MiMeDB: Showing metabocard for PG(19:iso/15:0) (MMDBc0031513)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 00:52:07 UTC

Update Date

2022-08-31 18:11:43 UTC

Metabolite ID

MMDBc0031513

Metabolite Identification

Common Name

PG(19:iso/15:0)

Description

PG(19:iso/15:0) 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(19:iso/15:0), in particular, consists of one 17-methylocatdecanoyl chain to the C-1 atom, and one pentadecanoyl 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 10241215472D          

 51 50  0  0  0  0            999 V2000
   33.8980   17.9210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   33.8980   17.0960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   16.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   17.0960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   15.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   15.4460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   14.6210    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   36.1519   14.6210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.5019   14.6210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   13.7960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   13.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8980   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.1835   12.5585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.4690   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.4690   11.3210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.7546   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.0401   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3256   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.6112   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.8967   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.1822   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.4677   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.7533   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.0388   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3243   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6099   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8954   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1809   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4664   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7520   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0375   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3230   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0375   11.3210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   12.1460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.0414   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.0414   13.3835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.7559   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.4703   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.1848   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.8993   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.6137   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.3282   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.0427   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.7572   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.4716   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.1861   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.9006   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.6150   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.3295   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   46.0440   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  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
 32 34  1  0  0  0  0
 12 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END


  Mrv0541 10241215472D          

 51 50  0  0  0  0            999 V2000
   33.8980   17.9210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   33.8980   17.0960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   16.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   17.0960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   15.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   15.4460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   14.6210    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   36.1519   14.6210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.5019   14.6210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   13.7960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   13.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.6124   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8980   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.1835   12.5585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.4690   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.4690   11.3210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.7546   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.0401   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3256   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.6112   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.8967   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.1822   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.4677   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.7533   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.0388   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3243   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6099   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8954   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1809   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4664   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7520   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0375   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3230   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0375   11.3210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3269   12.1460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.0414   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.0414   13.3835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.7559   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.4703   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.1848   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.8993   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   39.6137   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.3282   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.0427   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.7572   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.4716   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.1861   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.9006   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.6150   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.3295   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   46.0440   12.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  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
 32 34  1  0  0  0  0
 12 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0031513

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(C)C)COP(O)(=O)OCC(O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C40H79O10P/c1-4-5-6-7-8-9-10-15-19-22-25-28-31-40(44)50-38(35-49-51(45,46)48-33-37(42)32-41)34-47-39(43)30-27-24-21-18-16-13-11-12-14-17-20-23-26-29-36(2)3/h36-38,41-42H,4-35H2,1-3H3,(H,45,46)

> <INCHI_KEY>
OXHYXPPQIBTPHV-UHFFFAOYSA-N

> <FORMULA>
C40H79O10P

> <MOLECULAR_WEIGHT>
751.023

> <EXACT_MASS>
750.54108526

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
92.31765943296239

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2,3-dihydroxypropoxy)({3-[(17-methyloctadecanoyl)oxy]-2-(pentadecanoyloxy)propoxy})phosphinic acid

> <ALOGPS_LOGP>
7.99

> <JCHEM_LOGP>
11.668639280666666

> <ALOGPS_LOGS>
-6.84

> <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>
204.45850000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
41

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.10e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,3-dihydroxypropoxy(3-[(17-methyloctadecanoyl)oxy]-2-(pentadecanoyloxy)propoxy)phosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-OCT-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-OCT-12         0                                  
HETATM    1  O   UNK     0      63.276  33.453   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      63.276  31.913   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      64.610  31.143   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      65.944  31.913   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      64.610  29.603   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      65.944  28.833   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      65.944  27.293   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      67.484  27.293   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      64.404  27.293   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      65.944  25.753   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      64.610  24.983   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      64.610  23.443   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      63.276  22.673   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      61.943  23.443   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      60.609  22.673   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      60.609  21.133   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      59.275  23.443   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      57.942  22.673   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      56.608  23.443   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      55.274  22.673   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      53.941  23.443   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      52.607  22.673   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      51.273  23.443   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      49.939  22.673   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      48.606  23.443   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      47.272  22.673   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      45.938  23.443   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      44.605  22.673   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      43.271  23.443   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      41.937  22.673   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      40.604  23.443   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      39.270  22.673   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      37.936  23.443   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      39.270  21.133   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      65.944  22.673   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      67.277  23.443   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      67.277  24.983   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      68.611  22.673   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      69.945  23.443   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      71.278  22.673   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      72.612  23.443   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      73.946  22.673   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      75.279  23.443   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      76.613  22.673   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      77.947  23.443   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      79.280  22.673   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      80.614  23.443   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      81.948  22.673   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      83.281  23.443   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      84.615  22.673   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      85.949  23.443   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   35                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   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   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   12   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   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                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  100    0
END

Synonyms

Not Available

Molecular Formula

C₄₀H₇₉O₁₀P

Average Mass

751.023

Monoisotopic Mass

750.54108526

IUPAC Name

(2,3-dihydroxypropoxy)({3-[(17-methyloctadecanoyl)oxy]-2-(pentadecanoyloxy)propoxy})phosphinic acid

Traditional Name

2,3-dihydroxypropoxy(3-[(17-methyloctadecanoyl)oxy]-2-(pentadecanoyloxy)propoxy)phosphinic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(C)C)COP(O)(=O)OCC(O)CO

InChI Identifier

InChI=1S/C40H79O10P/c1-4-5-6-7-8-9-10-15-19-22-25-28-31-40(44)50-38(35-49-51(45,46)48-33-37(42)32-41)34-47-39(43)30-27-24-21-18-16-13-11-12-14-17-20-23-26-29-36(2)3/h36-38,41-42H,4-35H2,1-3H3,(H,45,46)

InChI Key

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

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00011 g/L	ALOGPS
logP	7.99	ALOGPS
logP	11.67	ChemAxon
logS	-6.8	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	41	ChemAxon
Refractivity	204.46 m³·mol⁻¹	ChemAxon
Polarizability	92.32 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

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0fc0-3190250600-e654755f94dddd7875f9	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0059-5391031100-45b3ca7457c044e42798	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a6r-9532120000-f1ec7bc20698991b1876	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-002b-0190020300-2864a293c40481f736a0	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004j-4290000000-8bcb2e15b464f9e09d91	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9130000000-842309d5d6d65788b9c1	2015-09-15	View Spectrum

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

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	Proteobacteria	1	Human ; Human feces; Human feces; pleural fluid plaque; bal; Human stool	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Casadei MA, Manas P, Niven G, Needs E, Mackey BM: Role of membrane fluidity in pressure resistance of Escherichia coli NCTC 8164. Appl Environ Microbiol. 2002 Dec;68(12):5965-72. doi: 10.1128/AEM.68.12.5965-5972.2002. [PubMed:12450817 ]
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 ]

Showing metabocard for PG(19:iso/15:0) (MMDBc0031513)

MOL for #<Metabolite:0x00007f46f809d8a0>

3D MOL for #<Metabolite:0x00007f46f809d8a0>

3D SDF for #<Metabolite:0x00007f46f809d8a0>

3D-SDF for #<Metabolite:0x00007f46f809d8a0>

PDB for #<Metabolite:0x00007f46f809d8a0>

3D PDB for #<Metabolite:0x00007f46f809d8a0>

SMILES for #<Metabolite:0x00007f46f809d8a0>

INCHI for #<Metabolite:0x00007f46f809d8a0>

Structure for #<Metabolite:0x00007f46f809d8a0>

3D Structure for #<Metabolite:0x00007f46f809d8a0>