NP-MRD: Showing NP-Card for (1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene (NP0301386)

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Record Information

Version

2.0

Created at

2022-09-10 14:18:31 UTC

Updated at

2022-09-10 14:18:31 UTC

NP-MRD ID

NP0301386

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene

Description

Phomopsene belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open. (1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene is found in Diaporthe amygdali. (1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene was first documented in 2009 (PMID: 19161275). Based on a literature review a small amount of articles have been published on phomopsene (PMID: 29758116) (PMID: 31034729) (PMID: 28270685).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
   -3.9717   -2.2361   -0.0567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6165   -1.6011    0.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3053   -0.4260   -0.2575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0071    0.6139   -1.0387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5556    1.9258   -0.3522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5274    1.4347    0.6806 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6485    2.4570    1.1878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9820    0.2232   -0.0127 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3434    0.6232   -1.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1158    0.3168   -1.2629 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5124   -0.4390   -2.5413 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0288    1.4886   -1.1764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6526    1.4947    0.2024 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4594    0.0942    0.6800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3803   -0.0562    2.1770 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7564   -0.6510    0.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3346   -0.5225   -0.0516 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0106   -0.5979    0.6991 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3065   -2.0836    0.7121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6992   -2.4461    1.0127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8708   -3.1440   -0.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6889   -1.5077   -0.4507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3434   -2.5398    0.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1080    0.5131   -1.0099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7304    0.5989   -2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426    2.6396   -1.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4482    2.3237    0.1442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1700    1.0434    1.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2572    3.2088    1.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0512    2.0318    1.9342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0866    3.0699    0.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8104    0.0109   -2.1572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4585    1.6769   -1.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1870   -1.4989   -2.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9726   -0.0365   -3.4146 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6065   -0.3976   -2.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4081    2.4237   -1.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8091    1.4998   -1.9736 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7448    1.7151    0.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1828    2.2681    0.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4424   -0.0466    2.5616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8765    0.7440    2.7083 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0032   -1.0729    2.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4889   -1.6762    0.0090 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1977   -0.1750   -0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4763   -0.6549    1.1029 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6721   -1.5249   -0.4150 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1138   -0.2513    1.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1016   -2.4269   -0.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4507   -2.6041    1.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8542   -3.5123    0.7040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9004   -2.3111    2.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 14  1  0
 14 15  1  0
 14 16  1  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  6
 10  9  1  0
  8  9  1  6
  8  6  1  0
  8  3  1  0
  8 18  1  0
 10 17  1  0
  7 29  1  0
  7 30  1  0
  7 31  1  0
  6 28  1  1
  5 26  1  0
  5 27  1  0
  4 24  1  0
  4 25  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
 20 51  1  0
 20 52  1  0
 19 49  1  0
 19 50  1  0
 18 48  1  1
 17 47  1  6
 15 41  1  0
 15 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 13 39  1  0
 13 40  1  0
 12 37  1  0
 12 38  1  0
 11 34  1  0
 11 35  1  0
 11 36  1  0
  9 32  1  0
  9 33  1  0
M  END


  Mrv1652309102216182D          

 20 23  0  0  1  0            999 V2000
   -1.7184   -1.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9371   -1.0668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7760   -0.2577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695    0.4034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932    1.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0054    0.8323    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6558    1.3258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0053    0.0074    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3311    0.7653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1526    0.6897    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9707    1.4943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8617    1.1113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4819    0.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561   -0.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9439   -0.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9949   -0.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3345   -0.1150    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6254   -0.5367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4643   -1.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3169   -1.6109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  6  0  0  0
  6  8  1  0  0  0  0
  8  3  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 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
 14 16  1  0  0  0  0
 17 14  1  1  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0301386

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CCC2=C(C)CC[C@H]3[C@@H]4C(C)(C)CC[C@]4(C)C[C@@]123

> <INCHI_IDENTIFIER>
InChI=1S/C20H32/c1-13-6-8-16-17-18(3,4)10-11-19(17,5)12-20(16)14(2)7-9-15(13)20/h14,16-17H,6-12H2,1-5H3/t14-,16-,17+,19+,20+/m0/s1

