NP-MRD: Showing NP-Card for methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate (NP0150232)

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Record Information

Version

2.0

Created at

2022-09-02 06:16:23 UTC

Updated at

2022-09-02 06:16:23 UTC

NP-MRD ID

NP0150232

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate

Description

Methyl (5e,17e)-18-bromo-octadeca-5,17-diene-15-ynoate belongs to the class of organic compounds known as fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group. methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate is found in Pleopsidium gobiense. Based on a literature review very few articles have been published on Methyl (5e,17e)-18-bromo-octadeca-5,17-diene-15-ynoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 50  0  0  0  0  0  0  0  0999 V2000
   -7.0776    2.9237    0.7317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1253    2.0648    0.1309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9743    0.7347    0.4647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7075    0.2294    1.3466 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9587   -0.1400   -0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0379   -1.5166    0.3794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0648   -2.4699   -0.1746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6384   -2.2829    0.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0821   -1.3954    0.8735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6627   -1.2289    1.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2787   -2.0544    0.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3949   -1.8172   -1.1182 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7490   -0.4658   -1.6082 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0214    0.1591   -1.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3303    0.5125    0.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6913    1.1823    0.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8348    0.3232   -0.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0585    1.1455    0.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0520    1.8099    0.1862 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2293    2.6156    0.3564 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1461    2.2233    1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7314    3.2899    1.4603 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -8.0293    2.9167    0.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2885    2.6148    1.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6127    3.9311    0.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1680   -0.1909   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9850    0.3182   -0.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0668   -1.9098    0.1095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9753   -1.5231    1.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1599   -2.4823   -1.3071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3155   -3.5208    0.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0002   -3.0418   -0.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8215   -0.7455    1.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4486   -1.3491    2.2346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3395   -0.1374    0.9689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2844   -2.1472    0.8151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1502   -3.1602    0.3765 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2413   -2.5440   -1.4405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4820   -2.2424   -1.6558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1239    0.2352   -1.3664 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6738   -0.5169   -2.7518 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8771   -0.5270   -1.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1824    1.1033   -1.8779 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6079    1.3431    0.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2605   -0.2338    0.9167 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843    1.4337    1.3368 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7306    2.1333   -0.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7100    0.1558   -1.2927 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9494   -0.6116    0.3564 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3904    3.5357   -0.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9866    1.3201    1.7630 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  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  3  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 17 49  1  0
 20 50  1  0
 21 51  1  0
M  END

  Mrv1652309022208162D          

 22 21  0  0  0  0            999 V2000
   -2.7177    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0033    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2888    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2888    3.3809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5743    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    2.1434    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4283    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1427    3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8572    2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5717    3.3809    0.0000 Br  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
  3  5  1  0  0  0  0
  5  6  1  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  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  3  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0150232

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CCC\C=C\CCCCCCCCC#C\C=C\Br

> <INCHI_IDENTIFIER>
InChI=1S/C19H29BrO2/c1-22-19(21)17-15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18-20/h9,11,16,18H,2-8,10,13,15,17H2,1H3/b11-9+,18-16+

> <INCHI_KEY>
RJHPNNYGRMJAPM-GEFYFZSISA-N

> <FORMULA>
C19H29BrO2

> <MOLECULAR_WEIGHT>
369.343

> <EXACT_MASS>
368.135093

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
41.22988201087262

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (5E,17E)-18-bromooctadeca-5,17-dien-15-ynoate

> <ALOGPS_LOGP>
6.78

> <JCHEM_LOGP>
6.692316661333333

> <ALOGPS_LOGS>
-5.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.024098185009097

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
99.19639999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.20e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (5E,17E)-18-bromooctadeca-5,17-dien-15-ynoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.073   4.771   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.739   4.001   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.406   4.771   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.406   6.311   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.072   4.001   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.262   4.771   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.595   4.001   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.929   4.771   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.263   4.001   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.266   4.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.599   5.541   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.933   6.311   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      20.267   5.541   0.000  0.00  0.00           C+0
HETATM   22 Br   UNK     0      21.600   6.311   0.000  0.00  0.00          Br+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    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                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   42    0
END

View in JSmol

Synonyms

Value	Source
Methyl (5E,17E)-18-bromo-octadeca-5,17-diene-15-ynoic acid	Generator

Chemical Formula

C₁₉H₂₉BrO₂

Average Mass

369.3430 Da

Monoisotopic Mass

368.13509 Da

IUPAC Name

methyl (5E,17E)-18-bromooctadeca-5,17-dien-15-ynoate

Traditional Name

methyl (5E,17E)-18-bromooctadeca-5,17-dien-15-ynoate

CAS Registry Number

Not Available

SMILES

COC(=O)CCC\C=C\CCCCCCCCC#C\C=C\Br

InChI Identifier

InChI=1S/C19H29BrO2/c1-22-19(21)17-15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18-20/h9,11,16,18H,2-8,10,13,15,17H2,1H3/b11-9+,18-16+

InChI Key

RJHPNNYGRMJAPM-GEFYFZSISA-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
Pleopsidium gobiense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid methyl esters

Alternative Parents

Substituents

Fatty acid methyl ester
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Vinyl bromide
Vinyl halide
Haloalkene
Bromoalkene
Organooxygen compound
Organobromide
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organohalogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Halogenated fatty acids (LMFA01090086 )

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	6.78	ALOGPS
logP	6.69	ChemAxon
logS	-5.9	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	99.2 m³·mol⁻¹	ChemAxon
Polarizability	41.23 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

78434931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15518451

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate (NP0150232)

MOL for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

3D MOL for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

3D SDF for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

3D-SDF for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

PDB for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

3D PDB for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

SMILES for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

INCHI for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

Structure for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)

3D Structure for NP0150232 (methyl (5e,17e)-18-bromooctadeca-5,17-dien-15-ynoate)