NP-MRD: Showing NP-Card for methyl octadeca-9,12-dienoate (NP0330497)

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Record Information

Version

1.0

Created at

2022-09-12 15:54:44 UTC

Updated at

2022-09-12 15:54:44 UTC

NP-MRD ID

NP0330497

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl octadeca-9,12-dienoate

Description

METHYL LINOLEATE 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 octadeca-9,12-dienoate is found in Acyrthosiphon pisum, Aegle marmelos, Ageratum conyzoides, Beilschmiedia erythrophloia, Beilschmiedia tsangii, Coreopsis grandiflora, Cyperus conglomeratus, Hygrophorus chrysodon, Kaempferia parviflora, Lycoris sanguinea, Paxillus involutus, Photinia lucida, Pueraria montana, Rhamnus formosana and Streptomyces piomogenus. METHYL LINOLEATE is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.7863    0.0482    0.5153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7282   -1.3446   -0.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3024   -1.8383   -0.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5736   -0.9456   -1.1329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1505   -1.4553   -1.2958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3783   -1.4962   -0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3048   -0.8829    0.2193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5620    0.0448   -0.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5267    1.3371    0.0774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4249    1.9237    0.4341 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9197    1.3929    0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6197    2.4715   -0.6876 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0110    2.0679   -1.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8277    1.8502    0.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2309    1.4619   -0.2878 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1173    1.2289    0.8950 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6201    0.1078    1.7654 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5794   -1.1459    0.9715 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6242   -1.3632    0.1956 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5795   -2.0963    1.0637 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6138   -3.2977    0.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7786    0.4134    0.8338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1743    0.7267   -0.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4654    0.1360    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2872   -2.0355    0.6653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1964   -1.3796   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7794   -1.8899    0.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3784   -2.8759   -0.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5412    0.0796   -0.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0828   -0.9074   -2.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6488   -0.8464   -2.0572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1943   -2.4990   -1.7718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8005   -2.1667    0.7269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8313   -1.0226    1.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5884   -0.3498   -0.9541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1800    0.1819   -1.5949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4952    1.8231    0.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4722    2.9046    0.9917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4973    1.2561    1.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9466    0.4966   -0.4559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6015    3.3827   -0.0463 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9615    2.6372   -1.5496 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9232    1.1085   -1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4705    2.8324   -1.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8870    2.7555    0.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4387    1.0119    0.7866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6778    2.3082   -0.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2072    0.5854   -0.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1260    0.9468    0.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2495    2.1564    1.4924 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6391    0.3287    2.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3333   -0.0810    2.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7823   -3.4390   -0.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5759   -4.1704    1.0567 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5715   -3.3145   -0.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  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
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
M  END


  Mrv1533004241511172D          

 21 20  0  0  0  0            999 V2000
   -0.7658    0.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0513    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632    0.3829    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  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
 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>
NP0330497

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h7-8,10-11H,3-6,9,12-18H2,1-2H3

> <INCHI_KEY>
WTTJVINHCBCLGX-UHFFFAOYSA-N

> <FORMULA>
C19H34O2

> <MOLECULAR_WEIGHT>
294.479

> <EXACT_MASS>
294.255880335

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
37.489955725038755

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl octadeca-9,12-dienoate

> <ALOGPS_LOGP>
6.95

> <JCHEM_LOGP>
6.567770850333332

> <ALOGPS_LOGS>
-6.76

> <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>
93.28789999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.14e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl octadeca-9,12-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -1.429   0.715   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.096   1.485   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.238   0.715   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 linoleic acid	Generator
Methyl linoleate, (Z,e)-isomer	MeSH
Linoleic acid methyl ester	MeSH
Methyl linoleate, (e,e)-isomer	MeSH
Methyl linoleate, (e,Z)-isomer	MeSH
Methyl linoleate, 1-(14)C-labeled, (Z,Z)-isomer	MeSH
Methyl octadeca-9,12-dienoic acid	Generator

Chemical Formula

C₁₉H₃₄O₂

Average Mass

294.4790 Da

Monoisotopic Mass

294.25588 Da

IUPAC Name

methyl octadeca-9,12-dienoate

Traditional Name

methyl octadeca-9,12-dienoate

CAS Registry Number

Not Available

SMILES

CCCCCC=CCC=CCCCCCCCC(=O)OC

InChI Identifier

InChI=1S/C19H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h7-8,10-11H,3-6,9,12-18H2,1-2H3

InChI Key

WTTJVINHCBCLGX-UHFFFAOYSA-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
Acyrthosiphon pisum	LOTUS Database	35616633
Aegle marmelos	LOTUS Database	35616633
Ageratum conyzoides	LOTUS Database	35616633
Beilschmiedia erythrophloia	LOTUS Database	35616633
Beilschmiedia tsangii	LOTUS Database	35616633
Coreopsis grandiflora	LOTUS Database	35616633
Cyperus conglomeratus	LOTUS Database	35616633
Hygrophorus chrysodon	LOTUS Database	35616633
Kaempferia parviflora	LOTUS Database	35616633
Lycoris sanguinea	LOTUS Database	35616633
Paxillus involutus	LOTUS Database	35616633
Photinia lucida	LOTUS Database	35616633
Pueraria montana	LOTUS Database	35616633
Rhamnus formosana	LOTUS Database	35616633
Streptomyces piomogenus	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	6.95	ALOGPS
logP	6.57	ChemAxon
logS	-6.8	ALOGPS
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	15	ChemAxon
Refractivity	93.29 m³·mol⁻¹	ChemAxon
Polarizability	37.49 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

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

8203

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl octadeca-9,12-dienoate (NP0330497)

MOL for NP0330497 (methyl octadeca-9,12-dienoate)

3D MOL for NP0330497 (methyl octadeca-9,12-dienoate)

3D SDF for NP0330497 (methyl octadeca-9,12-dienoate)

3D-SDF for NP0330497 (methyl octadeca-9,12-dienoate)

PDB for NP0330497 (methyl octadeca-9,12-dienoate)

3D PDB for NP0330497 (methyl octadeca-9,12-dienoate)

SMILES for NP0330497 (methyl octadeca-9,12-dienoate)

INCHI for NP0330497 (methyl octadeca-9,12-dienoate)

Structure for NP0330497 (methyl octadeca-9,12-dienoate)

3D Structure for NP0330497 (methyl octadeca-9,12-dienoate)