NP-MRD: Showing NP-Card for (1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one (NP0196592)

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Record Information

Version

2.0

Created at

2022-09-04 14:42:41 UTC

Updated at

2022-09-04 14:42:41 UTC

NP-MRD ID

NP0196592

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one

Description

Coulterone belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one was first documented in 2005 (PMID: 16149801). Based on a literature review very few articles have been published on Coulterone (PMID: 27896867).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    4.1636    3.2486   -0.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1760    1.8431   -0.1006 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0479    1.0365   -0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8083    1.6167   -0.2295 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6590    0.7887   -0.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8574   -0.5614   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1541   -1.1326   -0.0510 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2576   -0.3351   -0.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6449   -0.7954    0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0209   -1.7076   -1.0651 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7469   -1.7105    1.3957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1330   -1.6399   -0.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2030   -2.7598   -0.3982 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5278   -1.3767    0.5169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2144   -0.3698   -0.3730 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8841    1.0488   -0.0973 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3839    1.4690    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8913    1.4408    1.1967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3993    0.0631    0.8480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6888   -0.5821   -0.2966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0273   -2.0806   -0.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2631   -0.1533   -1.6388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5605    1.5550   -0.4780 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0232    3.6714    0.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912    3.5636   -0.9425 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1708    3.6172   -0.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6077    2.6718   -0.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2632   -2.1943    0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3481   -0.0112    0.2321 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6158   -1.0201   -1.7644 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7258   -2.4939   -0.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1305   -2.0244   -1.6152 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8764   -1.6475    2.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8980   -2.7644    1.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6715   -1.5104    1.9626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0577   -2.3366    0.4369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4918   -1.1028    1.5820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9108   -0.6748   -1.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147    1.6296   -0.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1190    2.5279    1.4139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9785    0.9230    2.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2928    1.6939    2.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2550    2.1903    0.4981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4764    0.1920    0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4379   -0.6005    1.7574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1126   -2.1877   -0.5050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0163   -2.3881    0.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4794   -2.6952   -0.9079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2242   -0.6934   -1.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5384   -0.5836   -2.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4294    0.9125   -1.7283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6298    1.8740   -1.5776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4236    2.5559    0.0328 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  2  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 16 23  1  0
  8  3  1  0
 20 15  1  0
 23  5  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  7 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  6
 16 39  1  6
 17 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
M  END


  Mrv1652309042216422D          

 23 25  0  0  1  0            999 V2000
    7.3332    1.9733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5448    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9401    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1517    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7305    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5189    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1237    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9120    0.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5168    1.1689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0956   -0.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5741   -0.8553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    0.5330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0604    1.3373    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4556    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0884    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5487   -0.3342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3040   -0.5065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6953    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  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  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 16 23  1  0  0  0  0
  5 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196592

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1C(C)C)C(=O)C[C@@H]1[C@@H](CCCC1(C)C)C2

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O2/c1-13(2)16-11-17-15(10-20(16)23-5)9-14-7-6-8-21(3,4)18(14)12-19(17)22/h10-11,13-14,18H,6-9,12H2,1-5H3/t14-,18+/m0/s1

> <INCHI_KEY>
GBHQYFDQBZMNFV-KBXCAEBGSA-N

> <FORMULA>
C21H30O2

> <MOLECULAR_WEIGHT>
314.469

> <EXACT_MASS>
314.224580206

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.5833142079965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,11R)-5-methoxy-12,12-dimethyl-6-(propan-2-yl)tricyclo[9.4.0.0^{3,8}]pentadeca-3(8),4,6-trien-9-one

> <JCHEM_LOGP>
5.399547054666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.272175643533625

> <JCHEM_PKA_STRONGEST_BASIC>
-4.838492759742019

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
95.10239999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,11R)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0^{3,8}]pentadeca-3(8),4,6-trien-9-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      13.689   3.683   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      12.217   4.137   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.088   3.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.617   3.544   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.488   2.496   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.830   0.995   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.302   0.541   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.431   1.588   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.902   1.135   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.031   2.182   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.245  -0.367   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.870  -0.209   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.538  -1.597   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.330  -0.209   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.370   0.995   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.713   2.496   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.584   3.544   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.112   3.090   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.770   1.588   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.898   0.541   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.891  -0.624   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.301  -0.946   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.100   3.165   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    6   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15   21   22                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   16    5                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₂

Average Mass

314.4690 Da

Monoisotopic Mass

314.22458 Da

IUPAC Name

(1S,11R)-5-methoxy-12,12-dimethyl-6-(propan-2-yl)tricyclo[9.4.0.0^{3,8}]pentadeca-3(8),4,6-trien-9-one

Traditional Name

(1S,11R)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0^{3,8}]pentadeca-3(8),4,6-trien-9-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1C(C)C)C(=O)C[C@@H]1[C@@H](CCCC1(C)C)C2

InChI Identifier

InChI=1S/C21H30O2/c1-13(2)16-11-17-15(10-20(16)23-5)9-14-7-6-8-21(3,4)18(14)12-19(17)22/h10-11,13-14,18H,6-9,12H2,1-5H3/t14-,18+/m0/s1

InChI Key

GBHQYFDQBZMNFV-KBXCAEBGSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Abeoabietane diterpenoid
Diterpenoid
Cumene
Anisole
Phenol ether
Aryl ketone
Aryl alkyl ketone
Alkyl aryl ether
Benzenoid
Ketone
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	5.4	ChemAxon
pKa (Strongest Acidic)	17.27	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.1 m³·mol⁻¹	ChemAxon
Polarizability	37.58 Å³	ChemAxon
Number of Rings	3	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

C00044673

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101666184

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Thommen C, Neuburger M, Gademann K: Collective Syntheses of Icetexane Natural Products Based on Biogenetic Hypotheses. Chemistry. 2017 Jan 1;23(1):120-127. doi: 10.1002/chem.201603932. Epub 2016 Nov 29. [PubMed:27896867 ]
Sengupta S, Drew MG, Mukhopadhyay R, Achari B, Banerjee AK: Stereoselective syntheses of (+/-)-komaroviquinone and (+/-)-faveline methyl ether through intramolecular Heck reaction. J Org Chem. 2005 Sep 16;70(19):7694-700. doi: 10.1021/jo051082i. [PubMed:16149801 ]
LOTUS database [Link]

Showing NP-Card for (1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one (NP0196592)

MOL for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

3D MOL for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

3D SDF for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

3D-SDF for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

PDB for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

3D PDB for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

SMILES for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

INCHI for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

Structure for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)

3D Structure for NP0196592 ((1s,11r)-6-isopropyl-5-methoxy-12,12-dimethyltricyclo[9.4.0.0³,⁸]pentadeca-3(8),4,6-trien-9-one)