NP-MRD: Showing NP-Card for TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3] (NP0338762)

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Record Information

Version

2.0

Created at

2024-09-11 17:35:08 UTC

Updated at

2024-09-11 17:35:09 UTC

NP-MRD ID

NP0338762

Secondary Accession Numbers

None

Natural Product Identification

Common Name

TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3]

Description

TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3] belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages. TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3] is an extremely weak basic (essentially neutral) compound (based on its pKa). TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3] can be biosynthesized from DG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/0:0) And eicosapentaenoyl-CoA through the action of the enzyme diacylglycerol O-acyltransferase. In humans, TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3] is involved in the metabolic disorder called de novo triacylglycerol biosynthesis pathway.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02251201162D          

 67 66  0  0  0  0            999 V2000
   -2.7477    9.8258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3953    9.0798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5731    9.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2207    8.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3985    8.1983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0462    7.4523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7760    7.3845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1284    6.6385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9506    6.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4205    7.2488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2427    7.1810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5347    7.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0045    8.4695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8267    8.4017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2966    9.0798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1188    9.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5886    9.6902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2362   10.4361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5283   11.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7061   11.1143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.1791   12.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6490   13.3522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7029   10.2327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0552    9.4867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8775    9.4189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3473   10.0971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2298    8.6730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0520    8.6051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.7536   11.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9314   11.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4615   10.6396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6393   10.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1695   10.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5219    9.2833    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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
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 18 19  2  0  0  0  0
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 20 21  1  0  0  0  0
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 64 65  2  0  0  0  0
 65 66  1  0  0  0  0
 66 67  1  0  0  0  0
M  END


  Mrv0541 02251201162D          

 67 66  0  0  0  0            999 V2000
   -2.7477    9.8258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3953    9.0798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5731    9.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2207    8.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1284    6.6385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9506    6.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4205    7.2488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2427    7.1810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6522    9.2155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8300    9.2833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3030   10.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4205   12.2671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8903   12.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0045   13.4878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 66 67  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0338762

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC=CCC=CCCCCCCCC(=O)OC(COC(=O)CCCC=CCC=CCC=CCC=CCC=CCC)COC(=O)CCCC=CCC=CCC=CCC=CCC=CCC

> <INCHI_IDENTIFIER>
InChI=1S/C61H94O6/c1-4-7-10-13-16-19-22-25-28-30-33-35-38-41-44-47-50-53-59(62)65-56-58(67-61(64)55-52-49-46-43-40-37-32-27-24-21-18-15-12-9-6-3)57-66-60(63)54-51-48-45-42-39-36-34-31-29-26-23-20-17-14-11-8-5-2/h7-8,10-11,16-21,25-29,32-36,41-42,44-45,58H,4-6,9,12-15,22-24,30-31,37-40,43,46-57H2,1-3H3

> <INCHI_KEY>
KKWBWRCIRQWSRS-UHFFFAOYSA-N

> <FORMULA>
C61H94O6

> <MOLECULAR_WEIGHT>
923.3955

> <EXACT_MASS>
922.70504074

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
113.86350096117043

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(icosa-5,8,11,14,17-pentaenoyloxy)-2-(octadeca-9,12-dienoyloxy)propyl icosa-5,8,11,14,17-pentaenoate

> <ALOGPS_LOGP>
9.44

> <JCHEM_LOGP>
19.02677445433333

> <ALOGPS_LOGS>
-8.04

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.565947185579763

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
300.6994999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
48

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.34e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(icosa-5,8,11,14,17-pentaenoyloxy)-2-(octadeca-9,12-dienoyloxy)propyl icosa-5,8,11,14,17-pentaenoate

