5608   -2.5232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3403   -3.8735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.6257   -2.8086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.3008   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9759   -2.8086    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   26.6511   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.5130   -4.3975    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   27.2889   -2.7719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.5523   -2.1237    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   25.3639   -2.1237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1433   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8578   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5723   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2868   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0013   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7157   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4302   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1447   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8591   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5736   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2881   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0025   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7170   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4315   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1460   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8605   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8605   -2.3507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6798   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3943   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1088   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8232   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5377   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2522   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9666   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6811   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3956   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1102   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8246   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5391   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2536   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9681   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6825   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3970   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1115   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8260   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5405   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2550   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9695   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6839   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6839   -5.6053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.0289   -3.1365    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.7690   -3.5011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.3935   -2.3964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.6644   -3.8765    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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33  5  1  0  0  0  0
 33 34  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  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  2  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  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56  6  1  0  0  0  0
 56 57  2  0  0  0  0
 59 58  2  0  0  0  0
 60 58  1  0  0  0  0
 61 58  1  0  0  0  0
 15 58  1  0  0  0  0
M  END


  Mrv1652303252017072D          

 61 60  0  0  1  0            999 V2000
   22.6003   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9252   -3.5882    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.2501   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2754   -3.5882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.5749   -3.5882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.3984   -4.3678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9505   -3.1984    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   23.5608   -2.5232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3403   -3.8735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.6257   -2.8086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.3008   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.9759   -2.8086    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   26.6511   -3.1984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.5130   -4.3975    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   27.2889   -2.7719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.5523   -2.1237    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   25.3639   -2.1237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1433   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8578   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5723   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2868   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0013   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7157   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4302   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1447   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8591   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5736   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2881   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0025   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7170   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4315   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1460   -3.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8605   -3.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8605   -2.3507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6798   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3943   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1088   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8232   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5377   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2522   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9666   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6811   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3956   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1102   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8246   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5391   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2536   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9681   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6825   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3970   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1115   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8260   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5405   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2550   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9695   -4.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6839   -4.7803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6839   -5.6053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.0289   -3.1365    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.7690   -3.5011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.3935   -2.3964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.6644   -3.8765    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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33  5  1  0  0  0  0
 33 34  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  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  2  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  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56  6  1  0  0  0  0
 56 57  2  0  0  0  0
 59 58  2  0  0  0  0
 60 58  1  0  0  0  0
 61 58  1  0  0  0  0
 15 58  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0339276

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@](O)(COP(O)(O)=O)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C44H80O13P2/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-24-26-28-30-32-34-36-44(47)57-42(40-56-59(51,52)55-38-41(45)37-54-58(48,49)50)39-53-43(46)35-33-31-29-27-25-23-16-14-12-10-8-6-4-2/h11,13,17-18,20-21,24,26,41-42,45H,3-10,12,14-16,19,22-23,25,27-40H2,1-2H3,(H,51,52)(H2,48,49,50)/b13-11-,18-17-,21-20-,26-24-/t41-,42+/m0/s1

> <INCHI_KEY>
AFMJWGBKSCTQSX-YGUNRICGSA-N

> <FORMULA>
C44H80O13P2

> <MOLECULAR_WEIGHT>
879.0457

> <EXACT_MASS>
878.50741567

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
139

> <JCHEM_AVERAGE_POLARIZABILITY>
98.87447331094242

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S)-3-({[(2R)-2-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-3-(hexadecanoyloxy)propoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy]phosphonic acid

> <ALOGPS_LOGP>
7.69

> <JCHEM_LOGP>
12.033210851333333

> <ALOGPS_LOGS>
-6.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
2.0402061436989327

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.354879296415124

> <JCHEM_PKA_STRONGEST_BASIC>
-3.410499386302644

> <JCHEM_POLAR_SURFACE_AREA>
195.35

> <JCHEM_REFRACTIVITY>
238.25420000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
44

