NP-MRD: Showing NP-Card for (11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one (NP0191102)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 07:56:02 UTC

Updated at

2022-09-04 07:56:02 UTC

NP-MRD ID

NP0191102

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one

Description

Faveline methyl ether belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. (11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one is found in Cnidoscolus quercifolius. (11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one was first documented in 2005 (PMID: 16149801). Based on a literature review very few articles have been published on Faveline methyl ether.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
    5.2363   -1.9583    0.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0150   -0.5831    0.1125 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7531   -0.0119   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6178   -0.7650   -0.2246 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927   -0.1476   -0.3460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2628    1.2224   -0.2659 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3939    1.9702   -0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6476    1.3782    0.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8862    2.1585    0.2909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0249    1.9856   -0.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1365    3.2197   -0.1941 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3443    1.4466   -0.7006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6381    0.2805    0.1957 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9927   -0.9381   -0.3344 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2927   -1.1193   -0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7936   -2.1638   -0.6893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1180   -1.7013   -1.2525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8697   -0.7806   -0.3675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0768    0.1040    0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1668   -0.5005    1.9361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7683    1.4697    0.6608 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2751   -2.2059   -0.2386 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5855   -2.4227   -0.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0424   -2.4421    1.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6892   -1.8302   -0.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3174    3.0277    0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6670    3.1799    0.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3936    2.2486   -0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5909    1.6510    0.9812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0467    2.2843   -0.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2919    1.0685   -1.7620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0993    0.5250    1.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5884   -2.0896   -0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2530   -2.6808   -1.5090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8962   -2.8585    0.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7284   -2.6259   -1.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0005   -1.2732   -2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6617   -1.3608    0.1963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4911   -0.1178   -1.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2518   -0.6658    2.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7730    0.1905    2.6860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6776   -1.4751    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1140    1.8492   -0.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6641    1.3122    1.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0918    2.1455    1.1946 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
  6 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 14 15  2  0
  8  3  1  0
 19 13  1  0
 15  5  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  7 26  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  1
 16 34  1  0
 16 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 18 39  1  0
 20 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  0
 21 44  1  0
 21 45  1  0
 15 33  1  0
M  END


  Mrv1652309042209562D          

 21 23  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
    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  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
    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
  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
  6 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  2  0  0  0  0
  5 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0191102

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H24O2/c1-12-8-15-14(10-18(12)21-4)9-13-6-5-7-19(2,3)16(13)11-17(15)20/h8-10,16H,5-7,11H2,1-4H3/t16-/m1/s1

> <INCHI_KEY>
RGZDNFGDHPPFAU-MRXNPFEDSA-N

> <FORMULA>
C19H24O2

> <MOLECULAR_WEIGHT>
284.399

> <EXACT_MASS>
284.177630013

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.6489380211283

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11S)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0^{3,8}]pentadeca-1,3(8),4,6-tetraen-9-one

> <JCHEM_LOGP>
4.345079812

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.09975958392374

> <JCHEM_PKA_STRONGEST_BASIC>
-4.8372840526155825

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
86.80280000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(11S)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0^{3,8}]pentadeca-1,3(8),4,6-tetraen-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       7.870  -0.209   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.538  -1.597   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.330  -0.209   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.370   0.995   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.713   2.496   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.100   3.165   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.584   3.544   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.112   3.090   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.770   1.588   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.898   0.541   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.891  -0.624   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.301  -0.946   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   15                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    6   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14    5                                                       
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   13   20   21                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄O₂

Average Mass

284.3990 Da

Monoisotopic Mass

284.17763 Da

IUPAC Name

(11S)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0^{3,8}]pentadeca-1,3(8),4,6-tetraen-9-one

Traditional Name

(11S)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0^{3,8}]pentadeca-1,3(8),4,6-tetraen-9-one

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C19H24O2/c1-12-8-15-14(10-18(12)21-4)9-13-6-5-7-19(2,3)16(13)11-17(15)20/h8-10,16H,5-7,11H2,1-4H3/t16-/m1/s1

InChI Key

RGZDNFGDHPPFAU-MRXNPFEDSA-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
Cnidoscolus quercifolius	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Aryl alkyl ketone
Aryl ketone
Anisole
Alkyl aryl ether
Ketone
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	4.35	ChemAxon
pKa (Strongest Acidic)	17.1	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	1	ChemAxon
Refractivity	86.8 m³·mol⁻¹	ChemAxon
Polarizability	33.65 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

Not Available

Chemspider ID

74111014

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101771120

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

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 (11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one (NP0191102)

MOL for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

3D MOL for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

3D SDF for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

3D-SDF for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

PDB for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

3D PDB for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

SMILES for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

INCHI for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

Structure for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)

3D Structure for NP0191102 ((11s)-5-methoxy-6,12,12-trimethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraen-9-one)