NP-MRD: Showing NP-Card for methyl elaidolinolenate (NP0323927)

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Record Information

Version

2.0

Created at

2022-09-12 03:40:22 UTC

Updated at

2022-09-12 03:40:22 UTC

NP-MRD ID

NP0323927

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl elaidolinolenate

Description

Methyl elaidolinolenate, also known as linolenic acid methyl ester, belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. methyl elaidolinolenate is found in Achillea millefolium, Ageratum conyzoides, Agrimonia pilosa, Anchietea pyrifolia, Azadirachta indica, Bellis perennis, Bidens pilosa, Coreopsis grandiflora, Daphne papyracea, Hamamelis virginiana, Krameria sonorae, Lepidium meyenii, Palafoxia arida, Raphanus sativus and Scolochloa festucacea. Based on a literature review very few articles have been published on Methyl elaidolinolenate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 52  0  0  0  0  0  0  0  0999 V2000
    6.7726   -1.0330    2.4859 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5043   -1.5918    1.2943 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1730   -0.8246    0.0731 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3381    0.1913    0.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.9713   -1.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5495    0.9525   -1.4019 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1460    0.4619   -2.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7238    0.3945   -2.9955 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8019    0.9436   -1.9639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8498    0.2091   -1.4103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0810    0.7703   -0.3663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5133    0.6828   -0.8485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4452    1.2445    0.1941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8982    1.1930   -0.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3843   -0.2079   -0.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8169   -0.1811   -0.9018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7306    0.4140    0.1211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7594   -0.3016    1.4060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1074   -1.3409    1.5773 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5160    0.1527    2.4837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5651   -0.5034    3.7177 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9819   -1.6391    3.4058 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0736    0.0253    2.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6754   -1.0822    2.3280 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1749   -2.6623    1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5897   -1.5397    1.5374 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6386   -1.1186   -0.8963 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8958    0.4657    1.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2527    2.0516   -0.8896 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6238    0.6769   -1.9401 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7919    1.3250   -0.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8934    0.0851   -3.2545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4263   -0.6380   -3.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6411    1.0014   -3.9436 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8997    1.9712   -1.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7681   -0.8187   -1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2116    1.8083   -0.1307 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0116    0.1052    0.5164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5981    1.3287   -1.7560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8109   -0.3272   -1.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1902    2.3207    0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3133    0.6986    1.1558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4645    1.5864    0.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0478    1.8210   -1.1135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2509   -0.8526    0.3845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7979   -0.6474   -1.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1159   -1.2621   -1.0614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9586    0.3070   -1.9011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4344    1.4786    0.3310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8062    0.4182   -0.2530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4970   -1.1193    3.7907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7036   -1.1929    3.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5974    0.2361    4.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
M  END


  Mrv1652309122205402D          

 21 20  0  0  0  0            999 V2000
    0.6632    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0921    0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802    3.2704    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  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  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0323927

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C\C\C=C\C\C=C\CCCCCCCC(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C19H32O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h4-5,7-8,10-11H,3,6,9,12-18H2,1-2H3/b5-4+,8-7+,11-10+

> <INCHI_KEY>
DVWSXZIHSUZZKJ-JSIPCRQOSA-N

> <FORMULA>
C19H32O2

> <MOLECULAR_WEIGHT>
292.463

> <EXACT_MASS>
292.24023027

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.79396133295754

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (9E,12E,15E)-octadeca-9,12,15-trienoate

> <JCHEM_LOGP>
6.2058491936666655

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.023980613669104

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
94.40449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl linolenate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       1.238   5.335   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.238   3.795   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.572   3.025   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.572   1.485   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.905   0.715   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.239   1.485   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.573   0.715   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.906   1.485   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.906   3.025   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.240   3.795   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.574   6.105   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.907   5.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.241   6.105   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.575   5.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.908   6.105   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.242   5.335   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.576   6.105   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      18.576   7.645   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      19.909   5.335   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      21.243   6.105   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                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
Methyl elaidolinolenic acid	Generator
Linolenic acid methyl ester	MeSH
Methyl linolenate	MeSH
9,12,15-Octadecatrienoic acid, methyl ester	MeSH
Methyl linolenate, (Z,Z,Z)-isomer	MeSH

Chemical Formula

C₁₉H₃₂O₂

Average Mass

292.4630 Da

Monoisotopic Mass

292.24023 Da

IUPAC Name

methyl (9E,12E,15E)-octadeca-9,12,15-trienoate

Traditional Name

methyl linolenate

CAS Registry Number

Not Available

SMILES

CC\C=C\C\C=C\C\C=C\CCCCCCCC(=O)OC

InChI Identifier

InChI=1S/C19H32O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h4-5,7-8,10-11H,3,6,9,12-18H2,1-2H3/b5-4+,8-7+,11-10+

InChI Key

DVWSXZIHSUZZKJ-JSIPCRQOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Achillea millefolium	LOTUS Database	35616633
Ageratum conyzoides	LOTUS Database	35616633
Agrimonia pilosa	LOTUS Database	35616633
Anchietea pyrifolia	LOTUS Database	35616633
Azadirachta indica	LOTUS Database	35616633
Bellis perennis	LOTUS Database	35616633
Bidens pilosa	LOTUS Database	35616633
Coreopsis grandiflora	LOTUS Database	35616633
Daphne papyracea	LOTUS Database	35616633
Hamamelis virginiana	LOTUS Database	35616633
Krameria sonorae	LOTUS Database	35616633
Lepidium meyenii	LOTUS Database	35616633
Palafoxia arida	LOTUS Database	35616633
Raphanus sativus	LOTUS Database	35616633
Scolochloa festucacea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Fatty acid methyl ester
Fatty acid ester
Methyl ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
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	6.21	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	94.4 m³·mol⁻¹	ChemAxon
Polarizability	36.79 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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4518968

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5367462

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl elaidolinolenate (NP0323927)

MOL for NP0323927 (methyl elaidolinolenate)

3D MOL for NP0323927 (methyl elaidolinolenate)

3D SDF for NP0323927 (methyl elaidolinolenate)

3D-SDF for NP0323927 (methyl elaidolinolenate)

PDB for NP0323927 (methyl elaidolinolenate)

3D PDB for NP0323927 (methyl elaidolinolenate)

SMILES for NP0323927 (methyl elaidolinolenate)

INCHI for NP0323927 (methyl elaidolinolenate)

Structure for NP0323927 (methyl elaidolinolenate)

3D Structure for NP0323927 (methyl elaidolinolenate)