MiMeDB: Showing metabocard for PC(16:1(9Z)/18:3(6Z,9Z,12Z)) (MMDBc0033788)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 05:03:14 UTC

Update Date

2024-04-30 20:17:13 UTC

Metabolite ID

MMDBc0033788

Metabolite Identification

Common Name

PC(16:1(9Z)/18:3(6Z,9Z,12Z))

Description

PC(16:1(9Z)/18:3(6Z,9Z,12Z)) 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(16:1(9Z)/18:3(6Z,9Z,12Z)), in particular, consists of one chain of palmitoleic acid at the C-1 position and one chain of g-linolenic acid at the C-2 position. The palmitoleic acid moiety is derived from animal fats and vegetable oils, while the g-linolenic acid moiety is derived from animal fats. 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


  Mrv1652305221922382D          

 53 52  0  0  1  0            999 V2000
   -4.1395    1.6643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7229    0.1891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9894    8.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3143    7.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1436    9.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4771    2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8176    1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7200    1.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1551    1.5003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0576    2.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2498    2.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3005    1.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5873    2.8116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6381    2.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6819    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1190    2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0195    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7815    2.6477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2624    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6868    3.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3493    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1063    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8429    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7688    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1805    4.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5258    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1883    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7610    4.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0936    5.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0039    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3366    5.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    4.7786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6741    4.9425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1601    7.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3406    7.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1649    4.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4029    5.9259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4975    5.1064    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5844    4.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9171    5.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6519    8.3728    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -1.4898    3.6312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8224    6.0898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7903    7.3319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8761    8.0568    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.9220    4.9425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1512    7.1426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    6.4177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    4.7786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    7.2372    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2595    5.4342    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  7  2  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  2  0  0  0  0
 17 15  1  0  0  0  0
 16 18  1  4  0  0  0
 19 17  2  0  0  0  0
 20 18  1  0  0  0  0
 21 20  2  0  0  0  0
 19 22  1  4  0  0  0
 21 23  1  4  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  2  0  0  0  0
 28 26  1  0  0  0  0
 27 29  1  4  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 32 30  1  0  0  0  0
 33 31  1  0  0  0  0
 34 32  1  0  0  0  0
 35 33  1  0  0  0  0
 37 36  1  0  0  0  0
 40 38  1  0  0  0  0
 40 39  1  0  0  0  0
 41 34  1  0  0  0  0
 42 35  1  0  0  0  0
 43  3  1  0  0  0  0
 43  4  1  0  0  0  0
 43  5  1  0  0  0  0
 43 36  1  0  0  0  0
 44 41  2  0  0  0  0
 45 42  2  0  0  0  0
 48 38  1  0  0  0  0
 48 41  1  0  0  0  0
 49 37  1  0  0  0  0
 50 39  1  0  0  0  0
 40 51  1  1  0  0  0
 51 42  1  0  0  0  0
 52 46  2  0  0  0  0
 52 47  1  0  0  0  0
 52 49  1  0  0  0  0
 52 50  1  0  0  0  0
 40 53  1  1  0  0  0
M  CHG  2  43   1  47  -1
M  END


  Mrv1652305221922382D          

 53 52  0  0  1  0            999 V2000
   -4.1395    1.6643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7229    0.1891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9894    8.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3143    7.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1436    9.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4771    2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8176    1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7200    1.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1551    1.5003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0576    2.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2498    2.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3005    1.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5873    2.8116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6381    2.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6819    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1190    2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0195    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7815    2.6477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2624    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6868    3.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3493    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1063    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8429    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7688    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1805    4.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5258    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1883    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7610    4.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0936    5.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0039    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3366    5.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3415    4.7786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6741    4.9425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1601    7.7104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3406    7.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1649    4.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4029    5.9259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4975    5.1064    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5844    4.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9171    5.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6519    8.3728    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -1.4898    3.6312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8224    6.0898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7903    7.3319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8761    8.0568    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -0.9220    4.9425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1512    7.1426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0654    6.4177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    4.7786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    7.2372    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2595    5.4342    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  7  2  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  2  0  0  0  0
 17 15  1  0  0  0  0
 16 18  1  4  0  0  0
 19 17  2  0  0  0  0
 20 18  1  0  0  0  0
 21 20  2  0  0  0  0
 19 22  1  4  0  0  0
 21 23  1  4  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  2  0  0  0  0
 28 26  1  0  0  0  0
 27 29  1  4  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 32 30  1  0  0  0  0
 33 31  1  0  0  0  0
 34 32  1  0  0  0  0
 35 33  1  0  0  0  0
 37 36  1  0  0  0  0
 40 38  1  0  0  0  0
 40 39  1  0  0  0  0
 41 34  1  0  0  0  0
 42 35  1  0  0  0  0
 43  3  1  0  0  0  0
 43  4  1  0  0  0  0
 43  5  1  0  0  0  0
 43 36  1  0  0  0  0
 44 41  2  0  0  0  0
 45 42  2  0  0  0  0
 48 38  1  0  0  0  0
 48 41  1  0  0  0  0
 49 37  1  0  0  0  0
 50 39  1  0  0  0  0
 40 51  1  1  0  0  0
 51 42  1  0  0  0  0
 52 46  2  0  0  0  0
 52 47  1  0  0  0  0
 52 49  1  0  0  0  0
 52 50  1  0  0  0  0
 40 53  1  1  0  0  0
M  CHG  2  43   1  47  -1
M  END
> <DATABASE_ID>
MMDBc0033788

