MiMeDB: Showing metabocard for PG(19:0/16:0) (MMDBc0030298)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 00:01:55 UTC

Update Date

2023-02-07 22:23:20 UTC

Metabolite ID

MMDBc0030298

Metabolite Identification

Common Name

PG(19:0/16:0)

Description

PG(16:0/19:0) is a phosphatidylglycerol. Phosphatidylglycerols consist of a glycerol 3-phosphate backbone esterified to either saturated or unsaturated fatty acids on carbons 1 and 2. As is the case with diacylglycerols, phosphatidylglycerols can have many different combinations of fatty acids of varying lengths and saturation attached to the C-1 and C-2 positions. PG(16:0/19:0), in particular, consists of one hexadecanoyl chain to the C-1 atom, and one nonadecanoyl to the C-2 atom. In E. coli glycerophospholipid metabolism, phosphatidylglycerol is formed from phosphatidic acid (1,2-diacyl-sn-glycerol 3-phosphate) by a sequence of enzymatic reactions that proceeds via two intermediates, cytidine diphosphate diacylglycerol (CDP-diacylglycerol) and phosphatidylglycerophosphate (PGP, a phosphorylated phosphatidylglycerol). Phosphatidylglycerols, along with CDP-diacylglycerol, also serve as precursor molecules for the synthesis of cardiolipin, a phospholipid found in membranes.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 05311207182D          

 54 53  0  0  0  0            999 V2000
  -13.5020   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6479   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7875   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9335   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0730   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2190   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3586   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5045   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6441   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7900   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9296   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0756   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2151   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3611   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5007   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6466   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7862   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0717   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3573   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9322   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6428   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9283   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2177   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2138   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5032   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7887   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7849   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0743   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0704   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3598   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3560   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6453   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6914  -11.3506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4539  -10.6362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7874   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -8.6842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2789  -10.6362    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5019   -7.8592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6415   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9309   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2789  -12.0651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6914   -9.9217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6415   -6.6217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9309   -8.6842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3914   -9.9217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164  -10.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0730   -7.8592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -9.9217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164   -9.0967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164   -7.4467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164   -9.9217    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    3.8664  -11.3506    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7874   -8.2717    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 16  1  0  0  0  0
 21 19  1  0  0  0  0
 22 21  1  0  0  0  0
 23 20  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 27  1  0  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 32 30  1  0  0  0  0
 33 31  1  0  0  0  0
 38 34  1  0  0  0  0
 38 35  1  0  0  0  0
 39 36  1  0  0  0  0
 39 37  1  0  0  0  0
 40 32  1  0  0  0  0
 41 33  1  0  0  0  0
 42 34  1  0  0  0  0
 38 43  1  6  0  0  0
 44 40  2  0  0  0  0
 45 41  2  0  0  0  0
 48 36  1  0  0  0  0
 48 40  1  0  0  0  0
 49 35  1  0  0  0  0
 50 37  1  0  0  0  0
 39 51  1  6  0  0  0
 51 41  1  0  0  0  0
 52 46  1  0  0  0  0
 52 47  2  0  0  0  0
 52 49  1  0  0  0  0
 52 50  1  0  0  0  0
 38 53  1  6  0  0  0
 39 54  1  6  0  0  0
M  END