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.01e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-3-{[(2R)-2-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-3-(hexadecanoyloxy)propoxy(hydroxy)phosphoryl]oxy}-2-hydroxypropoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-MAR-20         0                                  
HETATM    1  C   UNK     0      42.187  -5.970   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      40.927  -6.698   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      39.667  -5.970   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      43.447  -6.698   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      38.406  -6.698   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      39.944  -8.153   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      44.708  -5.970   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      43.980  -4.710   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      45.435  -7.231   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      45.968  -5.243   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      47.228  -5.970   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      48.488  -5.243   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      49.749  -5.970   0.000  0.00  0.00           C+0
HETATM   14  H   UNK     0      42.024  -8.209   0.000  0.00  0.00           H+0
HETATM   15  O   UNK     0      50.939  -5.174   0.000  0.00  0.00           O+0
HETATM   16  H   UNK     0      49.564  -3.964   0.000  0.00  0.00           H+0
HETATM   17  O   UNK     0      47.346  -3.964   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      17.067  -6.698   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.401  -5.928   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      19.735  -6.698   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.069  -5.928   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      22.402  -6.698   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      23.736  -5.928   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.070  -6.698   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.403  -5.928   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      27.737  -6.698   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      29.071  -5.928   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      30.404  -6.698   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      31.738  -5.928   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      33.072  -6.698   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      34.405  -5.928   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      35.739  -6.698   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      37.073  -5.928   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      37.073  -4.388   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      10.602  -8.153   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.936  -8.923   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.270  -8.153   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      14.603  -8.923   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      15.937  -8.153   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      17.271  -8.923   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      18.604  -8.923   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      19.938  -8.153   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      21.272  -8.923   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      22.606  -8.923   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      23.939  -8.153   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      25.273  -8.923   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      26.607  -8.923   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      27.940  -8.153   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      29.274  -8.923   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      30.608  -8.923   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      31.941  -8.153   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      33.275  -8.923   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      34.609  -8.153   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      35.943  -8.923   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      37.276  -8.153   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      38.610  -8.923   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      38.610 -10.463   0.000  0.00  0.00           O+0
HETATM   58  P   UNK     0      52.321  -5.855   0.000  0.00  0.00           P+0
HETATM   59  O   UNK     0      53.702  -6.535   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      53.001  -4.473   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      51.640  -7.236   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   33                                                       
CONECT    6    2   56                                                       
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   58                                                       
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    5   34                                                  
CONECT   34   33                                                            
CONECT   35   36                                                            
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56                                                       
CONECT   56   55    6   57                                                  
CONECT   57   56                                                            
CONECT   58   59   60   61   15                                             
CONECT   59   58                                                            
CONECT   60   58                                                            
CONECT   61   58                                                            
MASTER        0    0    0    0    0    0    0    0   61    0  120    0
END

View in JSmol

Synonyms

Value	Source
1-Palmitoyl-2-adrenoyl-sn-glycero-3-phospho-(1'-sn-glycerol-3'-phosphate)	HMDB
3-sn-Phosphatidyl-1'-sn-glycerol 3'-phosphoric acid	HMDB
PGP(16:0/22:4)	HMDB
PGP(16:0/22:4n6)	HMDB
PGP(16:0/22:4W6)	HMDB
PGP(38:4)	HMDB
1-Hexadecanoyl-2-(7Z,10Z,13Z,16Z-docosatetraenoyl)-sn-glycero-3-phospho-(1'-sn-glycerol-3'-phosphate)	HMDB
PGP(16:0/22:4(7Z,10Z,13Z,16Z))	Lipid Annotator
[(2S)-3-({[(2R)-2-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-3-(hexadecanoyloxy)propoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy]phosphonate	Generator

Chemical Formula

C₄₄H₈₀O₁₃P₂

Average Mass

879.0457 Da

Monoisotopic Mass

878.50742 Da

IUPAC Name

[(2S)-3-({[(2R)-2-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-3-(hexadecanoyloxy)propoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy]phosphonic acid

Traditional Name

(2S)-3-{[(2R)-2-[(7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoyloxy]-3-(hexadecanoyloxy)propoxy(hydroxy)phosphoryl]oxy}-2-hydroxypropoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

[H][C@](O)(COP(O)(O)=O)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC

InChI Identifier

InChI=1S/C44H80O13P2/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-24-26-28-30-32-34-36-44(47)57-42(40-56-59(51,52)55-38-41(45)37-54-58(48,49)50)39-53-43(46)35-33-31-29-27-25-23-16-14-12-10-8-6-4-2/h11,13,17-18,20-21,24,26,41-42,45H,3-10,12,14-16,19,22-23,25,27-40H2,1-2H3,(H,51,52)(H2,48,49,50)/b13-11-,18-17-,21-20-,26-24-/t41-,42+/m0/s1

InChI Key

AFMJWGBKSCTQSX-YGUNRICGSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phosphatidylglycerophosphates. These are glycerophosphoglycerophosphates in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoglycerophosphates

Direct Parent

Phosphatidylglycerophosphates

Alternative Parents

Substituents

Diacylglycerophosphoglycerophosphate
Sn-glycerol-3-phosphate
Fatty acid ester
Monoalkyl phosphate
Dialkyl phosphate
Dicarboxylic acid or derivatives
Organic phosphoric acid derivative
Phosphoric acid ester
Alkyl phosphate
Fatty acyl
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

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	7.69	ALOGPS
logP	12.03	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	1.35	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	195.35 Å²	ChemAxon
Rotatable Bond Count	44	ChemAxon
Refractivity	238.25 m³·mol⁻¹	ChemAxon
Polarizability	98.87 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

HMDB0013483

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB029483

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

53481803

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for PGP(16:0/22:4(7Z,10Z,13Z,16Z)) (NP0339276)

MOL for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

3D MOL for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

3D SDF for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

3D-SDF for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

PDB for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

3D PDB for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

SMILES for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

INCHI for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

Structure for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))

3D Structure for NP0339276 (PGP(16:0/22:4(7Z,10Z,13Z,16Z)))