> <INCHI_KEY>
WFXPJSKWJXCYJM-TWRRNRRFSA-N

> <FORMULA>
C20H32

> <MOLECULAR_WEIGHT>
272.476

> <EXACT_MASS>
272.25040103

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
34.48360345300061

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,9S,10R,14R)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0^{1,5}.0^{10,14}]pentadec-5-ene

> <JCHEM_LOGP>
5.356997101666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
86.39989999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,9S,10R,14R)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0^{1,5}.0^{10,14}]pentadec-5-ene

> <JCHEM_VEBER_RULE>
1

$$$$

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      -3.208  -2.486   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.749  -1.991   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.449  -0.481   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.370   0.753   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.481   2.011   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.010   1.554   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.224   2.475   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.010   0.014   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.618   1.429   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.152   1.287   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.812   2.789   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.475   2.074   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.633   1.059   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.025  -0.356   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.495  -0.813   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.724  -1.866   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.491  -0.215   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.167  -1.002   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.867  -2.512   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.592  -3.007   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    3    9   18                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   12   17                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   10   18                                                  
CONECT   18   17    8   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    2                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂

Average Mass

272.4760 Da

Monoisotopic Mass

272.25040 Da

IUPAC Name

(1S,2S,9S,10R,14R)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0^{1,5}.0^{10,14}]pentadec-5-ene

Traditional Name

(1S,2S,9S,10R,14R)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0^{1,5}.0^{10,14}]pentadec-5-ene

CAS Registry Number

Not Available

SMILES

C[C@H]1CCC2=C(C)CC[C@H]3[C@@H]4C(C)(C)CC[C@]4(C)C[C@@]123

InChI Identifier

InChI=1S/C20H32/c1-13-6-8-16-17-18(3,4)10-11-19(17,5)12-20(16)14(2)7-9-15(13)20/h14,16-17H,6-12H2,1-5H3/t14-,16-,17+,19+,20+/m0/s1

InChI Key

WFXPJSKWJXCYJM-TWRRNRRFSA-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
Fusicoccum amygdali	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Iridoids and derivatives

Alternative Parents

Substituents

11-noriridane monoterpenoid
Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.36	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	86.4 m³·mol⁻¹	ChemAxon
Polarizability	34.48 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

Not Available

Chemspider ID

58828720

KEGG Compound ID

Not Available

BioCyc ID

CPD-18470

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25229136

PDB ID

Not Available

ChEBI ID

156237

Good Scents ID

Not Available

References

General References

Toyomasu T, Kaneko A, Tokiwano T, Kanno Y, Kanno Y, Niida R, Miura S, Nishioka T, Ikeda C, Mitsuhashi W, Dairi T, Kawano T, Oikawa H, Kato N, Sassa T: Biosynthetic gene-based secondary metabolite screening: a new diterpene, methyl phomopsenonate, from the fungus Phomopsis amygdali. J Org Chem. 2009 Feb 20;74(4):1541-8. doi: 10.1021/jo802319e. [PubMed:19161275 ]
Lauterbach L, Rinkel J, Dickschat JS: Two Bacterial Diterpene Synthases from Allokutzneria albata Produce Bonnadiene, Phomopsene, and Allokutznerene. Angew Chem Int Ed Engl. 2018 Jul 2;57(27):8280-8283. doi: 10.1002/anie.201803800. Epub 2018 Jun 6. [PubMed:29758116 ]
Rinkel J, Steiner ST, Dickschat JS: Diterpene Biosynthesis in Actinomycetes: Studies on Cattleyene Synthase and Phomopsene Synthase. Angew Chem Int Ed Engl. 2019 Jul 1;58(27):9230-9233. doi: 10.1002/anie.201902950. Epub 2019 May 24. [PubMed:31034729 ]
Shinde SS, Minami A, Chen Z, Tokiwano T, Toyomasu T, Kato N, Sassa T, Oikawa H: Cyclization mechanism of phomopsene synthase: mass spectrometry based analysis of various site-specifically labeled terpenes. J Antibiot (Tokyo). 2017 May;70(5):632-638. doi: 10.1038/ja.2017.27. Epub 2017 Mar 8. [PubMed:28270685 ]
LOTUS database [Link]

Showing NP-Card for (1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene (NP0301386)

MOL for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

3D MOL for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

3D SDF for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

3D-SDF for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

PDB for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

3D PDB for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

SMILES for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

INCHI for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

Structure for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)

3D Structure for NP0301386 ((1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene)