NP-MRD: Showing NP-Card for 3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate (NP0270467)

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Record Information

Version

2.0

Created at

2022-09-08 16:23:43 UTC

Updated at

2022-09-08 16:23:43 UTC

NP-MRD ID

NP0270467

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate

Description

Farnesyl octanoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate is found in Ophrys arachnitiformis. 3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate was first documented in 2013 (PMID: 24197916). Based on a literature review a small amount of articles have been published on farnesyl octanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 65 64  0  0  0  0  0  0  0  0999 V2000
    8.2838   -1.8800   -3.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2103   -2.2312   -2.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7874   -0.9304   -1.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7265   -1.1721   -0.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3451    0.1280    0.2339 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8079    1.1289   -0.7283 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4238    2.4087   -0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3383    2.1887    0.9175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581    1.0942    1.1087 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    3.2426    1.7261 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8499    3.1033    2.6745 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5692    2.6608    2.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0915    1.5728    2.3563 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3905    0.6049    3.3796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3905    1.3071    1.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2331    0.0194    0.9003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3600   -0.4896    0.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5599   -0.0437   -0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1780    1.1774    0.5448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5289   -0.8185   -0.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6750   -1.2250   -0.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6500   -1.9895   -0.9117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8933   -1.5571   -1.0592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3776   -0.3256   -0.4226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8249   -2.3471   -1.8971 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3168   -2.6456   -3.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2626   -1.7558   -2.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0818   -0.9060   -3.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3558   -2.7064   -2.6269 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6768   -2.8790   -1.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6815   -0.4494   -1.0456 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3939   -0.2966   -2.2909 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8272   -1.6070   -0.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0501   -1.8590    0.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6520   -0.0934    1.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2933    0.5055    0.7022 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8798    0.7077   -1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5145    1.3213   -1.5735 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0854    3.1122   -0.8827 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3383    2.8300    0.4154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6559    4.1338    3.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1734    2.5086    3.5357 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1584    3.3340    1.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4549    0.0389    3.8305 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0540   -0.1159    2.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9419    1.0521    4.2074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1587    1.3768    2.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4774    2.1487    0.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3337    0.1464    0.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8825   -0.7613    1.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1430   -1.4462   -0.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3624    1.0455    1.6512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6785    2.1126    0.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2402    1.3367    0.1603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9778   -1.6408   -1.3830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8263   -0.1333   -1.7663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1952   -0.3986    0.4332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2572   -1.8871    0.7255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3035   -2.8991   -1.3858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3337   -0.4692    0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4218   -0.1052   -0.6803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7726    0.5635   -0.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8752   -1.9687   -1.8205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4716   -2.3755   -2.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8307   -3.3872   -1.4805 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  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 14 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
 19 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  0
 24 60  1  0
 24 61  1  0
 24 62  1  0
 25 63  1  0
 25 64  1  0
 25 65  1  0
M  END


  Mrv1652309082218232D          

 25 24  0  0  0  0            999 V2000
    4.2355    3.2704    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
    9.2368    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 C   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
   12.0947    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9526    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9526    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6671    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3815    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0960    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8105    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5249    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8105    2.0329    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
  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
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270467

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(=O)OCC=C(C)CCC=C(C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H40O2/c1-6-7-8-9-10-17-23(24)25-19-18-22(5)16-12-15-21(4)14-11-13-20(2)3/h13,15,18H,6-12,14,16-17,19H2,1-5H3

> <INCHI_KEY>
HHSVAJNBWYMLPB-UHFFFAOYSA-N

> <FORMULA>
C23H40O2

> <MOLECULAR_WEIGHT>
348.571

> <EXACT_MASS>
348.302830528

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
45.99011092105571

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate

> <JCHEM_LOGP>
7.526602153333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.043362508273769

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
111.7681

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate

> <JCHEM_VEBER_RULE>
0

$$$$

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       7.906   6.105   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.574   6.105   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.907   5.335   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.241   6.105   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.575   5.335   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.908   6.105   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.242   5.335   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      17.242   3.795   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      18.576   6.105   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      19.909   5.335   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.243   6.105   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      22.577   5.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      22.577   3.795   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      23.910   6.105   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      25.244   5.335   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.578   6.105   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      27.912   5.335   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      27.912   3.795   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.245   6.105   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      30.579   5.335   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      31.913   6.105   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      33.246   5.335   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      34.580   6.105   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      33.246   3.795   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   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Value	Source
Farnesyl octanoic acid	Generator

Chemical Formula

C₂₃H₄₀O₂

Average Mass

348.5710 Da

Monoisotopic Mass

348.30283 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCCC(=O)OCC=C(C)CCC=C(C)CCC=C(C)C

InChI Identifier

InChI=1S/C23H40O2/c1-6-7-8-9-10-17-23(24)25-19-18-22(5)16-12-15-21(4)14-11-13-20(2)3/h13,15,18H,6-12,14,16-17,19H2,1-5H3

InChI Key

HHSVAJNBWYMLPB-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
Ophrys x arachnitiformis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Farsesane sesquiterpenoid
Sesquiterpenoid
Fatty alcohol ester
Fatty acid ester
Fatty acyl
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

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

67031933

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

529263

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Tolasch T, Konig C, von Fragstein M, Steidle JL: Identification of the sex pheromone of Idolus picipennis (Bach, 1852) revealed the presence of a cryptic sibling species. J Chem Ecol. 2013 Dec;39(11-12):1433-40. doi: 10.1007/s10886-013-0360-6. Epub 2013 Nov 7. [PubMed:24197916 ]
LOTUS database [Link]

Showing NP-Card for 3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate (NP0270467)

MOL for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

3D MOL for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

3D SDF for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

3D-SDF for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

PDB for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

3D PDB for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

SMILES for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

INCHI for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

Structure for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)

3D Structure for NP0270467 (3,7,11-trimethyldodeca-2,6,10-trien-1-yl octanoate)