> <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      -5.129  18.341   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.471  16.949   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.936  16.822   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.279  15.430   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.744  15.303   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.086  13.911   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.449  13.784   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.106  12.392   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.641  12.265   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.518  13.531   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.053  13.405   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.930  14.671   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.465  14.544   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.342  15.810   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.877  15.683   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.754  16.949   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.288  16.822   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.165  18.088   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      13.508  19.481   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      15.700  17.962   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      16.577  19.228   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.919  20.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      14.385  20.747   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      13.727  22.139   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      14.604  23.405   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.192  22.266   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.315  21.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.973  19.607   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.096  18.341   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.561  18.468   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.684  17.202   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.149  17.329   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.492  18.721   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.957  18.848   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.299  20.240   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.176  21.506   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.518  22.899   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.395  24.165   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.930  24.038   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.807  25.304   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.342  25.177   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.000  23.785   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      11.534  23.658   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      12.411  24.924   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      18.112  19.101   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      18.770  17.709   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      20.305  17.582   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      21.182  18.848   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      20.962  16.190   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      22.497  16.063   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      23.155  14.671   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      24.690  14.544   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      25.347  13.151   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      26.882  13.025   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      27.759  14.291   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      29.294  14.164   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      30.171  15.430   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      29.513  16.822   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      30.390  18.088   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      29.733  19.481   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      28.198  19.607   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      27.540  21.000   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      26.005  21.126   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0      25.128  19.861   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0      23.593  19.987   0.000  0.00  0.00           C+0
HETATM   66  C   UNK     0      22.716  18.721   0.000  0.00  0.00           C+0
HETATM   67  C   UNK     0      23.374  17.329   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   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   45                                                  
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                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   21   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   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   61                                                       
CONECT   61   60   62                                                       
CONECT   62   61   63                                                       
CONECT   63   62   64                                                       
CONECT   64   63   65                                                       
CONECT   65   64   66                                                       
CONECT   66   65   67                                                       
CONECT   67   66                                                            
MASTER        0    0    0    0    0    0    0    0   67    0  132    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₆₁H₉₄O₆

Average Mass

923.3955 Da

Monoisotopic Mass

922.70504 Da

IUPAC Name

3-(icosa-5,8,11,14,17-pentaenoyloxy)-2-(octadeca-9,12-dienoyloxy)propyl icosa-5,8,11,14,17-pentaenoate

Traditional Name

3-(icosa-5,8,11,14,17-pentaenoyloxy)-2-(octadeca-9,12-dienoyloxy)propyl icosa-5,8,11,14,17-pentaenoate

CAS Registry Number

Not Available

SMILES

CCCCCC=CCC=CCCCCCCCC(=O)OC(COC(=O)CCCC=CCC=CCC=CCC=CCC=CCC)COC(=O)CCCC=CCC=CCC=CCC=CCC=CCC

InChI Identifier

InChI=1S/C61H94O6/c1-4-7-10-13-16-19-22-25-28-30-33-35-38-41-44-47-50-53-59(62)65-56-58(67-61(64)55-52-49-46-43-40-37-32-27-24-21-18-15-12-9-6-3)57-66-60(63)54-51-48-45-42-39-36-34-31-29-26-23-20-17-14-11-8-5-2/h7-8,10-11,16-21,25-29,32-36,41-42,44-45,58H,4-6,9,12-15,22-24,30-31,37-40,43,46-57H2,1-3H3

InChI Key

KKWBWRCIRQWSRS-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Triradylcglycerols

Direct Parent

Triacylglycerols

Alternative Parents

Substituents

Triacyl-sn-glycerol
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	9.44	ALOGPS
logP	19.03	ChemAxon
logS	-8	ALOGPS
pKa (Strongest Basic)	-6.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	48	ChemAxon
Refractivity	300.7 m³·mol⁻¹	ChemAxon
Polarizability	113.86 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB027687

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

76043001

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3] (NP0338762)

MOL for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

3D MOL for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

3D SDF for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

3D-SDF for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

PDB for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

3D PDB for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

SMILES for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

INCHI for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

Structure for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])

3D Structure for NP0338762 (TG(20:5(5Z,8Z,11Z,14Z,17Z)/18:2(9Z,12Z)/20:5(5Z,8Z,11Z,14Z,17Z))[iso3])