MiMeDB: Showing metabocard for PC(24:0/18:1(11Z)) (MMDBc0034112)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 05:16:31 UTC

Update Date

2024-04-30 20:21:18 UTC

Metabolite ID

MMDBc0034112

Metabolite Identification

Common Name

PC(24:0/18:1(11Z))

Description

PC(24:0/18:1(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(24:0/18:1(11Z)), in particular, consists of one chain of lignoceric acid at the C-1 position and one chain of vaccenic acid at the C-2 position. The lignoceric acid moiety is derived from groundnut oil, 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 02241223432D          

 61 60  0  0  1  0            999 V2000
   21.5605   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2750   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9895   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7039   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.4184   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1329   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.8474   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.5618   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2763   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.9908   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.7052   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.4197   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.1342   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.8487   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.5631   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.2776   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.9921   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.7065   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.4210   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.1355   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.8499   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.5644   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.2789   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.9934   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.9934   12.0355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   38.7078   13.2730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   39.4223   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.1368   13.2730    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   40.1368   14.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   14.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   15.3355    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   40.0262   15.3355    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   41.6762   15.3355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   16.1605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   16.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   17.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.2802   17.8105    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   42.6927   17.0960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.8677   18.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.9947   18.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   12.8605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   14.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   42.2802   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.9947   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.7091   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.4236   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.1381   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.8525   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   46.5670   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   47.2815   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   47.9960   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   48.7104   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   49.4249   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.1394   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.1394   14.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.8538   14.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.8538   15.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   51.5683   15.7480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   51.5683   16.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8513   13.6855    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
  6  7  1  0  0  0  0
  7  8  1  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  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  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
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 28 41  1  6  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 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
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
 28 61  1  1  0  0  0
M  CHG  2  32  -1  37   1
M  END


  Mrv0541 02241223432D          

 61 60  0  0  1  0            999 V2000
   21.5605   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2750   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9895   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7039   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.4184   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1329   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.8474   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.5618   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2763   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.9908   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.7052   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.4197   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.1342   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.8487   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.5631   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.2776   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.9921   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.7065   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.4210   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.1355   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.8499   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.5644   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.2789   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.9934   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.9934   12.0355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   38.7078   13.2730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   39.4223   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.1368   13.2730    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   40.1368   14.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   14.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   15.3355    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   40.0262   15.3355    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   41.6762   15.3355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   16.1605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   16.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   17.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.2802   17.8105    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   42.6927   17.0960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.8677   18.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.9947   18.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8512   12.8605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   41.5657   14.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   42.2802   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   42.9947   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   43.7091   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   44.4236   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.1381   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   45.8525   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   46.5670   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   47.2815   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   47.9960   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   48.7104   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   49.4249   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.1394   13.2730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.1394   14.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.8538   14.5105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   50.8538   15.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   51.5683   15.7480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   51.5683   16.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   40.8513   13.6855    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
  6  7  1  0  0  0  0
  7  8  1  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  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  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
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 28 41  1  6  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 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
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
 28 61  1  1  0  0  0
M  CHG  2  32  -1  37   1
M  END
> <DATABASE_ID>
MMDBc0034112

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C50H98NO8P/c1-6-8-10-12-14-16-18-20-22-23-24-25-26-27-29-30-32-34-36-38-40-42-49(52)56-46-48(47-58-60(54,55)57-45-44-51(3,4)5)59-50(53)43-41-39-37-35-33-31-28-21-19-17-15-13-11-9-7-2/h17,19,48H,6-16,18,20-47H2,1-5H3/t48-/m1/s1

> <INCHI_KEY>
GHQRIAPHRZOTFN-QSCHNALKSA-N

> <FORMULA>
C50H98NO8P

> <MOLECULAR_WEIGHT>
872.2888

> <EXACT_MASS>
871.703005629

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
112.33272389538072

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
trimethyl(2-{[(2R)-2-(octadec-11-enoyloxy)-3-(tetracosanoyloxy)propyl phosphonato]oxy}ethyl)azanium

> <ALOGPS_LOGP>
6.61

> <JCHEM_LOGP>
12.197561372528254

> <ALOGPS_LOGS>
-7.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309169687

