MiMeDB: Showing metabocard for PC(20:5(5Z,8Z,11Z,14Z,17Z)/16:1(9Z)) (MMDBc0034057)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 05:14:21 UTC

Update Date

2022-12-15 22:52:08 UTC

MiMeDB ID

MMDBc0034057

Metabolite Identification

Common Name

PC(20:5(5Z,8Z,11Z,14Z,17Z)/16:1(9Z))

Description

PC(20:5(5Z,8Z,11Z,14Z,17Z)/16:1(9Z)) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PC(20:5(5Z,8Z,11Z,14Z,17Z)/16:1(9Z)), in particular, consists of one chain of eicosapentaenoic acid at the C-1 position and one chain of palmitoleic acid at the C-2 position. The eicosapentaenoic acid moiety is derived from fish oils, liver and kidney, while the palmitoleic acid moiety is derived from animal fats and vegetable oils. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.‚Üµ‚ÜµWhile most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02251201442D          

 54 53  0  0  1  0            999 V2000
    2.2323    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9467    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6612    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3757    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0901    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8046    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    6.2388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    6.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    7.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    8.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    9.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    8.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    9.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    8.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    7.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    6.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    3.7638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.9388    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   15.9177    2.9388    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   14.2677    2.9388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.1138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    1.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    0.8763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    0.4638    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   13.2513    1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0763   -0.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    0.0513    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 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  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  6  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  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  4  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 33 32  1  4  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 36 35  1  4  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 39 38  1  4  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 19 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
 45 47  2  0  0  0  0
 45 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
 51 52  1  0  0  0  0
 51 53  1  0  0  0  0
 51 54  1  0  0  0  0
M  CHG  2  46  -1  51   1
M  END


  Mrv0541 02251201442D          

 54 53  0  0  1  0            999 V2000
    2.2323    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9467    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6612    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3757    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0901    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8046    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    6.2388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    6.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    7.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    8.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    9.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    8.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    9.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    8.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    7.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    7.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    6.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    6.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    3.7638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.9388    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   15.9177    2.9388    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   14.2677    2.9388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.1138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    1.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    0.8763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    0.4638    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   13.2513    1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0763   -0.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    0.0513    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 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  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  6  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  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  4  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 33 32  1  4  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 36 35  1  4  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 39 38  1  4  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 19 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
 45 47  2  0  0  0  0
 45 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
 51 52  1  0  0  0  0
 51 53  1  0  0  0  0
 51 54  1  0  0  0  0
M  CHG  2  46  -1  51   1
M  END
> <DATABASE_ID>
MMDBc0034057

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCCC=CCCCCCCCC(=O)O[C@H](COC(=O)CCCC=CCC=CCC=CCC=CCC=CCC)COP([O-])(=O)OCC[N+](C)(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C44H76NO8P/c1-6-8-10-12-14-16-18-20-21-22-23-25-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-24-19-17-15-13-11-9-7-2/h8,10,14,16-17,19-21,23,25,28,30,42H,6-7,9,11-13,15,18,22,24,26-27,29,31-41H2,1-5H3/t42-/m1/s1

> <INCHI_KEY>
SHMZMMGXODYRCN-HUESYALOSA-N

> <FORMULA>
C44H76NO8P

> <MOLECULAR_WEIGHT>
778.0499

> <EXACT_MASS>
777.530854925

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
91.69248596541895

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(icosa-5,8,11,14,17-pentaenoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
5.40

> <JCHEM_LOGP>
7.7205410991949215

> <ALOGPS_LOGS>
-7.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064467632

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744219009617128

> <JCHEM_POLAR_SURFACE_AREA>
111.19000000000001

> <JCHEM_REFRACTIVITY>
240.96869999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
38

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.33e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(icosa-5,8,11,14,17-pentaenoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
HETATM    1  C   UNK     0       4.167  10.106   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.501   9.336   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.834  10.106   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.168   9.336   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.502  10.106   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.835   9.336   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.169  10.106   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.503   9.336   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.836  10.106   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.504  10.106   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.837   9.336   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.171  10.106   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.505   9.336   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      22.838  10.106   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      24.172   9.336   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      24.172   7.796   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      25.506  10.106   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      26.839   9.336   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      28.173  10.106   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      29.507   9.336   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      30.841  10.106   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      30.841  11.646   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      32.174   9.336   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      33.508  10.106   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      34.842   9.336   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      36.175  10.106   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      37.509   9.336   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      38.843  10.106   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      38.843  11.646   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      40.176  12.416   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      40.176  13.956   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      38.843  14.726   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      38.843  16.266   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      37.509  17.036   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      36.175  16.266   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      34.842  17.036   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      33.508  16.266   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      33.508  14.726   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      32.174  13.956   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      32.174  12.416   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      33.508  11.646   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      26.839   7.796   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      28.173   7.026   0.000  0.00  0.00           O+0
HETATM   45  P   UNK     0      28.173   5.486   0.000  0.00  0.00           P+0
HETATM   46  O   UNK     0      29.713   5.486   0.000  0.00  0.00           O-1
HETATM   47  O   UNK     0      26.633   5.486   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      28.173   3.946   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      26.839   3.176   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      26.839   1.636   0.000  0.00  0.00           C+0
HETATM   51  N   UNK     0      25.506   0.866   0.000  0.00  0.00           N+1
HETATM   52  C   UNK     0      24.736   2.199   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      26.276  -0.468   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      24.172   0.096   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   43                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   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                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41                                                            
CONECT   43   19   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46   47   48                                             
CONECT   46   45                                                            
CONECT   47   45                                                            
CONECT   48   45   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52   53   54                                             
CONECT   52   51                                                            
CONECT   53   51                                                            
CONECT   54   51                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  106    0
END

