MiMeDB: Showing metabocard for PC(24:1(15Z)/16:1(9Z)) (MMDBc0034118)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 05:16:45 UTC

Update Date

2024-04-30 20:21:25 UTC

Metabolite ID

MMDBc0034118

Metabolite Identification

Common Name

PC(24:1(15Z)/16:1(9Z))

Description

PC(24:1(15Z)/16:1(9Z)) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PC(24:1(15Z)/16:1(9Z)), in particular, consists of one chain of nervonic acid at the C-1 position and one chain of palmitoleic acid at the C-2 position. The nervonic acid moiety is derived from fish oils, while the palmitoleic acid moiety is derived from animal fats and vegetable oils. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.‚Üµ‚ÜµWhile most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02251201562D          

 58 57  0  0  1  0            999 V2000
    6.9908    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7053    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4198    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1342    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8487    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5632    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2776    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9921    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7066    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4211    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1355    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5645    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2789    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9934    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7079    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4224    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1368    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8513    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5658    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2802    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9947    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7092    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4237    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4237    7.7487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.1381    8.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.8526    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5671    8.9862    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   25.5671    9.8112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815   10.2237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815   11.0487    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   25.4565   11.0487    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   27.1065   11.0487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815   11.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960   12.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960   13.1112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.7105   13.5237    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   28.1230   12.8092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2980   14.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.4249   13.9362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815    8.5737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960    9.8112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.7105    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.4249    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.1394    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.8539    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.5684    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.2828    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.9973    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7118    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.4262    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.1407    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.1407    9.8112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.8552   10.2237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.8552   11.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.5697   11.4612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.5697   12.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  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
 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
 51 50  1  4  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  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
M  CHG  2  32  -1  37   1
M  END


  Mrv0541 02251201562D          

 58 57  0  0  1  0            999 V2000
    6.9908    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7053    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4198    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1342    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8487    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5632    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2776    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9921    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7066    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4211    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1355    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5645    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2789    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9934    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7079    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4224    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1368    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8513    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5658    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2802    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9947    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7092    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4237    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4237    7.7487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.1381    8.9862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.8526    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5671    8.9862    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   25.5671    9.8112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815   10.2237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815   11.0487    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   25.4565   11.0487    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   27.1065   11.0487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815   11.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960   12.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960   13.1112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.7105   13.5237    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   28.1230   12.8092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2980   14.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.4249   13.9362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.2815    8.5737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9960    9.8112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.7105    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.4249    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.1394    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.8539    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.5684    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.2828    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.9973    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.7118    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.4262    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.1407    8.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.1407    9.8112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.8552   10.2237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.8552   11.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.5697   11.4612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.5697   12.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  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
 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
 51 50  1  4  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  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
M  CHG  2  32  -1  37   1
M  END
> <DATABASE_ID>
MMDBc0034118

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C48H92NO8P/c1-6-8-10-12-14-16-18-20-21-22-23-24-25-26-27-29-30-32-34-36-38-40-47(50)54-44-46(45-56-58(52,53)55-43-42-49(3,4)5)57-48(51)41-39-37-35-33-31-28-19-17-15-13-11-9-7-2/h17,19-21,46H,6-16,18,22-45H2,1-5H3/t46-/m1/s1

> <INCHI_KEY>
ZHHDWDXQYDFYKQ-YACUFSJGSA-N

> <FORMULA>
C48H92NO8P

> <MOLECULAR_WEIGHT>
842.2197

> <EXACT_MASS>
841.656055437

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
106.9474261065184

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(tetracos-15-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
6.38

> <JCHEM_LOGP>
10.946502385861589

> <ALOGPS_LOGS>
-7.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309169722

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
254.90630000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
46

