MiMeDB: Showing metabocard for PC(20:4(8Z,11Z,14Z,17Z)/18:1(11Z)) (MMDBc0034051)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 05:14:07 UTC

Update Date

2024-04-30 20:20:23 UTC

Metabolite ID

MMDBc0034051

Metabolite Identification

Common Name

PC(20:4(8Z,11Z,14Z,17Z)/18:1(11Z))

Description

PC(20:4(8Z,11Z,14Z,17Z)/18:1(11Z)) 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(20:4(8Z,11Z,14Z,17Z)/18:1(11Z)), in particular, consists of one chain of eicsoatetraenoic acid at the C-1 position and one chain of vaccenic acid at the C-2 position. The eicsoatetraenoic acid moiety is derived from fish oils, while the vaccenic acid moiety is derived from butter fat and animal fat. 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 02251201222D          

 57 56  0  0  1  0            999 V2000
  -13.8303   10.4760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1613   10.9588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4087   10.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3251    9.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5725    9.4621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4888    8.6414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7362    8.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6526    7.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9000    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2310    7.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4784    7.2895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8094    7.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0568    7.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3879    7.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6353    7.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9663    8.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2137    7.7241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5447    8.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6283    9.0276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7921    7.8689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1231    8.3517    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3705    8.0137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7015    8.4965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0511    8.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1347    7.3378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7201    8.6414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4727    8.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1416    8.7862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942    8.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779    7.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3089    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3925    6.3240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7235    5.8412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8072    5.0204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5598    4.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6434    3.8617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960    3.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0650    4.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8176    3.6686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4865    4.1514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4029    4.9721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0719    5.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9883    6.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6573    6.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2067    9.1724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5377    9.6552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6214   10.4760    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4421   10.3924    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.8006   10.5596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7050   11.2967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0360   11.7795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1196   12.6003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4507   13.0831    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    0.0321   12.4141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9335   13.7521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2183   13.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0395    7.5309    0.0000 H   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  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 21 20  1  1  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  2  0  0  0  0
 24 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
 32 31  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 35 34  1  4  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 38 37  1  4  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 41 40  1  4  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 21 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
 47 49  2  0  0  0  0
 47 50  1  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
 53 55  1  0  0  0  0
 53 56  1  0  0  0  0
 21 57  1  6  0  0  0
M  CHG  2  48  -1  53   1
M  END


  Mrv0541 02251201222D          

 57 56  0  0  1  0            999 V2000
  -13.8303   10.4760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1613   10.9588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4087   10.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3251    9.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5725    9.4621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4888    8.6414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7362    8.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6526    7.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9000    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2310    7.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4784    7.2895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8094    7.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0568    7.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3879    7.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6353    7.5792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9663    8.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2137    7.7241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5447    8.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6283    9.0276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7921    7.8689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1231    8.3517    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3705    8.0137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7015    8.4965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0511    8.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1347    7.3378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7201    8.6414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4727    8.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1416    8.7862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942    8.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9779    7.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3089    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3925    6.3240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7235    5.8412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8072    5.0204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5598    4.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6434    3.8617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960    3.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0650    4.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8176    3.6686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4865    4.1514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4029    4.9721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0719    5.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9883    6.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6573    6.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2067    9.1724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5377    9.6552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6214   10.4760    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4421   10.3924    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.8006   10.5596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7050   11.2967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0360   11.7795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1196   12.6003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4507   13.0831    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    0.0321   12.4141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9335   13.7521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2183   13.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0395    7.5309    0.0000 H   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  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 21 20  1  1  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  2  0  0  0  0
 24 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
 32 31  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 35 34  1  4  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 38 37  1  4  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 41 40  1  4  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 21 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
 47 49  2  0  0  0  0
 47 50  1  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
 53 55  1  0  0  0  0
 53 56  1  0  0  0  0
 21 57  1  6  0  0  0
M  CHG  2  48  -1  53   1
M  END
> <DATABASE_ID>
MMDBc0034051

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C46H82NO8P/c1-6-8-10-12-14-16-18-20-22-23-25-26-28-30-32-34-36-38-45(48)52-42-44(43-54-56(50,51)53-41-40-47(3,4)5)55-46(49)39-37-35-33-31-29-27-24-21-19-17-15-13-11-9-7-2/h8,10,14,16-17,19-20,22,25-26,44H,6-7,9,11-13,15,18,21,23-24,27-43H2,1-5H3/t44-/m1/s1

> <INCHI_KEY>
AKLWUKOTFBFPBC-USYZEHPZSA-N

> <FORMULA>
C46H82NO8P

> <MOLECULAR_WEIGHT>
808.1189

> <EXACT_MASS>
807.577805117

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
97.86956747020272

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
5.89

> <JCHEM_LOGP>
8.971600085861589

> <ALOGPS_LOGS>
-7.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309193598

> <JCHEM_POLAR_SURFACE_AREA>
111.19000000000001

> <JCHEM_REFRACTIVITY>
249.05409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
41