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C42H76NO8P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-42(45)51-40(39-50-52(46,47)49-37-36-43(3,4)5)38-48-41(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h14,16-17,19-21,25,27,40H,6-13,15,18,22-24,26,28-39H2,1-5H3/t40-/m1/s1

> <INCHI_KEY>
ZZLFVAJFRYBVSN-RRHRGVEJSA-N

> <FORMULA>
C42H76NO8P

> <MOLECULAR_WEIGHT>
754.0285

> <EXACT_MASS>
753.530854925

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
128

> <JCHEM_AVERAGE_POLARIZABILITY>
90.59786001113073

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-3-(hexadec-9-enoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
5.32

> <JCHEM_LOGP>
7.555247082528254

> <ALOGPS_LOGS>
-7.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469115

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744160237391408

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
229.53349999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
38

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.23e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-3-(hexadec-9-enoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 22-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-MAY-19         0                                  
HETATM    1  C   UNK     0      -7.727   3.107   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -18.149   0.353   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.847  16.547   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.320  14.711   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001  16.866   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.491   4.025   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -18.326   1.883   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.077   3.413   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -17.090   2.801   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.841   4.330   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -17.266   4.330   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.428   3.719   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -16.030   5.248   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.191   4.636   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -16.206   6.778   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.222   4.025   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -14.970   7.696   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.459   4.942   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -13.557   7.084   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.282   6.472   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.519   7.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -12.320   8.002   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.932   6.778   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -10.907   7.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.168   7.696   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -9.670   8.308   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.582   7.084   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.257   7.696   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.818   8.002   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.020   8.614   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.641   9.532   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.607   8.002   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.228  10.144   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -4.371   8.920   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.992   9.226   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.166  14.393   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.636  14.569   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.308   8.614   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.752  11.062   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.929   9.532   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.958   8.308   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.579   9.838   0.000  0.00  0.00           C+0
HETATM   43  N   UNK     0      -3.083  15.629   0.000  0.00  0.00           N+1
HETATM   44  O   UNK     0      -2.781   6.778   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       3.402  11.368   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       3.342  13.686   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       1.635  15.039   0.000  0.00  0.00           O-1
HETATM   48  O   UNK     0      -1.721   9.226   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       0.282  13.333   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       1.989  11.980   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       2.342   8.920   0.000  0.00  0.00           O+0
HETATM   52  P   UNK     0       1.812  13.509   0.000  0.00  0.00           P+0
HETATM   53  H   UNK     0      -0.484  10.144   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2    7                                                            
CONECT    3   43                                                            
CONECT    4   43                                                            
CONECT    5   43                                                            
CONECT    6    1    8                                                       
CONECT    7    2    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   14                                                       
CONECT   13   11   15                                                       
CONECT   14   12   16                                                       
CONECT   15   13   17                                                       
CONECT   16   14   18                                                       
CONECT   17   15   19                                                       
CONECT   18   16   20                                                       
CONECT   19   17   22                                                       
CONECT   20   18   21                                                       
CONECT   21   20   23                                                       
CONECT   22   19   24                                                       
CONECT   23   21   25                                                       
CONECT   24   22   26                                                       
CONECT   25   23   27                                                       
CONECT   26   24   28                                                       
CONECT   27   25   29                                                       
CONECT   28   26   30                                                       
CONECT   29   27   31                                                       
CONECT   30   28   32                                                       
CONECT   31   29   33                                                       
CONECT   32   30   34                                                       
CONECT   33   31   35                                                       
CONECT   34   32   41                                                       
CONECT   35   33   42                                                       
CONECT   36   37   43                                                       
CONECT   37   36   49                                                       
CONECT   38   40   48                                                       
CONECT   39   40   50                                                       
CONECT   40   38   39   51   53                                             
CONECT   41   34   44   48                                                  
CONECT   42   35   45   51                                                  
CONECT   43    3    4    5   36                                             
CONECT   44   41                                                            
CONECT   45   42                                                            
CONECT   46   52                                                            
CONECT   47   52                                                            
CONECT   48   38   41                                                       
CONECT   49   37   52                                                       
CONECT   50   39   52                                                       
CONECT   51   40   42                                                       
CONECT   52   46   47   49   50                                             
CONECT   53   40                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  104    0
END