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.34e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(tetracos-15-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      13.049  16.774   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.383  16.004   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.717  16.774   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.051  16.004   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.384  16.774   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.718  16.004   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.052  16.774   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.385  16.004   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.719  16.774   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      25.053  16.004   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      26.386  16.774   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      27.720  16.004   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      29.054  16.774   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      30.387  16.004   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      31.721  16.774   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      33.055  16.004   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      34.388  16.774   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      35.722  16.004   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      37.056  16.774   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      38.389  16.004   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      39.723  16.774   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      41.057  16.004   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      42.391  16.774   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      43.724  16.004   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      43.724  14.464   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      45.058  16.774   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      46.392  16.004   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      47.725  16.774   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      47.725  18.314   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      49.059  19.084   0.000  0.00  0.00           O+0
HETATM   31  P   UNK     0      49.059  20.624   0.000  0.00  0.00           P+0
HETATM   32  O   UNK     0      47.519  20.624   0.000  0.00  0.00           O-1
HETATM   33  O   UNK     0      50.599  20.624   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      49.059  22.164   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      50.393  22.934   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      50.393  24.474   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0      51.726  25.244   0.000  0.00  0.00           N+1
HETATM   38  C   UNK     0      52.496  23.911   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      50.956  26.578   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      53.060  26.014   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      49.059  16.004   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      50.393  16.774   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      50.393  18.314   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      51.726  16.004   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      53.060  16.774   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      54.394  16.004   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      55.727  16.774   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      57.061  16.004   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      58.395  16.774   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      59.728  16.004   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      61.062  16.774   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      62.396  16.004   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      63.729  16.774   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      63.729  18.314   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      65.063  19.084   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      65.063  20.624   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      66.397  21.394   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      66.397  22.934   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
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                                                  
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                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  114    0
END

Synonyms

Not Available

Molecular Formula

C₄₈H₉₂NO₈P

Average Mass

842.2197

Monoisotopic Mass

841.656055437

IUPAC Name

(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(tetracos-15-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

Traditional Name

(2-{[(2R)-2-(hexadec-9-enoyloxy)-3-(tetracos-15-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

CAS Registry Number

Not Available

SMILES

CCCCCCCCC=CCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCC

InChI Identifier

InChI=1S/C48H92NO8P/c1-6-8-10-12-14-16-18-20-21-22-23-24-25-26-27-29-30-32-34-36-38-40-47(50)54-44-46(45-56-58(52,53)55-43-42-49(3,4)5)57-48(51)41-39-37-35-33-31-28-19-17-15-13-11-9-7-2/h17,19-21,46H,6-16,18,22-45H2,1-5H3/t46-/m1/s1

InChI Key

ZHHDWDXQYDFYKQ-YACUFSJGSA-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	2.3e-05 g/L	ALOGPS
logP	6.38	ALOGPS
logP	10.95	ChemAxon
logS	-7.6	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	46	ChemAxon
Refractivity	254.91 m³·mol⁻¹	ChemAxon
Polarizability	106.95 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
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
Animal	Milk	Bos taurus	FooDB	31437929
Animal	Milk	Bos taurus	FooDB	31437929
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 Urine	Detected and Quantified			0.0	0.05	umol/mmol creatinine	Newborn (0-30 days old)	Both	Normal	HMDB	32340350
Human Urine	Detected and Quantified	0.0		0.0	0.03	umol/mmol creatinine	Newborn (0-30 days old)	Male	Normal	HMDB	32340350
Human Urine	Detected and Quantified	0.0		0.0	0.06	umol/mmol creatinine	Newborn (0-30 days old)	Female	Normal	HMDB	32340350
Human Feces	Detected and Quantified	0.08	0.04			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Feces	Detected and Quantified	0.09	0.06			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Blood	Detected and Quantified	0.25		0.2	0.37	uM	Newborn (0-30 days old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	0.29		0.25	0.35	uM	Infant (0-1 year old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	0.32	0.12			uM	Adult (>18 years old)	Both	Normal	HMDB	28278231
Human Blood	Detected and Quantified	0.36		0.05	1.88	uM	Adolescent (13-18 years old)	Both	Normal	HMDB	28959601
Human Blood	Detected and Quantified	0.296	0.142			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	0.297	0.119			uM	Children (1-13 years old)	Both	Obesity	HMDB	Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children
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

FDB025982

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(24:1(15Z)/16:1(9Z)) (MMDBc0034118)

MOL for #<Metabolite:0x00007fece0a45068>

3D MOL for #<Metabolite:0x00007fece0a45068>

3D SDF for #<Metabolite:0x00007fece0a45068>

3D-SDF for #<Metabolite:0x00007fece0a45068>

PDB for #<Metabolite:0x00007fece0a45068>

3D PDB for #<Metabolite:0x00007fece0a45068>

SMILES for #<Metabolite:0x00007fece0a45068>

INCHI for #<Metabolite:0x00007fece0a45068>

Structure for #<Metabolite:0x00007fece0a45068>

3D Structure for #<Metabolite:0x00007fece0a45068>