NP-MRD: Showing NP-Card for etherolenic acid (NP0292064)

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Record Information

Version

2.0

Created at

2022-09-09 23:25:08 UTC

Updated at

2022-09-09 23:25:08 UTC

NP-MRD ID

NP0292064

Secondary Accession Numbers

None

Natural Product Identification

Common Name

etherolenic acid

Description

Etherolenic acid, also known as etherolenate, belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. etherolenic acid is found in Allium sativum. etherolenic acid was first documented in 2014 (PMID: 24863619). Based on a literature review a small amount of articles have been published on Etherolenic acid (PMID: 30008094) (PMID: 26776054) (PMID: 26277770).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 48  0  0  0  0  0  0  0  0999 V2000
   -8.3343   -0.1709    0.3281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2838   -1.2380   -0.6783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1282   -1.5492   -1.4599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9742   -1.0048   -1.4531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5251    0.0960   -0.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2664    0.5586   -0.7455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9141    1.6183    0.0791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6433    2.1228   -0.0889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5601    1.6367    0.5355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2553    2.2102    0.3171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8082    1.7527    0.9141 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7904    0.6335    1.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6847   -0.4894    1.3264 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1211   -0.0577    1.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9067   -1.2449    0.6504 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3657   -0.9124    0.4508 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5721    0.1962   -0.5458 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0597    0.4505   -0.6568 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8242   -0.7257   -1.1060 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1347   -1.6557   -0.3224 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2090   -0.7987   -2.4430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4170   -0.2381    0.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3154    0.8737   -0.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7434   -0.3541    1.2433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1921   -1.0246   -1.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6388   -2.1993   -0.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2517   -2.3976   -2.1891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1987   -1.4051   -2.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0953    0.6318    0.1008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6034    0.0941   -1.4559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4767    2.9558   -0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7525    0.8143    1.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1778    3.0733   -0.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736    2.2215    0.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2143    0.9814    2.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1721    0.1816    2.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321   -0.8070    0.3596 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5761   -1.3537    2.0081 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1581    0.7917    0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5112    0.1794    2.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4585   -1.6167   -0.2673 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8485   -2.0326    1.4289 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8378   -1.8259    0.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8683   -0.6802    1.4000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2025   -0.1460   -1.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1077    1.1490   -0.2279 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2419    1.3496   -1.2781 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4035    0.7164    0.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0093   -1.3607   -2.6798 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  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  1  0
 19 21  1  0
 19 20  2  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
  6 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 21 49  1  0
M  END


  Mrv1652309102201252D          

 21 20  0  0  0  0            999 V2000
    0.1401    8.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    7.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5743    7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5743    6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    4.6184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    1.3184    0.0000 O   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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0292064

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H28O3/c1-2-3-4-13-16-21-17-14-11-9-7-5-6-8-10-12-15-18(19)20/h3-4,9,11,13-14,16-17H,2,5-8,10,12,15H2,1H3,(H,19,20)/b4-3-,11-9-,16-13+,17-14+

> <INCHI_KEY>
QWRJRLCIDLDGLM-GTTHPXIQSA-N

> <FORMULA>
C18H28O3

> <MOLECULAR_WEIGHT>
292.419

> <EXACT_MASS>
292.203844762

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
35.981872479979856

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9Z,11E)-12-[(1E,3Z)-hexa-1,3-dien-1-yloxy]dodeca-9,11-dienoic acid

> <JCHEM_LOGP>
5.1979071260000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.988167283934771

> <JCHEM_PKA_STRONGEST_BASIC>
-5.158770246611053

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
90.85449999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
etherolenic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       0.262  15.551   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.262  14.011   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.072  13.241   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.072  11.701   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.262  10.931   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.262   9.391   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.595   8.621   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.595   7.081   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.929   6.311   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.929   4.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.263   4.001   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      16.266   4.771   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      14.932   2.461   0.000  0.00  0.00           O+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   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
(9Z,11E,1'e,3'z)-12-(1',3'-Hexadienyloxy)-9,11-dodecadienoic acid	Kegg
(9Z,11E,1'e,3'z)-12-(1',3'-Hexadienyloxy)-9,11-dodecadienoate	Generator
Etherolenate	Generator

Chemical Formula

C₁₈H₂₈O₃

Average Mass

292.4190 Da

Monoisotopic Mass

292.20384 Da

IUPAC Name

(9Z,11E)-12-[(1E,3Z)-hexa-1,3-dien-1-yloxy]dodeca-9,11-dienoic acid

Traditional Name

etherolenic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C18H28O3/c1-2-3-4-13-16-21-17-14-11-9-7-5-6-8-10-12-15-18(19)20/h3-4,9,11,13-14,16-17H,2,5-8,10,12,15H2,1H3,(H,19,20)/b4-3-,11-9-,16-13+,17-14+

InChI Key

QWRJRLCIDLDGLM-GTTHPXIQSA-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
Allium sativum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Unsaturated fatty acid
Straight chain fatty acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

medium-chain fatty acid (CHEBI:80443 )

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	5.2	ChemAxon
pKa (Strongest Acidic)	4.99	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	90.85 m³·mol⁻¹	ChemAxon
Polarizability	35.98 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

26324016

KEGG Compound ID

C16319

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23724709

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Toporkova YY, Bessolitsyna EK, Smirnova EO, Gorina SS, Petrova OE, Mukhtarova LS, Grechkin AN: Antimicrobial Activity of Geometric Isomers of Etherolenic Acid-the Products of Plant Lipoxygenase Cascade. Dokl Biochem Biophys. 2018 May;480(1):139-142. doi: 10.1134/S1607672918030031. Epub 2018 Jul 14. [PubMed:30008094 ]
Gorina SS, Toporkova YY, Mukhtarova LS, Smirnova EO, Chechetkin IR, Khairutdinov BI, Gogolev YV, Grechkin AN: Oxylipin biosynthesis in spikemoss Selaginella moellendorffii: Molecular cloning and identification of divinyl ether synthases CYP74M1 and CYP74M3. Biochim Biophys Acta. 2016 Apr;1861(4):301-9. doi: 10.1016/j.bbalip.2016.01.001. Epub 2016 Jan 9. [PubMed:26776054 ]
Ogorodnikova AV, Mukhitova FK, Grechkin AN: Oxylipins in the spikemoss Selaginella martensii: Detection of divinyl ethers, 12-oxophytodienoic acid and related cyclopentenones. Phytochemistry. 2015 Oct;118:42-50. doi: 10.1016/j.phytochem.2015.08.003. Epub 2015 Aug 12. [PubMed:26277770 ]
Gorina SS, Toporkova YY, Mukhtarova LS, Chechetkin IR, Khairutdinov BI, Gogolev YV, Grechkin AN: Detection and molecular cloning of CYP74Q1 gene: identification of Ranunculus acris leaf divinyl ether synthase. Biochim Biophys Acta. 2014 Sep;1841(9):1227-33. doi: 10.1016/j.bbalip.2014.05.005. Epub 2014 May 24. [PubMed:24863619 ]
LOTUS database [Link]

Showing NP-Card for etherolenic acid (NP0292064)

MOL for NP0292064 (etherolenic acid)

3D MOL for NP0292064 (etherolenic acid)

3D SDF for NP0292064 (etherolenic acid)

3D-SDF for NP0292064 (etherolenic acid)

PDB for NP0292064 (etherolenic acid)

3D PDB for NP0292064 (etherolenic acid)

SMILES for NP0292064 (etherolenic acid)

INCHI for NP0292064 (etherolenic acid)

Structure for NP0292064 (etherolenic acid)

3D Structure for NP0292064 (etherolenic acid)