Synonyms

Not Available

Molecular Formula

C₄₂H₇₆NO₈P

Average Mass

754.0285

Monoisotopic Mass

753.530854925

IUPAC Name

(2-{[(2R)-3-(hexadec-9-enoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium

Traditional Name

(2-{[(2R)-3-(hexadec-9-enoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C42H76NO8P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-42(45)51-40(39-50-52(46,47)49-37-36-43(3,4)5)38-48-41(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h14,16-17,19-21,25,27,40H,6-13,15,18,22-24,26,28-39H2,1-5H3/t40-/m1/s1

InChI Key

ZZLFVAJFRYBVSN-RRHRGVEJSA-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	3.2e-05 g/L	ALOGPS
logP	5.32	ALOGPS
logP	7.56	ChemAxon
logS	-7.4	ALOGPS
pKa (Strongest Acidic)	1.86	ChemAxon
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	111.19 Å²	ChemAxon
Rotatable Bond Count	38	ChemAxon
Refractivity	229.53 m³·mol⁻¹	ChemAxon
Polarizability	90.6 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
MMDBr0036228	PC(16:1(9Z)/18:3(6Z,9Z,12Z))	gamma-Linolenic acid	Lipid droplet phospholipase 1	Hydrolysis	RHEA	34755880
MMDBr0037027	PC(16:1(9Z)/18:3(6Z,9Z,12Z))	(9Z)-hexadecenoic 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	Decreased	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	0.34	0.02			umol/mmol creatinine	Adolescent (13-18 years old)	Both	Obese	HMDB	26910390
Human Blood	Detected and Quantified	2.9268	1.229			uM	Adult (>18 years old)	Female	Pregnancy	HMDB	24704061
Human Urine	Detected and Quantified	0.0023		0.0002	0.018	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	24023812
Human Feces	Detected and Quantified	0.02	0.01			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Feces	Detected and Quantified	0.05	0.1			nmol/g wet feces	Adult (>18 years old)	Both	Normal	HMDB	27624970
Human Blood	Detected and Quantified	0.52		0.43	0.62	uM	Newborn (0-30 days old)		Normal	HMDB	25754623
Human Urine	Detected and Quantified	0.66	0.15			umol/mmol creatinine	Adolescent (13-18 years old)	Both	Normal	HMDB	26910390
Human Blood	Detected and Quantified	0.82		0.63	1.14	uM	Infant (0-1 year old)		Normal	HMDB	25754623
Human Blood	Detected and Quantified	1.87	0.66			uM	Adult (>18 years old)	Both	Normal	HMDB	28278231
Human Blood	Detected and Quantified	2.76	1.13			uM	Adult (>18 years old)	Both	Normal	HMDB	26010610
Human Blood	Detected and Quantified	1.40	0.61			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	1.74	0.59			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

FDB025198

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(16:1(9Z)/18:3(6Z,9Z,12Z)) (MMDBc0033788)

MOL for #<Metabolite:0x00007f9238659ec0>

3D MOL for #<Metabolite:0x00007f9238659ec0>

3D SDF for #<Metabolite:0x00007f9238659ec0>

3D-SDF for #<Metabolite:0x00007f9238659ec0>

PDB for #<Metabolite:0x00007f9238659ec0>

3D PDB for #<Metabolite:0x00007f9238659ec0>

SMILES for #<Metabolite:0x00007f9238659ec0>

INCHI for #<Metabolite:0x00007f9238659ec0>

Structure for #<Metabolite:0x00007f9238659ec0>

3D Structure for #<Metabolite:0x00007f9238659ec0>