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
262.9917

> <JCHEM_ROTATABLE_BOND_COUNT>
49

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.92e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
trimethyl(2-{[(2R)-2-(octadec-11-enoyloxy)-3-(tetracosanoyloxy)propyl phosphonato]oxy}ethyl)azanium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      40.246  24.776   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      41.580  24.006   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      42.914  24.776   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      44.247  24.006   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      45.581  24.776   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      46.915  24.006   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      48.248  24.776   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      49.582  24.006   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      50.916  24.776   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      52.249  24.006   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      53.583  24.776   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      54.917  24.006   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      56.251  24.776   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      57.584  24.006   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      58.918  24.776   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      60.252  24.006   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      61.585  24.776   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      62.919  24.006   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      64.253  24.776   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      65.586  24.006   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      66.920  24.776   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      68.254  24.006   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      69.587  24.776   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      70.921  24.006   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      70.921  22.466   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      72.255  24.776   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      73.588  24.006   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      74.922  24.776   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      74.922  26.316   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      76.256  27.086   0.000  0.00  0.00           O+0
HETATM   31  P   UNK     0      76.256  28.626   0.000  0.00  0.00           P+0
HETATM   32  O   UNK     0      74.716  28.626   0.000  0.00  0.00           O-1
HETATM   33  O   UNK     0      77.796  28.626   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      76.256  30.166   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      77.589  30.936   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      77.589  32.476   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0      78.923  33.246   0.000  0.00  0.00           N+1
HETATM   38  C   UNK     0      79.693  31.913   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      78.153  34.580   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      80.257  34.016   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      76.256  24.006   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      77.589  24.776   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      77.589  26.316   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      78.923  24.006   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      80.257  24.776   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      81.590  24.006   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      82.924  24.776   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      84.258  24.006   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      85.591  24.776   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      86.925  24.006   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      88.259  24.776   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      89.593  24.006   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      90.926  24.776   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      92.260  24.006   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      93.594  24.776   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      93.594  26.316   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      94.927  27.086   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      94.927  28.626   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      96.261  29.396   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      96.261  30.936   0.000  0.00  0.00           C+0
HETATM   61  H   UNK     0      76.256  25.546   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                                                       
CONECT   21   20   22                                                       
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   41   61                                             
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39   40                                             
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   37                                                            
CONECT   41   28   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   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   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59                                                            
CONECT   61   28                                                            
MASTER        0    0    0    0    0    0    0    0   61    0  120    0
END

Synonyms

Not Available

Molecular Formula

C₅₀H₉₈NO₈P

Average Mass

872.2888

Monoisotopic Mass

871.703005629

IUPAC Name

trimethyl(2-{[(2R)-2-(octadec-11-enoyloxy)-3-(tetracosanoyloxy)propyl phosphonato]oxy}ethyl)azanium

Traditional Name

trimethyl(2-{[(2R)-2-(octadec-11-enoyloxy)-3-(tetracosanoyloxy)propyl phosphonato]oxy}ethyl)azanium

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C50H98NO8P/c1-6-8-10-12-14-16-18-20-22-23-24-25-26-27-29-30-32-34-36-38-40-42-49(52)56-46-48(47-58-60(54,55)57-45-44-51(3,4)5)59-50(53)43-41-39-37-35-33-31-28-21-19-17-15-13-11-9-7-2/h17,19,48H,6-16,18,20-47H2,1-5H3/t48-/m1/s1

InChI Key

GHQRIAPHRZOTFN-QSCHNALKSA-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	1.9e-05 g/L	ALOGPS
logP	6.61	ALOGPS
logP	12.2	ChemAxon
logS	-7.7	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	49	ChemAxon
Refractivity	262.99 m³·mol⁻¹	ChemAxon
Polarizability	112.33 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

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	0.5457	0.1542			uM	Adult (>18 years old)	Female	Pregnancy	HMDB	24704061
Human Feces	Detected and Quantified	0.03	0.01			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Feces	Detected and Quantified	0.04	0.03			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Blood	Detected and Quantified	0.27		0.22	0.33	uM	Infant (0-1 year old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	0.28		0.22	0.34	uM	Newborn (0-30 days old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	0.32	0.08			uM	Adult (>18 years old)	Both	Normal	HMDB	28278231
Human Blood	Detected and Quantified	0.242	0.097			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	0.250	0.084			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	0.025	0.009			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

FDB025951

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(24:0/18:1(11Z)) (MMDBc0034112)

MOL for #<Metabolite:0x00007fecbabd9f58>

3D MOL for #<Metabolite:0x00007fecbabd9f58>

3D SDF for #<Metabolite:0x00007fecbabd9f58>

3D-SDF for #<Metabolite:0x00007fecbabd9f58>

PDB for #<Metabolite:0x00007fecbabd9f58>

3D PDB for #<Metabolite:0x00007fecbabd9f58>

SMILES for #<Metabolite:0x00007fecbabd9f58>

INCHI for #<Metabolite:0x00007fecbabd9f58>

Structure for #<Metabolite:0x00007fecbabd9f58>

3D Structure for #<Metabolite:0x00007fecbabd9f58>