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.85e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-3-(icosa-8,11,14,17-tetraenoyloxy)-2-(octadec-11-enoyloxy)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     -25.817  19.555   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -24.568  20.456   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -23.163  19.825   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -23.007  18.294   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -21.602  17.663   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -21.446  16.131   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -20.041  15.500   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -19.885  13.968   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -18.480  13.337   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -17.231  14.238   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -15.826  13.607   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -14.578  14.508   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -13.173  13.878   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -11.924  14.779   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.519  14.148   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -9.270  15.049   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.866  14.418   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.617  15.320   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.773  16.852   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -5.212  14.689   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.963  15.590   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.558  14.959   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.309  15.860   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.095  15.229   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.251  13.697   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.344  16.131   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.749  15.500   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.998  16.401   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.403  15.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.559  14.238   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.310  13.337   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.466  11.805   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.217  10.904   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.373   9.371   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.778   8.741   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.934   7.209   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.339   6.578   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.588   7.479   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.993   6.848   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.241   7.749   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.085   9.281   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      11.334  10.182   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      11.178  11.715   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      12.427  12.616   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -4.119  17.122   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -2.870  18.023   0.000  0.00  0.00           O+0
HETATM   47  P   UNK     0      -3.027  19.555   0.000  0.00  0.00           P+0
HETATM   48  O   UNK     0      -4.559  19.399   0.000  0.00  0.00           O-1
HETATM   49  O   UNK     0      -1.494  19.711   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      -3.183  21.087   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      -1.934  21.988   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -2.090  23.521   0.000  0.00  0.00           C+0
HETATM   53  N   UNK     0      -0.841  24.422   0.000  0.00  0.00           N+1
HETATM   54  C   UNK     0       0.060  23.173   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      -1.743  25.671   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       0.407  25.323   0.000  0.00  0.00           C+0
HETATM   57  H   UNK     0      -3.807  14.058   0.000  0.00  0.00           H+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                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   45   57                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   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   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   21   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48   49   50                                             
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   47   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54   55   56                                             
CONECT   54   53                                                            
CONECT   55   53                                                            
CONECT   56   53                                                            
CONECT   57   21                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  112    0
END

Synonyms

Not Available

Molecular Formula

C₄₆H₈₂NO₈P

Average Mass

808.1189

Monoisotopic Mass

807.577805117

IUPAC Name

(2-{[(2R)-3-(icosa-8,11,14,17-tetraenoyloxy)-2-(octadec-11-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

Traditional Name

(2-{[(2R)-3-(icosa-8,11,14,17-tetraenoyloxy)-2-(octadec-11-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C46H82NO8P/c1-6-8-10-12-14-16-18-20-22-23-25-26-28-30-32-34-36-38-45(48)52-42-44(43-54-56(50,51)53-41-40-47(3,4)5)55-46(49)39-37-35-33-31-29-27-24-21-19-17-15-13-11-9-7-2/h8,10,14,16-17,19-20,22,25-26,44H,6-7,9,11-13,15,18,21,23-24,27-43H2,1-5H3/t44-/m1/s1

InChI Key

AKLWUKOTFBFPBC-USYZEHPZSA-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	2.8e-05 g/L	ALOGPS
logP	5.89	ALOGPS
logP	8.97	ChemAxon
logS	-7.5	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	41	ChemAxon
Refractivity	249.05 m³·mol⁻¹	ChemAxon
Polarizability	97.87 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

Spectra

Not Available

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

All Tissues
Blood
Feces
Saliva
Urine

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
Obesity		Association	Human Blood	HMDB	Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children
Obesity		Association	Human Blood	HMDB	Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces; Human saliva	Unknown

Exposure Sources

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

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Blood	Detected and Quantified	76.975	21.930			uM	Adult (>18 years old)	Female	Pregnancy	HMDB	24704061
Human Urine	Detected and Quantified	0.0007		0.0002	0.002	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	24023812
Human Feces	Detected and Quantified	0.05	0.02			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Feces	Detected and Quantified	0.09	0.09			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Blood	Detected and Quantified	21.8		18.8	25.2	uM	Newborn (0-30 days old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	36.2		28.8	42.9	uM	Infant (0-1 year old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	54.2	13.2			uM	Adult (>18 years old)	Both	Normal	HMDB	28278231
Human Blood	Detected and Quantified	81.9	19.68			uM	Adult (>18 years old)	Both	Normal	HMDB	26010610
Human Blood	Detected and Quantified	39.8	13.1			uM	Children (1-13 years old)	Both	Obesity	HMDB	Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children
Human Blood	Detected and Quantified	48.5	15.2			uM	Children (1-13 years old)	Both	Obesity	HMDB	Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children
Human Saliva	Detected and Quantified	0.022	0.005			uM	Adult (>18 years old)	Both	Normal	HMDB	https://doi.org/10.1007/s11306-015-0840-5
Human All tissues	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	34986597

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB025655

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(20:4(8Z,11Z,14Z,17Z)/18:1(11Z)) (MMDBc0034051)

MOL for #<Metabolite:0x00007fece8024e00>

3D MOL for #<Metabolite:0x00007fece8024e00>

3D SDF for #<Metabolite:0x00007fece8024e00>

3D-SDF for #<Metabolite:0x00007fece8024e00>

PDB for #<Metabolite:0x00007fece8024e00>

3D PDB for #<Metabolite:0x00007fece8024e00>

SMILES for #<Metabolite:0x00007fece8024e00>

INCHI for #<Metabolite:0x00007fece8024e00>

Structure for #<Metabolite:0x00007fece8024e00>

3D Structure for #<Metabolite:0x00007fece8024e00>