Showing metabocard for PC(20:3(8Z,11Z,14Z)/18:3(6Z,9Z,12Z)) (MMDBc0034030)

Record Information
Version1.0
StatusDetected and Quantified
Creation Date2021-11-19 05:13:18 UTC
Update Date2024-04-30 20:20:03 UTC
Metabolite IDMMDBc0034030
Metabolite Identification
Common NamePC(20:3(8Z,11Z,14Z)/18:3(6Z,9Z,12Z))
DescriptionPC(20:3(8Z,11Z,14Z)/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(20:3(8Z,11Z,14Z)/18:3(6Z,9Z,12Z)), in particular, consists of one chain of homo-g-linolenic acid at the C-1 position and one chain of g-linolenic acid at the C-2 position. The homo-g-linolenic acid moiety is derived from fish oils, liver and kidney, 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.↵↵While 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
MOLSDFPDBSMILESInChI

MOL for #<Metabolite:0x0000556b6aea4068>


  Mrv0541 02251201402D          

 56 55  0  0  1  0            999 V2000
    0.0888    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8033    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5178    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2323    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9467    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6612    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3757    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0901    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0901    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8046    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8046    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    6.2388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   15.0927    3.7638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.9388    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   15.9177    2.9388    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   14.2677    2.9388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.1138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   14.3783    0.8763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.2513    1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0763   -0.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    0.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2374    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9519    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6664    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3809    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0953    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.8098    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.5243    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2387    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  6  5  1  4  0  0  0
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  7  8  1  0  0  0  0
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 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
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 24 37  1  1  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
 44 43  1  4  0  0  0
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 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
M  CHG  2  28  -1  33   1
M  END
Download

3D MOL for #<Metabolite:0x0000556b6aea4068>

Download
3D SDF for #<Metabolite:0x0000556b6aea4068>

  Mrv0541 02251201402D          

 56 55  0  0  1  0            999 V2000
    0.0888    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8033    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5178    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2323    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9467    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6612    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3757    2.5263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0901    2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0901    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8046    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8046    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    6.2388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.3783    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    3.7638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.9388    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   15.9177    2.9388    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   14.2677    2.9388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    2.1138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    1.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    0.8763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    0.4638    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   13.2513    1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0763   -0.2507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    0.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   16.5217    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0940    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8085    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5230    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.2374    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9519    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6664    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3809    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0953    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.8098    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.5243    3.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.2387    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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 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  1  0  0  0
 37 38  1  0  0  0  0
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 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
 44 43  1  4  0  0  0
 44 45  2  0  0  0  0
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 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
 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
M  CHG  2  28  -1  33   1
M  END
> <DATABASE_ID>
MMDBc0034030

> <DATABASE_NAME>
MIME

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

> <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/h14-17,20-22,24-26,29,31,44H,6-13,18-19,23,27-28,30,32-43H2,1-5H3/t44-/m1/s1

> <INCHI_KEY>
RIDIYDAFPMEWTP-USYZEHPZSA-N

> <FORMULA>
C46H80NO8P

> <MOLECULAR_WEIGHT>
806.1031

> <EXACT_MASS>
805.562155053

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
95.56690226743467

> <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-6,9,12-trienoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
5.71

> <JCHEM_LOGP>
8.609678429194922

> <ALOGPS_LOGS>
-7.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469115

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744160237415283

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
250.17069999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
40

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.08e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-3-(icosa-8,11,14-trienoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$

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3D-SDF for #<Metabolite:0x0000556b6aea4068>
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PDB for #<Metabolite:0x0000556b6aea4068>
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       0.166   4.716   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.499   5.486   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.833   4.716   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.167   5.486   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.501   4.716   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.834   5.486   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.168   4.716   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.502   5.486   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.502   7.026   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.835   7.796   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.835   9.336   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.169  10.106   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.503   9.336   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.836  10.106   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.504  10.106   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.837   9.336   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.171  10.106   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.505   9.336   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.838  10.106   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      22.838  11.646   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      24.172   9.336   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      25.506  10.106   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      26.839   9.336   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.839   7.796   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      28.173   7.026   0.000  0.00  0.00           O+0
HETATM   27  P   UNK     0      28.173   5.486   0.000  0.00  0.00           P+0
HETATM   28  O   UNK     0      29.713   5.486   0.000  0.00  0.00           O-1
HETATM   29  O   UNK     0      26.633   5.486   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      28.173   3.946   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      26.839   3.176   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      26.839   1.636   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      25.506   0.866   0.000  0.00  0.00           N+1
HETATM   34  C   UNK     0      24.736   2.199   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      26.276  -0.468   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      24.172   0.096   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      28.173  10.106   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      29.507   9.336   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      29.507   7.796   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      30.841  10.106   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      32.174   9.336   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      33.508  10.106   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      34.842   9.336   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      36.175  10.106   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      37.509   9.336   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      38.843  10.106   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      40.176   9.336   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      40.176   7.796   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      41.510   7.026   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      42.844   7.796   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      44.177   7.026   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      45.511   7.796   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      46.845   7.026   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      48.178   7.796   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      49.512   7.026   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      50.846   7.796   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   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   37                                                  
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                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  110    0
END

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3D PDB for #<Metabolite:0x0000556b6aea4068>
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SMILES for #<Metabolite:0x0000556b6aea4068>
CCCCCC=CCC=CCC=CCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCC=CCC=CCC=CCCCCC
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INCHI for #<Metabolite:0x0000556b6aea4068>
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/h14-17,20-22,24-26,29,31,44H,6-13,18-19,23,27-28,30,32-43H2,1-5H3/t44-/m1/s1
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SynonymsNot Available
Molecular FormulaC46H80NO8P
Average Mass806.1031
Monoisotopic Mass805.562155053
IUPAC Name(2-{[(2R)-3-(icosa-8,11,14-trienoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium
Traditional Name(2-{[(2R)-3-(icosa-8,11,14-trienoyloxy)-2-(octadeca-6,9,12-trienoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium
CAS Registry NumberNot Available
SMILES
CCCCCC=CCC=CCC=CCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCC=CCC=CCC=CCCCCC
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/h14-17,20-22,24-26,29,31,44H,6-13,18-19,23,27-28,30,32-43H2,1-5H3/t44-/m1/s1
InChI KeyRIDIYDAFPMEWTP-USYZEHPZSA-N