NP-MRD: Showing NP-Card for (1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one (NP0269101)

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Record Information

Version

2.0

Created at

2022-09-08 14:25:55 UTC

Updated at

2022-09-08 14:25:55 UTC

NP-MRD ID

NP0269101

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one

Description

Ecklonialactone A belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. (1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one is found in Egregia menziesii and Eisenia bicyclis. (1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one was first documented in 1994 (PMID: 8158161). Based on a literature review very few articles have been published on Ecklonialactone A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -0.9894    2.6951   -1.3791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5539    1.3021   -1.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7126    0.8792    0.1999 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6383    0.8166    0.9900 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2354    1.5073    1.7013 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2071    1.3773    2.9891 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2768    2.4373    1.2206 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074    1.8532    0.2036 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3518    1.0965    0.7731 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3413   -0.3845    0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3712   -0.6646   -0.9980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4467   -1.3243   -1.6770 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2752   -1.8264   -0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1283   -2.1723   -1.7487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0845   -2.0712   -1.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4488   -1.6374    0.1052 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4091   -0.4828    0.1358 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1439   -0.6255    1.4590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3690   -2.1137    1.5213 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3544   -2.8793    2.0728 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3312   -2.7522    0.6966 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0789    2.6723   -1.6168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2445    3.2893   -0.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4761    3.2294   -2.2445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9118    0.6033   -1.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5317    1.3040   -1.7735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5066    1.5621    0.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8985    2.8209    2.0516 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7940    3.3291    0.7812 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6614    1.2646   -0.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6413    2.7281   -0.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3418    1.1571    1.8921 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3378    1.4810    0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2899   -0.8029    0.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5363   -0.8415    1.0125 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2430   -0.2873   -1.5472 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4989   -1.5125   -2.7335 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9737   -0.9995   -0.2570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6207   -2.7224   -0.3650 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2764   -2.5038   -2.7574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9178   -2.3432   -1.9105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6522   -1.5038    0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1067   -0.5514   -0.7009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0900   -0.0519    1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5302   -0.2488    2.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4094   -2.5116    1.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6217   -3.5911    0.0661 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17  3  1  0
 17 16  1  0
 19 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  1
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  0
 16 42  1  1
 21 47  1  6
 19 46  1  6
 18 44  1  0
 18 45  1  0
 17 43  1  6
M  END


  Mrv1652309082216252D          

 21 23  0  0  1  0            999 V2000
    2.0431   -0.8492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8485   -0.6702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4062   -1.2781    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1230   -0.8696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9460   -0.8126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0736    0.0025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7123   -1.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2700   -1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5087   -2.5159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3812   -3.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9126   -4.0100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1958   -4.4185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3728   -4.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6065   -4.1698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0488   -3.5619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8101   -2.7722    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9376   -1.9571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2019   -1.5839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6196   -2.1683    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1715   -2.8611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9955   -2.9027    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 21 20  1  1  0  0  0
 19 21  1  0  0  0  0
 16 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0269101

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1OC(=O)CCCC\C=C/C\C=C/[C@@H]2[C@H]3O[C@H]3C[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O3/c1-2-15-14-12-16-18(21-16)13(14)10-8-6-4-3-5-7-9-11-17(19)20-15/h3-4,8,10,13-16,18H,2,5-7,9,11-12H2,1H3/b4-3-,10-8-/t13-,14+,15-,16-,18+/m0/s1

> <INCHI_KEY>
GZNRNQVZDUCYFB-SOVGUPCDSA-N

> <FORMULA>
C18H26O3

> <MOLECULAR_WEIGHT>
290.403

> <EXACT_MASS>
290.188194697

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.16184377352445

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,9Z,12Z,14S,15R,17S)-2-ethyl-3,16-dioxatricyclo[12.4.0.0^{15,17}]octadeca-9,12-dien-4-one

> <JCHEM_LOGP>
3.776793250333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.206412749342519

> <JCHEM_POLAR_SURFACE_AREA>
38.83

> <JCHEM_REFRACTIVITY>
84.156

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,9Z,12Z,14S,15R,17S)-2-ethyl-3,16-dioxatricyclo[12.4.0.0^{15,17}]octadeca-9,12-dien-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       3.814  -1.585   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.317  -1.251   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.358  -2.386   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.696  -1.623   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.233  -1.517   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.471   0.005   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.663  -2.088   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.704  -3.222   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.150  -4.696   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.912  -6.218   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.037  -7.485   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.699  -8.248   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.163  -8.354   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.732  -7.784   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.691  -6.649   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.245  -5.175   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.484  -3.653   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.110  -2.957   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.023  -4.048   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.187  -5.341   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.725  -5.418   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    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   21                                                  
CONECT   17   16    3   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19   21                                                       
CONECT   21   20   19   16                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₆O₃

Average Mass

290.4030 Da

Monoisotopic Mass

290.18819 Da

IUPAC Name

(1R,2S,9Z,12Z,14S,15R,17S)-2-ethyl-3,16-dioxatricyclo[12.4.0.0^{15,17}]octadeca-9,12-dien-4-one

Traditional Name

(1R,2S,9Z,12Z,14S,15R,17S)-2-ethyl-3,16-dioxatricyclo[12.4.0.0^{15,17}]octadeca-9,12-dien-4-one

CAS Registry Number

Not Available

SMILES

CC[C@@H]1OC(=O)CCCC\C=C/C\C=C/[C@@H]2[C@H]3O[C@H]3C[C@@H]12

InChI Identifier

InChI=1S/C18H26O3/c1-2-15-14-12-16-18(21-16)13(14)10-8-6-4-3-5-7-9-11-17(19)20-15/h3-4,8,10,13-16,18H,2,5-7,9,11-12H2,1H3/b4-3-,10-8-/t13-,14+,15-,16-,18+/m0/s1

InChI Key

GZNRNQVZDUCYFB-SOVGUPCDSA-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
Egregia menziesii	LOTUS Database	35616633
Eisenia bicyclis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Oxane
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	3.78	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	38.83 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	84.16 m³·mol⁻¹	ChemAxon
Polarizability	32.16 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00000410

Chemspider ID

10474881

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23428255

PDB ID

Not Available

ChEBI ID

168744

Good Scents ID

Not Available

References

General References

Todd JS, Proteau PJ, Gerwick WH: The absolute configuration of ecklonialactones A, B, and E, novel oxylipins from brown algae of the genera Ecklonia and Egregia. J Nat Prod. 1994 Jan;57(1):171-4. doi: 10.1021/np50103a028. [PubMed:8158161 ]
LOTUS database [Link]

Showing NP-Card for (1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one (NP0269101)

MOL for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

3D MOL for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

3D SDF for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

3D-SDF for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

PDB for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

3D PDB for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

SMILES for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

INCHI for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

Structure for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)

3D Structure for NP0269101 ((1r,2s,9z,12z,14s,15r,17s)-2-ethyl-3,16-dioxatricyclo[12.4.0.0¹⁵,¹⁷]octadeca-9,12-dien-4-one)