Synonyms

Not Available

Chemical Formula

C₄₄H₇₆NO₈P

Average Molecular Weight

778.0499

Monoisotopic Molecular Weight

777.530854925

IUPAC Name

(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(icosa-5,8,11,14,17-pentaenoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

Traditional Name

(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(icosa-5,8,11,14,17-pentaenoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

CAS Registry Number

Not Available

SMILES

CCCCCCC=CCCCCCCCC(=O)O[C@H](COC(=O)CCCC=CCC=CCC=CCC=CCC=CCC)COP([O-])(=O)OCC[N+](C)(C)C

InChI Identifier

InChI=1S/C44H76NO8P/c1-6-8-10-12-14-16-18-20-21-22-23-25-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-24-19-17-15-13-11-9-7-2/h8,10,14,16-17,19-21,23,25,28,30,42H,6-7,9,11-13,15,18,22,24,26-27,29,31-41H2,1-5H3/t42-/m1/s1

InChI Key

SHMZMMGXODYRCN-HUESYALOSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.

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

Not Available

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	3.3e-05 g/L	ALOGPS
logP	5.4	ALOGPS
logP	7.72	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	38	ChemAxon
Refractivity	240.97 m³·mol⁻¹	ChemAxon
Polarizability	91.69 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	Deposition Date
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

All Tissues
Blood
Feces
Urine

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference
Obesity		This associated disease is originally imported from HMDB metabolite HMDB0008496 concentration id 140708	Association	Human Blood		Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children	details
Obesity		This associated disease is originally imported from HMDB metabolite HMDB0008496 concentration id 140709	Association	Human Blood		Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children	details

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Fungi	Ascomycota	1	Human Feces	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details
Animal	Milk	Bos taurus	FooDB	31437929	details
Animal	Milk	Bos taurus	FooDB	31437929	details

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Age	Sex	Health Condition	Data Source	Reference
Human	Detected and Quantified	2.1289	0.9321			Adult (>18 years old)	Female	Pregnancy	HMDB	24704061	details
Human	Detected and Quantified	0.0037				Adult (>18 years old)	Both	Normal	HMDB	24023812	details
Human	Detected and Quantified	0.0	0.01			Newborn (0-30 days old)	Female	Normal	HMDB	32340350	details
Human	Detected and Quantified			0.0	0.02	Newborn (0-30 days old)	Both	Normal	HMDB	32340350	details
Human	Detected and Quantified	0.03	0.01			Adult (>18 years old)	Both	Normal	HMDB	27624970	details
Human	Detected and Quantified	0.17	0.35			Adult (>18 years old)	Both	Normal	HMDB	27624970	details
Human	Detected and Quantified	0.31		0.26	0.37	Newborn (0-30 days old)		Normal	HMDB	25754623	details
Human	Detected and Quantified	0.4		0.3	0.54	Infant (0-1 year old)		Normal	HMDB	25754623	details
Human	Detected and Quantified	1.16	0.47			Adult (>18 years old)	Both	Normal	HMDB	28278231	details
Human	Detected and Quantified	1.7	0.84			Adult (>18 years old)	Both	Normal	HMDB	26010610	details
Human	Detected and Quantified	0.574	0.243			Children (1-13 years old)	Both	Obesity	HMDB	Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children	details
Human	Detected and Quantified	0.725	0.281			Children (1-13 years old)	Both	Obesity	HMDB	Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children	details
Human All Tissues	Detected but not Quantified					Not Specified	Not Specified	Normal	HMDB	34986597	details

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB025686

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

Ramirez-Gaona M, Marcu A, Pon A, Guo AC, Sajed T, Wishart NA, Karu N, Djoumbou Feunang Y, Arndt D, Wishart DS: YMDB 2.0: a significantly expanded version of the yeast metabolome database. Nucleic Acids Res. 2017 Jan 4;45(D1):D440-D445. doi: 10.1093/nar/gkw1058. Epub 2016 Nov 28. [PubMed:27899612 ]

Showing metabocard for PC(20:5(5Z,8Z,11Z,14Z,17Z)/16:1(9Z)) (MMDBc0034057)

MOL for #<Metabolite:0x00007f09201854e0>

3D MOL for #<Metabolite:0x00007f09201854e0>

3D SDF for #<Metabolite:0x00007f09201854e0>

3D-SDF for #<Metabolite:0x00007f09201854e0>

PDB for #<Metabolite:0x00007f09201854e0>

3D PDB for #<Metabolite:0x00007f09201854e0>

SMILES for #<Metabolite:0x00007f09201854e0>

INCHI for #<Metabolite:0x00007f09201854e0>

Structure for #<Metabolite:0x00007f09201854e0>

3D Structure for #<Metabolite:0x00007f09201854e0>