MiMeDB: Showing metabocard for PC(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z)) (MMDBc0034031)

Microbial

Human

Animal

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-11-19 05:13:21 UTC

Update Date

2024-04-30 20:20:05 UTC

Metabolite ID

MMDBc0034031

Metabolite Identification

Common Name

PC(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z))

Description

PC(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z)) 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(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z)), in particular, consists of one chain of homo-g-linolenic acid at the C-1 position and one chain of a-linolenic acid at the C-2 position. The homo-g-linolenic acid moiety is derived from fish oils, liver and kidney, while the a-linolenic acid moiety is derived from seed oils, especially canola and soybean oil. 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 02251200012D          

 57 56  0  0  1  0            999 V2000
  -13.3698    7.3735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5771    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3790    6.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5863    6.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3882    5.3142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5955    5.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3974    4.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6047    4.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0103    4.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2176    4.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6232    4.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8213    5.7718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2268    6.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4250    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8305    7.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0379    7.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4434    8.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6508    7.8312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0563    8.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2637    8.1744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6692    8.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0655    7.3735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2729    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6784    7.7167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8766    8.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821    9.0896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802    9.8905    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2811    9.6923    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.6794   10.0886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6784   10.6913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0839   11.2634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821   12.0642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6876   12.6362    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -0.1156   12.0418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2596   13.2307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0931   13.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8858    7.4879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2913    8.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4894    8.8608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5013    7.8312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0958    8.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8885    8.1744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4829    8.7464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    8.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737    7.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8792    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0774    6.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4829    5.7718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6811    4.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737    4.7422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6719    3.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4645    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0590    4.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8516    4.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4461    4.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2387    4.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0839    8.2887    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  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  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 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
 27 29  2  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 24 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 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
 47 46  1  4  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 50 49  1  4  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 53 52  1  4  0  0  0
 53 54  2  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 24 57  1  1  0  0  0
M  CHG  2  28  -1  33   1
M  END


  Mrv0541 02251200012D          

 57 56  0  0  1  0            999 V2000
  -13.3698    7.3735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5771    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3790    6.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5863    6.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3882    5.3142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5955    5.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3974    4.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6047    4.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0103    4.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2176    4.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6232    4.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8213    5.7718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2268    6.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4250    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8305    7.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0379    7.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4434    8.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6508    7.8312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0563    8.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2637    8.1744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6692    8.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0655    7.3735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2729    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6784    7.7167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8766    8.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821    9.0896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4802    9.8905    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2811    9.6923    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.6794   10.0886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6784   10.6913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0839   11.2634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821   12.0642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6876   12.6362    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -0.1156   12.0418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2596   13.2307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0931   13.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8858    7.4879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2913    8.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4894    8.8608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5013    7.8312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0958    8.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8885    8.1744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4829    8.7464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    8.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737    7.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8792    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0774    6.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4829    5.7718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6811    4.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737    4.7422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6719    3.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4645    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0590    4.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8516    4.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4461    4.6278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2387    4.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0839    8.2887    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  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  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 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
 27 29  2  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 24 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 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
 47 46  1  4  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 50 49  1  4  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 53 52  1  4  0  0  0
 53 54  2  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 24 57  1  1  0  0  0
M  CHG  2  28  -1  33   1
M  END
> <DATABASE_ID>
MMDBc0034031

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C46H80NO8P/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/h9,11,14-17,20-22,24-26,44H,6-8,10,12-13,18-19,23,27-43H2,1-5H3/t44-/m1/s1

> <INCHI_KEY>
ONHNZXQSGXKTJD-USYZEHPZSA-N

> <FORMULA>
C46H80NO8P

> <MOLECULAR_WEIGHT>
806.1031

> <EXACT_MASS>
805.562155053

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
97.63930615037398

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-3-(icosa-8,11,14-trienoyloxy)-2-(octadeca-9,12,15-trienoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
5.70

> <JCHEM_LOGP>
8.609678429194922

> <ALOGPS_LOGS>
-7.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.7441593091936305

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
250.17069999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
40

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.11e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-3-(icosa-8,11,14-trienoyloxy)-2-(octadeca-9,12,15-trienoyloxy)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     -24.957  13.764   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -23.477  13.337   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -23.107  11.842   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -21.628  11.415   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -21.258   9.920   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -19.778   9.493   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -19.408   7.998   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -17.929   7.571   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -16.819   8.639   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -15.340   8.211   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -14.230   9.279   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -14.600  10.774   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -13.490  11.842   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -13.860  13.337   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -12.750  14.405   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -11.271  13.977   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -10.161  15.045   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -8.681  14.618   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -7.572  15.686   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.092  15.259   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.983  16.327   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -5.722  13.764   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.243  13.337   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.133  14.405   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.503  15.900   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.393  16.967   0.000  0.00  0.00           O+0
HETATM   27  P   UNK     0      -2.763  18.462   0.000  0.00  0.00           P+0
HETATM   28  O   UNK     0      -4.258  18.092   0.000  0.00  0.00           O-1
HETATM   29  O   UNK     0      -1.268  18.832   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -3.133  19.957   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.023  21.025   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.393  22.520   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      -1.284  23.588   0.000  0.00  0.00           N+1
HETATM   34  C   UNK     0      -0.216  22.478   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.351  24.697   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.174  24.655   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.653  13.977   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.544  15.045   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -0.914  16.540   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       0.936  14.618   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.045  15.686   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.525  15.259   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.635  16.327   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.114  15.900   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.484  14.405   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       5.375  13.337   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.744  11.842   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       4.635  10.774   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.005   9.279   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       6.484   8.852   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       6.854   7.357   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       8.334   6.930   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       9.443   7.998   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      10.923   7.571   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      12.033   8.639   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      13.512   8.211   0.000  0.00  0.00           C+0
HETATM   57  H   UNK     0      -2.023  15.472   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                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   37   57                                             
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33                                                            
CONECT   37   24   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56                                                       
CONECT   56   55                                                            
CONECT   57   24                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  112    0
END