  Mrv0541 05311207182D          

 54 53  0  0  0  0            999 V2000
  -13.5020   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6479   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7875   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9335   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0730   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2190   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3586   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5045   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6441   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7900   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9296   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0756   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2151   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3611   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5007   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6466   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7862   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0717   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3573   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9322   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6428   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9283   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2177   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2138   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5032   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4994   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7887   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7849   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0743   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0704   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3598   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3560   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6453   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6914  -11.3506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4539  -10.6362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7874   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5019   -8.6842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2789  -10.6362    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5019   -7.8592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6415   -7.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9309   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2789  -12.0651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6914   -9.9217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6415   -6.6217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9309   -8.6842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3914   -9.9217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164  -10.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0730   -7.8592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -9.9217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164   -9.0967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164   -7.4467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2164   -9.9217    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    3.8664  -11.3506    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7874   -8.2717    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 16  1  0  0  0  0
 21 19  1  0  0  0  0
 22 21  1  0  0  0  0
 23 20  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 27  1  0  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 32 30  1  0  0  0  0
 33 31  1  0  0  0  0
 38 34  1  0  0  0  0
 38 35  1  0  0  0  0
 39 36  1  0  0  0  0
 39 37  1  0  0  0  0
 40 32  1  0  0  0  0
 41 33  1  0  0  0  0
 42 34  1  0  0  0  0
 38 43  1  6  0  0  0
 44 40  2  0  0  0  0
 45 41  2  0  0  0  0
 48 36  1  0  0  0  0
 48 40  1  0  0  0  0
 49 35  1  0  0  0  0
 50 37  1  0  0  0  0
 39 51  1  6  0  0  0
 51 41  1  0  0  0  0
 52 46  1  0  0  0  0
 52 47  2  0  0  0  0
 52 49  1  0  0  0  0
 52 50  1  0  0  0  0
 38 53  1  6  0  0  0
 39 54  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0030298

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C41H81O10P/c1-3-5-7-9-11-13-15-17-18-19-21-22-24-26-28-30-32-40(44)48-36-39(37-50-52(46,47)49-35-38(43)34-42)51-41(45)33-31-29-27-25-23-20-16-14-12-10-8-6-4-2/h38-39,42-43H,3-37H2,1-2H3,(H,46,47)/t38-,39+/m0/s1

> <INCHI_KEY>
WXDNYCHHTCISSS-ZESVVUHVSA-N

> <FORMULA>
C41H81O10P

> <MOLECULAR_WEIGHT>
765.0496

> <EXACT_MASS>
764.556735324

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
93.73861022725966

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S)-2,3-dihydroxypropoxy][(2R)-2-(hexadecanoyloxy)-3-(nonadecanoyloxy)propoxy]phosphinic acid

> <ALOGPS_LOGP>
8.43

> <JCHEM_LOGP>
12.270757514333335

> <ALOGPS_LOGS>
-6.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.641245576372423

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8907737771908404

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9689647678483633

> <JCHEM_POLAR_SURFACE_AREA>
148.82

> <JCHEM_REFRACTIVITY>
209.11190000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
43

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.69e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,3-dihydroxypropoxy(2R)-2-(hexadecanoyloxy)-3-(nonadecanoyloxy)propoxyphosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 31-MAY-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-MAY-12         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   52  P   UNK     0       0.000   0.000   0.000  0.00  0.00           P+0
HETATM   53  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   14                                                       
CONECT   13   11   15                                                       
CONECT   14   12   16                                                       
CONECT   15   13   17                                                       
CONECT   16   14   20                                                       
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   21                                                       
CONECT   20   16   23                                                       
CONECT   21   19   22                                                       
CONECT   22   21   24                                                       
CONECT   23   20   25                                                       
CONECT   24   22   26                                                       
CONECT   25   23   27                                                       
CONECT   26   24   28                                                       
CONECT   27   25   29                                                       
CONECT   28   26   30                                                       
CONECT   29   27   31                                                       
CONECT   30   28   32                                                       
CONECT   31   29   33                                                       
CONECT   32   30   40                                                       
CONECT   33   31   41                                                       
CONECT   34   38   42                                                       
CONECT   35   38   49                                                       
CONECT   36   39   48                                                       
CONECT   37   39   50                                                       
CONECT   38   34   35   43   53                                             
CONECT   39   36   37   51   54                                             
CONECT   40   32   44   48                                                  
CONECT   41   33   45   51                                                  
CONECT   42   34                                                            
CONECT   43   38                                                            
CONECT   44   40                                                            
CONECT   45   41                                                            
CONECT   46   52                                                            
CONECT   47   52                                                            
CONECT   48   36   40                                                       
CONECT   49   35   52                                                       
CONECT   50   37   52                                                       
CONECT   51   39   41                                                       
CONECT   52   46   47   49   50                                             
CONECT   53   38                                                            
CONECT   54   39                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  106    0
END

Synonyms

Not Available

Molecular Formula

C₄₁H₈₁O₁₀P

Average Mass

765.0496

Monoisotopic Mass

764.556735324

IUPAC Name

[(2S)-2,3-dihydroxypropoxy][(2R)-2-(hexadecanoyloxy)-3-(nonadecanoyloxy)propoxy]phosphinic acid