Synonyms

Not Available

Molecular Formula

C₄₆H₈₀NO₈P

Average Mass

806.1031

Monoisotopic Mass

805.562155053

IUPAC Name

(2-{[(2R)-3-(icosa-8,11,14-trienoyloxy)-2-(octadeca-9,12,15-trienoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

Traditional Name

(2-{[(2R)-3-(icosa-8,11,14-trienoyloxy)-2-(octadeca-9,12,15-trienoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C46H80NO8P/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/h9,11,14-17,20-22,24-26,44H,6-8,10,12-13,18-19,23,27-43H2,1-5H3/t44-/m1/s1

InChI Key

ONHNZXQSGXKTJD-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	3.1e-05 g/L	ALOGPS
logP	5.7	ALOGPS
logP	8.61	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	40	ChemAxon
Refractivity	250.17 m³·mol⁻¹	ChemAxon
Polarizability	97.64 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

Chromatographic Retention Times and Retention Indices

Retention Times

Chromatography Type	Technique	Column	Deposition Date	Retention Time (s)
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (eluted)	2025-10-24	135.6
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-24	75.1
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-24	1272.2
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-24	1235.4
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-24	2120.6
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (eluted)	2025-10-24	409.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	5740.8
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	282.1
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-24	542.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	1533.5
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	556.8
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	307.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	374.2
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (void)	2025-10-24	11.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	258.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	1297.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	848.3
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-24	3547.4
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-24	4283.8

Retention Indices

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

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0036194	PC(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z))	alpha-Linolenic acid	Lipid droplet phospholipase 1	Hydrolysis	RHEA	34755880
MMDBr0036773	PC(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z))	Dihomo-gamma-linolenic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference
Obesity	Increased	Association	Human Urine	HMDB	26910390
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

Food Exposures

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
Human Urine	Detected and Quantified	0.78	0.08			umol/mmol creatinine	Adolescent (13-18 years old)	Both	Obese	HMDB	26910390
Human Blood	Detected and Quantified	178.280	54.427			uM	Adult (>18 years old)	Female	Pregnancy	HMDB	24704061
Human Urine	Detected and Quantified			0.0	0.1	umol/mmol creatinine	Newborn (0-30 days old)	Both	Normal	HMDB	32340350
Human Urine	Detected and Quantified	0.001		0.0005	0.0036	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	24023812
Human Urine	Detected and Quantified	0.01		0.0	0.05	umol/mmol creatinine	Newborn (0-30 days old)	Female	Normal	HMDB	32340350
Human Urine	Detected and Quantified	0.01		0.0	0.1	umol/mmol creatinine	Newborn (0-30 days old)	Male	Normal	HMDB	32340350
Human Feces	Detected and Quantified	0.07	0.04			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Feces	Detected and Quantified	0.12	0.11			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Urine	Detected and Quantified	0.13	0.15			umol/mmol creatinine	Adolescent (13-18 years old)	Both	Normal	HMDB	26910390
Human Blood	Detected and Quantified	103.41	31.68			uM	Adult (>18 years old)	Both	Normal	HMDB	26010610
Human Blood	Detected and Quantified	49.1		37.8	60.8	uM	Infant (0-1 year old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	60.6		50.1	72.9	uM	Newborn (0-30 days old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	88.0	25.0			uM	Adult (>18 years old)	Both	Normal	HMDB	28278231
Human Blood	Detected and Quantified	51.9	20.0			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	60.5	21.7			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	0.030	0.004			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

FDB025594

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

CMMC Knowledgebase

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(20:3(8Z,11Z,14Z)/18:3(9Z,12Z,15Z)) (MMDBc0034031)

MOL for #<Metabolite:0x00007f9ad19c45a0>

3D MOL for #<Metabolite:0x00007f9ad19c45a0>

3D SDF for #<Metabolite:0x00007f9ad19c45a0>

3D-SDF for #<Metabolite:0x00007f9ad19c45a0>

PDB for #<Metabolite:0x00007f9ad19c45a0>

3D PDB for #<Metabolite:0x00007f9ad19c45a0>

SMILES for #<Metabolite:0x00007f9ad19c45a0>

INCHI for #<Metabolite:0x00007f9ad19c45a0>

Structure for #<Metabolite:0x00007f9ad19c45a0>

3D Structure for #<Metabolite:0x00007f9ad19c45a0>