Traditional Name

(2S)-2,3-dihydroxypropoxy(2R)-2-(hexadecanoyloxy)-3-(nonadecanoyloxy)propoxyphosphinic acid

CAS Registry Number

Not Available

SMILES

[H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C41H81O10P/c1-3-5-7-9-11-13-15-17-18-19-21-22-24-26-28-30-32-40(44)48-36-39(37-50-52(46,47)49-35-38(43)34-42)51-41(45)33-31-29-27-25-23-20-16-14-12-10-8-6-4-2/h38-39,42-43H,3-37H2,1-2H3,(H,46,47)/t38-,39+/m0/s1

InChI Key

WXDNYCHHTCISSS-ZESVVUHVSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phosphatidylglycerols. These are glycerophosphoglycerols in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages. As is the case with diacylglycerols, phosphatidylglycerols can have many different combinations of fatty acids of varying lengths and saturation attached to the C-1 and C-2 positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoglycerols

Direct Parent

Phosphatidylglycerols

Alternative Parents

Substituents

1,2-diacylglycerophosphoglycerol
Fatty acid ester
Dialkyl phosphate
Dicarboxylic acid or derivatives
Organic phosphoric acid derivative
Phosphoric acid ester
Alkyl phosphate
Fatty acyl
1,2-diol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Organic oxide
Organooxygen compound
Alcohol
Organic oxygen compound
Primary alcohol
Carbonyl group
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Diacylglycerophosphoglycerols (LMGP04010954 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	9.7e-05 g/L	ALOGPS
logP	8.43	ALOGPS
logP	12.27	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Acidic)	1.89	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	148.82 Å²	ChemAxon
Rotatable Bond Count	43	ChemAxon
Refractivity	209.11 m³·mol⁻¹	ChemAxon
Polarizability	93.74 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

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0037788	PG(19:0/16:0)	2-Acyl-sn-glycero-3-phosphoglycerol (N-C16:0)	Unknown Protein		RHEA	34755880

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Proteobacteria	1	Human ; Human feces; Human feces; pleural fluid plaque; bal; Human stool	Unknown

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

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

52927217

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Keseler IM, Collado-Vides J, Santos-Zavaleta A, Peralta-Gil M, Gama-Castro S, Muniz-Rascado L, Bonavides-Martinez C, Paley S, Krummenacker M, Altman T, Kaipa P, Spaulding A, Pacheco J, Latendresse M, Fulcher C, Sarker M, Shearer AG, Mackie A, Paulsen I, Gunsalus RP, Karp PD: EcoCyc: a comprehensive database of Escherichia coli biology. Nucleic Acids Res. 2011 Jan;39(Database issue):D583-90. doi: 10.1093/nar/gkq1143. Epub 2010 Nov 21. [PubMed:21097882 ]
Kanehisa M, Goto S, Sato Y, Furumichi M, Tanabe M: KEGG for integration and interpretation of large-scale molecular data sets. Nucleic Acids Res. 2012 Jan;40(Database issue):D109-14. doi: 10.1093/nar/gkr988. Epub 2011 Nov 10. [PubMed:22080510 ]
Authors unspecified: Reorganizing the protein space at the Universal Protein Resource (UniProt). Nucleic Acids Res. 2012 Jan;40(Database issue):D71-5. doi: 10.1093/nar/gkr981. Epub 2011 Nov 18. [PubMed:22102590 ]

Showing metabocard for PG(19:0/16:0) (MMDBc0030298)

MOL for #<Metabolite:0x00007f9231f97b88>

3D MOL for #<Metabolite:0x00007f9231f97b88>

3D SDF for #<Metabolite:0x00007f9231f97b88>

3D-SDF for #<Metabolite:0x00007f9231f97b88>

PDB for #<Metabolite:0x00007f9231f97b88>

3D PDB for #<Metabolite:0x00007f9231f97b88>

SMILES for #<Metabolite:0x00007f9231f97b88>

INCHI for #<Metabolite:0x00007f9231f97b88>

Structure for #<Metabolite:0x00007f9231f97b88>

3D Structure for #<Metabolite:0x00007f9231f97b88>